3.8 Article

Renal Phosphate Handling: Independent Effects of Circulating FGF23, PTH, and Calcium

Journal

JBMR PLUS
Volume 5, Issue 2, Pages -

Publisher

WILEY
DOI: 10.1002/jbm4.10437

Keywords

FIBROBLAST GROWTH FACTOR 23; HYPERPARATHYROIDISM; HYPOPARATHYROIDISM; PARATHYROID HORMONE; X-LINKED HYPOPHOSPHATEMIA

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This study investigated the effects of FGF23, PTH, and calcium on TmP/GFR, finding that hypoparathyroidism can ameliorate the effects of FGF23 excess. The analysis revealed complex relationships among these physiological indicators, particularly during PTH deficiency.
Excess fibroblast growth factor 23 (FGF23), excess PTH, and an increase in extracellular calcium cause hypophosphatemia by lowering the maximum renal phosphate reabsorption threshold (TmP/GFR). We recently reported two cases of X-linked hypophosphatemia (XLH) with severe tertiary hyperparathyroidism who had normalization of TmP/GFR upon being rendered hypoparathyroid following total parathyroidectomy, despite marked excess in both C-terminal FGF23 (cFGF23) and intact FGF23 (iFGF23). We explored the effects of FGF23, PTH, and calcium on TmP/GFR in a cross-sectional study (n =74) across a spectrum of clinical cases with abnormalities in TmP/GFR, PTH, and FGF23. This comprised three groups: FGF23-dependent hypophosphatemia (n =27), hypoparathyroidism (HOPT; n =17), and chronic kidney disease (n =30). Measurements included TmP/GFR, cFGF23, PTH, ionized calcium, vitamin D metabolites, and bone turnover markers. The combined effect of cFGF23, PTH, and ionized calcium on TmP/GFR was modeled using hierarchical multiple regression and was probed by moderation analysis with PROCESS. Modeling analysis showed independent effects on TmP/GFR by cFGF23, PTH, and ionized calcium in conjunction with a weak but significant effect of the interaction term for PTH and FGF23; probing showed that the effect was most prominent during PTH deficiency. Teriparatide 20 mu g daily was self-administered for 28days by one case of X-linked hypophosphatemia with hypoparathyroidism (XLH-HOPT) to assess the response of TmP/GFR, cFGF23, iFGF23, nephrogenous cyclic adenosine monophosphate (NcAMP), vitamin D metabolites, and bone turnover markers. After 28days, TmP/GFR was lowered from 1.10mmol/L to 0.48mmol/L; this was accompanied by increases in NcAMP, ionized calcium, and bone turnover markers. In conclusion, the effect of FGF23 excess on TmP/GFR is altered by PTH such that the effect is ameliorated by hypoparathyroidism and the effect is augmented by hyperparathyroidism. (c) 2020 The Authors. JBMR Plus published by Wiley Periodicals LLC. on behalf of American Society for Bone and Mineral Research.

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