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The effect of vitamin D on fibroblast growth factor 23: a systematic review and meta-analysis of randomized controlled trials

Armin Zittermann, Heiner K. Berthold, Stefan Pilz

2020European Journal of Clinical Nutrition47 citationsDOIOpen Access PDF

Abstract

Abstract The phosphaturic hormone fibroblast growth factor 23 (FGF23) is a risk marker of cardiovascular and all-cause mortality. We therefore aimed to synthesize the evidence for the effect of vitamin D administration on circulating FGF23 concentrations. We performed a systematic review and meta-analysis of randomized, placebo-controlled trials (RCTs) in several databases from inception to January 2020. A total of 73 records were identified for full-text review, and 21 articles with 23 studies were included in the final analysis. The selected studies included 1925 participants with 8–156 weeks of follow-up. The weighted mean difference in FGF23 in the vitamin D versus placebo group was +21 pg/ml (95% CI: 13–28 pg/ml; P < 0.001) with considerable heterogeneity among studies ( I 2 = 99%). The FGF23 increment was higher in patients with end-stage kidney/heart failure than in other individuals (+300 pg/ml [95% CI: 41–558 pg/ml] vs. +20 pg/ml [95% CI: 12–28 pg/ml], P interaction = 0.03), and if baseline 25-hydroxyvitamin D concentrations were <50 nmol/l instead of ≥50 nmol/l (+34 pg/ml [95% CI: 18–51 pg/ml] vs. +9 pg/ml [95% CI: 3–14 pg/ml]; P interaction = 0.002). Moreover, the FGF23 increment was influenced by vitamin D dose/type (vitamin D dose equivalent ≤ 2000 IU/day: +2 pg/ml [95% CI: 0–3 pg/ml]; vitamin D dose equivalent > 2000 IU/day: +18 pg/ml [95% CI: 6–30 pg/ml]; administration of activated vitamin D: +67 pg/ml [95% CI: 16–117 pg/ml]; P interaction = 0.001). Results were not significantly influenced by study duration ( P interaction = 0.14), age class ( P interaction = 0.09), or assay provider ( P interaction = 0.11). In conclusion, this meta-analysis of RCTs demonstrates that vitamin D administration of >2000 IU/d vitamin D or activated vitamin D significantly increased concentrations of the cardiovascular risk marker FGF23, especially in patients with end-stage kidney/heart failure.

Topics & Concepts

MedicineVitamin D and neurologyPlaceboFibroblast growth factor 23Internal medicineMeta-analysisRandomized controlled trialVitaminGastroenterologyEndocrinologyCalciumParathyroid hormonePathologyAlternative medicineParathyroid Disorders and TreatmentsVitamin D Research StudiesPancreatitis Pathology and Treatment
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