PMID- 36387843 OWN - NLM STAT- MEDLINE DCOM- 20221121 LR - 20221222 IS - 1664-2392 (Print) IS - 1664-2392 (Electronic) IS - 1664-2392 (Linking) VI - 13 DP - 2022 TI - Perirenalfat thickness is associated with bone turnover markers and bone mineral density in postmenopausal women with type 2 diabetes mellitus. PG - 990667 LID - 10.3389/fendo.2022.990667 [doi] LID - 990667 AB - OBJECTIVES: Emerging evidence demonstrated that perirenal fat may modulate bone metabolism through several pathological pathways. This study was aimed to assess the associations between perirenal fat thickness (PrFT) and bone turnover markers (BTMs) and bone mineral density (BMD) in postmenopausal women with type 2 diabetes mellitus (T2DM) and further explore the correlation between PrFT and osteoporosis. METHODS: In this cross-sectional study, a total of 626 participants with complete data were enrolled in this study. Demographic and anthropometric information was collected. Biochemical parameters and BTMs were determined. PrFT and BMD were measured by computed tomography and dual-energy x-ray absorptiometry, respectively. Correlation analysis and regression models were used to assess the associations between PrFT and BTMs and BMD. The multiple binomial logistic regression model was used to estimate the independent variables of PrFT for osteoporosis. RESULTS: Overall, the prevalence of osteoporosis was 38.7%. PrFT was negatively correlated with beta-cross-linked C-telopeptide of type I collagen (beta-CTX) (r = -0.216,< 0.001), L1-L4 BMD (r = -0.351, < 0.001), and T-score (r = -0.396, < 0.001). PrFT also remained significantly correlated with beta-CTX (beta = -0.291, P< 0.001), L1-L4 BMD (beta = -0.109, P= 0.027), and L1-L4 T-score (beta = -0.149, P= 0.001) after adjustment for other confounding factors. Furthermore, PrFT was also independently associated with osteoporosis after adjustment for other confounding factors; the OR (95% CI) was 1.13 (1.04-1.23). PrFT also seems to have a relatively good identifying value for osteoporosis. The area under the curve (AUC) value of PrFT in identifying osteoporosis was 0.766 (95% CI: 0.705-0.826, P < 0.001). The optimal cutoff value of PrFT was 15.2 mm (sensitivity: 72.5%, specificity: 79.8%). CONCLUSIONS: PrFT was significantly associated with beta-CTX, BMD, and osteoporosis. These findings indicate that perirenal fat may play an important role in bone metabolism. CLINICAL TRIAL REGISTRATION: http://www.chictr.org.cn/, identifier (ChiCTR2100052032). CI - Copyright (c) 2022 Wang, Huang, Tang, Tu and Guo. FAU - Wang, Wei AU - Wang W AD - Department of Endocrinology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, China. FAU - Huang, Rong AU - Huang R AD - Department of Endocrinology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, China. FAU - Tang, Ping Tai AU - Tang PT AD - Department of Radiology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, China. FAU - Tu, Mei AU - Tu M AD - Department of Endocrinology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, China. FAU - Guo, Xiu Li AU - Guo XL AD - Department of Radiology, Longyan First Affiliated Hospital of Fujian Medical University, Longyan, China. LA - eng SI - ChiCTR/ChiCTR2100052032 PT - Journal Article DEP - 20221025 PL - Switzerland TA - Front Endocrinol (Lausanne) JT - Frontiers in endocrinology JID - 101555782 RN - 0 (Biomarkers) RN - 9007-34-5 (Collagen) SB - IM MH - Female MH - Humans MH - Bone Density MH - *Diabetes Mellitus, Type 2/complications MH - Postmenopause MH - Cross-Sectional Studies MH - Biomarkers MH - *Osteoporosis MH - Collagen MH - Bone Remodeling PMC - PMC9641290 OTO - NOTNLM OT - bone mineral density OT - bone turnover markers OT - perirenal fat thickness OT - postmenopausal women OT - type 2 diabetes mellitus COIS- The authors declare that the research was conducted in the absence of any commercial or financial relationships that could be construed as a potential conflict of interest. EDAT- 2022/11/18 06:00 MHDA- 2022/11/22 06:00 PMCR- 2022/01/01 CRDT- 2022/11/17 12:04 PHST- 2022/07/10 00:00 [received] PHST- 2022/10/06 00:00 [accepted] PHST- 2022/11/17 12:04 [entrez] PHST- 2022/11/18 06:00 [pubmed] PHST- 2022/11/22 06:00 [medline] PHST- 2022/01/01 00:00 [pmc-release] AID - 10.3389/fendo.2022.990667 [doi] PST - epublish SO - Front Endocrinol (Lausanne). 2022 Oct 25;13:990667. doi: 10.3389/fendo.2022.990667. eCollection 2022.