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PubMed Narrative Review Evidence Moderate

Fracture nonunion in long bones: A literature review of risk factors and surgical management.

Injury | 2021 | Nicholson JA, Makaram N, Simpson A, Keating JF

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PubMed
Type
Narrative Review
Evidence
Moderate

Abstract

[Indexed for MEDLINE] Conflict of interest statement: Declaration of Competing Interest There are no conflicts of interest to declare for any of the authors involved in this study. 2. Nat Genet. 2023 Nov;55(11):1820-1830. doi: 10.1038/s41588-023-01527-3. Epub 2023 Nov 2. An atlas of genetic determinants of forearm fracture. Nethander M(#)(1)(2), Movérare-Skrtic S(#)(1), Kämpe A(3)(4), Coward E(5), Reimann E(6), Grahnemo L(1), Borbély É(7)(8), Helyes Z(7)(8)(9), Funck-Brentano T(10), Cohen-Solal M(10), Tuukkanen J(11), Koskela A(11), Wu J(1), Li L(1), Lu T(12), Gabrielsen ME(5); Estonian Biobank Research Team; Mägi R(6), Hoff M(13)(14), Lerner UH(1), Henning P(1), Ullum H(15), Erikstrup C(16)(17), Brunak S(18); DBDS Genomic Consortium; Langhammer A(19), Tuomi T(4)(20)(21)(22)(23), Oddsson A(24), Stefansson K(24)(19), Pettersson-Kymmer U(25), Ostrowski SR(26)(27)(28), Pedersen OBV(28)(29), Styrkarsdottir U(24), Mäkitie O(3)(23)(30)(31), Hveem K(5)(32), Richards JB(12)(33)(34), Ohlsson C(35)(36). Author information: (1)Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Osteoporosis Centre, Centre for Bone and Arthritis Research at the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. (2)Bioinformatics Core Facility, Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. (3)Department of Molecular Medicine and Surgery, Karolinska Institutet, Stockholm, Sweden. (4)Institute for Molecular Medicine Finland (FIMM), University of Helsinki, Helsinki, Finland. (5)K.G. Jebsen Center for Genetic Epidemiology, Department of Public Health and Nursing, NTNU, Norwegian University of Science and Technology, Trondheim, Norway. (6)Estonian Genome Center, Institute of Genomics, University of Tartu, Tartu, Estonia. (7)Department of Pharmacology and Pharmacotherapy, Medical School, University of Pécs, Pécs, Hungary. (8)National Laboratory for Drug Research and Development, Budapest, Hungary. (9)Eotvos Lorand Research Network, Chronic Pain Research Group, University of Pécs, Pécs, Hungary. (10)BIOSCAR UMRS 1132, Université Paris Diderot, Sorbonne Paris Cité, INSERM, Paris, France. (11)Department of Anatomy and Cell Biology, Faculty of Medicine, Institute of Cancer Research and Translational Medicine, University of Oulu, Oulu, Finland. (12)Lady Davis Institute for Medical Research, Jewish General Hospital, Montreal, Quebec, Canada. (13)Department of Neuromedicine and Movement Science, Norwegian University of Science and Technology, Trondheim, Norway. (14)Department of Rheumatology, St Olavs Hospital, Trondheim, Norway. (15)Statens Serum Institut, Copenhagen, Denmark. (16)Department of Clinical Immunology, Aarhus University Hospital, Aarhus, Denmark. (17)Department of Clinical Medicine, Aarhus University, Aarhus, Denmark. (18)Novo Nordisk Foundation Center for Protein Research, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. (19)Faculty of Medicine, University of Iceland, Reykjavik, Iceland. (20)Folkhälsan Research Center, Helsinki, Finland. (21)Lund University Diabetes Centre, Department of Clinical Sciences, Lund University, Malmö, Sweden. (22)Department of Endocrinology, Abdominal Center, Helsinki University Hospital, Helsinki, Finland. (23)Research Program for Clinical and Molecular Metabolism, Faculty of Medicine, University of Helsinki, Helsinki, Finland. (24)deCODE genetics, Reykjavik, Iceland. (25)Department of Integrative Medical Biology, Clinical Pharmacology, Umea University, Umea, Sweden. (26)Department of Clinical Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark. (27)Department of Clinical Immunology, Copenhagen Hospital Biobank Unit, Copenhagen University Hospital Rigshospitalet, Copenhagen, Denmark. (28)Department of Clinical Medicine, Faculty of Health and Medical Science, University of Copenhagen, Copenhagen, Denmark. (29)Department of Clinical Immunology, Zealand University Hospital, Koege, Denmark. (30)Folkhälsan Institute of Genetics, Helsinki, Finland. (31)Children's Hospital and Pediatric Research Center, University of Helsinki and Helsinki University Hospital, Helsinki, Finland. (32)HUNT Research Centre, Department of Public Health and Nursing, Norwegian University of Science and Technology, and Levanger Hospital, Nord-Trøndelag Hospital Trust, Levanger, Norway. (33)Department of Human Genetics, McGill University, Montreal, Quebec, Canada. (34)Department of Twin Research and Genetic Epidemiology, King's College London, London, UK. (35)Department of Internal Medicine and Clinical Nutrition, Institute of Medicine, Sahlgrenska Osteoporosis Centre, Centre for Bone and Arthritis Research at the Sahlgrenska Academy, University of Gothenburg, Gothenburg, Sweden. claes.ohlsson@medic.gu.se. (36)Region Västra Götaland, Sahlgrenska University Hospital, Department of Drug Treatment, Gothenburg, Sweden. claes.ohlsson@medic.gu.se. (#)Contributed equally Osteoporotic fracture is among the most common and costly of diseases. While reasonably heritable, its genetic determinants have remained elusive. Forearm fractures are the most common clinically recognized osteoporotic fractures with a relatively high heritability. To establish an atlas of the genetic determinants of forearm fractures, we performed genome-wide association analyses including 100,026 forearm fracture cases. We identified 43 loci, including 26 new fracture loci. Although most fracture loci associated with bone mineral density, we also identified loci that primarily regulate bone quality parameters. Functional studies of one such locus, at TAC4, revealed that Tac4-/- mice have reduced mechanical bone strength. The strongest forearm fracture signal, at WNT16, displayed remarkable bone-site-specificity with no association with hip fractures. Tall stature and low body mass index were identified as new causal risk factors for fractures. The insights from this atlas may improve fracture prediction and enable therapeutic development to prevent fractures. © 2023. The Author(s). DOI: 10.1038/s41588-023-01527-3 PMCID: PMC10632131

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