Bone remodeling parameters in patients with type 1 diabetes mellitus and diabetic peripheral polyneuropathy of varying severity
https://doi.org/10.14341/osteo13168
Abstract
BACKGROUND: Diabetic peripheral polyneuropathy (DPPN) is a common and early chronic complication of diabetes mellitus (DM). This complication can be associated with bone tissue damage and low-trauma fractures, particularly in type 1 DM. Therefore, evaluating the relationship between DPPN and bone metabolism parameters is crucial for clinical practice.
AIM: To assess bone remodeling parameters in patients with type 1 DM with varying degrees of DPPN.
MATERIALS AND METHODS: The study included 90 patients with type 1 DM and DPPN aged 18 to 55 years on stable insulin therapy for the past 3 months. Assessment was conducted for levels of HbA1c, 25(OH)D, total calcium (Ca), phosphorus (P), parathyroid hormone (PTH), osteocalcin (OC), C-terminal telopeptide of type I collagen (CTX), fibroblast growth factor 23 (FGF-23) in serum. The degree of neurological deficit was determined using the Neuropathy Disability Score (NDS), Neuropathy Symptoms Score (NSS), and Michigan Neuropathy Screening Instrument (MNSI). Dual-energy X-ray absorptiometry (DXA) was performed to determine bone mineral density (BMD) and trabecular bone score (TBS).
RESULTS: Regardless of the degree of DPPN severity, patients with type 1 DM were comparable in HbA1c and 25(OH)D levels. A direct correlation was found between the severity of neurological disorders and BMI (r=0.214; p=0.044) and duration of DM (r=0.246, p=0.019). Vitamin D insufficiency and deficiency were diagnosed in 79% of examined patients with type 1 DM, but the level of 25(OH)D in serum did not depend on the degree of DPPN severity, HbA1c level, duration of DM, and daily insulin dose (p>0.05). A positive correlation was established between PTH level and severity of neurological symptoms, and a negative one with HbA1c level. Patients with type 1 DM and varying degrees of DPPN did not differ in BMD and TBS. A Z-score of less than -2.0 SD was only recorded in six patients, and partially degraded microarchitecture of bone tissue was observed in 8 patients.
CONCLUSION: Therefore, BMD, TBS, and bone remodeling markers in patients with type 1 DM and DPPN were independent of the degree of neurological deficit, degree of compensation, and duration of DM. Vitamin D deficiency is common in most patients with type 1 DM, but the 25(OH)D level is not influenced by HbA1c level, duration of the disease, and daily insulin dose.
About the Authors
N. V. TimkinaRussian Federation
Natalia V. Timkina - MD, junior scientific researcher.
194021, St. Petersburg, Parkhomenko Avenue, 15
Competing Interests:
none
A. V. Murasheva
Russian Federation
Anna V. Murasheva - MD, PhD, scientific researcher.
St. Petersburg
Competing Interests:
none
A. O. Ustyuzhanina
Russian Federation
Anna O. Ustyuzhanina - MD.
St. Petersburg
Competing Interests:
none
F. M. Radugin
Russian Federation
Fedor M. Radugin - MD.
St. Petersburg
Competing Interests:
none
A. T. Chernikova
Russian Federation
Alena T. Chernikova - MD, PhD, scientific researcher.
St. Petersburg
Competing Interests:
none
E. Yu. Vasilieva
Russian Federation
Elena Yu. Vasil’eva - MD, PhD, head of the central clinical diagnostic laboratory.
St. Petersburg
Competing Interests:
none
T. L. Karonova
Russian Federation
Tatiana L. Karonova - MD, PhD, Professor of the Endocrinology Department.
St. Petersburg
Competing Interests:
none
References
1. Ziegler D, Papanas N, Vinik AI, Shaw JE. Epidemiology of polyneuropathy in diabetes and prediabetes. Handb Clin Neurol. 2014;126:3-22. doi: https://doi.org/10.1016/B978-0-444-53480-4.00001-1
2. Brazill JM, Beeve AT, Craft CS, Ivanusic JJ, Scheller EL. Nerves in Bone: Evolving Concepts in Pain and Anabolism. J Bone Miner Res. 2019;34(8):1393-1406. doi: https://doi.org/10.1002/jbmr.3822
3. Liu C, Lv H, Niu P, Tan J, Ma Y. Association between diabetic neuropathy and osteoporosis in patients: a systematic review and meta-analysis. Arch Osteoporos. 2020;15(1):125. doi: https://doi.org/10.1007/s11657-020-00804-6
4. Povaliaeva AA, Pigarova EA, Dzeranova LK, Rozhinskaya LYa. The relationship of vitamin D status with the development and course of diabetes mellitus type 1. Obesity and metabolism. 2020;17(1):82-87. (In Russ.). doi: https://doi.org/10.14341/omet12206
5. Bouillon R, Marcocci C, Carmeliet G, et al. Skeletal and Extraskeletal Actions of Vitamin D: Current Evidence and Outstanding Questions. Endocr Rev. 2019;40(4):1109-1151. doi: https://doi.org/10.1210/er.2018-00126
6. Pigarova EA, Rozhinskaya LYa, Belaya JE, Dzeranova LK, et al. Russian Association of Endocrinologists recommendations for diagnosis, treatment and prevention of vitamin D deficiency in adults. Problems of Endocrinology. 2016;62(4):60-84. (In Russ.). doi: https://doi.org/10.14341/probl201662460-84
7. Belaya ZhE, Belova KYu, Biryukova EV, Dedov II, et al. Federal clinical guidelines for diagnosis, treatment and prevention of osteoporosis. Osteoporosis and Bone Diseases. 2021;24(2):4-47. (In Russ.). doi: https://doi.org/10.14341/osteo12930
8. Fan Y, Wei F, Lang Y, Liu Y. Diabetes mellitus and risk of hip fractures: a meta-analysis. Osteoporos Int. 2016;27(1):219-228. doi: https://doi.org/10.1007/s00198-015-3279-7
9. Ferrari SL, Abrahamsen B, Napoli N, et al. Diagnosis and management of bone fragility in diabetes: an emerging challenge. Osteoporos Int. 2018;29(12). doi: https://doi.org/10.1007/s00198-018-4650-2
10. Koromani F, Oei L, Shevroja E, et al. Vertebral fractures in individuals with type 2 diabetes: More than skeletal complications alone. Diabetes Care. 2020;43(1):137-144. doi: https://doi.org/10.2337/dc19-0925
11. Cavati G, Pirrotta F, Merlotti D, et al. Role of Advanced Glycation End-Products and Oxidative Stress in Type-2-Diabetes-Induced Bone Fragility and Implications on Fracture Risk Stratification. Antioxidants. 2023;12(4). doi: https://doi.org/10.3390/antiox12040928
12. Solis-Herrera C, Triplitt C, Cersosimo E, DeFronzo RA. Pathogenesis of Type 2 Diabetes Mellitus. 2021. https://www.ncbi.nlm.nih.gov/books/NBK279115/
13. Maser RE, Stabley JN, Lenhard MJ, Provost-Craig MA. Autonomic nerve fiber function and bone mineral density in individuals with type 1 diabetes: a cross-sectional study. Diabetes Res Clin Pract. 2009;84(3):252-258. doi: https://doi.org/10.1016/j.diabres.2009.02.012
14. Miazgowski T, Pynka S, Noworyta-Zietara M, Krzyzanowska-Swiniarska B, Pikul R. Bone mineral density and hip structural analysis in type 1 diabetic men. Eur J Endocrinol. 2007;156(1):123-127. doi: https://doi.org/10.1530/eje.1.02309
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For citations:
Timkina N.V., Murasheva A.V., Ustyuzhanina A.O., Radugin F.M., Chernikova A.T., Vasilieva E.Yu., Karonova T.L. Bone remodeling parameters in patients with type 1 diabetes mellitus and diabetic peripheral polyneuropathy of varying severity. Osteoporosis and Bone Diseases. 2024;27(3):20-27. (In Russ.) https://doi.org/10.14341/osteo13168

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