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引用本文的文献

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Reply to: "Before Coming to the Conclusion That Inclusion Body Myositis Is a Risk Factor for a Heart Attack, All Influencing Factors Must Be Taken Into Account".回复:“在得出包涵体肌炎是心脏病发作的危险因素这一结论之前,必须考虑所有影响因素”。
Eur J Neurol. 2025 Jul;32(7):e70295. doi: 10.1111/ene.70295.
2
Before Coming to the Conclusion That Inclusion Body Myositis Is a Risk Factor for a Heart Attack, All Influencing Factors Must Be Taken Into Account.在得出包涵体肌炎是心脏病发作的一个风险因素这一结论之前,必须考虑所有影响因素。
Eur J Neurol. 2025 Jul;32(7):e70297. doi: 10.1111/ene.70297.

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NLRP3 Inflammasome Activation and Altered Mitophagy Are Key Pathways in Inclusion Body Myositis.NLRP3炎性小体激活和线粒体自噬改变是包涵体肌炎的关键途径。
J Cachexia Sarcopenia Muscle. 2025 Feb;16(1):e13672. doi: 10.1002/jcsm.13672.
2
Mitochondrial dysfunction at the crossroad of cardiovascular diseases and cancer.线粒体功能障碍:心血管疾病与癌症的交汇点
J Transl Med. 2023 Sep 19;21(1):635. doi: 10.1186/s12967-023-04498-5.
3
Epidemiology, Survival, and Clinical Characteristics of Inclusion Body Myositis.包涵体肌炎的流行病学、生存情况和临床特征。
Ann Neurol. 2022 Aug;92(2):201-212. doi: 10.1002/ana.26412. Epub 2022 Jun 6.
4
Coronary Heart Disease and Cardiovascular Risk Factors in Patients With Idiopathic Inflammatory Myopathies: A Systemic Review and Meta-Analysis.特发性炎性肌病患者的冠心病和心血管危险因素:一项系统评价和荟萃分析
Front Med (Lausanne). 2022 Jan 14;8:808915. doi: 10.3389/fmed.2021.808915. eCollection 2021.
5
Inclusion body myositis: correlation of clinical outcomes with histopathology, electromyography and laboratory findings.包涵体肌炎:临床结果与组织病理学、肌电图和实验室检查的相关性。
Rheumatology (Oxford). 2022 May 30;61(6):2504-2511. doi: 10.1093/rheumatology/keab754.
6
Survival and associated comorbidities in inclusion body myositis.包涵体肌炎的生存状况及其相关合并症。
Rheumatology (Oxford). 2022 May 5;61(5):2016-2024. doi: 10.1093/rheumatology/keab716.
7
The risk of ischemic stroke in patients with idiopathic inflammatory myopathies: a systematic review and meta-analysis.特发性炎性肌病患者的缺血性卒中风险:系统评价和荟萃分析。
Clin Rheumatol. 2021 Oct;40(10):4101-4108. doi: 10.1007/s10067-021-05751-2. Epub 2021 May 1.
8
Epidemiology and Natural History of Inclusion Body Myositis: A 40-Year Population-Based Study.包涵体肌炎的流行病学和自然史:一项基于人群的 40 年研究。
Neurology. 2021 May 25;96(21):e2653-e2661. doi: 10.1212/WNL.0000000000012004. Epub 2021 Apr 20.
9
Effects of statins on mitochondrial pathways.他汀类药物对线粒体途径的影响。
J Cachexia Sarcopenia Muscle. 2021 Apr;12(2):237-251. doi: 10.1002/jcsm.12654. Epub 2021 Jan 29.
10
Similar risk of cardiovascular events in idiopathic inflammatory myopathy and rheumatoid arthritis in the first 5 years after diagnosis.特发性炎症性肌病和类风湿关节炎患者在确诊后 5 年内发生心血管事件的风险相似。
Clin Rheumatol. 2021 Jan;40(1):231-238. doi: 10.1007/s10067-020-05237-7. Epub 2020 Jun 22.

包涵体肌炎患者心肌梗死风险增加:一项非同期队列研究

Increased Risk of Myocardial Infarction in Inclusion Body Myositis: A Non-Concurrent Cohort Study.

作者信息

Beecher Grayson, Muhammad Sara, Shammas Ibrahim, Chamberlain Alanna M, Larson Kathryn, Mandrekar Jay, Harmsen William S, Naddaf Elie

机构信息

Department of Neurology, Mayo Clinic, Rochester, Minnesota, USA.

Division of Neurology, Department of Medicine, University of Alberta, Edmonton, Alberta, Canada.

出版信息

Eur J Neurol. 2025 May;32(5):e70177. doi: 10.1111/ene.70177.

DOI:10.1111/ene.70177
PMID:40297918
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC12038370/
Abstract

BACKGROUND

Idiopathic inflammatory myopathies, beyond inclusion body myositis (IBM), have demonstrated an increased risk of adverse cardiovascular outcomes, particularly myocardial infarction (MI). This study evaluated the risk of cardiovascular disease in IBM.

METHODS

We conducted a non-concurrent cohort study utilizing the expanded Rochester Epidemiologic Project, including 50 patients with IBM, matched 1:6 to age-, sex-, and calendar year-matched referents without IBM. Baseline cardiovascular risk factors were recorded. Differences in baseline covariates were adjusted by the inverse probability of treatment weighting method. Participants were followed from the index date forward to determine relative risks (RR) and hazard ratios (HR) for the development of cardiovascular outcomes including MI, ischemic stroke, cardiomyopathy, congestive heart failure (CHF), and peripheral vascular disease (PVD).

RESULTS

50 patients with IBM and 294 matched population referents were included. Baseline cardiovascular risk factors were similar between groups. Aspirin use was more common (28% vs. 18%, p = 0.03) and statin use less common (26% vs. 38%, p = 0.04) in IBM versus referents. Patients with IBM had an increased hazard of MI compared to referents [HR: 5.79, 95% CI (2.51, 13.36)]. The risk of MI remained consistently elevated across all models, after accounting for potential confounders. For PVD, 16/50 IBM patients versus 16/287 referents were excluded due to pre-existing PVD at index (p < 0.001). Among remaining participants, RR for PVD was 2.38 (0.82, 6.9). IBM was not associated with an increased risk of ischemic stroke, cardiomyopathy, or CHF.

CONCLUSIONS

IBM is associated with increased risk of MI compared to population referents. Heightened cardiovascular monitoring and prevention strategies are needed in IBM.

摘要

背景

除包涵体肌炎(IBM)外,特发性炎性肌病已显示出不良心血管结局风险增加,尤其是心肌梗死(MI)。本研究评估了IBM患者发生心血管疾病的风险。

方法

我们利用扩展的罗切斯特流行病学项目进行了一项非同期队列研究,纳入50例IBM患者,按1:6与年龄、性别和日历年份匹配的无IBM对照者配对。记录基线心血管危险因素。通过治疗权重逆概率法调整基线协变量差异。从索引日期开始对参与者进行随访,以确定发生心血管结局(包括MI、缺血性中风、心肌病、充血性心力衰竭(CHF)和外周血管疾病(PVD))的相对风险(RR)和风险比(HR)。

结果

纳入了50例IBM患者和294名匹配的人群对照者。两组间基线心血管危险因素相似。与对照者相比,IBM患者使用阿司匹林更为常见(28%对18%,p = 0.03),而使用他汀类药物则较少见(26%对38%,p = 0.04)。与对照者相比,IBM患者发生MI的风险更高[HR:5.79,95%CI(2.51,13.36)]。在考虑潜在混杂因素后,MI风险在所有模型中均持续升高。对于PVD,由于索引时已存在PVD,50例IBM患者中有16例被排除,287名对照者中有16例被排除(p < 0.001)。在其余参与者中,PVD的RR为2.38(0.82,6.9)。IBM与缺血性中风、心肌病或CHF风险增加无关。

结论

与人群对照者相比,IBM患者发生MI的风险增加。IBM患者需要加强心血管监测和预防策略。