Atherosclerotic cardiovascular disease following a diagnosis of idiopathic inflammatory myopathy: analysis from a retrospective cohort in the TriNetX registry.

IF 2.9 3区 医学 Q2 RHEUMATOLOGY Clinical Rheumatology Pub Date : 2024-10-01 Epub Date: 2024-08-24 DOI:10.1007/s10067-024-07109-w
Astia Allenzara, Katherine Jicha, Carolina Álvarez, Amanda Nelson, Galen Foulke
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Abstract

Objective: Idiopathic inflammatory myopathies (IIM) confer an increased risk of morbidity from atherosclerotic cardiovascular disease (ASCVD). While ASCVD risk has been studied in other countries, these results may not be applicable to patients with dermatomyositis (DM) and polymyositis (PM) in the United States. This retrospective analysis of a cohort of patients identified by ICD code from TriNetX investigated the incidence of ASCVD after International Classification of Disease (ICD) codes of DM, PM, dermatopolymyositis (DPM) or juvenile dermatomyositis (JDM).

Method: Patients were identified by entry of two ICD codes separated by at least 6 months, according to their first diagnosis code; ASCVD was defined as first ICD code for myocardial infarction, ischemic stroke, transient ischemic attack, or peripheral arterial disease. Cox proportional hazards regression modeled time from first IIM ICD code to ASCVD event.

Results: A total of 35,554 patients were identified with the mean age at first IIM code of 54 and 26.1% were male. The most common comorbidity for all groups except JDM was hyperlipidemia (39.9%) though 79.2% of patients were on no cholesterol lowering medication. ASCVD occurred in 30.4% of patients with PM, 24.3% of patients with DM and 0.9% of patients with JDM. Patients with PM had a median time to event of 9.7 years (95% Confidence interval (CI) 9.1, 10.7) and 14.3 years (95% CI 12.6, 14.8) for DM. This study demonstrates that ASCVD is a comorbidity occurring after a median of 12.5 years (95% CI 11.9, 13.6) in patients with IIM.

Conclusions: ASCVD appears to be a long-term complication for IIM patients occurring in nearly a quarter of US patients without prior ASCVD with at least two ICD codes for IIM, with a median time to event of 12.5 years. There appears to be a practice gap in the recognition and treatment of hyperlipidemia in these patients. Key Points • Hyperlipidemia was a common comorbidity identified in patients with IIM though most patients were not on cholesterol lowering medication. • Development of ASCVD appears to be a long-term complication for patients with IIM in the United States.

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特发性炎症性肌病诊断后的动脉粥样硬化性心血管疾病:TriNetX 登记处的回顾性队列分析。
目的:特发性炎症性肌病(IIM特发性炎症性肌病(IIM)会增加动脉粥样硬化性心血管疾病(ASCVD)的发病风险。虽然 ASCVD 风险已在其他国家进行过研究,但这些结果可能不适用于美国的皮肌炎(DM)和多发性肌炎(PM)患者。这项回顾性分析通过 TriNetX 中的 ICD 代码确定了一组患者,研究了国际疾病分类(ICD)代码为 DM、PM、皮肌炎(DPM)或幼年皮肌炎(JDM)后 ASCVD 的发病率:根据患者的首次诊断代码,输入两个间隔至少 6 个月的 ICD 代码来确定患者;心肌梗死、缺血性中风、短暂性脑缺血发作或外周动脉疾病的首次 ICD 代码定义为 ASCVD。Cox比例危险回归模拟了从首次IIM ICD编码到ASCVD事件发生的时间:共发现 35554 名患者,首次获得 IIM 编码时的平均年龄为 54 岁,26.1% 为男性。除JDM外,所有组别中最常见的合并症是高脂血症(39.9%),但79.2%的患者未服用降胆固醇药物。30.4%的PM患者、24.3%的DM患者和0.9%的JDM患者发生了ASCVD。PM 患者的中位发病时间为 9.7 年(95% 置信区间(CI)为 9.1 - 10.7),DM 患者的中位发病时间为 14.3 年(95% 置信区间(CI)为 12.6 - 14.8)。这项研究表明,ASCVD是IIM患者在中位数12.5年(95% CI 11.9, 13.6)后发生的一种合并症:ASCVD似乎是IIM患者的一种长期并发症,在至少有两个ICD代码为IIM的无ASCVD既往症的美国患者中,近四分之一的患者会出现ASCVD,中位发生时间为12.5年。在识别和治疗这些患者的高脂血症方面,似乎还存在实践差距。要点 - 高脂血症是 IIM 患者常见的合并症,但大多数患者并未服用降低胆固醇的药物。- 在美国,ASCVD 的发展似乎是 IIM 患者的长期并发症。
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来源期刊
Clinical Rheumatology
Clinical Rheumatology 医学-风湿病学
CiteScore
6.90
自引率
2.90%
发文量
441
审稿时长
3 months
期刊介绍: Clinical Rheumatology is an international English-language journal devoted to publishing original clinical investigation and research in the general field of rheumatology with accent on clinical aspects at postgraduate level. The journal succeeds Acta Rheumatologica Belgica, originally founded in 1945 as the official journal of the Belgian Rheumatology Society. Clinical Rheumatology aims to cover all modern trends in clinical and experimental research as well as the management and evaluation of diagnostic and treatment procedures connected with the inflammatory, immunologic, metabolic, genetic and degenerative soft and hard connective tissue diseases.
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