Evidence map›Paper›PMID 39736789›Full record

ArticleHereditas2024

Association between bone mineral density and scoliosis: a two-sample mendelian randomization study in european populations.

Fangjun Yang, Jiantao Wen

Abstract read
In one paragraph

Article in Hereditas, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

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2citing papers in PubMed
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1 · What the graph read from it

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3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

2 authors.

Fangjun YangDepartment of orthopedic, Gansu Provincial Hospital of Traditional Chinese Medicine, Lanzhou, China.
Jiantao WenDepartment of Pediatric Spine Surgery, Gansu Provincial Hospital of Traditional Chinese Medicine, Lanzhou, China. 465545037@qq.com.

Funding

.Major Project of Gansu Province Joint Scientific Research Fund .Major Project of Gansu Province Joint Scientific Research FundNatural Science Foundation of Gansu Province 22JR5 RA632
6 · The paper itself

Abstract

backgroundPrevious studies have shown that bone mineral density (BMD) has a certain impact on scoliosis. However, up to now, there is no clear evidence that there is a causal association between the two. The aim of this study is to investigate whether there is a causal association between BMD at different body positions and scoliosis by two-sample Mendelian randomization (MR).

methodsGenetic variants (SNPS) strongly associated with BMD (total body BMD (TB-BMD), lumbar spine BMD (LS-BMD), femoral neck BMD (FN-BMD), heel BMD (HE-BMD), and forearm BMD (FA-BMD)) were extracted from GEFOS and genome-wide association analysis (GWAS) databases SNPs) were used as instrumental variables (IVs). Scoliosis was also selected from the Finnish database as the outcome. Inverse variance weighting (IVW) method was used as the main analysis method, and multiple sensitivity analysis was performed by combining weighted median, MR-Egger, MR Multi-effect residuals and outliers.

resultsIVW results showed that TB-BMD (OR = 0.83, 95%CI: 0.66-1.55 P = 0.13), LS-BMD (OR = 0.72, 95%CI: 0.52-0.99, P = 0.04), FN-BMD (OR = 0.74, 95%CI: 0.50-1.09, P = 0.13), FA-BMD (OR = 0.95,95%CI: 0.70-1.28, P = 0.75), HE-BMD (OR = 0.91, 95%CI: 0.77-1.08, P = 0.29). Sensitivity analyses showed no evidence of pleiotropy or heterogeneity (p > 0.05) (MR-PRESSO and Cochrane). The results were further validated by leave-one-out test and MR-Egger intercept, which confirmed the robustness of the study results.

conclusionIn conclusion, the present study demonstrates that the causal role of genetic prediction of scoliosis increases with decreasing lumbar BMD. There was no evidence that BMD at the remaining sites has a significant causal effect on scoliosis. Our results suggest that the lumbar spine BMD should be routinely measured in the population at high risk of scoliosis. If osteoporosis occurs, appropriate treatment should be given to reduce the incidence of scoliosis. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Bone DensityGenome-Wide Association StudyMendelian Randomization AnalysisPolymorphism, Single NucleotideScoliosisEuropeFemaleGenetic Predisposition to DiseaseHumansLumbar VertebraeMaleWhite PeopleBone mineral densityCausalityMendelian randomizationScoliosis

Identifiers

PMID39736789
PMCPMC11687161

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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.