手部僵硬是否反映了糖尿病患者的内脏纤维化?

Frontiers in clinical diabetes and healthcare Pub Date : 2023-07-10 eCollection Date: 2023-01-01 DOI:10.3389/fcdhc.2023.1198782
Sanat Phatak, Jennifer L Ingram, Pranay Goel, Satyajit Rath, Chittaranjan Yajnik
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引用次数: 0

摘要

纤维化导致组织不可逆转的僵化和功能丧失,是导致慢性病发病率和死亡率的常见途径。糖尿病(1 型和 2 型糖尿病)与内脏器官的严重纤维化有关,主要是肾脏和心脏,也包括肺、肝脏和脂肪组织。糖尿病还与糖尿病手足病有关,这是一系列影响手部的临床表现,包括关节活动受限(LJM)、屈肌腱鞘炎、Duypuytren 病和腕管综合征。从组织形态学上看,这些都是影响手部各种软组织成分的组织坏死性疾病。我们假设,这些手部表现反映了全身性的坏死状态,是当前或未来内部器官纤维化的潜在临床生物标志物。从流行病学角度看,有证据表明一个器官的纤维化与另一个器官的纤维化有关;导致糖尿病患者纤维化的假定暴露(高级糖化终产物沉积、微血管疾病和缺氧、持续的先天性炎症)是 "系统性 "的;还暗示了纤维化的共同遗传易感性。这些数据表明,糖尿病患者中有一部分人容易发生多器官纤维化。手部是临床检测这种易感性的一个有吸引力的生物标志物,因为手部易于进行体格检查,并能承受反复的机械压力。检验这一假设有几个先决条件:能够使用临床评分或基于成像的评分来测量手部纤维化,这将有助于使用经过验证的方法寻找手部纤维化与内部器官纤维化之间的关联。纵向研究对于确定手部表现者的纤维化轨迹至关重要。由于逆转纤维化的疗法很少,因此有责任识别易感人群,采取预防措施。如果得到系统的验证,临床手部检查可提供一个低成本、普遍可及、易于重复的筛查步骤,用于选择糖尿病纤维化临床试验的患者。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Does hand stiffness reflect internal organ fibrosis in diabetes mellitus?

Does hand stiffness reflect internal organ fibrosis in diabetes mellitus?

Fibrosis leads to irreversible stiffening of tissue and loss of function, and is a common pathway leading to morbidity and mortality in chronic disease. Diabetes mellitus (both type 1 and type 2 diabetes) are associated with significant fibrosis in internal organs, chiefly the kidney and heart, but also lung, liver and adipose tissue. Diabetes is also associated with the diabetic cheirarthropathies, a collection of clinical manifestations affecting the hand that include limited joint mobility (LJM), flexor tenosynovitis, Duypuytren disease and carpal tunnel syndrome. Histo-morphologically these are profibrotic conditions affecting various soft tissue components in the hand. We hypothesize that these hand manifestations reflect a systemic profibrotic state, and are potential clinical biomarkers of current or future internal organ fibrosis. Epidemiologically, there is evidence that fibrosis in one organ associates with fibrosis with another; the putative exposures that lead to fibrosis in diabetes (advanced glycation end product deposition, microvascular disease and hypoxia, persistent innate inflammation) are 'systemic'; a common genetic susceptibility to fibrosis has also been hinted at. These data suggest that a subset of the diabetic population is susceptible to multi-organ fibrosis. The hand is an attractive biomarker to clinically detect this susceptibility, owing to its accessibility to physical examination and exposure to repeated mechanical stresses. Testing the hypothesis has a few pre-requisites: being able to measure hand fibrosis in the hand, using clinical scores or imaging based scores, which will facilitate looking for associations with internal organ fibrosis using validated methodologies for each. Longitudinal studies would be essential in delineating fibrosis trajectories in those with hand manifestations. Since therapies reversing fibrosis are few, the onus lies on identification of a susceptible subset for preventative measures. If systematically validated, clinical hand examination could provide a low-cost, universally accessible and easily reproducible screening step in selecting patients for clinical trials for fibrosis in diabetes.

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