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Femoral neck width genetic risk score is a novel independent risk factor for hip fractures.
Tobias, Jonathan H; Nethander, Maria; Faber, Benjamin G; Heppenstall, Sophie V; Ebsim, Raja; Cootes, Tim; Lindner, Claudia; Saunders, Fiona R; Gregory, Jenny S; Aspden, Richard M; Harvey, Nicholas C; Kemp, John P; Frysz, Monika; Ohlsson, Claes.
Afiliação
  • Tobias JH; Musculoskeletal Research Unit, Translational Health Sciences, Southmead Hospital, University of Bristol, Bristol BS10 5NB, United Kingdom.
  • Nethander M; Medical Research Council Integrative Epidemiology Unit, Population Health Sciences, University of Bristol, Bristol BS8 2BN, United Kingdom.
  • Faber BG; Sahlgrenska Osteoporosis Centre, Centre for Bone and Arthritis Research, Institute of Medicine, Sahlgrenska Academy at University of Gothenburg, 41345 Gothenburg, Sweden.
  • Heppenstall SV; Bioinformatics and Data Center, Sahlgrenska Academy at University of Gothenburg, 40530 Gothenburg, Sweden.
  • Ebsim R; Musculoskeletal Research Unit, Translational Health Sciences, Southmead Hospital, University of Bristol, Bristol BS10 5NB, United Kingdom.
  • Cootes T; Medical Research Council Integrative Epidemiology Unit, Population Health Sciences, University of Bristol, Bristol BS8 2BN, United Kingdom.
  • Lindner C; Musculoskeletal Research Unit, Translational Health Sciences, Southmead Hospital, University of Bristol, Bristol BS10 5NB, United Kingdom.
  • Saunders FR; Division of Informatics, Imaging and Data Sciences, School of Health Sciences, The University of Manchester, Manchester M13 9PT, United Kingdom.
  • Gregory JS; Division of Informatics, Imaging and Data Sciences, School of Health Sciences, The University of Manchester, Manchester M13 9PT, United Kingdom.
  • Aspden RM; Division of Informatics, Imaging and Data Sciences, School of Health Sciences, The University of Manchester, Manchester M13 9PT, United Kingdom.
  • Harvey NC; Centre for Arthritis and Musculoskeletal Health, University of Aberdeen, Aberdeen AB24 3FX, United Kingdom.
  • Kemp JP; Centre for Arthritis and Musculoskeletal Health, University of Aberdeen, Aberdeen AB24 3FX, United Kingdom.
  • Frysz M; Centre for Arthritis and Musculoskeletal Health, University of Aberdeen, Aberdeen AB24 3FX, United Kingdom.
  • Ohlsson C; Medical Research Council Lifecourse Epidemiology Centre, University of Southampton, Southampton SO16 6YD, United Kingdom.
J Bone Miner Res ; 39(3): 241-251, 2024 Apr 19.
Article em En | MEDLINE | ID: mdl-38477772
ABSTRACT
Femoral neck width (FNW) derived from DXA scans may provide a useful adjunct to hip fracture prediction. Therefore, we investigated whether FNW is related to hip fracture risk independently of femoral neck bone mineral density (FN-BMD), using a genetic approach. FNW was derived from points automatically placed on the proximal femur using hip DXA scans from 38 150 individuals (mean age 63.8 yr, 48.0% males) in UK Biobank (UKB). Genome-wide association study (GWAS) identified 71 independent genome-wide significant FNW SNPs, comprising genes involved in cartilage differentiation, hedgehog, skeletal development, in contrast to SNPs identified by FN-BMD GWAS which primarily comprised runx1/Wnt signaling genes (MAGMA gene set analyses). FNW and FN-BMD SNPs were used to generate genetic instruments for multivariable Mendelian randomization. Greater genetically determined FNW increased risk of all hip fractures (odds ratio [OR] 1.53; 95% CI, 1.29-1.82 per SD increase) and femoral neck fractures (OR 1.58;1.30-1.92), but not trochanteric or forearm fractures. In contrast, greater genetically determined FN-BMD decreased fracture risk at all 4 sites. FNW and FN-BMD SNPs were also used to generate genetic risk scores (GRSs), which were examined in relation to incident hip fracture in UKB (excluding the FNW GWAS population; n = 338 742, 3222 cases) using a Cox proportional hazards model. FNW GRS was associated with increased risk of all incident hip fractures (HR 1.08;1.05-1.12) and femoral neck fractures (hazard ratio [HR] 1.10;1.06-1.15), but not trochanteric fractures, whereas FN-BMD GRS was associated with reduced risk of all hip fracture types. We conclude that the underlying biology regulating FNW and FN-BMD differs, and that DXA-derived FNW is causally related to hip fractures independently of FN-BMD, adding information beyond FN-BMD for hip fracture prediction. Hence, FNW derived from DXA analyses or a FNW GRS may contribute clinically useful information beyond FN-BMD for hip fracture prediction.
Femoral neck width (FNW) derived from DXA scans may provide useful information about hip fracture prediction, over and above that provided by BMD measurements. Therefore, we investigated whether FNW is related to hip fracture risk independently of BMD, using a genetic approach. FNW was derived from points automatically placed on the hip in DXA scans obtained from 38 150 individuals (mean age 63.8 yr, 48.0% males) in UK Biobank. Seventy-one distinct genetic factors were found to be associated with FNW. Individuals who were predicted by their genes to have greater FNW had a higher risk of hip but not forearm fractures. In contrast, those with greater genetically determined BMD of the femoral neck had a lower risk of both hip and forearm fractures. We conclude that the underlying biology regulating FNW and BMD of the femoral neck differs, and that FNW derived from DXA analyses may contribute clinically useful information beyond BMD for hip fracture prediction.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fraturas do Colo Femoral / Fraturas do Quadril Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fraturas do Colo Femoral / Fraturas do Quadril Idioma: En Ano de publicação: 2024 Tipo de documento: Article