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本文引用的文献

1
Lipoprotein(a) is associated with the onset but not the progression of aortic valve calcification.脂蛋白(a)与主动脉瓣钙化的发生有关,但与进展无关。
Eur Heart J. 2022 Oct 14;43(39):3960-3967. doi: 10.1093/eurheartj/ehac377.
2
Sex Differences in Factors Associated With Progression of Aortic Valve Calcification in the General Population.主动脉瓣钙化进展的相关因素在普通人群中的性别差异。
Circ Cardiovasc Imaging. 2022 Jan;15(1):e013165. doi: 10.1161/CIRCIMAGING.121.013165. Epub 2022 Jan 5.
3
Calcific aortic valve disease: from molecular and cellular mechanisms to medical therapy.钙化性主动脉瓣疾病:从分子和细胞机制到医学治疗。
Eur Heart J. 2022 Feb 12;43(7):683-697. doi: 10.1093/eurheartj/ehab757.
4
Plasma biomarkers associated with adverse outcomes in patients with calcific aortic stenosis.与钙化性主动脉瓣狭窄患者不良预后相关的血浆生物标志物。
Eur J Heart Fail. 2021 Dec;23(12):2021-2032. doi: 10.1002/ejhf.2361. Epub 2021 Oct 21.
5
Global, Regional, and National Burden of Calcific Aortic Valve and Degenerative Mitral Valve Diseases, 1990-2017.钙化性主动脉瓣和退行性二尖瓣疾病的全球、区域和国家负担,1990-2017 年。
Circulation. 2020 May 26;141(21):1670-1680. doi: 10.1161/CIRCULATIONAHA.119.043391. Epub 2020 Mar 29.
6
Influence of metabolic syndrome and diabetes on progression of calcific aortic valve stenosis.代谢综合征和糖尿病对钙化性主动脉瓣狭窄进展的影响。
Int J Cardiol. 2017 Oct 1;244:248-253. doi: 10.1016/j.ijcard.2017.06.104. Epub 2017 Jun 30.
7
Biomarkers of Calcific Aortic Valve Disease.钙化性主动脉瓣疾病的生物标志物
Arterioscler Thromb Vasc Biol. 2017 Apr;37(4):623-632. doi: 10.1161/ATVBAHA.116.308615. Epub 2017 Feb 2.
8
Systolic hypertension and progression of aortic valve calcification in patients with aortic stenosis: results from the PROGRESSA study.主动脉瓣狭窄患者的收缩期高血压与主动脉瓣钙化进展:PROGRESSA研究结果
Eur Heart J Cardiovasc Imaging. 2017 Jan;18(1):70-78. doi: 10.1093/ehjci/jew013. Epub 2016 Feb 18.
9
TGF-β signalopathies as a paradigm for translational medicine.转化医学范式下的TGF-β信号病变
Eur J Med Genet. 2015 Dec;58(12):695-703. doi: 10.1016/j.ejmg.2015.10.010. Epub 2015 Oct 24.
10
Calcification in Aortic Stenosis: The Skeleton Key.主动脉瓣狭窄中的钙化:关键所在。
J Am Coll Cardiol. 2015 Aug 4;66(5):561-77. doi: 10.1016/j.jacc.2015.05.066.

与老年人主动脉瓣钙化进展相关的因素。

Factors associated with the progression of aortic valve calcification in older adults.

机构信息

Heart Institute, Hadassah Medical Center and Faculty of Medicine, Hebrew University of Jerusalem, Jerusalem, Israel.

Department of Medicine, Columbia University Irving Medical Center, New York, NY, USA.

出版信息

Int J Cardiol. 2023 Jun 15;381:76-80. doi: 10.1016/j.ijcard.2023.03.059. Epub 2023 Apr 6.

DOI:10.1016/j.ijcard.2023.03.059
PMID:37030403
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10161393/
Abstract

BACKGROUND

Aortic valve calcification (AVC) is a common valvular abnormality that predisposes to stenosis; AVC progression and factors associated with it remain unclear. We investigated the association of clinical factors and serum biomarkers with AVC progression in a population-based cohort of older adults.

METHODS

Participants enrolled in both the Cardiovascular Abnormalities and Brain Lesion study (CABL; years 2005-2010) and the Subclinical Atrial Fibrillation And Risk of Ischemic Stroke study (SAFARIS;2014-2019) represent the study cohort. AVC was defined as bright dense echoes >1 mm in size on ≥1 cusps; each cusp was graded on a scale of 0 (normal) to 3 (severe calcification) at baseline and follow up. Serum biomarkers were measured at the time of follow-up assessment.

RESULTS

373 participants (mean 68.1 ± 7.6 years of age, 146 M/ 227F) were included. 139 (37%) had AVC progression;93 (25%) had mild progression (1 grade), and 46 (12%) had moderate-severe progression (≥2 grades). The only significant clinical predictor of any progression was the use of anti-hypertensive medication which was associated with older age, higher BMI and more frequent hypertension, diabetes and hyperlipidemia. In multivariable analysis including biomarkers, transforming growth factor beta 1 (TGF-β1) was significantly associated with both all and moderate-severe AVC progression.

CONCLUSIONS

A significant number of elderly subjects with AVC show progression of their valve disease; individual vascular risk factors are not associated with AVC progression, although a combined effect may exist. Higher levels of TGF-β1 are observed in individuals with AVC progression.

摘要

背景

主动脉瓣钙化(AVC)是一种常见的瓣膜异常,可导致狭窄;AVC 的进展及其相关因素仍不清楚。我们研究了临床因素和血清生物标志物与老年人群基础队列中 AVC 进展的关系。

方法

参加心血管异常和脑损伤研究(CABL;2005-2010 年)和亚临床心房颤动和缺血性中风风险研究(SAFARIS;2014-2019 年)的参与者代表了研究队列。AVC 定义为≥1 个瓣叶上大小≥1mm 的亮而密集的回声;在基线和随访时,每个瓣叶均按 0(正常)至 3(严重钙化)的等级进行分级。在随访评估时测量血清生物标志物。

结果

共纳入 373 名参与者(平均年龄 68.1±7.6 岁,146 名男性/227 名女性)。139 名(37%)发生 AVC 进展;93 名(25%)发生轻度进展(1 级),46 名(12%)发生中重度进展(≥2 级)。任何进展的唯一显著临床预测因素是使用抗高血压药物,其与年龄较大、BMI 较高以及更频繁的高血压、糖尿病和高脂血症有关。在包括生物标志物的多变量分析中,转化生长因子-β1(TGF-β1)与所有和中重度 AVC 进展均显著相关。

结论

相当数量的患有 AVC 的老年患者其瓣膜疾病会出现进展;个体血管危险因素与 AVC 进展无关,但可能存在综合效应。在 AVC 进展的个体中观察到 TGF-β1 水平升高。