Common Variable Immunodeficiency Disorder: A Decade of Insights from a Cohort of 150 Patients in India and the Use of Machine Learning Algorithms to Predict Severity.

IF 5.7 2区 医学 Q1 IMMUNOLOGY
Umair Ahmed Bargir, Priyanka Setia, Mukesh Desai, Chandrakala S, Aparna Dalvi, Shweta Shinde, Maya Gupta, Neha Jodhawat, Amrutha Jose, Mayuri Goriwale, Reetika Malik Yadav, Disha Vedpathak, Lavina Temkar, Snehal Shabrish, Gouri Hule, Vijaya Gowri, Prasad Taur, Amita Athavale, Farah Jijina, Shobna Bhatia, Akash Shukla, Manas Kalra, Meena Sivasankaran, Sarath Balaji, Punit Jain, Sujata Sharma, Harikrishnan Gangadharan, Gaurav Narula, Ratna Sharma, Pranoti Kini, Mamta Mangalani, Abhishek Zanwar, Himanshi Chaudhary, Narendra Kumar Chaudhary, Ujjawal Khurana, Ashish Bavdekar, Girish Subramaniam, Revathi Raj, Subhaprakash Saniyal, Nitin Shah, Tehsin Petiwala, Prawin Kumar, Venkatesh Pai, Sagar Bhattad, Abhinav Sengupta, Manish Soneja, Dayanand Upase, Abhijeet Ganapule, Indrani Talukdar, Manisha Madkaikar
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引用次数: 0

Abstract

Common Variable Immunodeficiency (CVID) is a heterogeneous disorder characterized by impaired antibody production and recurrent infections. In this study we investigated the clinical and immunological features of CVID in Indian patients and develops a machine learning model for predicting disease severity. We retrospectively analyzed 150 patients diagnosed with CVID over a decade at a tertiary care center in India. The median age of diagnosis was 18 years, with a male predominance (62%). The majority of patients (66.6%) had a severe phenotype, with recurrent respiratory tract infections being the most common clinical manifestation (84.2%). Gastrointestinal complications were observed in 45% of patients, while autoimmune manifestations were seen in 21%. All patients exhibited hypogammaglobulinemia. IgA levels varied, with 7.8% normal and 14.5% undetectable. IgM levels were decreased in 85.5% of patients. B-cell analysis revealed 64.4% had reduced class-switched memory B cells, with 21.7% showing very low levels. Nine adult patients presented with late-onset combined immunodeficiency. Genetic testing, performed on 52 patients, identified underlying monogenic causes in 29 pediatric and 15 adult patients. LRBA deficiency was the most common genetic defect, found in seven pediatric and three adult patients. We developed a novel machine learning-based severity prediction model for CVID patients, utilizing readily available lymphocyte subsets, class-switched memory B cell counts, and serum immunoglobulin levels to provide an accessible and robust tool for predicting disease severity using Ameratunga's clinical severity score. Random Forest outperformed other models across all metrics, achieving an accuracy of 0.853 (95% CI: 0.840-0.866). Feature importance analysis across all models identified Th-Tc ratio, CD19, and IgM levels as the most influential predictors for severity prediction. Our study highlights the diverse clinical and immunological features of CVID in Indian patients, emphasizing the need for early diagnosis and individualized management strategies. The machine learning model developed using commonly available immune parameters provide a robust tool for predicting disease severity, potentially guiding treatment strategies to improve patient outcomes.

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常见的可变免疫缺陷障碍:来自印度150名患者队列的十年见解和使用机器学习算法预测严重程度。
常见变异性免疫缺陷(CVID)是一种异质性疾病,其特征是抗体产生受损和反复感染。在这项研究中,我们调查了印度患者CVID的临床和免疫学特征,并开发了一种预测疾病严重程度的机器学习模型。我们回顾性分析了印度一家三级医疗中心十多年来诊断为CVID的150例患者。中位诊断年龄为18岁,男性居多(62%)。大多数患者(66.6%)表型严重,以反复呼吸道感染为最常见的临床表现(84.2%)。45%的患者出现胃肠道并发症,21%的患者出现自身免疫表现。所有患者均表现为低丙种球蛋白血症。IgA水平变化,7.8%正常,14.5%检测不到。85.5%的患者IgM水平下降。B细胞分析显示,64.4%的B细胞类型转换记忆减少,21.7%的B细胞非常低。9例成人患者表现为迟发性联合免疫缺陷。对52名患者进行了基因检测,在29名儿科患者和15名成人患者中确定了潜在的单基因原因。LRBA缺乏症是最常见的遗传缺陷,在7名儿童和3名成人患者中发现。我们开发了一种新的基于机器学习的CVID患者严重程度预测模型,利用易于获得的淋巴细胞亚群、类别转换记忆B细胞计数和血清免疫球蛋白水平,为使用Ameratunga临床严重程度评分预测疾病严重程度提供了一种易于获取和强大的工具。随机森林在所有指标上都优于其他模型,达到0.853的准确率(95% CI: 0.840-0.866)。所有模型的特征重要性分析发现Th-Tc比率、CD19和IgM水平是对严重程度预测最具影响力的预测因子。我们的研究强调了印度患者CVID的不同临床和免疫学特征,强调了早期诊断和个性化管理策略的必要性。使用常用免疫参数开发的机器学习模型为预测疾病严重程度提供了强大的工具,可能指导治疗策略以改善患者的预后。
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来源期刊
CiteScore
12.20
自引率
9.90%
发文量
218
审稿时长
2 months
期刊介绍: The Journal of Clinical Immunology publishes impactful papers in the realm of human immunology, delving into the diagnosis, pathogenesis, prognosis, or treatment of human diseases. The journal places particular emphasis on primary immunodeficiencies and related diseases, encompassing inborn errors of immunity in a broad sense, their underlying genotypes, and diverse phenotypes. These phenotypes include infection, malignancy, allergy, auto-inflammation, and autoimmunity. We welcome a broad spectrum of studies in this domain, spanning genetic discovery, clinical description, immunologic assessment, diagnostic approaches, prognosis evaluation, and treatment interventions. Case reports are considered if they are genuinely original and accompanied by a concise review of the relevant medical literature, illustrating how the novel case study advances the field. The instructions to authors provide detailed guidance on the four categories of papers accepted by the journal.
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