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Association of Insulin Resistance and β-cell Function With Bone Turnover Biomarkers in Dysglycemia Patients

Authors :
Yingli Lu
Ji Zhou
Ying Zhou
Chiyu Wang
Tao Gu
Zengmei An
Hui Guo
Jian Cai
Boren Jiang
Chunfang Zhu
Kexi Zha
Shaohong Ge
Liqin Zhang
Yan Zhao
Rong Ying
Ningjian Wang
Chenyu Cao
Source :
Frontiers in Endocrinology, Vol 12 (2021), Frontiers in Endocrinology
Publication Year :
2021
Publisher :
Frontiers Media SA, 2021.

Abstract

BackgroundThe interrelation between glucose and bone metabolism is complex and has not been fully revealed. This study aimed to investigate the association between insulin resistance, β-cell function and bone turnover biomarker levels among participants with abnormal glycometabolism.MethodsA total of 5277 subjects were involved through a cross-sectional study (METAL study, http://www.chictr.org.cn, ChiCTR1800017573) in Shanghai, China. Homeostasis model assessment of insulin resistance (HOMA-IR) and β-cell dysfunction (HOMA-%β) were applied to elucidate the nexus between β-C-terminal telopeptide (β-CTX), intact N-terminal propeptide of type I collagen (P1NP) and osteocalcin (OC). β-CTX, OC and P1NP were detected by chemiluminescence.ResultsHOMA-IR was negatively associated with β-CTX, P1NP and OC (regression coefficient (β) -0.044 (-0.053, -0.035), Q4vsQ1; β -7.340 (-9.130, -5.550), Q4vsQ1 and β -2.885 (-3.357, -2.412), Q4vsQ1, respectively, all P for trend ConclusionsOur results support that lower bone turnover biomarker (β-CTX, P1NP and OC) levels were associated with a combination of higher prevalence of insulin resistance and worse β-cell function among dysglycemia patients. It is feasible to detect bone turnover in diabetes or hyperglycemia patients to predict the risk of osteoporosis and fracture, relieve patients’ pain and reduce the expenses of long-term cure.

Details

Language :
English
ISSN :
16642392
Volume :
12
Database :
OpenAIRE
Journal :
Frontiers in Endocrinology
Accession number :
edsair.doi.dedup.....92e87c538150a5313bbaece720ea008f
Full Text :
https://doi.org/10.3389/fendo.2021.554604