Interstitial lung diseases (ILD) in common variable immunodeficiency (CVID) patients: a study from Iran.

IF 2.9 4区 医学 Q3 IMMUNOLOGY BMC Immunology Pub Date : 2024-07-16 DOI:10.1186/s12865-024-00640-0
Ghamartaj Khanbabaee, Fatemeh Khazaii, Zahra Chavoshzadeh, Mahsa Rekabi, Zahra Ghomi, Vahide Zeinali, Matin Pourghasem, Maedeh Soflaee, Mahsa Ghadrdan
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Abstract

Introduction: Interstitial lung disease (ILD) is a prevalent complication in patients with common variable immunodeficiency (CVID) and is often related to other characteristics such as bronchiectasis and autoimmunity. Because the term ILD encompasses a variety of acute and chronic pulmonary conditions, diagnosis is usually based on imaging features. Histopathology is less available. This study was conducted with the aim of investigating the ILD in patients with CVID.

Materials and methods: In this retrospective cross-sectional study, sixty CVID patients who referred to the pulmonology and immunodeficiency clinics of Mofid Children's Hospital between 2013 and 2022 were included. The diagnosis of ILD were based on transbronchial lung biopsy (TBB) or clinical and radiological symptoms. The prevalence of ILD in CVID patients was determined. Also, the CVID patients with and without ILD were compared in terms of demographic characteristics, clinical, laboratory and radiologic findings.

Results: Among all patients, ten patients had ILD (16.6%). In terms of laboratory parameters, there was a significant difference between platelets in the two groups of CVID patients with and without ILD, and the level of platelets was higher in the group of patients with ILD. Moreover, in terms of clinical symptoms, pneumonia, diarrhea and hepatomegaly were significantly different between the two groups and were statistically higher in the group of patients with ILD (P < 0.05). Autoimmunity and malignancy were not significantly different in two groups. There was a significant difference in, hyperinflation between the two groups of CVID patients with and without ILD, and the frequency of, hyperinflation was higher in the patients without ILD (P = 0.040).

Conclusion: Understanding the pathogenesis of ILD plays an essential role in revealing non-infectious pulmonary complications that occur in CVID patients. Increasing efforts to understand ILD not only shed light on its hidden pathogenesis and clinical features, but also enhance our understanding of CVID in a broader sense.

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常见可变免疫缺陷病 (CVID) 患者的间质性肺病 (ILD):伊朗的一项研究。
导言:间质性肺病(ILD)是常见变异性免疫缺陷症(CVID)患者的一种常见并发症,通常与支气管扩张和自身免疫等其他特征有关。由于 ILD 一词包含各种急性和慢性肺部疾病,因此诊断通常基于影像学特征。组织病理学检查则较少。本研究旨在调查 CVID 患者的 ILD:在这项回顾性横断面研究中,纳入了 2013 年至 2022 年期间转诊到莫菲德儿童医院肺科和免疫缺陷门诊的 60 名 CVID 患者。ILD的诊断依据是经支气管肺活检(TBB)或临床和放射学症状。确定了CVID患者中ILD的患病率。此外,还比较了有 ILD 和无 ILD 的 CVID 患者的人口统计学特征、临床、实验室和放射学检查结果:在所有患者中,10 名患者患有 ILD(16.6%)。在实验室指标方面,有 ILD 和无 ILD 两组 CVID 患者的血小板有显著差异,有 ILD 的患者血小板水平更高。此外,在临床症状方面,肺炎、腹泻和肝肿大在两组患者中存在显著差异,且有 ILD 的患者组中的肺炎、腹泻和肝肿大显著高于无 ILD 的患者组:了解 ILD 的发病机制对于揭示 CVID 患者出现的非感染性肺部并发症至关重要。加强对 ILD 的了解不仅能揭示其隐藏的发病机制和临床特征,还能从更广泛的意义上加深我们对 CVID 的了解。
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来源期刊
BMC Immunology
BMC Immunology 医学-免疫学
CiteScore
5.50
自引率
0.00%
发文量
54
审稿时长
1 months
期刊介绍: BMC Immunology is an open access journal publishing original peer-reviewed research articles in molecular, cellular, tissue-level, organismal, functional, and developmental aspects of the immune system as well as clinical studies and animal models of human diseases.
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