Evidence map›Paper›PMID 35939175›Full record

ArticleClinical and experimental medicine2023

Genetic polymorphisms and decreased protein expression of ABCG2 urate transporters are associated with susceptibility to gout, disease severity and renal-overload hyperuricemia.

Márton Pálinkás, Edit Szabó, Anna Kulin, Orsolya Mózner, Rita Rásonyi, Péter Juhász, Krisztina Nagy, György Várady, Dóra Vörös, Boglárka Zámbó and 2 more

Open access · hybridAbstract read
In one paragraph

Article in Clinical and experimental medicine, 2023. 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
1.2field-weighted citation impact, top 23% of its field
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, 8 citations in OpenAlex.

  1. Genetic Variants of the Human Thiamine Transporter (International journal of molecular sciences · 2025
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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

12 authors at 2 institutions in 1 country.

Márton PálinkásNational Institute of Locomotor Diseases and Disabilities, Frankel Leo str. 38-40, 1023, Budapest, Hungary. mrpalinkas@gmail.com.ORCID https://orcid.org/0000-0002-9853-3117
Edit SzabóInstitute of Enzymology, Research Centre for Natural Sciences, Budapest, Hungary.ORCID https://orcid.org/0000-0002-0150-0926
Anna KulinDoctoral School of Molecular Medicine, Semmelweis University, Budapest, Hungary.ORCID https://orcid.org/0000-0002-2877-5831
Orsolya MóznerDoctoral School of Molecular Medicine, Semmelweis University, Budapest, Hungary.
Rita RásonyiNational Institute of Locomotor Diseases and Disabilities, Frankel Leo str. 38-40, 1023, Budapest, Hungary.
Péter JuhászNational Institute of Locomotor Diseases and Disabilities, Frankel Leo str. 38-40, 1023, Budapest, Hungary.
Krisztina NagyNational Institute of Locomotor Diseases and Disabilities, Frankel Leo str. 38-40, 1023, Budapest, Hungary.
György VáradyInstitute of Enzymology, Research Centre for Natural Sciences, Budapest, Hungary.ORCID https://orcid.org/0000-0003-2012-9680
Dóra VörösNational Institute of Locomotor Diseases and Disabilities, Frankel Leo str. 38-40, 1023, Budapest, Hungary.
Boglárka ZámbóInstitute of Enzymology, Research Centre for Natural Sciences, Budapest, Hungary.
Balázs SarkadiInstitute of Enzymology, Research Centre for Natural Sciences, Budapest, Hungary.ORCID https://orcid.org/0000-0003-0592-4539
Gyula PoórNational Institute of Locomotor Diseases and Disabilities, Frankel Leo str. 38-40, 1023, Budapest, Hungary. poor.gyula@orfi.hu.
Institute of Molecular Life Sciences · HUSemmelweis University · HU

Funding

Hungarian National Development and Innovation Office FIEK_16-1-2016-0005Hungarian National Development and Innovation Office NKFIH K-128011KDP doctoral scholarship from the Ministry for Innovation and Technology National Research, Development and Innovation FundPredoctoral Fellowship Grant of Semmelweis University EFOP-3.6.3.-VEKOP-16-2017-00009
6 · The paper itself

Abstract

Gout is a common crystal induced disease of high personal and social burden, characterised by severe arthritis and comorbidity if untreated. Impaired function of ABCG2 transporter is causative in gout and may be responsible for renal-overload type hyperuricemia. Despite its importance, there is limited information on how clinical parameters correlate with protein expression and that with genetic changes. Urate and clinical parameters of 78 gouty patients and healthy controls were measured among standardised circumstances from a Hungarian population. ABCG2 membrane expression of red blood cells was determined by flow cytometry-based method and SNPs of this protein were analysed by TaqMan-based qPCR. The prevalence of ABCG2 functional polymorphisms in gouty and control patients were 32.1 and 13.7%, respectively. Most common SNP was Q141K while one sample with R236X, R383C and the lately described M71V were found in the gouty population. These polymorphisms showed strong linkage with decreased protein expression while the latter was also associated with higher fractional urate excretion (FUE) and urinary urate excretion (UUE). This study firstly evaluated ABCG2 protein expression in a clinically defined gouty population while also proving its associations between ABCG2 genetic changes and renal-overload hyperuricemia. The paper also highlighted relations between ABCG2 SNPs, gout susceptibility and disease severity characterised by an early onset disease with frequent flares and tophi formation.

Indexed as

GoutHyperuricemiaATP Binding Cassette Transporter, Subfamily G, Member 2HumansNeoplasm ProteinsPatient AcuityPolymorphism, Single NucleotideUric AcidABCG2 protein, humanATP Binding Cassette Transporter, Subfamily G, Member 2Neoplasm ProteinsUric AcidABCG2 transportersGeneticsGout severityProtein expressionRenal-overload hyperuricemia

Identifiers

PMID35939175
PMCPMC10390358
OpenAlexW4290723003

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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.