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Abstract

In this single-center, randomized, placebo-controlled, single-blinded, crossover trial (Clinical Trial Registry-India: CTRI/2024/08/090041), we evaluated the efficacy and safety of low-dose hydrochlorothiazide (HCTZ) in adults with nonsurgical hypoparathyroidism (excluding autoimmune and obvious syndromic forms). After stabilization on fixed doses of calcium carbonate and calcitriol under a controlled low-sodium diet, 26 participants received HCTZ (12.5-25 mg/d) or placebo for 7 d, with a 15-d washout before crossover, followed by an optional 4-wk open-label HCTZ extension. The primary outcome was change in serum calcium; secondary outcomes included change in 24-h urinary calcium (UCa), fractional calcium excretion, urinary sodium, and bone turnover markers (β-CTX and P1NP). Compared to baseline (8.61 ± 0.32 mg/dL), serum calcium increased significantly with HCTZ at day 5 (9.01 ± 0.46 mg/dL) and day 8 (9.04 ± 0.52 mg/dL; p < .001), while no significant change occurred with placebo. Hydrochlorothiazide reduced 24-h UCa by −26.3% at day 8 (vs +4.7% with placebo; p < .001). These effects remained robust in sensitivity analyses adjusting for urinary sodium and when expressed per kg body weight. Fractional calcium excretion fell by 29.9% with HCTZ (p < .001). A small but statistically significant decline in serum potassium was observed at day 8 (from 4.18 to 3.95 mEq/L; p < .001), though values remained within the normal range, no participants developed hypokalemia; renal function and intact PTH (iPTH) were stable. During the extension phase, serum calcium levels rose while UCa excretion declined significantly, without any reported adverse effects. These findings indicate that low-dose HCTZ with sodium restriction safely improves calcium homeostasis in nonsurgical hypoparathyroidism—raising serum calcium and reducing calciuria—with good tolerability. Hydrochlorothiazide offers a cost-effective adjunct to standard therapy and warrants further investigation for long-term outcomes.

Lay Summary

In 26 adults with nonsurgical hypoparathyroidism, low-dose hydrochlorothiazide (12.5-25 mg daily) raised serum calcium levels and reduced calcium loss in urine within 1 wk, without causing harmful side effects. A 4-wk extension confirmed sustained benefits. This simple, safe, and affordable treatment may improve calcium control alongside standard therapy and may reduce kidney-related complications.

Details

1009240
Title
Hydrochlorothiazide with salt restriction in nonsurgical hypoparathyroidism: a placebo-controlled single-blinded randomized crossover trial assessing efficacy and safety
Author
Jha, Vivek 1   VIAFID ORCID Logo  ; Mukherjee, Soham 1 ; Bhadada, Sanjay Kumar 1   VIAFID ORCID Logo  ; Sahni, Nancy 2 ; Ram, Sant 3 ; Dutta, Pinaki 1   VIAFID ORCID Logo 

 Department of Endocrinology, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh 160012, India  [email protected]; [email protected]
 Department of Dietetics, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh 160012, India 
 Department of Biochemistry, Postgraduate Institute of Medical Education and Research (PGIMER), Chandigarh 160012, India 
Author e-mail address
Publication title
JBMR Plus; Hoboken
Volume
9
Issue
12
Number of pages
12
Publication year
2025
Publication date
Dec 2025
Section
Clinical Trial
Publisher
Oxford University Press
Place of publication
Hoboken
Country of publication
United Kingdom
e-ISSN
24734039
Source type
Scholarly Journal
Language of publication
English
Document type
Journal Article
Publication history
 
 
Online publication date
2025-11-03
Milestone dates
2025-09-08 (Received); 2025-10-27 (Rev-Recd); 2025-10-29 (Accepted); 2025-11-24 (Corrected-Typeset)
Publication history
 
 
   First posting date
03 Nov 2025
ProQuest document ID
3274967253
Document URL
https://www.proquest.com/scholarly-journals/hydrochlorothiazide-with-salt-restriction/docview/3274967253/se-2?accountid=208611
Copyright
© 2025 The Author(s) 2025. Published by Oxford University Press on behalf of the American Society for Bone and Mineral Research. This work is published under https://creativecommons.org/licenses/by-nc/4.0/ (the "License"). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Last updated
2025-11-25
Database
ProQuest One Academic