Evidence map›Paper›PMID 38458775›Full record

SynthesisLupus science & medicine2024

Association of genetic variation on X chromosome with systemic lupus erythematosus in both Thai and Chinese populations.

Pattarin Tangtanatakul, Yao Lei, Krisana Jaiwan, Wanling Yang, Manon Boonbangyang, Punna Kunhapan, Pimpayao Sodsai, Surakameth Mahasirimongkol, Prapaporn Pisitkun, Yi Yang and 6 more

Open access · goldAbstract readMeta-Analysis
In one paragraph

Synthesis in Lupus science & medicine, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
2.4field-weighted citation impact, top 13% 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

4 citing papers in PubMed, 5 citations in OpenAlex.

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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

16 authors at 7 institutions in 3 countries.

Pattarin Tangtanatakul *Department of Transfusion Medicine and Clinical Microbiology, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand.ORCID 0000-0001-8978-6916
Yao Lei *Department of Paediatrics and Adolescent Medicine, Hong Kong University, Hong Kong, People's Republic of China.
Krisana JaiwanMaster of Sciences Program in Molecular Science of Medical Microbiology and Immunology, Faculty of Allied Health Sciences, Chulalongkorn University, Bangkok, Thailand.
Wanling YangDepartment of Paediatrics and Adolescent Medicine, Hong Kong University, Hong Kong, People's Republic of China.ORCID 0000-0003-0063-6327
Manon BoonbangyangNational Biobank of Thailand (NBT), National Science and Technology Development Agency, Khlong Luang, Pathum Thani, Thailand.
Punna KunhapanDepartment of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand.
Pimpayao SodsaiCentre of Excellent in Immunology and Immune-Mediated Diseases, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.
Surakameth MahasirimongkolDepartment of Medical Sciences, Ministry of Public Health, Nonthaburi, Thailand.
Prapaporn PisitkunDivision of Allergy, Immunology, and Rheumatology, Department of Medicine, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand.
Yi YangDepartment of Nephrology, Fourth Affiliated Hospital, International Institutes of Medicine, Zhejiang University School of Medicine, Hangzhou, Zhejiang, China.
Jakris Eu-AhsunthornwattanaDepartment of Community Medicine, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand.
Wichai AekplakornDepartment of Community Medicine, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand.
Natini JinawathProgram in Translational Medicine, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand.
Nareemarn NeelapaichitRamathibodi School of Nursing, Mahidol University Faculty of Medicine Ramathibodi Hospital, Bangkok, Thailand.
Nattiya HirankarnCentre of Excellent in Immunology and Immune-Mediated Diseases, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand.ORCID 0000-0003-2224-6856
Yong-Fei WangWarshel Institute for Computational Biology, The Chinese University of Hong Kong, Shenzhen, Guangdong, People's Republic of China yfwang@cuhk.edu.cn.ORCID 0000-0002-1260-6291
Mahidol University · THChulalongkorn University · THMinistry of Public Health · THUniversity of Hong Kong · HKChinese University of Hong Kong, Shenzhen · CNNational Science and Technology Development Agency · THZhejiang University · CN

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesX chromosome has been considered as a risk factor for SLE, which is a prototype of autoimmune diseases with a significant sex difference (female:male ratio is around 9:1). Our study aimed at exploring the association of genetic variants in X chromosome and investigating the influence of trisomy X in the development of SLE.

methodsX chromosome-wide association studies were conducted using data from both Thai (835 patients with SLE and 2995 controls) and Chinese populations (1604 patients with SLE and 3324 controls). Association analyses were performed separately in females and males, followed by a meta-analysis of the sex-specific results. In addition, the dosage of X chromosome in females with SLE were also examined.

resultsOur analyses replicated the association of

conclusionOur study confirmed previous SLE associations in X chromosome, and identified two loci suggestively associated with SLE. More importantly, our study indicated a higher risk of SLE for females with trisomy X.

Indexed as

Lupus Erythematosus, SystemicSex Chromosome Disorders of Sex DevelopmentTrisomyChinaChromosomes, Human, XFemaleGenetic Predisposition to DiseaseHumansMaleMembrane ProteinsSex Chromosome AberrationsThailandMembrane ProteinsTMEM187 protein, humanautoimmune diseaseslupus erythematosus, systemicpolymorphism, genetic

Identifiers

PMID38458775
PMCPMC10928741
OpenAlexW4392767123

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC
Read underepoch 390

Registered trials

None linked

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.