血管缺陷导致1型糖尿病患者骨骼脆弱。

Frontiers in clinical diabetes and healthcare Pub Date : 2023-10-06 eCollection Date: 2023-01-01 DOI:10.3389/fcdhc.2023.1272804
Adina E Draghici, Bita Zahedi, J Andrew Taylor, Mary L Bouxsein, Elaine W Yu
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引用次数: 0

摘要

目前,超过100万美国人患有T1D,糖尿病管理的改善增加了成年T1D患者的数量,使他们能够活到晚年。越来越多的老年糖尿病患者更容易患上衰老合并症,包括血管疾病和骨质疏松症。事实上,与没有糖尿病的人相比,患有T1D的成年人发生任何骨折的风险要高出2到3倍,髋关节骨折的风险高出7倍。最近,糖尿病相关的血管缺陷已成为骨血流量受损和骨骼健康状况不佳的潜在风险因素,并且有人假设T1D的血管疾病和骨骼结果之间存在直接的病理生理学联系。事实上,微血管疾病(MVD)是糖尿病最严重的后果之一,与没有微血管疾病的老年人相比,患有T1D的老年人的骨微结构更差。微血管并发症的存在与骨骼微结构受损之间的关联表明,血管受损可能会产生直接的有害影响,导致骨骼血流量异常、骨骼重塑改变和骨骼结构缺陷。此外,血管性糖尿病并发症的特征是血管钙化增加,动脉扩张性降低,血管重塑,动脉硬度和血管壁厚度增加。血管结构的这些广泛变化导致肌源性控制受损,一氧化氮介导的血管舒张减少,影响几乎所有血管床的血流调节,并显著限制T1D患者的骨骼肌血流。T1D的血管缺陷很可能会延伸到骨骼,影响骨骼血流控制,并导致流向骨骼的血流减少,从而对骨骼健康产生负面影响。事实上,一些动物和离体人类研究报告称,糖尿病诱导的骨内微血管损伤与糖尿病疾病的严重程度和持续时间密切相关。在这篇综述文章中,我们将讨论糖尿病诱导的血管缺陷对骨密度、骨微结构和骨血流调节的贡献,并回顾血管疾病对T1D骨骼脆性的潜在贡献。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Vascular deficits contributing to skeletal fragility in type 1 diabetes.

Vascular deficits contributing to skeletal fragility in type 1 diabetes.

Over 1 million Americans are currently living with T1D and improvements in diabetes management have increased the number of adults with T1D living into later decades of life. This growing population of older adults with diabetes is more susceptible to aging comorbidities, including both vascular disease and osteoporosis. Indeed, adults with T1D have a 2- to 3- fold higher risk of any fracture and up to 7-fold higher risk of hip fracture compared to those without diabetes. Recently, diabetes-related vascular deficits have emerged as potential risks factors for impaired bone blood flow and poor bone health and it has been hypothesized that there is a direct pathophysiologic link between vascular disease and skeletal outcomes in T1D. Indeed, microvascular disease (MVD), one of the most serious consequences of diabetes, has been linked to worse bone microarchitecture in older adults with T1D compared to their counterparts without MVD. The association between the presence of microvascular complications and compromised bone microarchitecture indicates the potential direct deleterious effect of vascular compromise, leading to abnormal skeletal blood flow, altered bone remodeling, and deficits in bone structure. In addition, vascular diabetic complications are characterized by increased vascular calcification, decreased arterial distensibility, and vascular remodeling with increased arterial stiffness and thickness of the vessel walls. These extensive alterations in vascular structure lead to impaired myogenic control and reduced nitric-oxide mediated vasodilation, compromising regulation of blood flow across almost all vascular beds and significantly restricting skeletal muscle blood flow seen in those with T1D. Vascular deficits in T1D may very well extend to bone, compromising skeletal blood flow control, and resulting in reduced blood flow to bone, thus negatively impacting bone health. Indeed, several animal and ex vivo human studies report that diabetes induces microvascular damage within bone are strongly correlated with diabetes disease severity and duration. In this review article, we will discuss the contribution of diabetes-induced vascular deficits to bone density, bone microarchitecture, and bone blood flow regulation, and review the potential contribution of vascular disease to skeletal fragility in T1D.

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