Nature CommunicationsGenetic & Genomic MedicinePeer-reviewed journal article
Genome-wide meta-analysis conducted in three large biobanks expands the genetic landscape of lumbar disc herniations
Ville SaloiD, Juhani H. MäättäiD, Eeva SliziD, FinnGeniD, Aarno V. PalotieiD, Mark J. DalyiD, Bridget Riley-Gills, Howard J. JacobiD, Dirk S. PauliD, Slavé PetrovskiiD, Heiko RunziD, Sally John, George Okafo, Nathan LawlessiD, Heli Salminen‐Mankonen, Robert M. PlengeiD, Joseph MaranvilleiD, Mark McCarthy, Margaret G. EhmiD, Kirsi Auro, Simonne Longerich, Anders MälarstigiD, Katherine Klinger, Clément ChatelainiD, Matthias Gossel, , Jukka T. KoskelaiD
- Citations
- 14
- FWCI
- 1.04
- Field percentile
- top 27%
Abstract
Introductory paragraphGiven that lumbar disc herniation (LDH) is a prevalent spinal condition that causes significant individual suffering and societal costs1, the genetic basis of LDH has received relatively little research. Our aim was to increase understanding of the genetic factors influencing LDH. We performed a genome-wide association analysis (GWAS) of LDH in the FinnGen project and in Estonian and UK biobanks, followed by a genome-wide meta-analysis to combine the results. In the meta-analysis, we identified 41 loci that have not been associated with LDH in prior studies on top of the 23 known risk loci. We detected LDH-associated loci in the vicinity of genes related to inflammation, disc-related structures, and synaptic transmission. Overall, our research contributes to a deeper understanding of the genetic factors behind LDH, potentially paving the way for the development of new therapeutics, prevention methods, and treatments for symptomatic LDH in the future.
- organism: human
- assay: GWAS summary statistics
- research focus: GWAS / association mapping
- approach: statistical model
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