Literature DB >> 35171366

Retrospective study of 98 patients with X-linked agammaglobulinemia complicated with arthritis.

Ran Qing-Qi1, Li Ya-Wen1, Chen Huan1, Zhang Yu1,2,3,4,5, An Yun-Fei1,2,3,4,5, Tang Xue-Mei1,2,3,4,5, Zhao Xiao-Dong2,3,4,5,6, Zhang Zhi-Yong7,8,9,10,11.   

Abstract

OBJECTIVE: We preformed this retrospective study of clinical manifestation, imaging feature, and mutations to describe joint involvement in X-linked agammaglobulinemia (XLA) patients, aimed to provide recommendation for physicians.
METHODS: A total number of 98 XLA patients who have been diagnosed between January 2000 and February 2020 were enrolled and grouped based on whether they developed arthritis and analyzed for the clinical, imaging, and gene mutation data using the t test or the Mann-Whitney test.
RESULTS: Forty-five out of 98 patients (45.9%) had joint involvement, 40.8% had symptom prior to the diagnosis of XLA, and 54.1% had no articular symptom. Patients with joint involvement had a higher median diagnostic age of XLA and initial IgG level than patients without it, while their intravenous immunoglobulin was lower (p < 0.05). Knee, hip, and ankle were the most frequent joint, and oligoarthritis (≦ 4 joints) was more common than polyarthritis (88.9% vs 11.1%). Red and tenderness were the most frequent clinical symptoms (80%) with 24.4% reporting limited activity and 8.9% reporting deformity. Imaging data collected from 32 patients indicated that joint effusion (53.3%), synovitis (15.5%), and swollen soft tissue (15.5%) were the most common feature. Seventeen patients were treated by antibiotics plus intravenous immunoglobulin (IVIG) with an effective rate of 70.6%, and 28 patients only received IVIG with an effective rate of 67.9%. In comparison to patients without arthritis who have higher frequency nonsense and frameshift mutation, patients with arthritis had a higher incidence of missense mutation (p < 0.05).
CONCLUSION: High prevalence of arthritis among X-linked agammaglobulinemia patients and subsequent progression through IVIG replacement therapy highlight the importance of timely diagnosis and better management of these patients. Our finding indicated a potential correlation between genotype and phenotype, and further research on the mechanism of arthritis in XLA patients could increase physicians' awareness and improve patients' prognosis. Key Points • This study described the feature of arthritis in XLA patients and indicated a potential correlation between this complication and genotype.
© 2022. International League of Associations for Rheumatology (ILAR).

Entities:  

Keywords:  Arthritis; Gene mutation; Intravenous immunoglobulin; X-linked agammaglobulinemia

Mesh:

Substances:

Year:  2022        PMID: 35171366     DOI: 10.1007/s10067-022-06095-1

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   3.650


  37 in total

Review 1.  Classification of childhood arthritis.

Authors:  Michaël Hofer; Taunton R Southwood
Journal:  Best Pract Res Clin Rheumatol       Date:  2002-07       Impact factor: 4.098

2.  Development and preliminary validation of a paediatric-targeted MRI scoring system for the assessment of disease activity and damage in juvenile idiopathic arthritis.

Authors:  Clara Malattia; Maria Beatrice Damasio; Angela Pistorio; Maka Ioseliani; Iris Vilca; Maura Valle; Nicolino Ruperto; Stefania Viola; Antonella Buoncompagni; Gian Michele Magnano; Angelo Ravelli; Paolo Tomà; Alberto Martini
Journal:  Ann Rheum Dis       Date:  2010-11-24       Impact factor: 19.103

3.  A genotype-phenotype correlation study in a group of 54 patients with X-linked agammaglobulinemia.

Authors:  Eduardo López-Granados; Rebeca Pérez de Diego; Antonio Ferreira Cerdán; Gumersindo Fontán Casariego; Maria Cruz García Rodríguez
Journal:  J Allergy Clin Immunol       Date:  2005-09       Impact factor: 10.793

Review 4.  Bruton's tyrosine kinase: cell biology, sequence conservation, mutation spectrum, siRNA modifications, and expression profiling.

Authors:  Jessica M Lindvall; K Emelie M Blomberg; Jouni Väliaho; Leonardo Vargas; Juhana E Heinonen; Anna Berglöf; Abdalla J Mohamed; Beston F Nore; Mauno Vihinen; C I Edvard Smith
Journal:  Immunol Rev       Date:  2005-02       Impact factor: 12.988

5.  Clinical and mutational characteristics of X-linked agammaglobulinemia and its carrier identified by flow cytometric assessment combined with genetic analysis.

Authors:  H Kanegane; T Futatani; Y Wang; K Nomura; K Shinozaki; H Matsukura; T Kubota; S Tsukada; T Miyawaki
Journal:  J Allergy Clin Immunol       Date:  2001-12       Impact factor: 10.793

6.  The European Society for Immunodeficiencies (ESID) Registry Working Definitions for the Clinical Diagnosis of Inborn Errors of Immunity.

Authors:  Markus G Seidel; Gerhard Kindle; Benjamin Gathmann; Isabella Quinti; Matthew Buckland; Joris van Montfrans; Raphael Scheible; Stephan Rusch; Lukas M Gasteiger; Bodo Grimbacher; Nizar Mahlaoui; Stephan Ehl
Journal:  J Allergy Clin Immunol Pract       Date:  2019-02-15

7.  Hypogammaglobulinemia and rheumatic disease.

Authors:  A H Lee; A I Levinson; H R Schumacher
Journal:  Semin Arthritis Rheum       Date:  1993-02       Impact factor: 5.532

Review 8.  B-cell antigen-receptor signalling in lymphocyte development.

Authors:  Leo D Wang; Marcus R Clark
Journal:  Immunology       Date:  2003-12       Impact factor: 7.397

9.  Deficient expression of a B cell cytoplasmic tyrosine kinase in human X-linked agammaglobulinemia.

Authors:  S Tsukada; D C Saffran; D J Rawlings; O Parolini; R C Allen; I Klisak; R S Sparkes; H Kubagawa; T Mohandas; S Quan
Journal:  Cell       Date:  1993-01-29       Impact factor: 41.582

10.  Primary immunodeficiency diseases: an update on the classification from the international union of immunological societies expert committee for primary immunodeficiency.

Authors:  Waleed Al-Herz; Aziz Bousfiha; Jean-Laurent Casanova; Helen Chapel; Mary Ellen Conley; Charlotte Cunningham-Rundles; Amos Etzioni; Alain Fischer; Jose Luis Franco; Raif S Geha; Lennart Hammarström; Shigeaki Nonoyama; Luigi Daniele Notarangelo; Hans Dieter Ochs; Jennifer M Puck; Chaim M Roifman; Reinhard Seger; Mimi L K Tang
Journal:  Front Immunol       Date:  2011-11-08       Impact factor: 7.561

View more

北京卡尤迪生物科技股份有限公司 © 2022-2023.