TY - JOUR
T1 - Elevated serum homocysteine is a predictor of accelerated decline in renal function and chronic kidney disease
T2 - A historical prospective study
AU - Levi, Amos
AU - Cohen, Eytan
AU - Levi, Micha
AU - Goldberg, Elad
AU - Garty, Moshe
AU - Krause, Ilan
PY - 2014/12/1
Y1 - 2014/12/1
N2 - Objective To estimate the effect of elevated serum homocysteine level on renal function decline and on the incidence of chronic kidney disease (CKD) in the general population. copy; 2014 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved.Methods A historical prospective study on 3602 subjects attending a screening center in Israel between the years 2000 and 2012. Only subjects with normal estimated glomerular filtration rate (eGFR) and without proteinuria were included. Subjects were divided to two groups according to mean total serum homocysteine level (≤ 15, > 15 μmol/l). Linear mixed effect model was used to estimate the annual eGRF decline in respect to homocysteine group. Cox proportional hazards models were used to estimate hazard ratios for CKD in the normal compared to the elevated homocysteine group.Results Annual eGFR decline was 25% higher in subjects with elevated versus normal mean homocysteine level (0.90 ± 0.16 ml/min/1.37 m bsupesup vs. 0.72 ± 0.14 ml/min/1.37 m bsupesup, p < 0.001). In a median follow up of 7.75 years, 38 subjects developed CKD (1.05%). Elevated mean homocysteine level was highly associated with developing CKD (HR 4.85, 95% CI 2.48-9.49, p < 0.001). In a multivariate analysis which adjusted for age, baseline kidney function, HDL cholesterol, BMI, vitamin B12 and folic acid levels, these relationships remained substantially unchanged.Conclusions Elevated mean serum homocysteine level is associated with an accelerated decline in renal function in both men and women, and is an independent risk factor for the development of CKD in the general population. Further prospective randomized clinical trials are needed to clarify whether the reduction in serum homocysteine concentrations will result in an improved renal prognosis.
AB - Objective To estimate the effect of elevated serum homocysteine level on renal function decline and on the incidence of chronic kidney disease (CKD) in the general population. copy; 2014 European Federation of Internal Medicine. Published by Elsevier B.V. All rights reserved.Methods A historical prospective study on 3602 subjects attending a screening center in Israel between the years 2000 and 2012. Only subjects with normal estimated glomerular filtration rate (eGFR) and without proteinuria were included. Subjects were divided to two groups according to mean total serum homocysteine level (≤ 15, > 15 μmol/l). Linear mixed effect model was used to estimate the annual eGRF decline in respect to homocysteine group. Cox proportional hazards models were used to estimate hazard ratios for CKD in the normal compared to the elevated homocysteine group.Results Annual eGFR decline was 25% higher in subjects with elevated versus normal mean homocysteine level (0.90 ± 0.16 ml/min/1.37 m bsupesup vs. 0.72 ± 0.14 ml/min/1.37 m bsupesup, p < 0.001). In a median follow up of 7.75 years, 38 subjects developed CKD (1.05%). Elevated mean homocysteine level was highly associated with developing CKD (HR 4.85, 95% CI 2.48-9.49, p < 0.001). In a multivariate analysis which adjusted for age, baseline kidney function, HDL cholesterol, BMI, vitamin B12 and folic acid levels, these relationships remained substantially unchanged.Conclusions Elevated mean serum homocysteine level is associated with an accelerated decline in renal function in both men and women, and is an independent risk factor for the development of CKD in the general population. Further prospective randomized clinical trials are needed to clarify whether the reduction in serum homocysteine concentrations will result in an improved renal prognosis.
KW - CKD-EPI equation
KW - Chronic kidney disease (CKD)
KW - General population
KW - Glomerular filtration rate (GFR)
KW - Longitudinal cohort study
UR - http://www.scopus.com/inward/record.url?scp=84916210726&partnerID=8YFLogxK
U2 - 10.1016/j.ejim.2014.10.014
DO - 10.1016/j.ejim.2014.10.014
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AN - SCOPUS:84916210726
VL - 25
SP - 951
EP - 955
JO - European Journal of Internal Medicine
JF - European Journal of Internal Medicine
SN - 0953-6205
IS - 10
ER -