The negative effect of unloading exceeds the bone-sparing effect of alkaline supplementation: a bed rest study

Summary Potassium bicarbonate was administrated to an already alkaline diet in seven male subjects during a 21-day bed rest study and was able to decrease bed rest induced increased calcium excretion but failed to prevent bed rest-induced bone resorption. Introduction Supplementation with alkali sal...

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Veröffentlicht in:Osteoporosis international 2019-02, Vol.30 (2), p.431-439
Hauptverfasser: Frings-Meuthen, P., Bernhardt, G., Buehlmeier, J., Baecker, N., May, F., Heer, M.
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Sprache:eng
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Zusammenfassung:Summary Potassium bicarbonate was administrated to an already alkaline diet in seven male subjects during a 21-day bed rest study and was able to decrease bed rest induced increased calcium excretion but failed to prevent bed rest-induced bone resorption. Introduction Supplementation with alkali salts appears to positively influence calcium and bone metabolism and, thus, could be a countermeasure for population groups with an increased risk for bone loss. However, the extent to which alkalization counteracts acid-induced bone resorption or whether it merely has a calcium and bone maintenance effect is still not completely understood. In the present study, we hypothesized that additional alkalization to an already alkaline diet can further counteract bed rest-induced bone loss. Methods Seven healthy male subjects completed two parts of a crossover designed 21-day bed rest study: bed rest only (control) and bed rest supplemented with 90 mmol potassium bicarbonate (KHCO 3 ) daily. Results KHCO 3 supplementation during bed rest resulted in a more alkaline status compared to the control intervention, demonstrated by the increase in pH and buffer capacity level (pH p  = 0.023, HCO 3 p  = 0.02, ABE p  = 0.03). Urinary calcium excretion was decreased during KHCO 3 supplementation (control 6.05 ± 2.74 mmol/24 h; KHCO 3 4.87 ± 2.21 mmol/24 h, p  = 0.03); whereas, bone formation was not affected by additional alkalization (bAP p  = 0.58; PINP p  = 0.60). Bone resorption marker UCTX tended to be lower during alkaline supplementation (UCTX p  = 0.16). Conclusions The more alkaline acid-base status, achieved by KHCO 3 supplementation, reduced renal calcium excretion during bed rest, but was not able to prevent immobilization-induced bone resorption. However, advantages of alkaline salts on bone metabolism may occur under acidic metabolic conditions or with respect to the positive effect of reduced calcium excretion within a longer time frame. Trial registration Trial number: NCT01509456
ISSN:0937-941X
1433-2965
DOI:10.1007/s00198-018-4703-6