Jiyu Sun , Hyo Jin Lee , Jung-Kyu Lee , Tae Yeon Park , Eun Young Heo , Deog Kyeom Kim , Hyun Woo Lee
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Additionally, subgroup analyses were conducted according to the duration of ICS exposure and the various components of ICS.</div></div><div><h3>Results</h3><div>A total of 442,880 COPD patients were included in the study, with 95,695 in ICS group and 347,185 in non-ICS group. The incidence rate of MASLD was higher in the ICS group compared to the non-ICS group (859.3 vs<em>.</em> 440.4 per 100,000 person-years). After adjusting for potential confounding factors, ICS use was associated with a significantly increased risk of MASLD (hazard ratio [HR]=1.630, 95 % confidence interval [CI]=1.560–1.704). Fluticasone furoate showed a higher risk of MASLD compared to other ICS components, and a longer duration of ICS exposure was associated with an increased MASLD risk.</div></div><div><h3>Conclusions</h3><div>In COPD patients, long-term use of ICS may be associated with an increased risk of developing MASLD. Further studies are needed to explore strategies to mitigate the potential risk of MASLD in COPD patients requiring ICS therapy.</div></div>","PeriodicalId":48479,"journal":{"name":"Respiratory Medicine and Research","volume":"87 ","pages":"Article 101171"},"PeriodicalIF":2.2000,"publicationDate":"2025-05-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Impact of inhaled corticosteroids on metabolic dysfunction-associated steatotic liver disease risk in COPD patients\",\"authors\":\"Jiyu Sun , Hyo Jin Lee , Jung-Kyu Lee , Tae Yeon Park , Eun Young Heo , Deog Kyeom Kim , Hyun Woo Lee\",\"doi\":\"10.1016/j.resmer.2025.101171\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div><h3>Background</h3><div>The systemic impact of long-term use of inhaled corticosteroid (ICS) on the liver remains poorly understood in patients with chronic obstructive pulmonary disease (COPD). Our study aimed to identify whether long-term ICS therapy impacts the risk of Metabolic dysfunction-associated steatotic liver disease (MASLD) in patients with COPD.</div></div><div><h3>Methods</h3><div>A retrospective cohort study was conducted using claims records from a large population-based database. We included COPD patients ≥40 years old who had no previous history of chronic liver disease. Patients were divided into two groups based on their ICS use. The primary outcome was the development of MASLD. Additionally, subgroup analyses were conducted according to the duration of ICS exposure and the various components of ICS.</div></div><div><h3>Results</h3><div>A total of 442,880 COPD patients were included in the study, with 95,695 in ICS group and 347,185 in non-ICS group. The incidence rate of MASLD was higher in the ICS group compared to the non-ICS group (859.3 vs<em>.</em> 440.4 per 100,000 person-years). After adjusting for potential confounding factors, ICS use was associated with a significantly increased risk of MASLD (hazard ratio [HR]=1.630, 95 % confidence interval [CI]=1.560–1.704). Fluticasone furoate showed a higher risk of MASLD compared to other ICS components, and a longer duration of ICS exposure was associated with an increased MASLD risk.</div></div><div><h3>Conclusions</h3><div>In COPD patients, long-term use of ICS may be associated with an increased risk of developing MASLD. Further studies are needed to explore strategies to mitigate the potential risk of MASLD in COPD patients requiring ICS therapy.</div></div>\",\"PeriodicalId\":48479,\"journal\":{\"name\":\"Respiratory Medicine and Research\",\"volume\":\"87 \",\"pages\":\"Article 101171\"},\"PeriodicalIF\":2.2000,\"publicationDate\":\"2025-05-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Respiratory Medicine and Research\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://www.sciencedirect.com/science/article/pii/S2590041225000182\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"RESPIRATORY SYSTEM\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Respiratory Medicine and Research","FirstCategoryId":"3","ListUrlMain":"https://www.sciencedirect.com/science/article/pii/S2590041225000182","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"RESPIRATORY SYSTEM","Score":null,"Total":0}
引用次数: 0
摘要
长期使用吸入性皮质类固醇(ICS)对慢性阻塞性肺疾病(COPD)患者肝脏的全身性影响尚不清楚。我们的研究旨在确定长期ICS治疗是否会影响COPD患者代谢功能障碍相关脂肪变性肝病(MASLD)的风险。方法回顾性队列研究采用基于人口的大型数据库中的索赔记录。我们纳入了年龄≥40岁且无慢性肝病病史的COPD患者。根据ICS的使用情况将患者分为两组。主要成果是MASLD的发展。此外,根据ICS暴露的持续时间和ICS的各种成分进行亚组分析。结果共纳入442,880例COPD患者,其中ICS组95,695例,非ICS组347,185例。与非ICS组相比,ICS组MASLD的发病率更高(859.3 vs 440.4 / 100000人年)。在调整了潜在的混杂因素后,ICS的使用与MASLD的风险显著增加相关(风险比[HR]=1.630, 95%可信区间[CI]= 1.560-1.704)。与其他ICS成分相比,糠酸氟替卡松显示出更高的MASLD风险,并且更长的ICS暴露时间与MASLD风险增加相关。结论慢性阻塞性肺病患者长期使用ICS可能与发生MASLD的风险增加有关。需要进一步的研究来探索降低需要ICS治疗的COPD患者发生MASLD的潜在风险的策略。
Impact of inhaled corticosteroids on metabolic dysfunction-associated steatotic liver disease risk in COPD patients
Background
The systemic impact of long-term use of inhaled corticosteroid (ICS) on the liver remains poorly understood in patients with chronic obstructive pulmonary disease (COPD). Our study aimed to identify whether long-term ICS therapy impacts the risk of Metabolic dysfunction-associated steatotic liver disease (MASLD) in patients with COPD.
Methods
A retrospective cohort study was conducted using claims records from a large population-based database. We included COPD patients ≥40 years old who had no previous history of chronic liver disease. Patients were divided into two groups based on their ICS use. The primary outcome was the development of MASLD. Additionally, subgroup analyses were conducted according to the duration of ICS exposure and the various components of ICS.
Results
A total of 442,880 COPD patients were included in the study, with 95,695 in ICS group and 347,185 in non-ICS group. The incidence rate of MASLD was higher in the ICS group compared to the non-ICS group (859.3 vs. 440.4 per 100,000 person-years). After adjusting for potential confounding factors, ICS use was associated with a significantly increased risk of MASLD (hazard ratio [HR]=1.630, 95 % confidence interval [CI]=1.560–1.704). Fluticasone furoate showed a higher risk of MASLD compared to other ICS components, and a longer duration of ICS exposure was associated with an increased MASLD risk.
Conclusions
In COPD patients, long-term use of ICS may be associated with an increased risk of developing MASLD. Further studies are needed to explore strategies to mitigate the potential risk of MASLD in COPD patients requiring ICS therapy.