Metabolic features of young patients with primary hyperparathyroidism
https://doi.org/10.14341/omet12771
Abstract
Background: The main components of mineral metabolism can influence non-classical target organs such as adipose tissue, pancreas, vascular wall. The «metabolic» effects of parathyroid hormone (PTH) and other participants of phosphorus-calcium metabolism in the hyperfunction of parathyroid glands remain unclear. The study of disorders of carbohydrate, fat and other types of metabolism in primary hyperparathyroidism (PHPT) will help to develop effective measures for prophylaxis and treatment of the patients in order to improve the quality and life span of the population.
Aim: To study the main parameters of metabolism in young patients with an active stage of PHPT before surgical treatment.
Materials and methods: A one-stage comparative study of young patients with PHPT and healthy volunteers matched by sex, age and body mass index (BMI) was carried out. The participants underwent a comprehensive biochemical and hormonal examination, a hyperinsulinemic euglycemic clamp and a bioimpedance analysis of the body composition.
Results: 21 patients with PHPT and 18 healthy volunteers were included in the study. Patients with PHPT have higher level of serum triglycerides (p=0.003) without statistically differences of the main carbohydrate and purine parameters comparing with the control group. Visceral obesity were revealed in 42.9% of patients, including those with a normal BMI. Insulin resistance in the PHPT group was noted in 52.4% of cases, while the M-index was statistically lower than in the control subgroup (p=0.008), despite of the comparable body composition of the participants. The M-index showed a positive correlation with blood phosphorus level (p=0.010) only in the general group. Statistically positive correlations of PTH, albumin-corrected calcium and osteocalcin with triglyceride levels, calcium with fasting glycaemia, and PTH with uric acid levels were determined.
Conclusion: PHPT is associated with insulin resistance in patients that is the main risk factor for the development of serious carbohydrate and fat disorders. The positive correlation of PTH and blood calcium levels with triglycerides, as well as the tendency to hypertriglyceridemia comparing with healthy volunteers, suggest the disease effect on the development of dyslipidemia.
About the Authors
E. E. BibikRussian Federation
Ekaterina E. Bibik, MD
11 Dm. Ulyanova street, 117036 Moscow, Russia
E. A. Dobreva
Russian Federation
Ekaterina A. Dobreva, MD, PhD
Moscow
A. R. Ajnetdinova
Russian Federation
Alina R. Ajnetdinova, MD
Moscow
A. K. Eremkina
Russian Federation
Anna K. Eremkina, MD, PhD
Moscow
N. G. Mokrysheva
Russian Federation
Natalia G. Mokrysheva, MD, PhD, Professor
Moscow
References
1. Corbetta S, Mantovani G, Spada A. Metabolic Syndrome in Parathyroid Diseases. Front Horm Res. 2018;49:67-84. doi: https://doi.org/10.1159/000486003
2. DeFronzo RA, Tobin JD, Andres R. Glucose clamp technique: a method for quantifying insulin secretion and resistance. Am J Physiol. 1979;237(3):E214-223. doi: https://doi.org/10.1152/ajpendo.1979.237.3.E214
3. Mayorov A.Y. Sostojanie insulinorezistentnosti v jevoljucii saharnogo diabeta 2 tipa. [dissertation]. Moscow; 2009. (In Russ.)
4. Klinicheskie rekomendacii Ministerstva zdravoohranenija Rossijskoj Federacii “Pervichnyj giperparatireoz” of 2020. (In Russ.)
5. Procopio M, Barale M, Bertaina S, et al. Cardiovascular risk and metabolic syndrome in primary hyperparathyroidism and their correlation to different clinical forms. Endocrine. 2014;47(2):581-589. doi: https://doi.org/10.1007/s12020-013-0091-z
6. Mokrysheva NG. Pervichnyj giperparatireoz. Jepidemiologija, klinika, sovremennye principy diagnostiki i lechenija. [dissertation] Moscow; 2011. (In Russ.)
7. Wannamethee SG, Welsh P, Papacosta O, et al. Elevated parathyroid hormone, but not vitamin D deficiency, is associated with increased risk of heart failure in older men with and without cardiovascular disease. Circ Heart Fail. 2014;7(5):732-739. doi: https://doi.org/10.1161/CIRCHEARTFAILURE.114.001272
8. Mokrysheva NG, Dobreva EA, Mirnaya SS, Dedov II. Carbohydrate and lipid metabolism disorders in women with primary hyperparathyroidism: results of cross-sectional study. Diabetes mellitus. 2019;22(1):8-13. (In Russ.). doi: https://doi.org/10.14341/DM9450
9. Tassone F, Procopio M, Gianotti L, et al. Insulin resistance is not coupled with defective insulin secretion in primary hyperparathyroidism. Diabet Med. 2009;26(10):968-973. doi: https://doi.org/10.1111/j.1464-5491.2009.02804.x
10. Haap M, Heller E, Thamer C, et al. Association of serum phosphate levels with glucose tolerance, insulin sensitivity and insulin secretion in non-diabetic subjects. Eur J Clin Nutr. 2006;60(6):734-739. doi: https://doi.org/10.1038/sj.ejcn.1602375
11. Hagstrom E, Hellman P, Lundgren E, et al. Serum calcium is independently associated with insulin sensitivity measured with euglycaemic-hyperinsulinaemic clamp in a community-based cohort. Diabetologia. 2007;50(2):317-324. doi: https://doi.org/10.1007/s00125-006-0532-9
12. Osadnik K, Osadnik T, Delijewski M, et al. Calcium and Phosphate Levels are Among Other Factors Associated with Metabolic Syndrome in Patients with Normal Weight. Diabetes Metab Syndr Obes. 2020;13:1281-1288. doi: https://doi.org/10.2147/DMSO.S232497
13. Kim H, Kalkhoff RK, Costrini NV, et al. Plasma insulin disturbances in primary hyperparathyroidism. J Clin Invest. 1971;50(12):2596-2605. doi: https://doi.org/10.1172/JCI106760
14. Sun G, Vasdev S, Martin GR, et al. Altered calcium homeostasis is correlated with abnormalities of fasting serum glucose, insulin resistance, and beta-cell function in the Newfoundland population. Diabetes. 2005;54(11):3336-3339. doi: https://doi.org/10.2337/diabetes.54.11.3336
15. Chang E, Donkin SS, Teegarden D. Parathyroid hormone suppresses insulin signaling in adipocytes. Mol Cell Endocrinol. 2009;307(1-2):77-82. doi: https://doi.org/10.1016/j.mce.2009.03.024
16. Reusch JE, Begum N, Sussman KE, Draznin B. Regulation of GLUT-4 phosphorylation by intracellular calcium in adipocytes. Endocrinology. 1991;129(6):3269-3273. doi: https://doi.org/10.1210/endo-129-6-3269
17. Kanazawa I. Interaction between bone and glucose metabolism [Review]. Endocr J. 2017;64(11):1043-1053. doi: https://doi.org/10.1507/endocrj.EJ17-0323
18. Bao Y, Ma X, Yang R, et al. Inverse relationship between serum osteocalcin levels and visceral fat area in Chinese men. J Clin Endocrinol Metab. 2013;98(1):345-351. doi: https://doi.org/10.1210/jc.2012-2906
19. Mendonca ML, Batista SL, Nogueira-Barbosa MH, et al. Primary Hyperparathyroidism: The Influence of Bone Marrow Adipose Tissue on Bone Loss and of Osteocalcin on Insulin Resistance. Clinics (Sao Paulo). 2016;71(8):464-469. doi: https://doi.org/10.6061/clinics/2016(08)09
20. Gianotti L, Piovesan A, Croce CG, et al. Interplay between serum osteocalcin and insulin sensitivity in primary hyperparathyroidism. Calcif Tissue Int. 2011;88(3):231-237. doi: https://doi.org/10.1007/s00223-010-9453-1
21. Paik JM, Farwell WR, Taylor EN. Demographic, dietary, and serum factors and parathyroid hormone in the National Health and Nutrition Examination Survey. Osteoporos Int. 2012;23(6):1727-1736. doi: https://doi.org/10.1007/s00198-011-1776-x
22. Ponvilawan B, Charoenngam N, Ungprasert P. Primary hyperparathyroidism is associated with a higher level of serum uric acid: A systematic review and meta-analysis. Int J Rheum Dis. 2020;23(2):174-180. doi: https://doi.org/10.1111/1756-185X.13740
23. Sugimoto R, Watanabe H, Ikegami K, et al. Down-regulation of ABCG2, a urate exporter, by parathyroid hormone enhances urate accumulation in secondary hyperparathyroidism. Kidney Int. 2017;91(3):658-670. doi: https://doi.org/10.1016/j.kint.2016.09.041
24. Girardi AC, Titan SM, Malnic G, Reboucas NA. Chronic effect of parathyroid hormone on NHE3 expression in rat renal proximal tubules. Kidney Int. 2000;58(4):1623-1631. doi: https://doi.org/10.1046/j.1523-1755.2000.00323.x
25. Carroll R, Matfin G. Endocrine and metabolic emergencies: hypercalcaemia. Ther Adv Endocrinol Metab. 2010;1(5):225-234. doi: https://doi.org/10.1177/2042018810390260
26.
Supplementary files
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1. Figure 1. Comparison of serum triglyceride levels in the examined groups. | |
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2. Figure 2. M-index comparison in the examined groups. | |
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3. Figure 3. The relationship between the level of glycated hemoglobin and the duration of primary hyperparathyroidism. | |
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4. Figure 4. Relationship of serum triglyceride level with indicators of mineral metabolism. | |
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5. Figure 5. The relationship between the M-index and serum phosphorus level. | |
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Type | Результаты исследования | |
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Review
For citations:
Bibik E.E., Dobreva E.A., Ajnetdinova A.R., Eremkina A.K., Mokrysheva N.G. Metabolic features of young patients with primary hyperparathyroidism. Obesity and metabolism. 2021;18(3):236-244. (In Russ.) https://doi.org/10.14341/omet12771

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