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Spine (Phila Pa 1976). 2018 Feb 1;43(3):172-178. doi: 10.1097/BRS.0000000000002280.

A Replication Study for Association of LBX1 Locus With Adolescent Idiopathic Scoliosis in French-Canadian Population.

Author information

1
Viscogliosi Laboratory in Molecular Genetics of Musculoskeletal Diseases, Sainte-Justine, University Hospital, Research Center, Montreal, QC, Canada.
2
Program of Biomedical Sciences, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada.
3
Sainte-Justine University Hospital Research Center, Montreal, QC, Canada.
4
Department of Medicine, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada.
5
Department of Biochemistry and Molecular Medicine, Faculty of Medicine, Université de Montréal, Montreal, QC, Canada.
6
Department of Stomatology, Faculty of Dentistry, Université de Montréal, Montreal, QC, Canada.

Abstract

STUDY DESIGN:

A case-control association study.

OBJECTIVES:

To investigate the relationship between LBX1 (lady bird homeobox1) polymorphisms and adolescent idiopathic scoliosis (AIS) in French-Canadian population.

SUMMARY OF BACKGROUND DATA:

It is widely accepted that genetic factors contribute to AIS. Although the LBX1 locus is so far the most successfully replicated locus in different AIS cohorts, these associations were replicated mainly in Asian populations, with few studies in Caucasian populations of European descent.

METHODS:

We recruited 1568 participants (667 AIS patients and 901 healthy controls) in the French-Canadian population. Genomic data were generated using the Illumina Human Omni 2.5M BeadChip. An additional 121 AIS cases and 51 controls were genotyped for specific single-nucleotide polymorphisms (SNPs) by multiplex polymerase chain reaction using standard procedures. BEAGLE 3 was used to impute the following markers: rs7893223, rs11190878, and rs678741 against the 1000-genomes European cohort phased genotypes given that they were absent in our genome wide association studies (GWAS) panel. Resulting genotypes were combined then used for single marker and haplotyped-based association.

RESULTS:

Four markers showed association with AIS in our cohort at this locus; rs11190870 the most studied marker, rs7893223, rs594791, and rs11190878. When we restricted the analysis to severe cases only, four additional SNPs showed associations: rs11598177, rs1322331, rs670206, and rs678741. In addition, we analyzed the associations of the observed haplotypes and dihaplotypes formed by these SNPs. The haplotype TTAAGAAA and its homozygous dihaplotype showed the highest association with our severe group and was the highest risk haplotype. The haplotype CCGCAGGG was significantly more associated with the control group, and its homozygous or heterozygous dihaplotype was less frequent in the severe group compared with the control group, suggesting that CCGCAGGG may represent a protective haplotype.

CONCLUSION:

We have replicated the association of the LBX1 locus with AIS in French-Canadian population, a novel European descent cohort, which is known for its unique genetic architecture.

LEVEL OF EVIDENCE:

3.

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