Lower bicarbonate level is associated with CKD progression and all-cause mortality: a propensity score matching analysis.

BMC Nephrol

Renal Division, Department of Internal Medicine, Iwata City Hospital, 512-3 Ohkubo, Iwata, Shizuoka, 438-8550, Japan.

Published: March 2022

Background: Although metabolic acidosis is known as a potential complication of chronic kidney disease (CKD), there is limited information concerning the association between metabolic acidosis and clinical outcomes.

Methods: Five hundred fifty-two patients referred to renal division of Iwata City Hospital from 2015 to 2017 were included as a retrospective CKD cohort, and finally 178 patients with CKD stage III or IV and 20 to 80 years of age were analyzed. We examined the association between serum bicarbonate (HCO) levels and clinical outcomes using Kaplan-Meier methods after the matching of baseline characteristics by propensity scores.

Results: Of 178 patients with CKD, patients with lower HCO levels (N = 94), as compared with patients with higher HCO levels (N = 84), were more likely to be male (P < 0.05), had more severe CKD stages (P < 0.05), more frequent use of renin-angiotensin system inhibitor (P < 0.05) or uric acid lowering agent (P < 0.001), heavier body weight (P < 0.001) and lower estimated glomerular filtration rate (P < 0.05). In Kaplan-Meier analysis after propensity score matching, the incidence of composite outcome as the doubling of serum creatinine level from baseline, end-stage kidney disease requiring the initiation of dialysis, or death from any causes was significantly fewer in the higher HCO group than the lower HCO group (N = 57 each group, P = 0.016).

Conclusions: Lower HCO level is significantly associated with the doubling of serum creatinine level, end-stage kidney disease or all-cause mortality in patients with CKD.

Trial Registration: This study was registered with the Clinical Trial Registry of the University Hospital Medical Information Network ( http://www.umin.ac.jp/ , study number: UMIN000044861 ).

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC8895620PMC
http://dx.doi.org/10.1186/s12882-022-02712-yDOI Listing

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