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2型糖尿病伴骨密度异常患者中沉默调节蛋白1减少。

Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMD.

作者信息

Xu Yao, Hu Tianxiao, Jiang Peiwu, Wang Xiujing, Yao Jiaqi, Shen Huiling, Zhang Zhenying, Zheng Bojing, Wang Ting, Ren Yanxia, Wang Jing, Tan Qingying

机构信息

Department of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, China.

Department of Vascular Surgery, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, China.

出版信息

Front Endocrinol (Lausanne). 2025 Jan 29;15:1480847. doi: 10.3389/fendo.2024.1480847. eCollection 2024.

Abstract

INTRODUCTION

Sirtuin 1, a class III histone deacetylase, plays a critical role in the pathophysiology of both diabetes mellitus and bone metabolism by promoting osteoblast differentiation and inhibiting osteoclast maturation. However, its exact impact on bone mineral density (BMD) and bone metabolism in type 2 diabetes mellitus (T2DM) remains unclear. This study investigates the relationship between Sirtuin 1 levels, BMD, and bone metabolism in newly diagnosed T2DM patients, specifically examining alterations in Sirtuin 1 levels in those with concomitant osteoporosis or osteopenia.

METHODS

A total of 69 newly diagnosed T2DM patients and 82 control subjects with normal glucose tolerance (NGT) were enrolled. Serum Sirtuin 1 levels and bone turnover markers, including osteocalcin (OC), procollagen type 1 N-terminal propeptide (P1NP), and β-C-terminal telopeptide of type I collagen (β-CTX), were measured using enzyme-linked immunosorbent assay (ELISA). BMD was assessed via dual-energy X-ray absorptiometry (DXA). Comparisons of these parameters were made between the T2DM and NGT groups.

RESULTS

T2DM patients were further categorized into a normal BMD group (DMn) and an osteopenia or osteoporosis group (DMo), and differences in Sirtuin 1 levels between these subgroups were analyzed. Risk factors for osteoporosis/osteopenia in T2DM patients were also evaluated. Serum Sirtuin 1 levels were found to be significantly diminished in the T2DM group relative to the control group (P < 0.05), with no significant differences in lumbar spine BMD, OC, 25(OH)D, and β-CTX between groups (P > 0.05). Osteoporosis incidence was higher in T2DM subjects compared to controls (34.8% vs. 18.3%, P = 0.026). Subgroup analysis revealed that SIRT1 levels in T2DM patients with osteoporosis or osteopenia exhibited a significant reduction compared to those with normal BMD (P < 0.05). Logistic regression indicated that Sirtuin 1, age, HDL-C, P1NP, and β-CTX were independent risk factors for osteoporosis in T2DM patients.

DISCUSSION

In conclusion, decreased serum Sirtuin 1 levels are associated with bone turnover markers in T2DM patients and may serve as an independent risk factor and potential biomarker for diagnosing bone metabolism disorders in newly diagnosed T2DM patients.

摘要

引言

沉默调节蛋白1是一种III类组蛋白脱乙酰酶,通过促进成骨细胞分化和抑制破骨细胞成熟,在糖尿病和骨代谢的病理生理学中发挥关键作用。然而,其对2型糖尿病(T2DM)患者骨密度(BMD)和骨代谢的确切影响仍不清楚。本研究调查新诊断的T2DM患者中沉默调节蛋白1水平、BMD和骨代谢之间的关系,特别研究伴有骨质疏松或骨量减少患者的沉默调节蛋白1水平变化。

方法

共纳入69例新诊断的T2DM患者和82例糖耐量正常(NGT)的对照者。采用酶联免疫吸附测定(ELISA)法检测血清沉默调节蛋白1水平和骨转换标志物,包括骨钙素(OC)、I型前胶原N端前肽(P1NP)和I型胶原β羧基端肽(β-CTX)。通过双能X线吸收法(DXA)评估BMD。对T2DM组和NGT组的这些参数进行比较。

结果

将T2DM患者进一步分为骨密度正常组(DMn)和骨量减少或骨质疏松组(DMo),分析这些亚组之间沉默调节蛋白1水平的差异。还评估了T2DM患者骨质疏松/骨量减少的危险因素。发现T2DM组血清沉默调节蛋白1水平相对于对照组显著降低(P < 0.05),两组间腰椎BMD、OC、25(OH)D和β-CTX无显著差异(P > 0.05)。T2DM患者的骨质疏松发生率高于对照组(34.8%对18.3%,P = 0.026)。亚组分析显示,与骨密度正常的T2DM患者相比,伴有骨质疏松或骨量减少的T2DM患者的SIRT1水平显著降低(P < 0.05)。逻辑回归表明,沉默调节蛋白1、年龄、高密度脂蛋白胆固醇、P1NP和β-CTX是T2DM患者骨质疏松的独立危险因素。

讨论

总之,血清沉默调节蛋白1水平降低与T2DM患者的骨转换标志物相关,可能作为新诊断T2DM患者诊断骨代谢紊乱的独立危险因素和潜在生物标志物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e080/11813776/85110837c675/fendo-15-1480847-g001.jpg

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