Genome-wide association study identifies genetic variants which predict the response of bone mineral density to teriparatide therapy.


Journal

Annals of the rheumatic diseases
ISSN: 1468-2060
Titre abrégé: Ann Rheum Dis
Pays: England
ID NLM: 0372355

Informations de publication

Date de publication:
07 2023
Historique:
received: 11 11 2022
accepted: 15 02 2023
medline: 14 6 2023
pubmed: 21 3 2023
entrez: 20 3 2023
Statut: ppublish

Résumé

Teriparatide (TPTD) is an effective treatment for osteoporosis but the individual response to therapy is variable for reasons that are unclear. This study aimed to determine whether the response to TPTD might be influenced by genetic factors. We searched for predictors of the response of bone mineral density (BMD) to TPTD using a two-stage genome-wide association study in 437 patients with osteoporosis from three referral centres. Demographic and clinical data including the response of BMD to treatment at the lumbar spine and hip were extracted from the medical records of each participant. Allelic variation at rs6430612 on chromosome 2, close Genetic factors influence the response to TPTD at the lumbar spine and hip with a magnitude of effect that is clinically relevant. Further studies are required to identify the causal genetic variants and underlying mechanisms as well as to explore how genetic testing for these variants might be implemented in clinical practice.

Identifiants

pubmed: 36941031
pii: ard-2022-223618
doi: 10.1136/ard-2022-223618
doi:

Substances chimiques

Teriparatide 10T9CSU89I
Bone Density Conservation Agents 0

Types de publication

Journal Article Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

985-991

Subventions

Organisme : Chief Scientist Office
ID : ETM/426
Pays : United Kingdom

Informations de copyright

© Author(s) (or their employer(s)) 2023. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: BLL has served on advisory boards and received lecture honoraria from Amgen, UCB, Gideon-Richter, Astellas and Astra-Zeneca. She holds research grants from Novo Nordisk and Amgen. SHR holds research grants from Amgen, Eli Lilly and UCB.

Auteurs

Nerea Alonso (N)

Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Clinical Institute of Medical and Chemical Laboratory Diagnostics, Medical University of Graz, Graz, Austria.

Omar M E Albagha (OME)

Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
College of Health and Life Sciences, Hamad Bin Khalifa University, Doha, Qatar.

Asim Azfer (A)

Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.

Beatriz Larraz-Prieto (B)

Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.

Kathryn Berg (K)

Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.

Philip L Riches (PL)

Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK.
Rheumatic Diseases Unit, Western General Hospital, Edinburgh, UK.

Barbara Ostanek (B)

Department of Clinical Biochemistry, Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.

Tomaz Kocjan (T)

Department of Endocrinology, Diabetes and Metabolic Diseases, University Medical Centre Ljubljana, Ljubljana, Slovenia.
Department of Internal Medicine, Faculty of Medicine, University of Ljubljana, Ljubljana, Slovenia.

Janja Marc (J)

Department of Clinical Biochemistry, Faculty of Pharmacy, University of Ljubljana, Ljubljana, Slovenia.

Bente L Langdahl (BL)

Department of Endocrinology and Internal Medicine, Aarhus University Hospital, Aarhus, Denmark.

Stuart H Ralston (SH)

Centre for Genomic and Experimental Medicine, Institute of Genetics and Cancer, University of Edinburgh, Edinburgh, UK stuart.ralston@ed.ac.uk.
Rheumatic Diseases Unit, Western General Hospital, Edinburgh, UK.

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Classifications MeSH