Hydrochlorothiazide and Bone Mineral Density in Patients with Kidney Stones: A Post-Hoc Analysis of the NOSTONE Trial.

Details

Serval ID
serval:BIB_B870327E5514
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
Hydrochlorothiazide and Bone Mineral Density in Patients with Kidney Stones: A Post-Hoc Analysis of the NOSTONE Trial.
Journal
Clinical journal of the American Society of Nephrology
Author(s)
Christe A., Primetis E., Cereghetti G.M., Drakopoulos D., Dhayat N.A., Bonny O., Ritter A., Mohebbi N., Faller N., Pellegrini L., Bedino G., Venzin R.M., Grosse P., Hüsler C., Koneth I., Bucher C., Del Giorno R., Gabutti L., Mayr M., Odermatt U., Buchkremer F., Ernandez T., Stoermann-Chopard C., Teta D., Tamò L., Trelle S., Roth B., Bargagli M., Fuster D.G.
ISSN
1555-905X (Electronic)
ISSN-L
1555-9041
Publication state
In Press
Peer-reviewed
Oui
Language
english
Notes
Publication types: Journal Article
Publication Status: aheadofprint
Abstract
Low bone mass and fractures are common among kidney stone formers, yet it remains unclear whether thiazides can help preserve bone mass. We aimed to evaluate the effectiveness of a range of hydrochlorothiazide (HCTZ) doses compared to a placebo on bone mineral density (BMD) over a three-year period.
This post-hoc analysis was conducted on data from the NOSTONE trial, a multicenter, randomized, controlled study. A total of 416 adults with recurrent calcium stones participated in the study, receiving either placebo or HCTZ at doses of 12.5 mg, 25 mg or 50 mg daily. BMD was measured using computed tomography (CT) at the T12-L3 vertebrae both at baseline and the end of the study.
Over a median follow-up period of 2.92 years, the mean BMD decreased by 6.4±15.7 Hounsfield Units (HU) in the placebo group, 5.1±15.1 HU in the 12.5 mg HCTZ group (β coefficient vs placebo, 0.37 HU, 95% CI -1.74; 2.47, p = 0.73), 4.1±16.3 HU in the 25 mg HCTZ group (β 0.93 HU, 95% CI -1.34; 3.19, p = 0.42), and 4.8±15.9 HU in the 50 mg HCTZ group (β 0.70 HU, 95% CI -1.45; 2.85, p = 0.52). No association was observed between HCT dose and BMD at the end of the study (p = 0.43). The results were confirmed in sensitivity analyses for eGFR, urine calcium, net gastrointestinal alkali absorption, body mass index (BMI), in subgroup and in per-protocol analyses.
In patients with recurrent calcium kidney stones, loss of BMD was similar in patients receiving HCTZ at a dose of 12.5 mg, 25 mg, or 50 mg, or placebo once daily.
Pubmed
Create date
14/03/2025 16:54
Last modification date
15/03/2025 8:09
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