评论:使用BACTRAC蛋白质组学数据库-缺血性卒中尿调蛋白表达。

Journal of experimental neurology Pub Date : 2021-03-01
Gabriella-Salome K Armstrong, Jacqueline A Frank, Christopher J McLouth, Ann Stowe, Jill M Roberts, Amanda L Trout, Justin F Fraser, Keith Pennypacker
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引用次数: 0

摘要

尿调素(UMOD)是肾Henle’s袢厚升肢上皮细胞表达的一种糖蛋白。研究表明,尿调蛋白表达增加可能与成人心血管疾病风险降低有关。利用血液和血栓切除登记与协作(BACTRAC) (clinicaltrials.gov NCT03153683),一个持续招募的组织库,我们旨在研究血清尿调素、年龄和高BMI (BMI>25)之间的关系及其与卒中的关系。方法:在取栓过程中,使用BACTRAC协议收集血栓远端和近端动脉血,并将其发送给Olink (Boston, MA),通过邻近延伸法测定蛋白质组学表达。用双尾t检验和线性回归分析尿调素的表达。结果:评估全身和颅内尿调素与年龄、高BMI和高血压的关系。全身和颅内尿调素随年龄的增长而降低(p2=0.343, p=0.0416, r2=0.102)。BMI>25时,全身尿调素表达增加(p=0.014)。高血压降低尿调素的全身表达(p=0.018)和颅内表达(p=0.007)。结论:尿调素在超重患者中显著升高,在老年患者中显著降低,在高血压患者中显著降低。高BMI人群尿调蛋白的增加可能是肾脏对更容易发生缺血性中风的恶化情况的一种保护性反应,目的是延迟危险的结果。老年人尿调蛋白表达的降低可能与伴随衰老的一般肾功能下降有关。高血压可通过减少肾脏灌注,从而降低肾功能和尿调素的产生而导致AKI。需要进一步分析了解尿调蛋白在缺血性脑卒中中的作用。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Commentary: Use of BACTRAC Proteomic Database-Uromodulin Protein Expression During Ischemic Stroke.

Commentary: Use of BACTRAC Proteomic Database-Uromodulin Protein Expression During Ischemic Stroke.

Commentary: Use of BACTRAC Proteomic Database-Uromodulin Protein Expression During Ischemic Stroke.

Commentary: Use of BACTRAC Proteomic Database-Uromodulin Protein Expression During Ischemic Stroke.

Introduction: Uromodulin (UMOD) is a glycoprotein expressed by the epithelial cells of the thick ascending limb of Henle's loop in the kidney. Research has shown that increased uromodulin expression may be associated with lower risk of cardiovascular disease in adults. Utilizing the Blood and Clot Thrombectomy Registry and Collaboration (BACTRAC) (clinicaltrials.gov NCT03153683), a continuously enrolling tissue bank, we aimed to examine the associations between serum uromodulin, age, and high BMI (BMI>25) and its relationship to stroke in patients.

Methods: Arterial blood distal and proximal to the thrombus was collected during a thrombectomy procedure using the BACTRAC protocol and sent to Olink (Boston, MA) to determine proteomic expression via proximity extension assay. Uromodulin expression was recorded and analyzed using two tailed T-tests and linear regressions.

Results: The relationship between systemic and intracranial uromodulin, age, high BMI and hypertension were assessed. Systemic and intracranial uromodulin decreased with age (p<0.0001 and r2=0.343, p=0.0416 and r2=0.102) respectively. Systemic uromodulin expression increased with BMI>25 (p=0.014). Presence of hypertension decreased uromodulin's expression systemically (p=0.018) and intracranially (p=0.007).

Conclusions: Uromodulin was increased significantly in overweight patients, decreased significantly in older patients, and decreased in patients with hypertension. The increase in uromodulin in people with high BMI could be a protective reaction of the kidney to worsening conditions that make ischemic stroke more likely, with a goal of delaying dangerous outcomes. The decreased expression of uromodulin in older adults could be associated with the decline of general kidney function that accompanies aging. Hypertension can contribute to an AKI by decreasing perfusion to the kidney, therefore decreasing kidney function and uromodulin production. Further analyses are needed to understand the role of uromodulin following ischemic stroke.

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