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Evaluating the impact of type 2 diabetes mellitus on interstitial lung disease prevalence in patients with systemic lupus erythematosus: A national inpatient sample analysis

医学 内科学 间质性肺病 2型糖尿病 特发性肺纤维化 队列 回顾性队列研究 糖尿病 倾向得分匹配 内分泌学
作者
Fares Saliba,Georges Khattar,Omar Mourad,Laurence Aoun,Elie Bou Sanayeh,Fatema Arafa,Ibrahim Al Saidi,Erica Abidor,Michel Al Achkar,Taqi A Rizvi,KOUSHIK V SANGARAJU,Gaetano Di Pietro,Fadi Haddadin,Shaza Almardini,Khalil El Gharib,Halim El-Hage
出处
期刊:Lupus [SAGE Publishing]
标识
DOI:10.1177/09612033241292162
摘要

Background Systemic lupus erythematosus (SLE) increases the risk of interstitial lung disease (ILD). SLE is also linked to an elevated risk of type 2 diabetes mellitus (T2DM). However, the impact of T2DM on ILD risk in patients with SLE is still unclear. This study aimed to compare the prevalence of ILD in patients with SLE based on the presence of T2DM (SLE + T2DM+) or its absence (SLE + T2DM−). Methods This was a retrospective cohort study using the 2019–2020 National Inpatient Sample database. Adult SLE patients were identified and stratified by T2DM status. Comparable cohorts were created using propensity score matching, resulting in 10,532 patients in each cohort. Multivariate logistic regression assessed the association between T2DM and ILD. Results T2DM was associated with a lower prevalence of ILD in patients with SLE (OR 0.798, 95% CI: 0.695–0.918, p = .002), occurring in 371 (3.5%) patients with T2DM compared to 463 (4.4%) patients without T2DM. Specifically, this difference was mainly driven by pulmonary fibrosis, which was significantly less frequent in the T2DM group (1.3% vs 1.8%, OR 0.7, 95% CI: 0.560–0.875, p = .002). No differences were found in secondary outcomes, including death rates, length of hospital stay, ARDS, pneumothorax, pleural effusion, or pulmonary arterial hypertension. Conclusion Our study suggests that T2DM significantly reduced ILD risk in patients with SLE, specifically diminishing pulmonary fibrosis prevalence. Further research should explore mechanisms for this protective association between T2DM and ILD development in SLE. These findings may guide management strategies for this vulnerable population.

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