Generalized Weakness Due to Hypocalcemia and Hypophosphatemia From Potent Acid Suppression

Potent gastric acid suppression can disrupt mineral homeostasis. An older woman receiving alfacalcidol developed weakness accompanied by profound hypophosphatemia with hypocalcemia and secondary hyperparathyroidism after initiation of the potassium-competitive acid blocker vonoprazan. Laboratory findings showed an elevated intact parathyroid hormone level and renal phosphate wasting, whereas her serum magnesium level was 2.7 mg/dL (reference range, 1.7–2.6 mg/dL) and her intact fibroblast growth factor 23 was 41.7 pg/mL (reference range, 19.9–52.9 pg/mL). The patient's weakness and calcium–phosphate abnormalities resolved with mineral repletion and switching from vonoprazan to a proton-pump inhibitor. This case highlights that strong acid suppression may precipitate significant calcium–phosphate derangements despite active vitamin D therapy. Early evaluation of mineral metabolism and reassessment of acid-suppressive therapy are especially important in patients with unexplained weakness.

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Publication Details

Journal
Annals of Internal Medicine Clinical Cases
Published
2026-05-01
DOI
https://doi.org/10.7326/aimcc.2026.0119
Primary Topic
Parathyroid Disorders and Treatments
Type
article
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article

Generalized Weakness Due to Hypocalcemia and Hypophosphatemia From Potent Acid Suppression

Ryo KONOIKE, Tetsuo Shoji, Osamu Hamada
Annals of Internal Medicine Clinical Cases
Parathyroid Disorders and Treatments
article

Generalized Weakness Due to Hypocalcemia and Hypophosphatemia From Potent Acid Suppression

Ryo KONOIKE, Tetsuo Shoji, Osamu Hamada
article en

Abstract

Potent gastric acid suppression can disrupt mineral homeostasis. An older woman receiving alfacalcidol developed weakness accompanied by profound hypophosphatemia with hypocalcemia and secondary hyperparathyroidism after initiation of the potassium-competitive acid blocker vonoprazan. Laboratory findings showed an elevated intact parathyroid hormone level and renal phosphate wasting, whereas her serum magnesium level was 2.7 mg/dL (reference range, 1.7–2.6 mg/dL) and her intact fibroblast growth factor 23 was 41.7 pg/mL (reference range, 19.9–52.9 pg/mL). The patient's weakness and calcium–phosphate abnormalities resolved with mineral repletion and switching from vonoprazan to a proton-pump inhibitor. This case highlights that strong acid suppression may precipitate significant calcium–phosphate derangements despite active vitamin D therapy. Early evaluation of mineral metabolism and reassessment of acid-suppressive therapy are especially important in patients with unexplained weakness.

Annals of Internal Medicine Clinical CasesVol. 5(5)
Kyoto University (JP), Inoue Hospital (JP), The University of Osaka (JP)
Zero hunger
Openalex Percentile: Top 7%
Parathyroid Disorders and Treatments
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