Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMD

IntroductionSirtuin 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...

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Main Authors: Yao Xu, Tianxiao Hu, Peiwu Jiang, Xiujing Wang, Jiaqi Yao, Huiling Shen, Zhenying Zhang, Bojing Zheng, Ting Wang, Yanxia Ren, Jing Wang, Qingying Tan
Format: Article
Language:English
Published: Frontiers Media S.A. 2025-01-01
Series:Frontiers in Endocrinology
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Online Access:https://www.frontiersin.org/articles/10.3389/fendo.2024.1480847/full
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author Yao Xu
Tianxiao Hu
Peiwu Jiang
Xiujing Wang
Jiaqi Yao
Huiling Shen
Zhenying Zhang
Bojing Zheng
Ting Wang
Yanxia Ren
Jing Wang
Qingying Tan
author_facet Yao Xu
Tianxiao Hu
Peiwu Jiang
Xiujing Wang
Jiaqi Yao
Huiling Shen
Zhenying Zhang
Bojing Zheng
Ting Wang
Yanxia Ren
Jing Wang
Qingying Tan
author_sort Yao Xu
collection DOAJ
description IntroductionSirtuin 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.MethodsA 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.ResultsT2DM 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.DiscussionIn 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.
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spelling doaj-art-27bcc0e5291849c8b8e7827ce67fc6852025-01-29T05:21:18ZengFrontiers Media S.A.Frontiers in Endocrinology1664-23922025-01-011510.3389/fendo.2024.14808471480847Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMDYao Xu0Tianxiao Hu1Peiwu Jiang2Xiujing Wang3Jiaqi Yao4Huiling Shen5Zhenying Zhang6Bojing Zheng7Ting Wang8Yanxia Ren9Jing Wang10Qingying Tan11Department of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Vascular Surgery, Hangzhou TCM Hospital Affiliated to Zhejiang Chinese Medical University, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaDepartment of Endocrinology, No.903 Hospital of PLA Joint Logistic Support Force, Hangzhou, ChinaIntroductionSirtuin 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.MethodsA 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.ResultsT2DM 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.DiscussionIn 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.https://www.frontiersin.org/articles/10.3389/fendo.2024.1480847/fullSirtuin 1bone mineral densitybone turnover markerstype 2 diabetes mellitusbone metabolism
spellingShingle Yao Xu
Tianxiao Hu
Peiwu Jiang
Xiujing Wang
Jiaqi Yao
Huiling Shen
Zhenying Zhang
Bojing Zheng
Ting Wang
Yanxia Ren
Jing Wang
Qingying Tan
Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMD
Frontiers in Endocrinology
Sirtuin 1
bone mineral density
bone turnover markers
type 2 diabetes mellitus
bone metabolism
title Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMD
title_full Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMD
title_fullStr Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMD
title_full_unstemmed Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMD
title_short Decreased sirtuin 1 in type 2 diabetes patients with abnormal BMD
title_sort decreased sirtuin 1 in type 2 diabetes patients with abnormal bmd
topic Sirtuin 1
bone mineral density
bone turnover markers
type 2 diabetes mellitus
bone metabolism
url https://www.frontiersin.org/articles/10.3389/fendo.2024.1480847/full
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