Submitted:
07 September 2023
Posted:
14 September 2023
You are already at the latest version
Abstract
Keywords:
Introduction
Discussion
Mechanism of action and types of ketogenic diet
Neuroprotective Role of KD in Neurological Disorders:
Epilepsy
Stroke
Alzheimer’s disease (AD)
Traumatic brain injury (TBI)
Migraine
Brain Tumor
Amyotrophic Lateral Sclerosis (ALS)
Autism Spectrum Disorder (ASD)
Role of Intermittent Fasting (IF) in Neuroprotection and Neurological Disorders:
Role of KD & IF in Cancers
Role of KD in Obesity:
Role of IF in Obesity
Evidence-based Recommendations:
Conclusion
Authors' contributions
Grant Support/Funding
Ethical approval
Informed Consent
Availability of data and material
Disclosure of potential conflict of interest
References
- Agarwal N, Arkilo D, Farooq O, Gillogly C, Kavak KS, Weinstock A. Ketogenic diet: Predictors of seizure control. SAGE Open Med. 2017 Dec 6;5:205031211771288. [CrossRef]
- Anton SD, Moehl K, Donahoo WT, Marosi K, Lee SA, Mainous AG, et al. Flipping the Metabolic Switch: Understanding and Applying the Health Benefits of Fasting. Obesity. 2018 Feb;26(2):254–68. [CrossRef]
- Arciero PJ, Arciero KM, Poe M, Mohr AE, Ives SJ, Arciero A, et al. Intermittent fasting two days versus one day per week, matched for total energy intake and expenditure, increases weight loss in overweight/obese men and women. Nutr J. 2022 Dec 4;21(1):36. [CrossRef]
- Augustin K, Khabbush A, Williams S, Eaton S, Orford M, Cross JH, et al. Mechanisms of action for the medium-chain triglyceride ketogenic diet in neurological and metabolic disorders. Lancet Neurol. 2018 Jan;17(1):84–93. [CrossRef]
- Augustus E, Granderson I, Rocke KD. The Impact of a Ketogenic Dietary Intervention on the Quality of Life of Stage II and III Cancer Patients: A Randomized Controlled Trial in the Caribbean. Nutr Cancer. 2021 Oct 21;73(9):1590–600. [CrossRef]
- Barbanti P, Fofi L, Aurilia C, Egeo G, Caprio M. Ketogenic diet in migraine: rationale, findings and perspectives. Neurol Sci. 2017 May 19;38(S1):111–5. [CrossRef]
- BARBORKA, CJ. BARBORKA CJ. KETOGENIC DIET TREATMENT OF EPILEPSY IN ADULTS. J Am Med Assoc. 1928 Jul 14;91(2):73.
- Bergqvist AC, Schall JI, Stallings VA, Zemel BS. Progressive bone mineral content loss in children with intractable epilepsy treated with the ketogenic diet. Am J Clin Nutr. 2008 Dec;88(6):1678–84. [CrossRef]
- Bruci A, Tuccinardi D, Tozzi R, Balena A, Santucci S, Frontani R, et al. Very Low-Calorie Ketogenic Diet: A Safe and Effective Tool for Weight Loss in Patients with Obesity and Mild Kidney Failure. Nutrients. 2020 Jan 27;12(2):333. [CrossRef]
- Cervenka MC, Henry-Barron BJ, Kossoff EH. Is there a role for diet monotherapy in adult epilepsy? Epilepsy Behav Case Reports. 2017;7:6–9. [CrossRef]
- Challa HJ, Ameer MA, Uppaluri KR. DASH Diet To Stop Hypertension. 2023.
- Choi H-R, Kim J, Lim H, Park Y. Two-Week Exclusive Supplementation of Modified Ketogenic Nutrition Drink Reserves Lean Body Mass and Improves Blood Lipid Profile in Obese Adults: A Randomized Clinical Trial. Nutrients. 2018 Dec 3;10(12):1895. [CrossRef]
- Cicero AFG, Benelli M, Brancaleoni M, Dainelli G, Merlini D, Negri R. Middle and Long-Term Impact of a Very Low-Carbohydrate Ketogenic Diet on Cardiometabolic Factors: A Multi-Center, Cross-Sectional, Clinical Study. High Blood Press Cardiovasc Prev. 2015 Dec 19;22(4):389–94. [CrossRef]
- Cohen CW, Fontaine KR, Arend RC, Gower BA. A Ketogenic Diet Is Acceptable in Women with Ovarian and Endometrial Cancer and Has No Adverse Effects on Blood Lipids: A Randomized, Controlled Trial. Nutr Cancer. 2020 May 18;72(4):584–94. [CrossRef]
- Cunha GM, Guzman G, Correa De Mello LL, Trein B, Spina L, Bussade I, et al. Efficacy of a 2-Month Very Low-Calorie Ketogenic Diet (VLCKD) Compared to a Standard Low-Calorie Diet in Reducing Visceral and Liver Fat Accumulation in Patients With Obesity. Front Endocrinol (Lausanne). 2020 Sep 14;11. [CrossRef]
- D’Abbondanza M, Ministrini S, Pucci G, Migliola EN, Martorelli EE, Gandolfo V, et al. VERY LOW-CARBOHYDRATE KETOGENIC DIET FOR THE TREATMENT OF SEVERE OBESITY AND ASSOCIATED NON-ALCOHOLIC FATTY LIVER DISEASE: THE ROLE OF SEX DIFFERENCES. Nutrition. 2021 Aug;87–88:111327. [CrossRef]
- de Oliveira Maranhão Pureza IR, da Silva Junior AE, Silva Praxedes DR, Lessa Vasconcelos LG, de Lima Macena M, Vieira de Melo IS, et al. Effects of time-restricted feeding on body weight, body composition and vital signs in low-income women with obesity: A 12-month randomized clinical trial. Clin Nutr. 2021 Mar;40(3):759–66. [CrossRef]
- Devathasan G, Koh C. WERNICKE’S ENCEPHALOPATHY IN PROLONGED FASTING. Lancet. 1982 Nov;320(8307):1108–9. [CrossRef]
- Di Lorenzo C, Coppola G, Bracaglia M, Di Lenola D, Sirianni G, Rossi P, et al. A ketogenic diet normalizes interictal cortical but not subcortical responsivity in migraineurs. BMC Neurol. 2019 Dec 22;19(1):136. [CrossRef]
- Di Lorenzo C, Coppola G, Di Lenola D, Evangelista M, Sirianni G, Rossi P, et al. Efficacy of Modified Atkins Ketogenic Diet in Chronic Cluster Headache: An Open-Label, Single-Arm, Clinical Trial. Front Neurol. 2018 Feb 12;9. [CrossRef]
- Di Lorenzo C, Coppola G, Sirianni G, Di Lorenzo G, Bracaglia M, Di Lenola D, et al. Migraine improvement during short lasting ketogenesis: a proof-of-concept study. Eur J Neurol. 2015 Jan;22(1):170–7. [CrossRef]
- Di Lorenzo C, Pinto A, Ienca R, Coppola G, Sirianni G, Di Lorenzo G, et al. A Randomized Double-Blind, Cross-Over Trial of very Low-Calorie Diet in Overweight Migraine Patients: A Possible Role for Ketones? Nutrients. 2019 Jul 28;11(8):1742. [CrossRef]
- Di Rosa C, Lattanzi G, Spiezia C, Imperia E, Piccirilli S, Beato I, et al. Mediterranean Diet versus Very Low-Calorie Ketogenic Diet: Effects of Reaching 5% Body Weight Loss on Body Composition in Subjects with Overweight and with Obesity—A Cohort Study. Int J Environ Res Public Health. 2022 Oct 11;19(20):13040. [CrossRef]
- Domaszewski P, Konieczny M, Dybek T, Łukaniszyn-Domaszewska K, Anton S, Sadowska-Krępa E, et al. Comparison of the effects of six-week time-restricted eating on weight loss, body composition, and visceral fat in overweight older men and women. Exp Gerontol. 2023 Apr;174:112116. [CrossRef]
- Elia M, Klepper J, Leiendecker B, Hartmann H. Ketogenic Diets in the Treatment of Epilepsy. Curr Pharm Des. 2018 Feb 9;23(37):5691–701. [CrossRef]
- Finnell JS, Saul BC, Goldhamer AC, Myers TR. Is fasting safe? A chart review of adverse events during medically supervised, water-only fasting. BMC Complement Altern Med. 2018 Dec 20;18(1):67. [CrossRef]
- Freeman JM, Vining EPG, Pillas DJ, Pyzik PL, Casey JC, Kelly L and MT. The Efficacy of the Ketogenic Diet—1998: A Prospective Evaluation of Intervention in 150 Children. Pediatrics. 1998 Dec 1;102(6):1358–63. [CrossRef]
- Gasior M, Rogawski MA, Hartman AL. Neuroprotective and disease-modifying effects of the ketogenic diet. Behav Pharmacol. 2006 Sep;17(5–6):431–9. [CrossRef]
- GENUTH, SM. GENUTH SM. Insulin Secretion in Obesity and Diabetes: An Illustrative Case. Ann Intern Med. 1977 Dec 1;87(6):714. [CrossRef]
- Gilbert DL, Pyzik PL, Freeman JM. The Ketogenic Diet: Seizure Control Correlates Better With Serum β-Hydroxybutyrate Than With Urine Ketones. J Child Neurol. 2000 Dec 2;15(12):787–90. [CrossRef]
- Gooch CL, Pracht E, Borenstein AR. The burden of neurological disease in the United States: A summary report and call to action. Ann Neurol. 2017 Apr;81(4):479–84. [CrossRef]
- Grandl G, Straub L, Rudigier C, Arnold M, Wueest S, Konrad D, et al. Short-term feeding of a ketogenic diet induces more severe hepatic insulin resistance than an obesogenic high-fat diet. J Physiol. 2018 Oct;596(19):4597–609. [CrossRef]
- Greenfield M, Kolterman O, Olefsky JM, Reaven GM. The effect of ten days of fasting on various aspects of carbohydrate metabolism in obese diabetic subjects with significant fasting hyperglycemia. Metabolism. 1978 Dec;27(12):1839–52. [CrossRef]
- Groesbeck DK, Bluml RM, Kossoff EH. Long-term use of the ketogenic diet in the treatment of epilepsy. Dev Med Child Neurol. 2006 Dec 17;48(12):978. [CrossRef]
- Guisado Rosa, JP. Guisado Rosa JP. Importance of a Blood Test Before Starting a Protein Ketogenic Diet. Obes Control Ther Open Access. 2015 Sep 20;2(2):1–2. [CrossRef]
- Headland ML, Clifton PM, Keogh JB. Effect of intermittent compared to continuous energy restriction on weight loss and weight maintenance after 12 months in healthy overweight or obese adults. Int J Obes. 2019 Oct 23;43(10):2028–36. [CrossRef]
- Hee Seo J, Mock Lee Y, Soo Lee J, Chul Kang H, Dong Kim H. Efficacy and Tolerability of the Ketogenic Diet According to Lipid:Nonlipid Ratios?Comparison of 3:1 with 4:1 Diet. Epilepsia. 2007 Apr;48(4):801–5. [CrossRef]
- Hemingway C, Freeman JM, Pillas DJ, Pyzik PL. The Ketogenic Diet: A 3- to 6-Year Follow-Up of 150 Children Enrolled Prospectively. Pediatrics. 2001 Oct 1;108(4):898–905. [CrossRef]
- Henderson ST, Vogel JL, Barr LJ, Garvin F, Jones JJ, Costantini LC. Study of the ketogenic agent AC-1202 in mild to moderate Alzheimer’s disease: a randomized, double-blind, placebo-controlled, multicenter trial. Nutr Metab (Lond). 2009;6(1):31. [CrossRef]
- Husain AM, Yancy WS, Carwile ST, Miller PP, Westman EC. Diet therapy for narcolepsy. Neurology. 2004 Jun 22;62(12):2300–2. [CrossRef]
- Jagust W, Harvey D, Mungas D, Haan M. Central Obesity and the Aging Brain. Arch Neurol. 2005 Oct 1;62(10). [CrossRef]
- Johnson RK, Appel LJ, Brands M, Howard B V., Lefevre M, Lustig RH, et al. Dietary Sugars Intake and Cardiovascular Health. Circulation. 2009 Sep 15;120(11):1011–20. [CrossRef]
- Kang J, Shi X, Fu J, Li H, Ma E, Chen W. Effects of an Intermittent Fasting 5:2 Plus Program on Body Weight in Chinese Adults with Overweight or Obesity: A Pilot Study. Nutrients. 2022 Nov 9;14(22):4734. [CrossRef]
- Kerndt PR, Naughton JL, Driscoll CE, Loxterkamp DA. Fasting: the history, pathophysiology and complications. West J Med. 1982 Nov;137(5):379–99.
- Khodabakhshi A, Akbari ME, Mirzaei HR, Mehrad-Majd H, Kalamian M, Davoodi SH. Feasibility, Safety, and Beneficial Effects of MCT-Based Ketogenic Diet for Breast Cancer Treatment: A Randomized Controlled Trial Study. Nutr Cancer. 2020 May 18;72(4):627–34. [CrossRef]
- Khodabakhshi A, Akbari ME, Mirzaei HR, Seyfried TN, Kalamian M, Davoodi SH. Effects of Ketogenic metabolic therapy on patients with breast cancer: A randomized controlled clinical trial. Clin Nutr. 2021 Mar;40(3):751–8. [CrossRef]
- Klement RJ, Kämmerer U. Is there a role for carbohydrate restriction in the treatment and prevention of cancer? Nutr Metab (Lond). 2011;8(1):75. [CrossRef]
- Klement RJ, Koebrunner PS, Meyer D, Kanzler S, Sweeney RA. Impact of a ketogenic diet intervention during radiotherapy on body composition: IV. Final results of the KETOCOMP study for rectal cancer patients. Clin Nutr. 2021 Jul;40(7):4674–84. [CrossRef]
- Klement RJ, Sweeney RA. Impact of a ketogenic diet intervention during radiotherapy on body composition: V. Final results of the KETOCOMP study for head and neck cancer patients. Strahlentherapie und Onkol. 2022 Nov 2;198(11):981–93. [CrossRef]
- Klement RJ, Weigel MM, Sweeney RA. A ketogenic diet consumed during radiotherapy improves several aspects of quality of life and metabolic health in women with breast cancer. Clin Nutr. 2021 Jun;40(6):4267–74. [CrossRef]
- Koppel SJ, Swerdlow RH. Neuroketotherapeutics: A modern review of a century-old therapy. Neurochem Int. 2018 Jul;117:114–25. [CrossRef]
- Kossoff EH, Dorward JL, Turner Z, Pyzik PL. Prospective Study of the Modified Atkins Diet in Combination With a Ketogenic Liquid Supplement During the Initial Month. J Child Neurol. 2011 Feb 10;26(2):147–51. [CrossRef]
- Kossoff EH, Dorward JL. The Modified Atkins Diet. Epilepsia. 2008 Nov;49:37–41.
- Kossoff EH, McGrogan JR, Bluml RM, Pillas DJ, Rubenstein JE, Vining EP. A Modified Atkins Diet Is Effective for the Treatment of Intractable Pediatric Epilepsy. Epilepsia. 2006 Feb;47(2):421–4.
- Kossoff EH, Zupec-Kania BA, Auvin S, Ballaban-Gil KR, Christina Bergqvist AG, Blackford R, et al. Optimal clinical management of children receiving dietary therapies for epilepsy: Updated recommendations of the International Ketogenic Diet Study Group. Epilepsia Open. 2018 Jun;3(2):175–92. [CrossRef]
- Kotarsky CJ, Johnson NR, Mahoney SJ, Mitchell SL, Schimek RL, Stastny SN, et al. Time-restricted eating and concurrent exercise training reduces fat mass and increases lean mass in overweight and obese adults. Physiol Rep. 2021 May 27;9(10). [CrossRef]
- Kowalski LM, Bujko J. [Evaluation of biological and clinical potential of paleolithic diet]. Rocz Panstw Zakl Hig. 2012;63(1):9–15.
- Krikorian R, Shidler MD, Dangelo K, Couch SC, Benoit SC, Clegg DJ. Dietary ketosis enhances memory in mild cognitive impairment. Neurobiol Aging. 2012 Feb;33(2):425.e19-425.e27. [CrossRef]
- Kverneland M, Selmer KK, Nakken KO, Iversen PO, Taubøll E. A prospective study of the modified Atkins diet for adults with idiopathic generalized epilepsy. Epilepsy Behav. 2015 Dec;53:197–201. [CrossRef]
- Kwan P, Arzimanoglou A, Berg AT, Brodie MJ, Allen Hauser W, Mathern G, et al. Definition of drug resistant epilepsy: Consensus proposal by the ad hoc Task Force of the ILAE Commission on Therapeutic Strategies. Epilepsia. 2009 Nov 3;51(6):1069–77. [CrossRef]
- Lawlor T, Mount SJ, Defelici S. DEATH DURING THERAPEUTIC STARVATION. Lancet. 1968 Jul;292(7558):44. [CrossRef]
- Li S, Lin G, Chen J, Chen Z, Xu F, Zhu F, et al. The effect of periodic ketogenic diet on newly diagnosed overweight or obese patients with type 2 diabetes. BMC Endocr Disord. 2022 Dec 3;22(1):34. [CrossRef]
- Liu H, Yang Y, Wang Y, Tang H, Zhang F, Zhang Y, et al. Ketogenic diet for treatment of intractable epilepsy in adults: A meta-analysis of observational studies. Epilepsia Open. 2018 Mar;3(1):9–17. [CrossRef]
- Luchsinger JA, Tang M-X, Shea S, Mayeux R. Caloric Intake and the Risk of Alzheimer Disease. Arch Neurol. 2002 Aug 1;59(8):1258. [CrossRef]
- Ma DC, Anderson CM, Rodman SN, Buranasudja V, McCormick ML, Davis A, et al. Ketogenic Diet with Concurrent Chemoradiation in Head and Neck Squamous Cell Carcinoma: Preclinical and Phase 1 Trial Results. Radiat Res. 2021 Jun 4;196(2). [CrossRef]
- Maalouf M, Sullivan PG, Davis L, Kim DY, Rho JM. Ketones inhibit mitochondrial production of reactive oxygen species production following glutamate excitotoxicity by increasing NADH oxidation. Neuroscience. 2007 Mar;145(1):256–64. [CrossRef]
- Maaloul R, Marzougui H, Ben Dhia I, Ghroubi S, Tagougui S, Kallel C, et al. Effectiveness of Ramadan diurnal intermittent fasting and concurrent training in the management of obesity: is the combination worth the weight? Nutr Metab Cardiovasc Dis. 2023 Mar;33(3):659–66. [CrossRef]
- Mahdi, GS. Mahdi GS. The Atkin’s diet controversy. Ann Saudi Med. 2006 May;26(3):244–5. [CrossRef]
- Malinowski B, Zalewska K, Węsierska A, Sokołowska MM, Socha M, Liczner G, et al. Intermittent Fasting in Cardiovascular Disorders—An Overview. Nutrients. 2019 Mar 20;11(3):673. [CrossRef]
- Manzanero S, Gelderblom M, Magnus T, Arumugam T V. Calorie restriction and stroke. Exp Transl Stroke Med. 2011 Dec 12;3(1):8. [CrossRef]
- Marsh EB, Freeman JM, Kossoff EH, Vining EPG, Rubenstein JE, Pyzik PL, et al. The Outcome of Children with Intractable Seizures: A 3- to 6-Year Follow-up of 67 Children Who Remained on the Ketogenic Diet Less Than One Year. Epilepsia. 2006 Feb;47(2):425–30. [CrossRef]
- Mattson MP, Longo VD, Harvie M. Impact of intermittent fasting on health and disease processes. Ageing Res Rev. 2017 Oct;39:46–58. [CrossRef]
- McDougall A, Bayley M, Munce SE. The ketogenic diet as a treatment for traumatic brain injury: a scoping review. Brain Inj. 2018 Mar 21;32(4):416–22. [CrossRef]
- McKenzie AL, Hallberg SJ, Creighton BC, Volk BM, Link TM, Abner MK, et al. A Novel Intervention Including Individualized Nutritional Recommendations Reduces Hemoglobin A1c Level, Medication Use, and Weight in Type 2 Diabetes. JMIR Diabetes. 2017 Mar 7;2(1):e5. [CrossRef]
- Michalczyk MM, Klonek G, Maszczyk A, Zajac A. The Effects of a Low Calorie Ketogenic Diet on Glycaemic Control Variables in Hyperinsulinemic Overweight/Obese Females. Nutrients. 2020 Jun 22;12(6):1854. [CrossRef]
- Michalsen A, Li C. Fasting Therapy for Treating and Preventing Disease - Current State of Evidence. Complement Med Res. 2013;20(6):444–53. [CrossRef]
- Napoli E, Dueñas N, Giulivi C. Potential Therapeutic Use of the Ketogenic Diet in Autism Spectrum Disorders. Front Pediatr. 2014 Jun 30;2. [CrossRef]
- Neal EG, Chaffe H, Schwartz RH, Lawson MS, Edwards N, Fitzsimmons G, et al. The ketogenic diet for the treatment of childhood epilepsy: a randomised controlled trial. Lancet Neurol. 2008 Jun;7(6):500–6. [CrossRef]
- Nei M, Ngo L, Sirven JI, Sperling MR. Ketogenic diet in adolescents and adults with epilepsy. Seizure. 2014 Jun;23(6):439–42. [CrossRef]
- Nordmann AJ, Nordmann A, Briel M, Keller U, Yancy WS, Brehm BJ, et al. Effects of Low-Carbohydrate vs Low-Fat Diets on Weight Loss and Cardiovascular Risk Factors. Arch Intern Med. 2006 Feb 13;166(3):285. [CrossRef]
- Okamoto K, Kihira T, Kondo T, Kobashi G, Washio M, Sasaki S, et al. Nutritional status and risk of amyotrophic lateral sclerosis in Japan. Amyotroph Lateral Scler. 2007 Jan 10;8(5):300–4. [CrossRef]
- Paoli A, Bianco A, Damiani E, Bosco G. Ketogenic Diet in Neuromuscular and Neurodegenerative Diseases. Biomed Res Int. 2014;2014:1–10. [CrossRef]
- Paoli A, Bosco G, Camporesi EM, Mangar D. Ketosis, ketogenic diet and food intake control: a complex relationship. Front Psychol. 2015 Feb 2;6. [CrossRef]
- Paoli A, Rubini A, Volek JS, Grimaldi KA. Beyond weight loss: a review of the therapeutic uses of very-low-carbohydrate (ketogenic) diets. Eur J Clin Nutr. 2013 Aug 26;67(8):789–96. [CrossRef]
- Patterson RE, Sears DD. Metabolic Effects of Intermittent Fasting. Annu Rev Nutr. 2017 Aug 21;37(1):371–93. [CrossRef]
- Perissiou M, Borkoles E, Kobayashi K, Polman R. The Effect of an 8 Week Prescribed Exercise and Low-Carbohydrate Diet on Cardiorespiratory Fitness, Body Composition and Cardiometabolic Risk Factors in Obese Individuals: A Randomised Controlled Trial. Nutrients. 2020 Feb 14;12(2):482. [CrossRef]
- Phillips MCL, Murtagh DKJ, Gilbertson LJ, Asztely FJS, Lynch CDP. Low-fat versus ketogenic diet in Parkinson’s disease: A pilot randomized controlled trial. Mov Disord. 2018 Aug;33(8):1306–14. [CrossRef]
- Picot M-C, Baldy-Moulinier M, Daurs J-P, Dujols P, Crespel A. The prevalence of epilepsy and pharmacoresistant epilepsy in adults: A population-based study in a Western European country. Epilepsia. 2008 Jul;49(7):1230–8. [CrossRef]
- Pinto A, Bonucci A, Maggi E, Corsi M, Businaro R. Anti-Oxidant and Anti-Inflammatory Activity of Ketogenic Diet: New Perspectives for Neuroprotection in Alzheimer’s Disease. Antioxidants. 2018 Apr 28;7(5):63. [CrossRef]
- Pitt CE. Cutting through the Paleo hype: The evidence for the Palaeolithic diet. Aust Fam Physician. 2016;45(1):35–8.
- Porper K, Shpatz Y, Plotkin L, Pechthold RG, Talianski A, Champ CE, et al. A Phase I clinical trial of dose-escalated metabolic therapy combined with concomitant radiation therapy in high-grade glioma. J Neurooncol. 2021 Jul 21;153(3):487–96. [CrossRef]
- Prins M, Greco T, Alexander D, Giza CC. The pathophysiology of traumatic brain injury at a glance. Dis Model Mech. 2013 Jan 1. [CrossRef]
- Reddy ST, Wang C-Y, Sakhaee K, Brinkley L, Pak CYC. Effect of low-carbohydrate high-protein diets on acid-base balance, stone-forming propensity, and calcium metabolism. Am J Kidney Dis. 2002 Aug;40(2):265–74. [CrossRef]
- Reger MA, Henderson ST, Hale C, Cholerton B, Baker LD, Watson GS, et al. Effects of β-hydroxybutyrate on cognition in memory-impaired adults. Neurobiol Aging. 2004 Mar;25(3):311–4. [CrossRef]
- Roberts RO, Roberts LA, Geda YE, Cha RH, Pankratz VS, O’Connor HM, et al. Relative Intake of Macronutrients Impacts Risk of Mild Cognitive Impairment or Dementia. J Alzheimer’s Dis. 2012 Oct 9;32(2):329–39. [CrossRef]
- Roehl K, Falco-Walter J, Ouyang B, Balabanov A. Modified ketogenic diets in adults with refractory epilepsy: Efficacious improvements in seizure frequency, seizure severity, and quality of life. Epilepsy Behav. 2019 Apr;93:113–8. [CrossRef]
- Roehl K, Sewak SL. Practice Paper of the Academy of Nutrition and Dietetics: Classic and Modified Ketogenic Diets for Treatment of Epilepsy. J Acad Nutr Diet. 2017 Aug;117(8):1279–92. [CrossRef]
- Salis S, Shefa S, Sharma N, Vora N, Anjana RM, Mohan V, et al. Effects of Intermittent Fasting on Weight Loss in Asian Indian Adults with Obesity. J Assoc Physicians India. 2022 Sep;70(9):11–2. [CrossRef]
- Shaafi S, Mahmoudi J, Pashapour A, Farhoudi M, Sadigh-Eteghad S, Akbari H. Ketogenic Diet Provides Neuroprotective Effects against Ischemic Stroke Neuronal Damages. Adv Pharm Bull. 2014 Dec;4(Suppl 2):479–81. [CrossRef]
- Shaafi S, Sharifi-Bonab M, Ghaemian N, Mokhtarkhani M, Akbari H. Early Motor-Behavioral Outcome of Ischemic Stroke with Ketogenic Diet Preconditioning: Interventional Animal Study. J Stroke Cerebrovasc Dis. 2019 Apr;28(4):1032–9. [CrossRef]
- Sharma S, Jain P, Gulati S, Sankhyan N, Agarwala A. Use of the Modified Atkins Diet in Lennox Gastaut Syndrome. J Child Neurol. 2015 Apr 20;30(5):576–9. [CrossRef]
- Sharma S, Sankhyan N, Gulati S, Agarwala A. Use of the modified Atkins diet for treatment of refractory childhood epilepsy: A randomized controlled trial. Epilepsia. 2013 Mar;54(3):481–6. [CrossRef]
- Steriade C, Andrade DM, Faghfoury H, Tarnopolsky MA, Tai P. Mitochondrial Encephalopathy With Lactic Acidosis and Stroke-like Episodes (MELAS) May Respond to Adjunctive Ketogenic Diet. Pediatr Neurol. 2014 May;50(5):498–502. [CrossRef]
- Sumithran P, Prendergast LA, Delbridge E, Purcell K, Shulkes A, Kriketos A, et al. Ketosis and appetite-mediating nutrients and hormones after weight loss. Eur J Clin Nutr. 2013 Jul 1;67(7):759–64. [CrossRef]
- Summaries for patients. Effectiveness and safety of low-carbohydrate diets. Ann Intern Med. 2004 May 18;140(10):I10. [CrossRef]
- Taylor MK, Sullivan DK, Mahnken JD, Burns JM, Swerdlow RH. Feasibility and efficacy data from a ketogenic diet intervention in Alzheimer’s disease. Alzheimer’s Dement Transl Res Clin Interv. 2018 Jan 4;4(1):28–36. [CrossRef]
- Tefera TW, Tan KN, McDonald TS, Borges K. Alternative Fuels in Epilepsy and Amyotrophic Lateral Sclerosis. Neurochem Res. 2017 Jun 21;42(6):1610–20. [CrossRef]
- U.S. Department of Health and Human Services C for DC and P and NCI https://www.cdc.gov/cancer/datavi. U.S. Cancer Statistics Working Group. U.S. Cancer Statistics Data Visualizations Tool, based on 2022 submission data (1999-2020). 2023 Jun.
- Urbain P, Bertz H. Monitoring for compliance with a ketogenic diet: what is the best time of day to test for urinary ketosis? Nutr Metab (Lond). 2016 Dec 4;13(1):77. [CrossRef]
- VanItallie TB, Nonas C, Di Rocco A, Boyar K, Hyams K, Heymsfield SB. Treatment of Parkinson disease with diet-induced hyperketonemia: A feasibility study. Neurology. 2005 Feb 22;64(4):728–30. [CrossRef]
- Vasconcelos AR, Yshii LM, Viel TA, Buck HS, Mattson MP, Scavone C, et al. Intermittent fasting attenuates lipopolysaccharide-induced neuroinflammation and memory impairment. J Neuroinflammation. 2014 Dec 6;11(1):85. [CrossRef]
- Vecchia D, Pietrobon D. Migraine: a disorder of brain excitatory–inhibitory balance? Trends Neurosci. 2012 Aug;35(8):507–20. [CrossRef]
- Veldink JH, Kalmijn S, Groeneveld G-J, Wunderink W, Koster A, de Vries JHM, et al. Intake of polyunsaturated fatty acids and vitamin E reduces the risk of developing amyotrophic lateral sclerosis. J Neurol Neurosurg Psychiatry. 2006 Oct 3;78(4):367–71. [CrossRef]
- Verrotti A, Iapadre G, Pisano S, Coppola G. Ketogenic diet and childhood neurological disorders other than epilepsy: an overview. Expert Rev Neurother. 2017 May 4;17(5):461–73. [CrossRef]
- Voss M, Wenger KJ, von Mettenheim N, Bojunga J, Vetter M, Diehl B, et al. Short-term fasting in glioma patients: analysis of diet diaries and metabolic parameters of the ERGO2 trial. Eur J Nutr. 2022 Feb 6;61(1):477–87. [CrossRef]
- Witjaksono F, Prafiantini E, Rahmawati A. Effect of intermittent fasting 5:2 on body composition and nutritional intake among employees with obesity in Jakarta: a randomized clinical trial. BMC Res Notes. 2022 Oct 12;15(1):323. [CrossRef]
- Woolf EC, Syed N, Scheck AC. Tumor Metabolism, the Ketogenic Diet and β-Hydroxybutyrate: Novel Approaches to Adjuvant Brain Tumor Therapy. Front Mol Neurosci. 2016 Nov 16;9. [CrossRef]
- YUDKOFF M, DAIKHIN Y, NISSIM I, HORYN O, LAZAROW A, LUHOVYY B, et al. Response of brain amino acid metabolism to ketosis. Neurochem Int. 2005 Jul;47(1–2):119–28. [CrossRef]
| Type of Diet | Description | Pros | Cons |
|---|---|---|---|
| Atkins (Husain et al., 2004; Kossoff & Dorward, 2008; Mahdi, 2006; Reddy et al., 2002; Roberts et al., 2012) | Initially, carbohydrate intake must be restricted to 20g/day, with the allowance to consume as much protein and fat as desired. | · No limitation on the amount of protein and fat consumed · Weight loss and seizure reduction in epilepsy patients · Risk of dementia or mild cognitive impairment (high carbohydrate levels) · Modest improvement in day-time sleepiness for narcolepsy patients |
· Side effects associated with ketosis: nausea, dizziness, constipation, headache, fatigue, smelly breath · Metabolic dehydration · Risk of hyperuricemia (leading to joint pain and gout), hypercalciuria (leading to kidney stones, hypocalcemia, and osteoporosis · Risk of permanent loss of kidney function in anyone with reduced kidney function |
| Modified Atkins Diet(Kossoff et al., 2006, 2011; Kossoff & Dorward, 2008; Sharma et al., 2013, 2015) | Carbohydrate intake is restricted to 10-15g/day for children and 15-20g/day for adolescents/adults with encouragement of high-fat foods (~65% of calories from fat sources) | · Less restrictive than the ketogenic diet · Decreased risk of growth impairment, kidney stones, dyslipidemia, gastroesophageal reflux · Seizure frequency reduction with about 45% of patients with epilepsy responding with greater than 50% seizure reduction |
· Approximate 25-50 mg/dl increase in total cholesterol in both pediatric and adult studies · Increase in Blood Urea Nitrogen (BUN) levels |
| DASH (Challa et al., 2023) | Promotes consumption of vegetables and fruits, lean meat, and dairy products and the inclusion of micronutrients in the diet and advocates in the reduction of sodium in the diet to about 1500 mg/day | · Lowers blood pressure · Lowers risk of adverse cardiac events and stroke · Lowers blood glucose levels, triglycerides, LDL cholesterol, and insulin resistance · Improvements in control of type 2 diabetes · and reduction in the incidence of colorectal cancer (mainly in the white population) |
· Not designed for weight loss |
| Paleo (Kowalski & Bujko, 2012; Pitt, 2016) | Dietary plan is based on foods similar to foods that might have been eaten in the Paleolithic era, which dates to approximately 2.5 million to 10,000 years ago. Diet includes lean meats, fish, fruits, vegetables, nuts, and seeds. | · Reduce the risk of cardiovascular disease, metabolic syndrome, type 2 diabetes, cancer, acne vulgaris, and myopia. · Favorable changes in risk factors, such as weight, waist circumference, glucose tolerance, insulin secretion, insulin sensitivity, and lipid profiles. |
· Low calcium intake. (risk for individuals at risk for osteoporosis) |
| Ketogenic Diet (Cicero et al., 2015; Grandl et al., 2018; Henderson et al., 2009; McKenzie et al., 2017) | High-fat, low carbohydrate diet (20-50gm/day) in which carbohydrates are nearly eliminated, thus enabling fatty acids to become the required obligatory source of cellular energy production by peripheral tissues and the brain. | · Increased Weight loss during the first 3-6 months compared with those who follow more balanced diets. · Reversal/control of Type 2 diabetes for primary and secondary prevention of cerebrovascular and cardiovascular disorders. · Reduction of serum triglycerides and improvement of lipid profiles. · Increase in the level of HDL cholesterol in obese patients. · Improvement of lipid disorders that are characteristic of atherogenic dyslipidemia. · Beneficial effects on neurological disorders include epilepsy and Alzheimer’s disease. |
· Muscle cramps, bad breath, changes in bowel habits, Keto-flu, and energy loss. · Long-term low-carbohydrate diets with increased fat consumption could stimulate inflammatory pathways and oxidative stress and promote biological aging, induction of hepatic insulin, micronutrient deficiencies, and cardiovascular safety. |
| Fasting (Devathasan & Koh, 1982; GENUTH, 1977; Greenfield et al., 1978; Kerndt et al., 1982; Lawlor et al., 1968) | 24-hour-fast, Intermittent daily fasting 16:8 (Restriction: Intake) or 18:6, Skipping meals, One Meal A Day Fast, Water or egg fasting | · Control of Type 2 diabetes to mitigate cardiovascular and cerebrovascular disorders · Improvement in glucose tolerance. · Improvement of insulin sensitivity and glucose tolerance in people with diabetes immediately following a fast weight loss. |
· Nausea and vomiting · Edema · Alopecia and motor neuropathy · Hyperuricemia and urate nephropathy · Irregular menses · Abnormal liver function tests and decreased bone density · Thiamine deficiency and Wernicke’s encephalopathy · Mild metabolic acidosis · Possible death (due to lactic acidosis, small bowel obstruction, renal failure, and cardiac arrhythmias) |
| Type of Fasting | Description |
|---|---|
| 24-hour-fast | Fast in which no food is consumed for 24 hours. Individuals can consume water, and in most cases, black coffee and/or green tea is allowed. |
| Intermittent daily fasting 16:8 (Anton et al., 2018) | Restricting food intake/fasting for 16 hours a day and consuming food for 8 hours a day |
| Skipping meals | Occasionally skipping meals such as breakfast, lunch, and/or dinner according to the individual’s level of hunger or time restraints. |
| One Meal A Day Fast (OMAD) | Type of intermittent fasting is referred to as 23:1, in which an individual spends 23 hours fasting and leaves 1 hour a day to consume calories by eating and drinking. |
| Water fasting (Finnell et al., 2018) | Fasting is when a person does not eat and drink anything other than pure water; a “zero calorie diet.” |
| Eggs fasting | Fast in which eggs are prepared without butter/oil and beverages such as water and zero-calorie beverages are permitted (use of artificial sugar is not recommended) |
| Clinical Conditions | Study, Country (Year) | Sample Size/Timeline | · Methods | · Findings | |
|---|---|---|---|---|---|
| Epilepsy (Groesbeck et al., 2006) | Groesbeck et al., USA (2006) | 28 patients (15 males, 13 females), currently aged 7 to 23 years | · Retrospective chart review of children treated with the KD for more than six years at the Johns Hopkins Hospital | · Twenty-four children experienced more than a 90% reduction in seizures over prolonged periods on KD, and 3 achieved complete freedom from seizures. | |
| Epilepsy (Cervenka et al., 2017) | Cervenka et al., USA (2017) |
Ten adults were treated with KD monotherapy for epilepsy (4 patients were naïve to anti-seizure drugs (ASDs), and six previously tried and stopped ASDs) |
· Adults (age ≥ 18 years) evaluated in the Johns Hopkins Adult Epilepsy Diet Center (AEDC) from August 2010 to August 2016 were followed, and descriptive statistics were used to represent patient characteristics and outcomes. | · 50% of treatment-naïve participants were free from disabling seizures on the Modified Atkins Diet (MAD) monotherapy for > 1 year. · 67% (4 out of 6) of patients who previously tried ASDs became seizure-free on diet monotherapy. Two patients experienced >50% seizure reduction. |
|
| Epilepsy (Freeman et al., 1998) | Freeman et al., USA (1998) | 150 consecutive children, ages 1 to 16 years, all of whom continued to have more than two seizures per week despite therapy with at least two anticonvulsant medications | · Children were treated with the KD and followed for at least one year. · Seizure frequency was tabulated from patients' daily seizure calendars. · Furthermore, seizure reduction was calculated as a percentage of baseline frequency. |
· The children (mean age, 5.3 years) averaged 410 seizures per month before the diet. · Three months after diet initiation, 83% remained on the diet, and 34% had a >90% decrease in seizures. · At six months, 71% still remained on the diet, and 32% had a >90% decrease in seizures. · At one year, 55% remained on the diet, and 27% had a >90% decrease in seizure frequency. |
|
| Epilepsy (Hemingway et al., 2001) | Hemingway et al., USA (2001) | 150 consecutive children entered prospectively into a study of the KDs efficacy and tolerability | · 3 to 6 years after diet initiation, all 150 families were sent a survey inquiring about their child's health status, seizure frequency, and anticonvulsant medications. | · Of the original 150-patient cohort, 20 (13%) were seizure-free, and 21 (14%) had a 90% -99% decrease in their seizures. · Twenty-nine were free of medications, and 28 were on only one; 15 remained on the diet. |
|
| Epilepsy (Marsh et al., 2006) | Marsh et al., USA (2006) | 150 children with epilepsy, refractory to at least two medications, who initiated the KD between 1994 and 1996 | · 3 to 6 years after diet initiation, all the families were contacted by telephone or questionnaire to assess their child's current seizure status, medications, and therapies. | · Almost half of the children who discontinued the diet during the first year had fewer seizures when assessed 3-6 years later. 22% of these had become seizure-free without surgery. | |
| Stroke/ Mitochondrial encephalopathy with lactic acidosis and stroke-like episodes (MELAS) (Steriade et al., 2014) | Steriade et al., USA (2014) | A 22-year-old woman with multiple episodes of generalized and focal status epilepticus and migratory cortical stroke-like lesions who underwent muscle biopsy for mitochondrial genome sequencing |
· Clinical, electrophysiologic, and radiologic data of the patient were analyzed. |
· KD improves mitochondrial dysfunction in MELAS, which may promote better seizure control and less frequent stroke-like episodes. |
|
| Alzheimer’s Diseases (Reger et al., 2004) | Reger et al., USA (2004) | 20 subjects with AD or mild cognitive impairment | · Subjects consumed a drink containing emulsified MCTs or placebo and cognitive tests were administered, and levels of the ketone body β-hydroxybutyrate were observed through blood draws. | · MCT treatment facilitated performance on the Alzheimer's Disease Assessment Scale-Cognitive Subscale (ADAS-cog) for APOE4(-) subjects but not for APOE4(+) subjects. · Higher ketone values were associated with greater improvement in paragraph recall with MCT treatment relative to placebo across all subjects. |
|
| Alzheimer’s Diseases (Henderson et al., 2009) | Henderson et al., USA (2009) | 152 subjects diagnosed with mild to moderate AD | · Daily administration of AC-1202, an oral ketogenic compound, was evaluated in subjects in a US-based, 90-day, randomized, double-blinded, placebo-controlled, parallel-group study. · Participants received one dose of the agent during the first seven days of the study, followed by two doses (20 g of MCT) administered at breakfast from day 8 to day 90. |
· AC-1202 rapidly elevated serum ketone bodies in AD patients, resulting in significant differences in ADAS-Cog scores compared to the placebo. Effects were most notable in APOE4(-) dosage-compliant subjects. | |
| Alzheimer’s Diseases (Luchsinger et al., 2002) | Luchsinger et al., USA (2002) | 80 Elderly individuals free of dementia were followed for four years. | · Daily intake of calories, carbohydrates, fats, and protein was recalled using a semiquantitative food frequency questionnaire between baseline and first follow-up visits. | · Individuals with the highest calorie intake compared to the lowest quartile had an increased risk of AD. (HR:1.5; 95% CI:1.0-2.2). · For individuals with the apolipoprotein E 4 allele, the hazard ratios of AD for the highest quartiles of calorie and fat intake were 2.3 (95% CI, 1.1-4.7) and 2.3 (95% CI: 1.1-4.9), respectively, compared with the lowest quartiles. |
|
| Alzheimer’s Diseases (Taylor et al., 2018) | Taylor et al., USA (2017) | 7- Clinical Dementia Rating (CDR) 0.5, 4- CDR 1, and 4- CDR 2 participants (a total of 15 patients with AD) were enrolled in the KD Retention and Feasibility Trial | · 3-month, medium-chain triglyceride-supplemented KD followed by 1-month washout participants. Administered the Alzheimer's Disease Assessment Scale-cognitive subscale and Mini-Mental State Examination before the KD and following the intervention and washout. | · In achieving ketosis, the mean of the Alzheimer’s Disease Assessment Scale cognitive subscale score improved significantly during the diet and reverted to baseline after the washout. | |
| Alzheimer’s Diseases (Krikorian et al., 2012) |
Krikorian et al., USA (2012) |
23 older adults with Mild Cognitive Impairment |
· Patients were randomly assigned either a high carbohydrate or very low carbohydrate diet in a 6-week intervention. | · Improved verbal memory performance for the subjects on the low-carbohydrate diet was noted. The levels of ketone bodies were positively correlated with memory performance. | |
| Migraine (Cherubino Di Lorenzo, Coppola, et al., 2019) | Di Lorenzo et al., Italy (2019) | 18 migraine patients without aura before and after a 1-month of KD | · To prove if the KD-related cortical excitability changes are primarily due to cerebral cortex activity or are modulated by the brainstem. The study concurrently recorded the interictally nociceptive blink reflex (nBR) and the pain-related evoked potentials (PREP). | · Following 1-month on KD, the mean number of attacks and headache duration reduced significantly. KD significantly normalized the interictal PREP habituation, while the nBR habituation deficit did not change. | |
| Migraine (C. Di Lorenzo et al., 2015) | Di Lorenzo et al., Italy (2017) | 96 overweight female migraineurs patients (45: KD and 51: standard diet) for three months | · Mean monthly attack frequency, number of days with headaches, and tablet intake were assessed before and 1, 2, 3, and 6 months after diet initiation. |
· Drastic improvement in attack frequency, days, and medication use during the one-month · (p<0.0001) followed by a worsening during the transitional diet and subsequent standard diet period. According to the authors, KD efficacy's underlying mechanisms could be related to its ability to enhance mitochondrial energy metabolism and counteract neural inflammation. |
|
| Migraine (Cherubino Di Lorenzo, Pinto, et al., 2019) | Di Lorenzo et al., Italy (2019) | Randomized Double-Blind, Cross-Over Trial of 35 overweight obese migraines. | · To determine the therapeutic effect of a very low-calorie diet in overweight episodic migraine patients during a weight-loss intervention in which subjects alternated randomly between a very low-calorie KD (VLCKD) and a very low-calorie non-KD(VLCnKD) each for one month. The primary outcome was reducing migraine days each month compared to a 1-month pre-diet baseline. Secondary outcome measures were a 50% responder rate for migraine days, reduction of monthly migraine attacks, abortive drug intake, and body mass index (BMI) change. | · VLCKD patients experienced fewer migraine days with respect to VLCnKD (p < 0.0001). · The 50% responder rate for migraine days was 74.28% (26/35 patients) during the VLCKD period but only 8.57% (3/35 patients) during VLCnKD. Migraine attacks decreased during VLCKD with respect to VLCnKD (p < 0.00001). · The two diets showed no differences in acute anti-migraine drug consumption (p = 0.112) and BMI (p = 0.354) between the two diets. · A VLCKD has a preventive effect in overweight episodic migraine patients that appears within one month, suggesting that ketogenesis may be a useful therapeutic strategy for migraines. VLCKD is effective for rapid, short-term improvement of migraines in overweight patients, while VLCnKD is not. · Whether this dietary strategy should be applied to all overweight migraine patients and for how long remains to be determined in future studies. |
|
| Chronic Cluster Headache (Cherubino Di Lorenzo et al., 2018) | Di Lorenzo et al., Italy (2018) | 18 drug-resistant chronic cluster headache (CCH) patients | · Patients underwent a 12-week KD (Modified Atkins Diet, MAD), and the clinical response was evaluated in terms of response (≥50% attack reduction). | · 3-month KD ameliorated clinical features of chronic cluster headache | |
| Parkinson’s Disease (VanItallie et al., 2005) | Vanitaille et al., USA (2005) | Seven patients with Parkinson’s Disease | · Patients prepared a "hyperketogenic" diet at home for 28 days. Used the Unified Parkinson's Disease Rating Scale (UPDRS) to measure effects. | · A hyperketogenic diet at home and adherence for 28 days resulted in high ketogenic bodies, which improved the Unified Parkinson's Disease Rating Scale scores. | |
| Parkinson’s Disease (Phillips et al., 2018) | Phillips et al., USA (2018) | Forty-seven patients with Parkinson's disease (38 individuals completed the study). | · This study assessed the effect of a low-fat versus KD in patients. Diets were followed for eight weeks. | · Both diet groups showed significantly improved motor and non-motor symptoms; however, the ketogenic group showed greater improvements in non-motor symptoms. | |
| Amyotrophic lateral sclerosis (ALS) (Veldink et al., 2006) | Veldink et al., Netherlands (2007) | A case-control study (132 patients and 220 healthy controls) between 2001–2002. | · Patients' dietary intake for the nutrients of fatty acids, cholesterol, glutamate, or antioxidants was assessed using a food-frequency questionnaire to evaluate their link with the risk of developing ALS. | · A high intake of PUFAs and vitamin E is associated with a 50–60% decreased risk of developing ALS, and these nutrients appear synergistically. | |
| ALS (Okamoto et al., 2007) | Okamoto et al., Japan (2007) | The study comprised 153 patients and 306 gender- and age-matched controls randomly selected from the general population. | · A self-administered food frequency questionnaire was used to estimate pre-illness intakes of food groups and nutrients. | · The high intakes of carbohydrates and low intakes of fat and some kinds of fatty acids may, when combined, increase the risk of ALS. | |
| Behavioral Disease (Jagust et al., 2005) |
Jagust et al., USA (2005) |
112 Latino individuals aged 60 years and above were selected from an ongoing larger cohort of 1789 individuals. | · Baseline anthropomorphic measures (WHR) and measurements of fasting blood glucose, cholesterol, insulin levels, and blood pressure were obtained. Baseline anthropomorphic measures (WHR) and measurements of fasting blood glucose, cholesterol, insulin levels, and blood pressure were obtained. | · The WHR and age were positively related to white matter hyperintensities (p = 0.02 and p = 0.001, respectively). A 1-SD increase in WHR was associated with a 0.2-SD decrease in hippocampal volume and a 27% increase in white matter hyperintensities. · A larger WHR may be related to neurodegenerative, vascular, or metabolic processes that affect brain structures underlying cognitive decline and dementia. |
|
| KD: Ketogenic Diet; IF: Intermittent Fasting | |||||
| Type of Cancer | References / Studies included | Type of Diet | Total Patients & Intervention | Role of KD |
|---|---|---|---|---|
| Head and neck cancer (Klement & Sweeney, 2022) | Klement et al., Germany (2022) | KD (7) + SD (21) | 28; with radiotherapy and chemotherapy | KD may partially counteract the detrimental effects of both radio and chemotherapy on body composition in HNC patients. |
| Brain Tumors (Voss et al., 2022) | Voss et al., Germany (2022) | KD + IF | 20; with irradiation | The short diet schedule led to significant metabolic changes, with low glucose emerging as a marker of better prognosis. |
| Non- metastasized Rectal Cancer (Klement, Koebrunner, et al., 2021) | Klement et al., Germany (2021) | KD (18) + SD (23) | 41; during radiotherapy | This study demonstrated a trend for KDs contributing synergistically to pathological tumor response. |
| High-grade glioma- new (6), recurrent (7) (Porper et al., 2021) | Porper et al., Israel (2021) | KD + KD & Metformin | 13; with radiotherapy | Higher serum ketone levels were associated with both dietary intake and metformin use. |
| Head and Neck Squamous Cell Carcinoma (Ma et al., 2021) | Ma et al., USA (2021) | KD | 12; 8 patients with concurrent radiation and platinum-chemotherapy | This study demonstrated difficulty with diet compliance when combined with standard-of-care radiation therapy and cisplatin chemotherapy. |
| Breast Cancer (Klement, Weigel, et al., 2021) | Klement et al., Germany (2021) | KD (29) + SD (30) | 59; during radiotherapy | It supports that consuming a KD during radiotherapy is safe for women with breast cancer and has the potential to improve quality of life and metabolic health. |
| Locally advanced and metastatic breast cancer (Khodabakhshi et al., 2021) | Khodabakhshi et al., Iran (2020) | KD + SD | 80; with chemotherapy | KD in breast cancer patients might exert beneficial effects by decreasing TNF-α and insulin and increasing IL-10. KD may result in a better response through reductions in tumor size and downstaging in patients with locally advanced disease. |
| Locally advanced and metastatic breast cancer (Khodabakhshi et al., 2020) | Khodabakhshi et al., Iran (2019) | KD + SD | 60; with chemotherapy | Results suggested that a combination of chemotherapy and KDs could improve the biochemical parameters, body composition, and overall survival with no substantial side effects in breast cancer patients. |
| Ovarian and Endometrial Cancer (Cohen et al., 2020) | Cohen et al., USA (2020) | KD + SD | 57; with usual care | The findings suggest that KD may be a safe and achievable component of treatment for some cancer patients. |
| Stage II and III Cancer Patients (Augustus et al., 2021) | Augustus et al., West Indies (2020) | KD | NA | KD was suitable for Stage II and III cancer patients in improving their quality of life and nutritional, functional, and psychosocial statuses. |
| KD: Ketogenic Diet; IF: Intermittent Fasting; SD-Standard Diet | ||||
| Study, Country (Year) | Sample Size/Timeline | Methods | Findings | |
|---|---|---|---|---|
| Obesity, Visceral fat, and Liver fat Accumulation (Cunha et al., 2020) | Cunha et al., Brazil, (2020) | 39 patients (20 VLCKD, 19 LC) for two months | · Prospective study to determine the efficacy of VLCKD compared to LCD in reducing Visceral and Liver fat accumulation in patients with obesity. | · At two months, the VLCKD group had a relative weight reduction of 9.59 2.87%, while the LC group had a relative weight loss of 1.87 2.4% (p 0.001). The average VAT reductions were 32 cm2 for the VLCKD group and 12 cm2 for the LC group (p 0.05). The VLCKD group experienced reductions in the liver fat fraction that were noticeably more severe than those in the LC group (4.77 vs. 0.79%; p<0.005). |
| Obesity and Mild kidney failure (Bruci et al., 2020) | Bruci et al., Rome, (2020) | 92 individuals (38 – mild renal disease, 54-no renal disease), for three months | · A prospective observational study where participants underwent VLCKD for three months. Anthropometric parameters, bioelectrical impedance, and biochemistry were gathered before and after dietary intervention. | · Notable decrease in fat mass, average weight loss close to 20% of initial weight, improvement in metabolic markers, and GFR returned to normal at 27.7% after intervention in the group with mild renal disease. |
| Severe obesity and NAFLD (D’Abbondanza et al., 2021) | Abbondanza et al., Italy (2020) | 100 subjects- 72 severely obese women, 28 severely obese men (BMI ≥ 40, BMI ≥ 35 with obesity-related comorbidities, age between 18 and 65 years, followed for 25 days | · All subjects were evaluated at enrolment and 25 days after following VLCKD. Statistical analysis determined the difference in primary endpoints (Excess of body weight loss (EBWL), reduction in GGT). Secondary endpoints (variations of obesity grade according to EOSS, degree of liver steatosis). | · Significant weight loss, fat mass, and degree of steatosis were observed in all groups. Males experienced significantly larger EBWL, and greater GGT reduction, and higher waist circumference, insulin resistance, and HbA1c reduction than females. |
| Obesity or overweight with newly diagnosed Type 2 DM (Li et al., 2022) | Li et al., China (2022) | 60 patients with overweight or obesity newly diagnosed with Type 2 DM, 30 on KD, 30 on standard diabetes diet for twelve weeks. | · Variables such as uric acid, insulin, blood lipids, body weight, and blood glucose were measured before and after intervention. | · A significant decrease in rates of weight, BMI, waist circumference, TG, Cholesterol, LDL, HDL, FBG, Fasting insulin, and HbA1C was noted in the KD group compared to the control group. |
| Obesity and Overweight (Di Rosa et al., 2022) | Rosa et al., Italy (2022) | 268 obese patients randomly assigned to MLCKD or VLCKD, maximum of 3 months, or lose 5 % body weight | · Population stratified according to gender, BMI, and age.· Follow-up visits were done monthly until 5% body weight loss, anthropometric parameters, and body composition were obtained at the end of the study. | · Both groups lost 5 %body weight but required different periods (VLCKD – 1 month, MD group- 3 months)· Higher waist circumference and fat mass percentage reduction in the MD group compared to the VLCKD group. |
| Obesity- Cardiorespiratory fitness, Body composition, Cardiometabolic risk factors (Perissiou et al., 2020) | Perissiou et al., Australia (2020) | 64 obese men and women were randomly assigned to experimental (structured exercise +low carbohydrate meals) and control (structured exercise+ standard dietary advice) for eight weeks | · Blocked randomization stratification applied by gender, Anthropometric parameters, blood biomarkers, and cardiorespiratory fitness obtained at the study's beginning and end, data was statistically analyzed between the experimental and control groups. | · A more significant increase in cardiorespiratory fitness (measured by delta V O2 peak – mean diff -3.4), a greater reduction in fat mass index, lean muscle mass, fasting blood glucose, triglycerides, and CRP was noted in the experimental group than the control group. Reaching a ketogenic status was associated with a significant decrease in total body fat, visceral adipose tissue, fat mass index, and lean muscle mass. |
| Hyperinsulinemic overweight / Obese (Michalczyk et al., 2020) | Michalczyk et al., 2020, Poland | 100 females who reported to the clinic were randomly assigned to LCKD and control group followed for 12 weeks, 4 in LCKD, 5 in control resigned | · A tailor-made hypocaloric diet was prescribed for each subject, where daily caloric consumption was 20 % less than total daily energy expenditure. Blood biochemical analysis, body mass measurement, and circumference measurement were measured at the beginning and end of the study. | · Compared to baseline, there was a decrease in glucose, insulin, HbA1c, TG, insulin resistance, body mass, waist circumference, hip circumference, thigh circumference, increase in HDL- C among the LCKD group after intervention. These changes are not observed in the control group. The LCKD group had lower glucose, insulin, HbA1c, insulin resistance, body mass, waist circumference, hip and thigh circumference, and an increase in HDL-C compared to the control group after the intervention. |
| Obesity (Choi et al., 2018) | Choi et al., 2018, South Korea | 46 subjects between 19- 49 years, BMI>25, intervention for two weeks | · Subjects were randomly assigned to 3 groups with equal gender distribution – 1. Ketogenic nutrition drink (fat: carb – 4:1), 2. Modified ketogenic nutrition drink (1.7:1), 3. Balanced nutrition drink. Measurements like anthropometric measurements, body composition analysis, blood lipid profile, and ketone bodies were performed before the intervention, during (after one week), and after (2 weeks) intervention. Changes in physical activity and body symptoms were surveyed through questionnaires. | · Saturated fat intake was high among KD 4:1 compared to KD 1.7:1. All groups showed a decrease in body water and minerals from 0 weeks to 1 week, with no significant change from 1 to 2 weeks. Protein and skeletal muscle mass decreased significantly in KD 4:1, BD groups. All groups showed decreased BMI, Body fat mass, and weight. A decrease in total cholesterol and LDL cholesterol was seen in KD 1.7:1 and BD groups, with no significant changes in KD 4:1 group. Ketone bodies significantly increased in KD 4:1 and KD 1.7:1 from 0 to 1 week, with no change from 1 to 2 weeks. Nausea, decreased appetite significantly increased from 0 to 1 week in KD 4:1, KD 1.7:1. Constipation significantly increased in KD 4:1 group. |
| Very Low-Calorie Ketogenic Diets (VLCKDs); Low-Calorie Diets (LC diets) | ||||
| Study, Country, (Year) | Sample size/ Timeline | Methods | Findings | |
|---|---|---|---|---|
| IF + protein pacing (Arciero et al., 2022) | Arciero et al., USA (2022) | 42 participants, 21 to intervention (10 assigned to IF1-P, 10 to IF2-P), five weeks of intervention. | · Randomized controlled trial where 42 were eligible, 20 IF-P matched for weight, BMI, randomly assigned to either a) IF diet for one day/week (36 hours), protein pacing diet for remaining six days/week, or b) Intermittent diet for two consecutive days (60 hours) and protein pacing for remaining five days/week. All lab testing procedures were performed at baseline control (week 0), and in week 5, ITT analysis was conducted. | · Dietary energy and macronutrient intake decreased; specifically, total energy intake decreased significantly (40%) during weight loss, with no difference in groups. IF2-P group had greater body weight and waist circumference than IF1-P; Fat-free mass increased by 2%. No significant hormone changes in both groups from baseline were noted. Both groups had significant reductions in BP, fasting total cholesterol, LDL-C, and triglycerides from baseline, with no differences between groups. Significant reduction in desire to eat and quantity of food to eat, the tendency of hunger ratings lower in IF2P compared to IF1-P· |
| Intermittent vs. continuous energy restriction (Headland et al., 2019) | Headland et al., Australia (2018) | 332 overweight and obese adults between 18-72 years, randomly assigned to 1 of 3 groups 1) Continuous energy restriction, 2) week on week off restriction, 3) 5:2 restriction for a total of 12 months. | · Randomized, parallel trial design to compare three different dietary patterns 146 completed study, all three groups visited the clinic every three months, a total of eight visits. Participants were grouped based on gender, BMI, and age, randomized 1:1 to intervention groups,· Only 56%of participants finished the trial. Primary outcome was weight loss. Secondary outcomes were changes in body composition, weight loss, and glucose. | · ITT analysis showed a significant effect of interventions on weight loss at 12 months, although there were no differences between the three groups. Fat and lean mass decreased significantly over time, with no differences between the dietary groups. HDL increased, and triglycerides decreased by a similar degree in all groups. |
| IF and concurrent exercise (Kotarsky et al., 2021) | Kotarsky et al., USA, (2021) | Twenty-one participants with a BMI of 25-34.9 were randomly assigned to normal eating (NE) or time-restricted eating (TRE), resistance training, and aerobic exercise standardized for both groups for eight weeks. | · Randomized control trials. Body composition, muscle performance, energy intake, macronutrient intake, physical activity, and physiological variables were assessed between both groups. | · Mild energy restriction was observed in TRE and NE. Loss of total body mass was more significant for the TRE group compared to both the NE group and pre-intervention. Lean mass increased during intervention for both TRE and NE with no differences. |
| IF on body weight, composition, vital signs in low-income women with obesity (de Oliveira Maranhão Pureza et al., 2021) | Puerza et al., Brazil, (2021) | 58 women were randomized to hypo energetic diet and time-restricted diet for 12 months.31 lost to follow up. | · Randomized controlled trial.· Body fat and waist circumference were measured at baseline and after 4,6, and 12 months of intervention. Systolic and diastolic blood pressure, heart rate, and axillary temperature were measured at baseline and 12 months of intervention. | · ITT analysis showed no significant changes in body weight after 12 months. An increase in axillary temperature, a reduction in percentage body fat, and waist circumference were observed in the interventional group compared to the control group. |
| IF – overweight older men and women(Domaszewski et al., 2023) | Domaszewski et al., Poland, (2023) | 116 healthy, non-smoking participants assigned to time-restricted eating (TRE) or educational control participants for six weeks | · TRE group were advised not to consume calories for 16 hrs/day, control group to continue the previous diet. Changes in body weight and composition were compared. | · TRE group had a decrease in body weight in both men and women. A significant reduction in visceral fat mass and waist circumference was observed in men. No changes in visceral fat or waist circumference were seen in women. |
| IF vs. IF with concurrent training (Maaloul et al., 2023) | Maaloul et al., Tunisia (2023) | Twenty obese men regularly performing Ramadan diurnal intermittent fasting (RDIF) were randomized into two groups: a) RDIF with concurrent training (RDIF-CT) and b) RDIF without training (RDIF-NCT) for four weeks. | · Randomized controlled trial. Body composition, blood glucose, lipid profile, and inflammation were assessed before and after the 4-week RDIF. | · Both groups had decreased weight, fat mass, fat percentage, and waist circumference and improved blood glucose, lipid profile, and inflammation. Fat-free mass decreased significantly in RDIF-NCT compared to the RDIF-CT group. RDIF-CT group showed more remarkable improvement in body composition (weight, fat mass, fat percentage, waist circumference) and a more significant decrease in lipid biomarkers, inflammation, and liver damage compared to RDIF -NCT group pre -post-intervention. |
| IF, weight loss (Salis et al., 2022) | Salis et al., India, (2022) | 32 overweight /obese adults were assigned consecutively to an IF plan and followed up for three months | · Demographic, anthropometric, and dietary assessments were done pre and post-intervention. Qualitative interviews were done at the end of the study to record the participants' overall well-being, experience, and sustainability of IF | · Significant reductions in mean body weight, waist circumference, BMI, daily calories, carbohydrate intake, and increased protein intake were noted. Participants reported positive experiences of practicing IF, such as improved fitness, sleep cycle, and adoption of healthy eating habits. |
| IF 5:2 plus program (Kang et al., 2022) | Kang et al., China (2022) | 131 participants in three groups 1) IF group (n= 42) 2) Daily calorie restriction group (CR)(n=1) 3) Daily calorie restriction with high protein meal replacement group (HP) (n=48); 12-week weight loss data analyzed | · In this retrospective cohort study, participants were divided into two groups: 1) IF 5:2 plus groups – 30% of energy requirement on fast days, 70% on rest, 2) Daily calories restriction group: 70% of daily energy requirement given. Clinical data such as age, sex, weight, and body composition at 0 and 12 weeks, data on adverse events were also collected | · A mean weight loss of 7.8 after 12 weeks was noted. Weight change from baseline is higher in IF and HP groups compared to the CR group. BMI, fat mass, and total mass of all three groups were significantly decreased at 12 weeks compared to baseline. No serious adverse events were reported in the three groups. |
| IF 5:2 (Witjaksono et al., 2022) | Witjaksono et al, Indonesia (2022) | 50 participants, 25 allocated to the fasting group, and 25 to the control group for eight weeks | · Non-blinded 1:1 two-arm randomized control trial, the fasting group fasted twice a week (5:2) while the control group did not fast. Interviews were conducted before, during, and after an intervention to gather data on education, income, knowledge, physical activity, and food intake history. Per protocol, analyses were done. | · Significant differences in total calories, carbohydrate, protein, and fat intake between intervention and control groups after intervention. No significant difference in fat mass, skeletal muscle, and visceral fat rating before and after the study in intervention and control groups. Fat-free mass before and after showed a significant difference. |
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