Evidence map›Paper›PMID 40856873›Full record

ArticleJournal of clinical immunology2025

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.

Umair Ahmed Bargir, Priyanka Setia, Mukesh Desai, Chandrakala S, Aparna Dalvi, Shweta Shinde, Maya Gupta, Neha Jodhawat, Amrutha Jose, Mayuri Goriwale and 40 more

Abstract read
In one paragraph

Article in Journal of clinical immunology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 3 papers.

0numbers the graph read from it
0cells of the map it votes in
3citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

3 citing papers in PubMed.

  1. Article
  2. Article
  3. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

50 authors.

Umair Ahmed BargirICMR National Institute of Immunohaematology, Mumbai, India.
Priyanka SetiaICMR National Institute of Immunohaematology, Mumbai, India.
Mukesh DesaiBai Jerbai Wadia Hospital for Children, Mumbai, India.
Chandrakala SKing Edward Memorial Hospital and Seth G.S. Medical College, Mumbai, India.
Aparna DalviICMR National Institute of Immunohaematology, Mumbai, India.
Shweta ShindeICMR National Institute of Immunohaematology, Mumbai, India.
Maya GuptaICMR National Institute of Immunohaematology, Mumbai, India.
Neha JodhawatICMR National Institute of Immunohaematology, Mumbai, India.
Amrutha JoseICMR National Institute of Immunohaematology, Mumbai, India.
Mayuri GoriwaleICMR National Institute of Immunohaematology, Mumbai, India.
Reetika Malik YadavICMR National Institute of Immunohaematology, Mumbai, India.
Disha VedpathakICMR National Institute of Immunohaematology, Mumbai, India.
Lavina TemkarICMR National Institute of Immunohaematology, Mumbai, India.
Snehal ShabrishICMR National Institute of Immunohaematology, Mumbai, India.
Gouri HuleICMR National Institute of Immunohaematology, Mumbai, India.
Vijaya GowriBai Jerbai Wadia Hospital for Children, Mumbai, India.
Prasad TaurBai Jerbai Wadia Hospital for Children, Mumbai, India.
Amita AthavaleKing Edward Memorial Hospital and Seth G.S. Medical College, Mumbai, India.
Farah JijinaKing Edward Memorial Hospital and Seth G.S. Medical College, Mumbai, India.
Shobna BhatiaKing Edward Memorial Hospital and Seth G.S. Medical College, Mumbai, India.
Akash ShuklaKing Edward Memorial Hospital and Seth G.S. Medical College, Mumbai, India.
Manas KalraSir Ganga Ram Hospital, New Delhi, India.
Meena SivasankaranKanchi Kamakoti CHILDS Trust Hospital, Chennai, India.
Sarath BalajiMadras Medical College, Chennai, India.
Punit JainApollo Hospitals, Chennai, India.
Sujata SharmaLokmanya Tilak Municipal General Hospital and Lokmanya Tilak Municipal Medical College, Mumbai, India.
Harikrishnan GangadharanGovernment Medical College, Kottayam, Kottayam, India.
Gaurav NarulaTata Memorial Hospital, Mumbai, India.
Ratna SharmaMCGM - Comprehensive Thalassemia Care, Mumbai, India.
Pranoti KiniMCGM - Comprehensive Thalassemia Care, Mumbai, India.
Mamta MangalaniMCGM - Comprehensive Thalassemia Care, Mumbai, India.
Abhishek ZanwarRuby Hall Clinic, Pune, India.
Himanshi ChaudharyRuby Hall Clinic, Pune, India.
Narendra Kumar ChaudharyAll India Institute of Medical Sciences Bhopal, Bhopal, India.
Ujjawal KhuranaAll India Institute of Medical Sciences Bhopal, Bhopal, India.
Ashish BavdekarKing Edward Memorial Hospital Research Centre, Pune, India.
Girish SubramaniamColours hospital, Nagpur, India.
Revathi RajApollo Hospitals Cancer Center, Chennai, India.
Subhaprakash SaniyalFortis Hospital, Noida, India.
Nitin ShahP. D. Hinduja Hospital and Medical Research Centre, Mumbai, India.
Tehsin PetiwalaMasina Hospital, Mumbai, India.
Prawin KumarAll India Institute of Medical Sciences Jodhpur, Jodhpur, India.
Venkatesh PaiAll India Institute of Medical Sciences Rishikesh, Rishikesh, India.
Sagar BhattadAster CMI Hospital, Bangalore, India.
Abhinav SenguptaAll India Institute of Medical Sciences, New Delhi, India.
Manish SonejaAll India Institute of Medical Sciences, New Delhi, India.
Dayanand UpaseSassoon General Hospital, Pune, India.
Abhijeet GanapuleNiche Haematology Care, Kolhapur, India.
Indrani TalukdarBirla Institute of Technology and Science, Pilani - Goa Campus, Sancoale, India.
Manisha MadkaikarICMR National Institute of Immunohaematology, Mumbai, India. madkaikarmanisha@gmail.com.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

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.

Indexed as

Common Variable ImmunodeficiencyMachine LearningAdolescentAdultAlgorithmsB-LymphocytesChildChild, PreschoolFemaleHumansIndiaMaleMiddle AgedRetrospective StudiesSeverity of Illness IndexYoung AdultClass switched memory B cellsCVIDIEIMachine learning

Identifiers

PMID40856873
PMCPMC12380919

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.