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Sarcopenia in postmenopausal patients with type 1 diabetes mellitus: characteristics of functional, laboratory, and instrumental indicators

https://doi.org/10.14341/DM13462

Abstract

BACKGROUND. Patients with type 1 diabetes mellitus (T1DM) are prone to earlier development of sarcopenia due to insulin deficiency, hyperglycemia, oxidative stress, and mitochondrial dysfunction. A pressing challenge in the  management of these patients is the search for standardized diagnostic tools for the timely detection and monitoring of sarcopenia.

OBJECTIVE. Comparative assessment of laboratory serum myokine levels in relation to muscle mass, strength, and function in postmenopausal women with type 1 diabetes and controls without diabetes.

MATERIALS AND METHODS. A single-center, cross-sectional comparative study was conducted in women with type 1 diabetes (n=40) and a control group (n=40) aged 50–75 years. The SARC-F questionnaire, laboratory parameters (myostatin, follistatin, cystatin C, lipocalin 2, IGF-1), muscle mass (iDXA densitometry), strength (wrist dynamometry), and function (short-form exercise battery) were assessed. Statistical processing was performed in Statistica 14.0.0.15, IBM SPSS Statistics 23 using the Mann-Whitney, Fisher, and Spearman correlation tests.

RESULTS. The age of the patients was 60 [56;64] years in the T1DM group and 64 [60;66] years in the control group (p=0.029). Glycated hemoglobin (HbA1c) in the T1DM group was 8.0% [7.6;9.3] with a diabetes duration of 26 [13;42] years. The myostatin level was significantly higher in T1DM 52.73 [46.45;58.26] mg/ml versus 21.46 [19.07;24.74] in the control (p < 0.001) and positively correlated with HbA1c (r=0.544, p < 0.001), but not with muscle strength and mass. HbA1c negatively correlated with the time it took to get up from a chair 5 times. No differences were found in the levels of follistatin, lipocalin 2, cystatin C. Wrist dynamometry strength and walking speed were lower in the T1DM group with a tendency to statistical significance. The median IGF-1 was lower in diabetes (92.7 vs. 114.1 ng/ml, p=0.014) and positively correlated with muscle strength (r=0.472, p < 0.001). The sarcopenia index negatively correlated with muscle strength (r=-0.402, p=0.021) and positively with HbA1c (r=0.514, p=0.035). Severe sarcopenia (according to EWGSOP2) was diagnosed in only one patient with T1DM, whose myostatin level did not differ from the range of patients without sarcopenia.

CONCLUSION. Thus, patients with type 1 diabetes have higher myostatin levels, which correlates with with the level of HbA1c. Low functional capacity in patients with type 1 diabetes is associated with HbA1c levels, but is not directly related to myostatin levels.

About the Authors

A. S. Zhdanova
Endocrinology Research Centre
Russian Federation

Anastasiia S. Zhdanova, PhD student

11 Dmitria Uljanova street, 117292 Moscow


Competing Interests:

none



Z. E. Belaya
Endocrinology Research Centre
Russian Federation

Zhanna E. Belaya, MD, PhD, Professor

Moscow


Competing Interests:

none



M. S. Shamkhalova
Endocrinology Research Centre
Russian Federation

Minara S. Shamkhalova, MD, PhD

Moscow


Competing Interests:

none



N. V. Rusyaeva
Endocrinology Research Centre
Russian Federation

Nadezhda V. Rusyaeva, MD, PhD

Moscow


Competing Interests:

none



A. A. Zhdanova
Endocrinology Research Centre
Russian Federation

Anastasia A. Zhdanova, MD

Moscow


Competing Interests:

none



N. P. Trubitsyna
Endocrinology Research Centre
Russian Federation

Natalia P. Trubitsyna, MD, PhD, leading research associate

Moscow


Competing Interests:

none



O. Y. Sukhareva
Endocrinology Research Centre
Russian Federation

Olga Y. Sukhareva, MD, PhD, Associate Professor

Moscow


Competing Interests:

none



D. E. Mironenkov
Endocrinology Research Centre
Russian Federation

Dmitrii E. Mironenkov, MD

Moscow


Competing Interests:

none



L. I. Ibragimova
Endocrinology Research Centre
Russian Federation

Liudmila I. Ibragimova, MD, PhD

Moscow


Competing Interests:

none



O. G. Melnikova
Endocrinology Research Centre
Russian Federation

Olga G. Melnikova, MD, PhD, leading research associate

Moscow


Competing Interests:

none



O. M. Schmidt
Endocrinology Research Centre
Russian Federation

Olga M. Schmidt, MD

Moscow


Competing Interests:

none



L. V. Nikankina
Endocrinology Research Centre
Russian Federation

Larisa V. Nikankina, MD, PhD

Moscow


Competing Interests:

none



A. I. Sleptsova
Endocrinology Research Centre
Russian Federation

Arina I. Sleptsova

Moscow


Competing Interests:

none



V. V. Gunkina
Endocrinology Research Centre
Russian Federation

Victoria V. Gunkina, MD

Moscow


Competing Interests:

none



G. A. Melnichenko
Endocrinology Research Centre
Russian Federation

Galina A. Melnichenko, MD, PhD, Academician of the RAS

Moscow


Competing Interests:

none



References

1. Shatskaya OA, Bondarenko IZ, Kushnarenko SS. Changes in skeletal muscle in diabetes mellitus. Medical Council. 2024;(16):148–153. (In Russ.) doi: https://doi.org/10.21518/ms2024-376

2. D'Souza DM, Al-Sajee D, Hawke TJ. Diabetic myopathy: impact of diabetes mellitus on skeletal muscle progenitor cells. Front Physiol. 2013;4:379. doi: https://doi.org/10.3389/fphys.2013.00379

3. Alway SE. Mitochondrial Dysfunction: Linking Type 1 Diabetes and Sarcopenia. Exerc Sport Sci Rev. 2019;47(2):63. doi: https://doi.org/10.1249/JES.0000000000000186

4. Cruz-Jentoft AJ, Bahat G, Bauer J, et al. Writing Group for the European Working Group on Sarcopenia in Older People 2 (EWGSOP2), and the Extended Group for EWGSOP2. Sarcopenia: revised European consensus on definition and diagnosis. Age Ageing. 2019;48(1):16–31. doi: https://doi.org/10.1093/ageing/afy169

5. Chen LK, Woo J, Assantachai P, et al. Asian Working Group for Sarcopenia: 2019 Consensus Update on Sarcopenia Diagnosis and Treatment. Journal of the American Medical Directors Association. 2020;21(3):300–307. e2. doi: https://doi.org/10.1016/j.jamda.2019.12.012

6. Bhasin S, Travison TG, Manini TM, et al. Sarcopenia Definition: The Position Statements of the Sarcopenia Definition and Outcomes Consortium. Journal of the American Geriatrics Society. 2020;68(7):1410–1418. doi: https://doi.org/10.1111/jgs.16372

7. Zhdanova AS, Belaya ZE, Omelchenko KA., et al. Clinical, laboratory and instrumental aspects of sarcopenia diagnostics. Osteoporosis and Bone Diseases. 2025;28(3):12–23 (In Russ.). doi: https://doi.org/10.14341/osteo13206

8. Ladang A, Beaudart C, Reginster JY, et al. Biochemical Markers of Musculoskeletal Health and Aging to be Assessed in Clinical Trials of Drugs Aiming at the Treatment of Sarcopenia: Consensus Paper from an Expert Group Meeting Organized by the European Society for Clinical and Economic Aspects of Osteoporosis, Osteoarthritis and Musculoskeletal Diseases (ESCEO) and the Centre Académique de Recherche et d'Expérimentation en Santé (CARES SPRL), Under the Auspices of the World Health Organization Collaborating Center for the Epidemiology of Musculoskeletal Conditions and Aging. Calcif Tissue Int. 2023 ;112(2):197–217. doi: https://doi.org/10.1007/s00223-022-01054-z.

9. Дистанционная абилитация реабилитация [интернет]. [доступ от 09.06.2026]. Доступ по ссылке: https://telereabilitacia.ru/docs/info/тесты_шкалы_опросники_10.pdf

10. Naumenava YL, Makhlina AS, Haurylenka DI, et al. Sarcopenia: features of manifestation in patients with diabetes mellitus. Health and Ecology Issues. 2023;20(4):26–34. (In Russ.) doi: https://doi.org/10.51523/2708-6011.2023-20-4-03

11. Российская Ассоциация геронтологов и гериатров. Проект клинических рекомендаций по саркопении. 2025.

12. Moriwaki, K, Matsumoto, H, Tanishima, S, et al. Association of serum bone- and muscle-derived factors with age, sex, body composition, and physical function in community-dwelling middle-aged and elderly adults: a cross-sectional study. BMC Musculoskelet Disord. 2019;20(1):276. doi: https://doi.org/10.1186/s12891-019-2650-9

13. Bergen HR, Farr JN, Vanderboom PM, et al. Myostatin as a mediator of sarcopenia versus homeostatic regulator of muscle mass: insights using a new mass spectrometry-based assay. Skeletal Muscle. 2015;5:21. doi: https://doi.org/10.1186/s13395-015-0047-5

14. Hofmann M, Halper B, Oesen S, et al. Serum concentrations of insulin-like growth factor-1, members of the TGF-beta superfamily and follistatin do not reflect different stages of dynapenia and sarcopenia in elderly women. Exp Gerontol. 2015;64:35–45. doi: https://doi.org/10.1016/j.exger.2015.02.008

15. Dydyshko YV. Changes in the condition of the muscle component in patients with type 1 diabetes mellitus. Medical Journal. 2016;1:101–106 (In Russ.)

16. Dial AG, Monaco CMF, Grafham GK, et al. Muscle and serum myostatin expression in type 1 diabetes. Physiol Rep. 2020;8(13):e14500. doi: https://doi.org/10.14814/phy2.14500

17. Fife E, Kostka J, Kroc Ł, et al. Relationship of muscle function to circulating myostatin, follistatin and GDF11 in older women and men. BMC Geriatrics. 2018;18(1):200. doi: https://doi.org/10.1186/s12877-018-0888-y

18. Pellegrino R, Paganelli R, Di Iorio A, et al. Muscle quality, physical performance, and comorbidity are predicted by circulating procollagen type III N-terminal peptide (P3NP): the InCHIANTI follow-up study. GeroScience. 2024;46:1259–1369. doi: https://doi.org/10.1007/s11357-023-00894-3

19. Cheng Y, Xu C, Wang S, et al. Serum cystatin C levels are decreased in type 1 diabetes mellitus patients with diabetic ketoacidosis. Minerva Endocrinol. 2020;45(2):106–116. doi: https://doi.org/10.23736/S0391-1977.20.03147-8

20. Gkiourtzis N, Stoimeni A, Michou P, et al. The role of cystatin C in kidney injury in children and adolescents with type 1 diabetes mellitus: a systematic review. J Bras Nefrol. 2025;47(4):e20240236. doi: https://doi.org/10.1590/2175-8239-JBN-2024-0236en

21. Ponzetti M, Aielli F, Ucci A, et al. Lipocalin 2 increases after highintensity exercise in humans and influences muscle gene expression and differentiation in mice. J Cell Physiol. 2022 ;237(1):551–565. doi: https://doi.org/10.1002/jcp.30501

22. Rebalka IA, Monaco C, Varah NE, et al. Loss of the adipokine lipocalin-2 impairs satellite cell activation and skeletal muscle regeneration. American Journal of Physiology-Cell Physiology. 2018;315(5):C714–C721. doi: https://doi.org/10.1152/ajpcell.00195.2017

23. Tay L, Ding YY, Leung BP, et al. Sex-specific differences in risk factors for sarcopenia amongst communitydwelling older adults. Age (Dordr). 2015;37(6):121. doi: https://doi.org/10.1007/s11357-015-9860-3


Supplementary files

1. Рисунок 1. Линейная регрессия влияния HbA1c на миостатин.
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Zhdanova A.S., Belaya Z.E., Shamkhalova M.S., Rusyaeva N.V., Zhdanova A.A., Trubitsyna N.P., Sukhareva O.Y., Mironenkov D.E., Ibragimova L.I., Melnikova O.G., Schmidt O.M., Nikankina L.V., Sleptsova A.I., Gunkina V.V., Melnichenko G.A. Sarcopenia in postmenopausal patients with type 1 diabetes mellitus: characteristics of functional, laboratory, and instrumental indicators. Diabetes mellitus. 2026;29(3):245-255. (In Russ.) https://doi.org/10.14341/DM13462

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ISSN 2072-0351 (Print)
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