The DOI matches its Crossref record; 27 of the 27 references it cites were found in a registry or an index.
The Effects of Very Low Energy Diets and Low Energy Diets with Exercise Training on Skeletal Muscle Mass: A Narrative Review
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
A 25% lean mass loss as a result of VLEDs and LEDs is commonly reported.
“A 25% lean mass loss as a result of VLEDs and LEDs is commonly reported [32–34].”
From International Society of Sports Nutrition position stand: diets for body weight reduction (2026) · cites this paper as [33]
In ‘An Introduction to Very-Low-Energy Diets,’ the review says that approximately 25% of total weight loss with LEDs is lean body mass; Table 1 also lists 25% lean body mass loss for VLEDs as a share of weight lost. The citing sentence omits that denominator and could be read as a 25% reduction in lean mass itself, which the source does not establish. (LLM, conf=0.86)
Experimental — accuracy not yet measuredSerious adverse effects of VLEDs, including sudden death precipitated by cardiac arrhythmias, were more prevalent in earlier research.
“Serious adverse effects of VLEDs (including sudden death precipitated by cardiac arrhythmias) were more prevalent in earlier research [33,46].”
From International Society of Sports Nutrition position stand: diets for body weight reduction (2026) · cites this paper as [33]
Weight regain after VLED cessation is a concern, ranging from 2-14 kg in post-intervention periods ranging from 8 days to 5 years.
“weight regain after VLED cessation is a concern, ranging from 2–14 kg in post-intervention periods ranging from 8 days to 5 years [33].”
From International Society of Sports Nutrition position stand: diets for body weight reduction (2026) · cites this paper as [33]
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Skeletal muscle mass and distribution in 468 men and women aged 18–88 yr
Janssen, I., Heymsfield, S. B., Wang, Z., & Ross, R. (2000) · Journal of Applied Physiology · doi:10.1152/jappl.2000.89.1.81 · Cited by 3,087
Lean, M. E., Leslie, W. S., Barnes, A. C., Brosnahan, N., Thom, G., McCombie, L., Peters, C., Zhyzhneuskaya, S., Al-Mrabeh, A., Hollingsworth, K. G., et al. (2018) · The Lancet · doi:10.1016/s0140-6736(17)33102-1 · Cited by 2,095
Multiple types of skeletal muscle atrophy involve a common program of changes in gene expression
Lecker, S. H., Jagoe, R. T., Gilbert, A., Gomes, M., Baracos, V., Bailey, J., Price, S. R., Mitch, W. E., & Goldberg, A. L. (2004) · The FASEB Journal · doi:10.1096/fj.03-0610com · Cited by 1,539
Morton, R. W., Murphy, K. T., McKellar, S. R., Schoenfeld, B. J., Henselmans, M., Helms, E., Aragon, A. A., Devries, M. C., Banfield, L., Krieger, J. W., et al. (2018) · British Journal of Sports Medicine · doi:10.1136/bjsports-2017-097608 · Cited by 1,269
Lean, M. E. J., Leslie, W. S., Barnes, A. C., Brosnahan, N., Thom, G., McCombie, L., Peters, C., Zhyzhneuskaya, S., Al-Mrabeh, A., Hollingsworth, K. G., et al. (2019) · The Lancet Diabetes & Endocrinology · doi:10.1016/s2213-8587(19)30068-3 · Cited by 1,017
Nutritional recommendations for the management of sarcopenia
Morley, J. E., Argiles, J. M., Evans, W. J., Bhasin, S., Cella, D., Deutz, N. E. P., Doehner, W., Fearon, K. C. H., Ferrucci, L., Hellerstein, M. K., et al. (2010) · Journal of the American Medical Directors Association · doi:10.1016/j.jamda.2010.04.014 · Cited by 664 · cited 4×
“However, these guidelines are inappropriate for the sarcopenic individual [46, 47], given their differing physiological milieu.”
BackgroundInfluentialDietary protein for athletes: From requirements to optimum adaptation
Phillips, S. M., & Van Loon, L. J. C. (2011) · Journal of Sports Sciences · doi:10.1080/02640414.2011.619204 · Cited by 530
Changes in fat-free mass during significant weight loss: a systematic review
Chaston, T. B., Dixon, J. B., & O'Brien, P. E. (2007) · International Journal of Obesity · doi:10.1038/sj.ijo.0803483 · Cited by 493
The developmental origins of sarcopenia
Sayer, A. A., Syddall, H., Martin, H., Patel, H., Baylis, D., & Cooper, C. (2008) · The Journal of nutrition, health and aging · doi:10.1007/bf02982703 · Cited by 450
Dietary protein: its role in satiety, energetics, weight loss and health.
Westerterp-Plantenga, M. S., Lemmens, S. G., & Westerterp, K. R. (2012) · British Journal of Nutrition · doi:10.1017/s0007114512002589 · Cited by 443
Drummond, M. J., Fry, C. S., Glynn, E. L., Dreyer, H. C., Dhanani, S., Timmerman, K. L., Volpi, E., & Rasmussen, B. B. (2009) · The Journal of Physiology · doi:10.1113/jphysiol.2008.163816 · Cited by 439
Control of the size of the human muscle mass
Rennie, M. J., Wackerhage, H., Spangenburg, E. E., & Booth, F. W. (2004) · Annual Review of Physiology · doi:10.1146/annurev.physiol.66.052102.134444 · Cited by 399
Ohanna, M., Sobering, A. K., Lapointe, T., Lorenzo, L., Praud, C., Petroulakis, E., Sonenberg, N., Kelly, P. A., Sotiropoulos, A., & Pende, M. (2005) · Nature Cell Biology · doi:10.1038/ncb1231 · Cited by 392
Pasiakos, S. M., Cao, J. J., Margolis, L. M., Sauter, E. R., Whigham, L. D., McClung, J. P., Rood, J. C., Carbone, J. W., Combs, G. F., & Young, A. J. (2013) · The FASEB Journal · doi:10.1096/fj.13-230227 · Cited by 312
Longland, T. M., Oikawa, S. Y., Mitchell, C. J., Devries, M. C., & Phillips, S. M. (2016) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.115.119339 · Cited by 271
Johansson, K., Neovius, M., & Hemmingsson, E. (2014) · The American Journal of Clinical Nutrition · doi:10.3945/ajcn.113.070052 · Cited by 243
Muscle sparing in muscle RING finger 1 null mice: response to synthetic glucocorticoids
Baehr, L. M., Furlow, J. D., & Bodine, S. C. (2011) · The Journal of Physiology · doi:10.1113/jphysiol.2011.212845 · Cited by 234
Areta, J. L., Burke, L. M., Camera, D. M., West, D. W. D., Crawshay, S., Moore, D. R., Stellingwerff, T., Phillips, S. M., Hawley, J. A., & Coffey, V. G. (2014) · American Journal of Physiology-Endocrinology and Metabolism · doi:10.1152/ajpendo.00590.2013 · Cited by 227
Willoughby, D., Hewlings, S., & Kalman, D. (2018) · Nutrients · doi:10.3390/nu10121876 · Cited by 221
Garthe, I., Raastad, T., Refsnes, P. E., Koivisto, A., & Sundgot-Borgen, J. (2011) · International Journal of Sport Nutrition and Exercise Metabolism · doi:10.1123/ijsnem.21.2.97 · Cited by 209
Gibson, A., & Sainsbury, A. (2017) · Behavioral Sciences · doi:10.3390/bs7030044 · Cited by 181
Glycogen availability and skeletal muscle adaptations with endurance and resistance exercise
Knuiman, P., Hopman, M. T. E., & Mensink, M. (2015) · Nutrition & Metabolism · doi:10.1186/s12986-015-0055-9 · Cited by 113
Molecular Mechanisms of Skeletal Muscle Insulin Resistance in Type 2 Diabetes
Bouzakri, K., Koistinen, H., & Zierath, J. (2005) · Current Diabetes Reviews · doi:10.2174/1573399054022785 · Cited by 106
ROY, M., WILLIAMS, S. M., BROWN, R. C., MEREDITH-JONES, K. A., OSBORNE, H., JOSPE, M., & TAYLOR, R. W. (2018) · Medicine & Science in Sports & Exercise · doi:10.1249/mss.0000000000001642 · Cited by 86
Antonio, J., Ellerbroek, A., Silver, T., Vargas, L., & Peacock, C. (2016) · Journal of the International Society of Sports Nutrition · doi:10.1186/s12970-016-0114-2 · Cited by 81
Washburn, R. A., Szabo, A. N., Lambourne, K., Willis, E. A., Ptomey, L. T., Honas, J. J., Herrmann, S. D., & Donnelly, J. E. (2014) · PLoS ONE · doi:10.1371/journal.pone.0109849 · Cited by 74
Pugh, J. K., Faulkner, S. H., Jackson, A. P., King, J. A., & Nimmo, M. A. (2015) · Physiological Reports · doi:10.14814/phy2.12364 · Cited by 63
Flagged first, then by citations
Research works printed but not linked: 63
- Saris WH. Very-low-calorie diets and sustained weight loss. Obes Res. 2001;9(Suppl 4):295S-301S. · DOI · Paper page
- Sellahewa L, Khan C, Lakkunarajah S, et al. A systematic review of evidence on the use of very low calorie diets in people with diabetes. Curr Diabetes Rev. 2017;13:35–46. · DOI · Paper page
- Brochu M, Malita MF, Messier V, et al. Resistance training does not contribute to improving the metabolic profile after a 6-month weight loss program in overweight and obese postmenopausal women. J Clin Endocrinol Metab. 2009;94:3226–33. · DOI · Paper page
- Krotkiewski M, Grimby G, Holm G, et al. Increased muscle dynamic endurance associated with weight reduction on a very-low-calorie diet. Am J Clin Nutr. 1990;51:321–30. · DOI
- Davies MJ, Alessio DAD, Fradkin J, et al. Management of hyperglycaemia in type 2 diabetes, 2018. A consensus report by the American Diabetes Association (ADA) and the European Association for the Study of Diabetes (EASD). Consens Rep Published Online First: 2018. · DOI · Paper page
- Dhindsa P, Scott A, Donnelly R. Metabolic and cardiovascular effects of very-low-calorie diet therapy in obese patients with Type 2 diabetes in secondary failure: outcomes after 1 year. Diabet Med. 2003;20:319–24. · DOI
- Sours HE, Frattali VP, Brand CD, et al. Sudden death associated with very low calorie weight reduction regimens. Am J Clin Nutr. 1981;34:453–61. · DOI
- Rudrappa SS, Wilkinson DJ, Greenhaff PL, et al.Human skeletal muscle disuse atrophy: effects on muscle protein synthesis, breakdown, and insulin resistance—a qualitative review. Front Physiol. 2016;7:361. · DOI
- Bodine SC, Stitt TN, Gonzalez M, et al. Akt/mTOR pathway is a crucial regulator of skeletal muscle hypertrophy and can prevent muscle atrophy in vivo. Nat Cell Biol. 2001;3:1014–9. · DOI · Paper page
- Gannon MC1, Nuttall FQ. Amino acid ingestion and glucose metabolism—a review. IUBMB Life. 2010;62(9):660–8. · DOI
- de Boer MD, Selby A, Atherton P, Smith K, Seynnes OR, Maganaris CN, Maffulli N, Movin T, Narici MV, Rennie MJ. The temporal responses of protein synthesis, gene expression and cell signalling in human quadriceps muscle and patellar tendon to disuse. J Physiol. 2007;585:241–51. · DOI
- Breen L, Stokes KA, Churchward-Venne TA, Moore DR, Baker SK, Smith K, Atherton PJ, Phillips SM. Two weeks of reduced activity decreases leg lean mass and induces “anabolic resistance” of myofibrillar protein synthesis in healthy elderly. J Clin Endocrinol Metab. 2013;98:2604–12. · DOI · Paper page
- Hunter GR, Plaisance EP, Carter SJ, Fisher G. Why intensity is not a bad word: optimizing health status at any age. Clin Nutr. 2018;37(1):56–60. doi: https://doi.org/10.1016/j.clnu.2017.02.004. Epub 2017 Feb 9. PMID: 28214041; PMCID: PMC5550361. · DOI
- Jacinto E, Loewith R, Schmidt A, et al. Mammalian TOR complex 2 controls the actin cytoskeleton and is rapamycin insensitive. Nat Cell Biol. 2004;6:1122–8. · DOI
- Sarbassov DD, Ali SM, Sengupta S, et al. Prolonged rapamycin treatment inhibits mTORC2 assembly and Akt/PKB. Mol Cell. 2006;22:159–68. · DOI · Paper page
- Jewell JL, Guan K-L. Nutrient signaling to mTOR and cell growth. Trends Biochem Sci. 2013;38:233–42. · DOI
- Jung CH, Jun CB, Ro S-H, et al. ULK-Atg13-FIP200 Complexes Mediate mTOR signaling to the autophagy machinery. Mol Biol Cell. 2009;20:1992–2003. · DOI · Paper page
- Ganley IG, Lam DH, Wang J, et al. ULK1{middle dot}ATG13{middle dot}FIP200 complex mediates mTOR signaling and is essential for autophagy. J Biol Chem. 2009;284:12297–305. · DOI · Paper page
- Mitchell WK, Williams J, Atherton P, et al. Sarcopenia, dynapenia, and the impact of advancing age on human skeletal muscle size and strength; a quantitative review. Front Physiol. 2012;3:1–18. · DOI · Paper page
- Bodine SC, Latres E, Baumhueter S, et al. Identification of ubiquitin ligases required for skeletal muscle atrophy. Science. 2001;294:1704–8. · DOI · Paper page
- Sandri M, Sandri C, Gilbert A, et al. Foxo transcription factors induce the atrophy- related ubiquitin ligase atrogin-1 and cause skeletal muscle atrophy. Cell. 2004;117:1–2. · DOI · Paper page
- Stitt TN, Drujan D, Clarke BA, et al. The IGF-1/PI3K/Akt pathway prevents expression of muscle atrophy-induced ubiquitin ligases by inhibiting FOXO transcription factors. Mol Cell. 2004;14:395–403. · DOI · Paper page
- Clausen T. Regulation of active Na + -K + transport in skeletal muscle. Physiol Rev. 1986;66:542–80. · DOI
- Sinacore DR, Gulve EA. The role of skeletal muscle in glucose transport, glucose homeostasis, and insulin resistance: implications for physical therapy. Phys Ther. 1993;73:878–91. · DOI
- Straznicky NE, Lambert EA, Grima MT, et al. The effects of dietary weight loss with or without exercise training on liver enzymes in obese metabolic syndrome subjects. Diabetes Obes Metab. 2012;14:139–48. · DOI
- Baron AD, Brechtel G, Wallace P, et al. Rates and tissue sites of non-insulin- and insulin-mediated glucose uptake in humans. Am J Physiol. 1988;255:E769–74.
- Cruz-Jentoft AJ, Bahat G, Bauer J, et al. Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing. 2019;48:16–31. · DOI · Paper page
- Reidy PT, Rasmussen BB. Role of ingested amino acids and protein in the promotion of resistance exercise-induced muscle protein anabolism. J Nutr. 2016;146(2):155–83. · DOI · Paper page
- Elena Volpi, Wayne W. Campbell, Johanna T. Dwyer, Mary Ann Johnson, Gordon L. Jensen, John E. Morley, Robert R. Wolfe. Is the optimal level of protein intake for older adults greater than the recommended dietary allowance? J Gerontol Ser A 2013;68(6): 677–681.
- Il-Young Kim, Scott Schutzler, Amy Schrader, Horace Spencer, Patrick Kortebein, Nicolaas E. P. Deutz, Robert R. Wolfe, and Arny A. Ferrando. Quantity of dietary protein intake, but not pattern of intake, affects net protein balance primarily through differences in protein synthesis in older adults. Am J Physiol Endocrinol Metab 2015 308(1):E21–E28. · DOI · Paper page
- Paddon-Jones D, Rasmussen BB. Dietary protein recommendations and the prevention of sarcopenia. Curr Opin Clin Nutr Metab Care. 2009;12(1):86–90. · DOI · Paper page
- Cuenca-Sánchez M, Navas-Carrillo D, Orenes-Piñero E. Controversies surrounding high-protein diet intake: satiating effect and kidney and bone health. Adv Nutr. 2015;6(3):260–6. · DOI
- Long-Term Effects of High-Protein Diets on Renal Function. Anne-lise kamper and svend strandgaard. Annu Rev Nutr. 2017;37(1):347–69. · DOI
- Esmeijer K, Geleijnse JM, de Fijter JW, Kromhout D, Hoogeveen EK. Dietary protein intake and kidney function decline after myocardial infarction: the Alpha Omega Cohort. Nephrol Dial Transp. 2020;35(1):106–15. · DOI
- Delimaris I. Adverse effects associated with protein intake above the recommended dietary allowance for adults. 2013; 2013:126929 · DOI
- Barrows K, Snook JT. Effect of a high-protein, very-low-calorie diet on body composition and anthropometric parameters of obese middle-aged women. Am J Clin Nutr. 1987;45:381–90. · DOI
- Larsen AE, Bibby BM, Hansen M. Effect of a whey protein supplement on preservation of fat free mass in overweight and obese individuals on an energy restricted very low caloric diet. Nutrients. 2018. https://doi.org/10.3390/nu10121918. · DOI
- Zurlo F, Larson K, Bogardus C, Ravussin E. Skeletal muscle metabolism is a major determinant of resting energy expenditure. J Clin Invest. 1990;86(5):1423–7. · DOI · Paper page
- Dasso NA. How is exercise different from physical activity? A concept analysis Nurs Forum. 2019;54(1):45–52. https://doi.org/10.1111/nuf.12296 (Epub 2018 Oct 17 PMID: 30332516). · DOI
- Ashutosh K, Methrotra K, Fragale-Jackson J. Effects of sustained weight loss and exercise on aerobic fitness in obese women. J Sports Med Phys Fit. 1997;37:252–7.
- Burd N, Holwerda AM, Selby KC, et al. Resistance exercise volume affects myofibrillar protein synthesis and anabolic signalling molecule phosphorylation in young men. J Physiol. 2010;588:3119–30. · DOI
- Song Z, Moore DR, Hodson N, Ward C, Dent JR, O’Leary MF, et al. Resistance exercise initiates mechanistic target of rapamycin (mTOR) translocation and protein complex co-localisation in human skeletal muscle. Sci Rep. 2017;7(1):5028. · DOI
- Carroll KM, Bazyler CD, Bernards JR, Taber CB, Stuart CA, DeWeese BH, et al. Skeletal muscle fiber adaptations following resistance training using repetition maximums or relative intensity. Sports (Basel). 2019. https://doi.org/10.3390/sports7070169. · DOI
- Kumar V, Atherton PJ, Selby A, Rankin D, Williams J, Smith K, et al. Muscle protein synthetic responses to exercise: effects of age, volume, and intensity. J Gerontol A Biol Sci Med Sci. 2012;67(11):1170–7. · DOI
- Weinheimer EM, Sands LP, Campbellnure WW. A systematic review of the separate and combined effects of energy restriction and exercise on fat-free mass in middle-aged and older adults: Implications for sarcopenic obesity. Nutr Rev. 2010;68:375–88. · DOI · Paper page
- Bryner RW, Ullrich IH, Sauers J, et al. Effects of resistance vs aerobic training combined with an 800 calorie liquid diet on lean body mass and resting metabolic rate. J Am Coll Nutr. 1999;18:115–21. · DOI · Paper page
- Svendsen OL, Hassager C, Christiansen C. Six months’ follow-up on exercise added to a short-term diet in overweight postmenopausal women–effects on body composition, resting metabolic rate, cardiovascular risk factors and bone. Int J Obes Relat Metab Disord. 1994;18(10):692–8.
- Donnelly JE, Sharp T, Houmard J, et al. Muscle hypertrophy with large-scale weight loss and resistance training. Am J Clin Nutr. 1993;58:561–5. · DOI · Paper page
- Hunter GR, Bryan DR, Borges JH, David Diggs M, Carter SJ. Racial differences in relative skeletal muscle mass loss during diet-induced weight loss in women. Obes (Silver Spring). 2018;26(8):1255–60. https://doi.org/10.1002/oby.22201. · DOI
- Heymsfield SB, Casper K, Hearn J, et al. Rate of weight loss during underfeeding: relation to level of physical activity. Metabolism. 1989;38:215–23. · DOI
- Hill JO, Sparling PB, Shields TW, et al. Effects of exercise and food restriction on body composition and metabolic rate in obese women 1–3. Am J Clin Nutr. 1987;46:622–30. · DOI
- Phinney SD, LaGrange BM, O’Connell M, et al. Effects of aerobic exercise on energy expenditure and nitrogen balance during very low calorie dieting. Metabolism. 1988;37:758–65. · DOI
- Pavlou KN, Steffee WP, Lerman RH, et al. Effects of dieting and exercise on lean body mass, oxygen uptake, and strength. Med Sci Sports Exerc. 1985;17:466–71. · DOI
- Engelke S, Koch F, Sciascia Q. Exercise and muscle protein synthesis: not all roads lead to mTORC1. J Physiol. 2016;594(12):3179–80. · DOI
- Milanović Z, Sporiš G, Weston M. Effectiveness of high-intensity interval training (HIT) and continuous endurance training for VO2max improvements: a systematic review and meta-analysis of controlled trials. Sports Med. 2015;45(10):1469–81. · DOI · Paper page
- Berryman N, Mujika I, Bosquet L. Concurrent training for sports performance: the 2 sides of the medal. Int J Sports Physiol Perform. 2019;14(3):279–85. · DOI
- Maillard F, Rousset S, Pereira B, et al. High-intensity interval training reduces abdominal fat mass in postmenopausal women with type 2 diabetes. Diabetes Metab. 2016;42:433–41. · DOI
- Tremblay A, Simoneau JA, Bouchard C. Impact of exercise intensity on body fatness and skeletal muscle metabolism. Metabolism. 1994;43:814–8. · DOI
- Frontera WR, Meredith CN, O’Reilly KP, et al. Strength conditioning in older men: skeletal muscle hypertrophy and improved function. J Appl Physiol. 1988;64:1038–44. · DOI
- Garrow JS, Summerbell CD. Meta-analysis: effect of exercise, with or without dieting, on the body composition of overweight subjects. Eur J Clin Nutr. 1995;49:1–10.
- Tsai AG, Wadden TA. The evolution of very-low-calorie diets: an update and meta-analysis. Obes (Silver Spring). 2006;14(8):1283–93. · DOI · Paper page
- Festi D, Colecchia A, Orsini M, Sangermano A, Sottili S, Simoni P, et al. Gallbladder motility and gallstone formation in obese patients following very low calorie diets: use it (fat) to lose it (well). Int J Obes Relat Metab Disord. 1998;22(6):592–600. · DOI · Paper page
- Anderson JW, Hamilton CC, Brinkman-Kaplan V. Benefits and risks of an intensive very-low-calorie diet program for severe obesity. Am J Gastroenterol. 1992;87(1):6–15.
Cited by
Sorted by citations
Proportion of caloric restriction‐induced weight loss as skeletal muscle
Heymsfield, S. B., Yang, S., McCarthy, C., Brown, J. B., Martin, C. K., Redman, L. M., Ravussin, E., Shen, W., Müller, M. J., & Bosy‐Westphal, A. (2024) · Obesity · doi:10.1002/oby.23910 · Cited by 53
Volek, J. S., Kackley, M. L., & Buga, A. (2024) · Current Nutrition Reports · doi:10.1007/s13668-024-00548-6 · Cited by 48
Janssen, T. A. H., Van Every, D. W., & Phillips, S. M. (2023) · Current Opinion in Clinical Nutrition & Metabolic Care · doi:10.1097/mco.0000000000000980 · Cited by 33
Lowrie, F. J., Rahimi, M. M., Hogan, C. M., Tran, D. L., Marshall, N. S., Phillips, C. L., Gordon, C. J., Yee, B. J., & Machan, E. A. (2025) · Obesity Research & Clinical Practice · doi:10.1016/j.orcp.2025.10.001 · Cited by 6
International Society of Sports Nutrition position stand: diets for body weight reduction
Aragon, A. A., Campbell, B. I., Schoenfeld, B. J., Stout, J. R., Kalman, D., Arciero, P. J., Arent, S. M., Kreider, R. B., Taylor, L. W., Bannock, L., et al. (2026) · Journal of the International Society of Sports Nutrition · doi:10.1080/15502783.2026.2740266
Metadata
- Authors
- Ardavani, A., Aziz, H., Smith, K., Atherton, P. J., Phillips, B. E., & Idris, I.
- Venue
- Advances in Therapy
- Published
- 2020-11-19
- Volume
- 38
- Issue
- 1
- Pages
- 149-163
- ISSN
- 0741-238X
- 1865-8652
- PMC
- PMC7854408
- Cited by
- 23
- References
- 27
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review