Evidence map›Paper›PMID 40943538›Full record

ArticleInternational journal of molecular sciences2025

The Presence of Risk and Protective HLA-DQ Haplotype Combinations and PLA2R1 Risk SNP in Hungarian Patients with Membranous Nephropathy.

Dóra Bajcsi, Zoltán Maróti, Emőke Endreffy, Péter Légrády, György Ábrahám, Béla Iványi

Abstract read
In one paragraph

Article in International journal of molecular sciences, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

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

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Review
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Dóra BajcsiDepartment of Internal Medicine, Albert Szent-Györgyi Medical Centre, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
Zoltán MarótiDepartment of Pediatrics, Albert Szent-Györgyi Medical Centre, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary.ORCID 0000-0002-0515-117X
Emőke EndreffyDepartment of Pediatrics, Albert Szent-Györgyi Medical Centre, Albert Szent-Györgyi Medical School, University of Szeged, 6720 Szeged, Hungary.
Péter LégrádyDepartment of Internal Medicine, Albert Szent-Györgyi Medical Centre, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
György ÁbrahámDepartment of Internal Medicine, Albert Szent-Györgyi Medical Centre, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.
Béla IványiDepartment of Pathology, Albert Szent-Györgyi Medical Centre, Albert Szent-Györgyi Medical School, University of Szeged, 6725 Szeged, Hungary.ORCID 0000-0003-4546-6253

Funding

Hungarian Society of Nephrology MANET-2012 research grantThe project was supported by the European Union and co-financed by the European Social Fund and the Hungarian State within the framework of the Social Renewal Operational Programme (TÁMOP) TÁMOP 4.2.2.A-11/1/KONV-2012-0035
6 · The paper itself

Abstract

With primary membranous nephropathy (pMN), the genetic background is not precisely known. Certain HLA-DQ serotypes however like HLA-DQ 2.5, and single-nucleotide polymorphisms (SNPs) in the phospholipase A2 receptor 1 (PLA2R1) gene pose a risk for the development of pMN. As antigen presentation is linked to a 3-dimensional conformation of the HLA-DQA/DQB dimer, we thought that the specific HLA-DQ haplotype combinations might also be risk factors in the evolution of MN. The HLA-DQ haplotype combinations and the PLA2R1 gene risk variant (rs4664308) genotypes were examined in 67 patients with MN (52 primary, 15 secondary [sMN]) and 77 controls. Based on the presence or absence of PLA2R1 risk alleles, we used a scoring system to assess the risk and to identify protective HLA-DQ haplotype combinations. The HLA-DQ 2.5 serotype was significantly enriched in both pMN and sMN patients compared to the controls. The pMN group had a significantly higher frequency of the PLA2R1 risk allele compared to the sMN group and the controls. HLA-DQ 2.5 appeared to carry the highest risk for the development of pMN, while HLA-DQ 7.5 and 6.2 seemed to be protective. Our results indicate that the HLA-DQ 2.5 probably carries the highest risk in both pMN and sMN, suggesting that this serotype has less specificity for antigens, and it induces an autoimmune response. Here, PLA2R1 played a role in the development of pMN but not in sMN.

Indexed as

Genetic Predisposition to DiseaseGlomerulonephritis, MembranousHaplotypesHLA-DQ AntigensPolymorphism, Single NucleotideReceptors, Phospholipase A2AdultAgedAllelesCase-Control StudiesFemaleGene FrequencyGenotypeHumansMaleMiddle AgedHLA-DQ AntigensPLA2R1 protein, humanReceptors, Phospholipase A2HLA-DQA/DQB haplotypesPLA2R1primary membranous nephropathyprotective haplotyperisk haplotypesecondary membranous nephropathy

Identifiers

PMID40943538
PMCPMC12429780

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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.