Evidence map›Paper›PMID 40098426›Full record

ArticleJournal of bone metabolism2025

Pharmacogenetics of Response to Bisphosphonate Treatment in Postmenopausal Osteoporosis: A Prospective Study.

Sirin Akbulut Ayturk, Ozden Ozyemisci Taskiran, Ebru Koseoglu Tohma, Aylin Sepici Dincel, Nesrin Demirsoy, Vesile Sepici

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Article in Journal of bone metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

6 authors.

Sirin Akbulut AyturkDepartment of Physical Medicine and Rehabilitation, Kartal Dr. Lütfi Kırdar City Hospital, İstanbul, Türkiye.
Ozden Ozyemisci TaskiranDepartment of Physical Medicine and Rehabilitation, Koç University School of Medicine, İstanbul, Türkiye.
Ebru Koseoglu TohmaDepartment of Physical Medicine and Rehabilitation, Muğla Training and Research Hospital, Muğla, Türkiye.
Aylin Sepici DincelDepartment of Medical Biochemistry, Gazi University Faculty of Medicine, Ankara, Türkiye.
Nesrin DemirsoyDepartment of Physical Medicine and Rehabilitation, Gazi University Faculty of Medicine, Ankara, Türkiye.
Vesile SepiciDepartment of Physical Medicine and Rehabilitation, Gazi University Faculty of Medicine, Ankara, Türkiye.

Funding

Gazi University Medical School
6 · The paper itself

Abstract

backgroundThis study aims to investigate the effect of genetic polymorphisms of vitamin D receptor (VDR), estrogen receptor 1 (ER1), and Col1a1 on the response to bisphosphonate (BP) therapy in women with postmenopausal osteoporosis (OP).

methodsTwenty-one women with postmenopausal OP who received alendronate, ibandronate, or zoledronic acid for one year were enrolled in this study. Bone mineral density (BMD) at the lumbar spine and femoral neck were assessed by dual energy X-ray absorptiometry at baseline and after 12 months. Serum osteocalcin levels were measured at baseline and after 12 months. Polymorphic sites of the genes encoding ER1, VDR and Col1a1 proteins were amplified by polymerase chain reaction and examined using restriction fragment length polymorphism. Response to BP treatment and change in osteocalcin levels were compared among women with different gene polymorphisms.

resultsRatio of responders to treatment regarding improvements in the BMD of lumbar spine and femoral neck was adequate in 76% and 62%, respectively. There was no significant difference in treatment response regarding BMD in either region or change in serum osteocalcin levels among different gene polymorphisms.

conclusionsThese findings did not support the potential role of VDR BsmI, Col1a1 Sp1, ER1 PvuII, or XbaI polymorphisms in predicting the response to BP therapy in women with postmenopausal OP. Further investigation with larger prospective studies is required.

Indexed as

Diphosphonates · Osteoporosis · Pharmacogenetics · Polymorphism, genetic · Vitamin D

Identifiers

PMID40098426
PMCPMC11960302

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