The efficacy of pharmacotherapy in postmenopausal osteoporosis: a longitudinal observational study.


Journal

Endokrynologia Polska
ISSN: 2299-8306
Titre abrégé: Endokrynol Pol
Pays: Poland
ID NLM: 0370674

Informations de publication

Date de publication:
2019
Historique:
received: 15 06 2019
accepted: 29 07 2019
entrez: 8 1 2020
pubmed: 8 1 2020
medline: 30 5 2020
Statut: ppublish

Résumé

The aim of the study was an assessment of longitudinal changes in fracture probability in postmenopausal women. A group of 226 postmenopausal women at baseline mean age 66.46 ± 7.96 years were studied. There were 21 women without therapy, 102 taking calcium + vitamin D, and 103 women on antiresorptive therapy, in the study group. Data concerning clinical risk factors for osteoporosis and hip BMD were gathered. Fracture probability for major and hip fractures was established using FRAXTM. Mean follow-up time was 2.43 ± 0.59 years. Baseline FRAX value in the whole group for major fracture was 7.1 ± 4.18, and at follow-up it was 7.44 ± 4.04. Respective results for FRAX for hip fracture were 3.17 ± 2.69 and 3.02 ± 2.35. In the whole group the probability for major fractures significantly increased during follow-up (p < 0.05) and for hip fracture did not change. In non-treated patients and patients taking calcium + vitamin D the fracture probability increased significantly. In patients on antiresorptive therapy the fracture probability did not change, which was connected with an improvement in bone status assessed by DXA. Femoral neck T-score in the whole group did not change, in those not treated and taking calcium + vitamin D it decreased significantly (p < 0.05), while in treated women it increased significantly (p < 0.05). In patients with improved bone status the FRAX values for major and hip fractures decreased by 0.44 ± 1.62 and 0.36 ± 1.19, respectively. Conversely, in patients with worsening T-score value the FRAX values increased by 1.33 ± 1.42 and 0.66 ± 1.25, respectively. Antiresorptive therapy stabilises fracture probability in postmenopausal women due to improvement in bone status.

Identifiants

pubmed: 31909456
pii: VM/OJS/J/64683
doi: 10.5603/EP.a2019.0058
doi:

Substances chimiques

Bone Density Conservation Agents 0
Vitamin D 1406-16-2
Calcium SY7Q814VUP

Types de publication

Journal Article Observational Study

Langues

eng

Sous-ensembles de citation

IM

Pagination

473-477

Auteurs

Wojciech Pluskiewicz (W)

Department and Clinic of Internal Diseases, Diabetology, and Nephrology, Metabolic Bone Diseases Unit, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland. osteolesna@poczta.onet.pl.

Piotr Adamczyk (P)

Department of Paediatrics, Faculty of Medical Sciences in Katowice, Medical University of Silesia in Katowice, Poland.

Edward Franek (E)

Mossakowski Medical Research Centre, Polish Academy of Sciences, Warsaw, Poland.

Ewa Sewerynek (E)

Department of Endocrine Disorders and Bone Metabolism, Medical University of Łódź, Poland.

Hanna Wichrowska (H)

Department of Internal Diseases, Endocrinology, and Diabetology, Central Clinical Hospital MSWiA, Warsaw, Poland.

Luiza Napiórkowska (L)

Department of Internal Diseases, Endocrinology, and Diabetology, Central Clinical Hospital MSWiA, Warsaw, Poland.

Michał Stuss (M)

Department of Endocrine Disorders and Bone Metabolism, Medical University of Łódź, Poland.

Aleksandra Rozwandowicz (A)

Department of Endocrine Disorders and Bone Metabolism, Medical University of Łódź, Poland.

Bogna Drozdzowska (B)

Department and Chair of Pathomorphology, Faculty of Medical Sciences in Zabrze, Medical University of Silesia, Katowice, Poland.

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Classifications MeSH