慢性广泛的肌肉骨骼疼痛与动脉粥样硬化和动脉僵硬有高度遗传性的潜在途径。

IF 5.9 1区 医学 Q1 ANESTHESIOLOGY
PAIN® Pub Date : 2025-06-01 Epub Date: 2024-12-03 DOI:10.1097/j.pain.0000000000003486
Maryam Kazemi Naeini, Marina Cecelja, Maxim B Freidin, Isabelle Granville Smith, Pirro Hysi, Christopher Sivert Nielsen, Frances M K Williams
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引用次数: 0

摘要

摘要:慢性广泛性疼痛(CWP)普遍存在,并与预期寿命降低有关。心血管疾病是一个可能的机制。本研究的目的是检查CWP与动脉僵硬度和颈动脉斑块的关联,以确定共同的环境或遗传因素是否可能解释任何观察到的关联。来自TwinsUK的约3000名参与者接受了CWP信息,并测量了颈动脉-股动脉脉搏波速度(cfPWV)、颈动脉内膜-中膜厚度(cIMT)和斑块。确定CWP与cfPWV、cIMT和斑块之间的关系。英国生物银行的数据被用来复制这种关联。检验了Cholesky分解和多元通路双胞胎模型。采用双样本孟德尔随机化方法,评估CWP与冠状动脉疾病之间的因果关系。TwinsUK参与者表现出CWP和cfPWV增加之间的显著关联,与动脉硬化一致(OR = 1.35, p值= 0.012),以及颈动脉斑块的存在(OR = 1.45, p值= 0.8e-5)。双胞胎模型显示CWP、cfPWV和颈动脉斑块具有共同的潜在成分和途径,遗传因素分别占潜在因素变异的68%和90%。双样本MR显示CWP与冠状动脉疾病之间存在潜在的因果关系。该研究发现,患有CWP的人动脉僵硬和动脉粥样硬化的风险增加,并表明CWP通过遗传因素导致心血管疾病风险增加。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Chronic widespread musculoskeletal pain shares a highly heritable latent pathway with atherosclerosis and arterial stiffness.

Abstract: Chronic widespread pain (CWP) is prevalent and associated with reduced life expectancy. Cardiovascular disease is one possible mechanism for this. The purpose of this study was to examine the association of CWP with arterial stiffness and carotid plaque measured using ultrasound to determine if shared environmental or genetic factors might account for any observed association. Around 3000 participants from the TwinsUK with CWP information and measures of carotid-femoral pulse wave velocity (cfPWV), carotid intima-media thickness (cIMT), and plaque were considered. The relationship between CWP and cfPWV, cIMT, and plaque was determined. UK Biobank data were used to replicate the association. Cholesky decomposition and multivariate pathway twin models were examined. Using a 2-sample Mendelian randomisation approach, the causal association between CWP and coronary artery disease was assessed. TwinsUK participants demonstrated a significant association between CWP and increased cfPWV consistent with arterial stiffening (OR = 1.35, P -value = 0.012), as well as the presence of carotid plaque (OR = 1.45, P -value = 0.8e-5). The twin modelling showed a common latent component and pathway underlying CWP, cfPWV, and carotid plaque, with genetic factors accounting for 68% and 90% of the latent factor variation, respectively. The 2-sample MR revealed a potential causal association between CWP and coronary artery disease. This study found that those with CWP have increased the risk of arterial stiffness and atherosclerosis and suggests that CWP leads to an increased risk of cardiovascular disease through genetic factors.

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来源期刊
PAIN®
PAIN® 医学-临床神经学
CiteScore
12.50
自引率
8.10%
发文量
242
审稿时长
9 months
期刊介绍: PAIN® is the official publication of the International Association for the Study of Pain and publishes original research on the nature,mechanisms and treatment of pain.PAIN® provides a forum for the dissemination of research in the basic and clinical sciences of multidisciplinary interest.
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