Evidence map›Paper›PMID 39113043›Full record

ArticleJournal of orthopaedic surgery and research2024

Two genetic variants in the HIBCH and FTCDNL1 genes are associated with susceptibility to developmental dysplasia of the hips among the Han Chinese population of Southwest China.

Xu-Han Meng, Yu-Ting Weng, Yu Rao, Yong-Qing Xu, Hao Sun, Chuan Li

Abstract read
In one paragraph

Article in Journal of orthopaedic surgery and research, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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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

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. [Study on Salter osteotomy combined with subtrochanteric shortening and derotational osteotomy in treatment of Tönnis typeZhongguo xiu fu chong jian wai ke za zhi = Zhongguo xiufu chongjian waike zazhi = Chinese journal of reparative and reconstructive surgery · 2025
    Article
4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Xu-Han Meng *Department of Orthopaedic, 920th Hospital of Joint Logistics Support Force of Chinese People's Liberation Army, 212 Daguan Road, Xishan District, Kunming, 650032, Yunnan, China.
Yu-Ting Weng *Department of Urology, Enze Hospital, Taizhou Enze Medical Center (Group), Taizhou Hospital of Zhejiang Province Affiliated to Wenzhou Medical University, Affiliate to Hangzhou Medical College, Taizhou, 318000, Zhejiang, China.
Yu RaoDepartment of Orthopaedic, 920th Hospital of Joint Logistics Support Force of Chinese People's Liberation Army, 212 Daguan Road, Xishan District, Kunming, 650032, Yunnan, China.
Yong-Qing XuDepartment of Orthopaedic, 920th Hospital of Joint Logistics Support Force of Chinese People's Liberation Army, 212 Daguan Road, Xishan District, Kunming, 650032, Yunnan, China.
Hao SunThe Department of Medical Genetics, Institute of Medical Biology, Chinese Academy of Medical Sciences & Peking Union Medical College, 935 Jiaoling Road, Kunming, 650118, Yunnan, China. sunhao@imbcams.com.cn.
Chuan LiDepartment of Orthopaedic, 920th Hospital of Joint Logistics Support Force of Chinese People's Liberation Army, 212 Daguan Road, Xishan District, Kunming, 650032, Yunnan, China. lichuankaka@163.com.

Funding

CAMS Innovation Fund for Medical Sciences CIFMS, 2021-I2M-1-024Yunnan Major Science and Technology Project - Biomedical Major Project 2018ZF008Yunnan Provincial Health Commission Clinical Center Construction Major Project ZX20191001Yunnan Science and Technology talents and platform Project 202005AC160011Yunnan Training Programme for the advanced Talents of Health and Medical Technology D-2018013
6 · The paper itself

Abstract

backgroundDevelopmental dysplasia of the hip (DDH) is a common cause of childhood disability, and the incidence of DDH shows significant familial aggregation. As the genetic factors of DDH remain unknown, the correlation between five candidate single nucleotide polymorphisms (SNPs) and DDH was evaluated in the Han Chinese population of Southwest China.

methodsA case‒control association study was conducted in 276 patients with DDH and 318 healthy controls. SNP genotyping in the case and control groups was performed by SNPshot and multiple PCR. SNPs were genotyped in the case and control groups by multiplex PCR. The relationship between DDH and candidate SNPs was evaluated using the χ2 test.

resultsThe genotype distributions of rs291412 in HIBCH and rs769956 in FTCDNL1 were different between the case and control groups (P < 0.05). After genetic model analysis, logistic regression analysis revealed that the C allele of rs291412 had a protective effect on DDH (OR = 0.605, P = 0.010) and that the G allele of rs769956 was a risk factor (OR = 2.939, P = 0.010).s.

conclusionThese SNPs could be associated with susceptibility to DDH but larger population-based studies should confirm the current results.

Indexed as

Developmental Dysplasia of the HipGenetic Predisposition to DiseaseHydroxymethyl and Formyl TransferasesThiolester HydrolasesCase-Control StudiesChild, PreschoolChinaEast Asian PeopleFemaleGenetic Association StudiesGenotypeHip Dislocation, CongenitalHumansInfantMalePolymorphism, Single Nucleotide3-hydroxyisobutyryl-CoA hydrolaseFTCDNL1 protein, humanHydroxymethyl and Formyl TransferasesThiolester HydrolasesDevelopmental dysplasia of the hipFTCDNL1HIBCHSingle-nucleotide polymorphismSusceptibility

Identifiers

PMID39113043
PMCPMC11304665

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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.