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Beyond the metabolic syndrome: Visceral and marrow adipose tissues impair bone quantity and quality in Cushing’s disease

机译:超越代谢综合征:内脏和骨髓脂肪组织损害库欣病的骨骼数量和质量

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摘要

The present study was designed to evaluate the relationship between bone traits [bone mineral density (BMD) and trabecular bone score (TBS)] and the accumulation of fat in adipose tissues [abdominal subcutaneous (SAT), visceral (VAT), marrow (MAT) and intrahepatic lipids (IHL)], as well as insulin resistance, in subjects with Cushing’s disease (CD). The study included control (C = 27), paired (P = 16) and Cushing’s disease (CD = 10) groups, which underwent biochemical assessment, dual X-ray absorptiometry, TBS, and magnetic resonance imaging to determine fat deposits. The CD group showed higher serum levels of glucose and insulin, as well as HOMA-IR values, but lower circulatory levels of osteocalcin, in comparison to C and P. The CD group exhibited lower L1-L4 BMD than P (P = 1.059 ± 0.141 vs CD = 0.935 ± 0.093 g/cm2, p < 0.05) (). The lumbar spine BMD from the C group was similar to the other groups. TBS was lower in CD than in P and C (C = 1.512±0.077 vs P = 1.405±0.150 vs CD = 1.135±0.136; p<0.05); there was also significant difference between C and P (p<0.05). MAT, VAT, and IHL were higher in CD than in C and P (p<0.05). Considering all subjects, there was a positive association between TBS with both lumbar spine BMD (R2 = 0.45; p<0.0001) and osteocalcin (R2 = 0.44; p = 0.05). TBS was negatively associated with MAT (R2 = 0.49; p = 0.01), VAT (R2 = 0.55; p<0.05), and HOMA-IR (R2 = 0.44; p<0.01). MAT was positively related with VAT (R2 = 0.44; p<0.01) and IHL (R2 = 0.41; p<0.05). In CD, insulin resistance and adipose tissue dysfunction, including high MAT, are active players in bone deterioration, as confirmed by lower lumbar spine BMD and lower TBS. Thus, our findings point to an additional component of the already well-known complex mechanisms of osteoporosis associated with hypercortisolism.Box-plots of (a) lumbar spine (L1-L4) bone mineral density (BMD) and (b) lumbar spine (L1-L4) trabecular bone score (TBS) in control (C), paired (P) and Cushing’s disease (CD) groups.
机译:本研究旨在评估骨质性状[骨矿物质密度(BMD)和小梁骨评分(TBS)]与脂肪组织[腹部皮下(SAT),内脏(VAT),骨髓(MAT)]中脂肪堆积的关系。 )和肝内脂质(IHL)],以及患有库欣氏病(CD)的受试者的胰岛素抵抗。该研究包括对照组(C = 27),成对(P = 16)和库欣氏病(CD = 10)组,这些组接受了生化评估,双X线吸收法,TBS和磁共振成像以确定脂肪沉积。与C和P相比,CD组显示较高的血清葡萄糖和胰岛素水平以及HOMA-IR值,但骨钙素的循环水平较低。CD组显示的L1-L4 BMD低于P(P = 1.059± 0.141 vs CD = 0.935±0.093 g / cm 2 ,p <0.05)()。 C组的腰椎BMD与其他组相似。 CD中的TBS低于P和C(C = 1.512±0.077 vs P = 1.405±0.150 vs CD = 1.135±0.136; p <0.05); C和P之间也存在显着差异(p <0.05)。 CD中的MAT,VAT和IHL高于C和P(p <0.05)。考虑到所有受试者,TBS与腰椎BMD(R 2 = 0.45; p <0.0001)和骨钙素(R 2 = 0.44; p = 0.05)。 TBS与MAT(R 2 = 0.49; p = 0.01),增值税(R 2 = 0.55; p <0.05)和HOMA-IR(R < sup> 2 = 0.44; p <0.01)。 MAT与增值税(R 2 = 0.44; p <0.01)和IHL(R 2 = 0.41; p <0.05)正相关。在CD中,低腰椎BMD和TBS降低证实了胰岛素抵抗和脂肪组织功能障碍(包括高MAT)是导致骨质退化的积极因素。因此,我们的发现指向与皮质醇过多症相关的骨质疏松症的众所周知复杂机制的其他组成部分。<!-fig ft0-> <!-fig mode = article f1-> <! -标题a7->(a)对照(C)的腰椎(L1-L4)骨矿物质密度(BMD)和(b)腰椎(L1-L4)小梁骨评分(TBS)的方框图, (P)和库欣氏病(CD)组。

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