Uncovering Risk Factors of Premature Mortality in Common Variable Immunodeficiency

IF 6.6 1区 医学 Q1 ALLERGY Journal of Allergy and Clinical Immunology-In Practice Pub Date : 2025-05-01 Epub Date: 2025-03-14 DOI:10.1016/j.jaip.2025.03.009
Patrick Bez MD , Bas Smits MD , Christoph Geier MD , Aleksandra Hirsch MD , Andrés Caballero de Oyteza PhD , Michele Proietti MD, PhD , Bodo Grimbacher MD , Martin Wolkewitz PhD , Sigune Goldacker MD , Klaus Warnatz MD
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Abstract

Background

Among patients with common variable immunodeficiency (CVID), patients with complications of immune dysregulation (CVIDc) have higher mortality rates than those with infection-only presentation (CVIDio). Therefore, identifying predictive markers of premature mortality among patients with CVIDc is crucial.

Objective

The purpose of this retrospective exploratory study was to describe the mortality in a large tertiary referral center and compare the clinical and laboratory characteristics of patients with CVIDc who died prematurely with a group of matched living CVIDc control patients to identify potential indicators of premature death.

Methods

The study included patients diagnosed with CVID according to European Society for Immunodeficiencies criteria and active follow-up. In a case-control analysis, we identified patients who died before the age of 70 years as cases and then randomly selected controls who were matched for sex, age, and CVID phenotype.

Results

We were able to confirm the poor prognosis of CVIDc compared with CVIDio in 497 patients, including 57 who had died. The most common causes of death were infections and neoplasia. The exploratory case-control analysis of 37 cases and 73 controls suggests that cases had a higher prevalence of severe enteropathy, hepatopathy, and neoplasia than controls 3 years before death. This was associated with a higher frequency of lymphopenia, thrombocytopenia, and liver enzyme elevation.

Conclusions

Hepatopathy and severe enteropathy need to be confirmed in a multicenter, prospective study as the most relevant factors associated with premature mortality in patients with CVIDc. Their early evaluation will hopefully allow for better and possibly more definitive treatment options.
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揭示共同可变免疫缺陷(CVID)患者过早死亡的危险因素。
背景:在常见变异性免疫缺陷(CVID)患者中,伴有免疫失调(CVIDc)并发症的患者死亡率高于单纯感染(CVIDio)患者。因此,确定CVIDc患者过早死亡的预测指标至关重要。目的:本回顾性探索性研究的目的是描述大型三级转诊中心的死亡率,并比较过早死亡的CVIDc患者与一组匹配的CVIDc对照患者的临床和实验室特征,以确定过早死亡的潜在指标。方法:纳入符合ESID诊断标准的CVID患者,并进行积极随访。在病例对照分析中,我们将70岁前死亡的患者作为病例,然后随机选择性别、年龄和CVID表型相匹配的对照组。结果:在497例患者中,我们能够确认CVIDc与CVIDio相比预后较差,其中57例死亡。最常见的死亡原因是感染和肿瘤。37例病例和73例对照的探索性病例-对照分析表明,与死亡前3年的对照组相比,这些病例有更高的严重肠病、肝病和肿瘤的患病率。这与淋巴细胞减少、血小板减少和肝酶升高的频率较高有关。结论:肝病和严重肠病是与CVIDc患者过早死亡最相关的因素,需要在多中心前瞻性研究中得到证实。他们的早期评估有望提供更好的、可能更明确的治疗方案。
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来源期刊
CiteScore
11.10
自引率
9.60%
发文量
683
审稿时长
50 days
期刊介绍: JACI: In Practice is an official publication of the American Academy of Allergy, Asthma & Immunology (AAAAI). It is a companion title to The Journal of Allergy and Clinical Immunology, and it aims to provide timely clinical papers, case reports, and management recommendations to clinical allergists and other physicians dealing with allergic and immunologic diseases in their practice. The mission of JACI: In Practice is to offer valid and impactful information that supports evidence-based clinical decisions in the diagnosis and management of asthma, allergies, immunologic conditions, and related diseases. This journal publishes articles on various conditions treated by allergist-immunologists, including food allergy, respiratory disorders (such as asthma, rhinitis, nasal polyps, sinusitis, cough, ABPA, and hypersensitivity pneumonitis), drug allergy, insect sting allergy, anaphylaxis, dermatologic disorders (such as atopic dermatitis, contact dermatitis, urticaria, angioedema, and HAE), immunodeficiency, autoinflammatory syndromes, eosinophilic disorders, and mast cell disorders. The focus of the journal is on providing cutting-edge clinical information that practitioners can use in their everyday practice or to acquire new knowledge and skills for the benefit of their patients. However, mechanistic or translational studies without immediate or near future clinical relevance, as well as animal studies, are not within the scope of the journal.
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