TY - JOUR
T1 - Serum uric acid levels and mortality in the Japanese population
T2 - the Yamagata (Takahata) study
AU - Kamei, Keita
AU - Konta, Tsuneo
AU - Ichikawa, Kazunobu
AU - Sato, Hiroko
AU - Suzuki, Natsuko
AU - Kabasawa, Asami
AU - Suzuki, Kazuko
AU - Hirayama, Atsushi
AU - Shibata, Yoko
AU - Watanabe, Tetsu
AU - Kato, Takeo
AU - Ueno, Yoshiyuki
AU - Kayama, Takamasa
AU - Kubota, Isao
N1 - Funding Information:
This study was supported in part by a Grant-in-Aid from the 21st Century Center of Excellence (COE) and Global COE program of the Japan Society for the Promotion of Science and by a Grant-in-Aid for Scientific Research (C) (15K09240).
Publisher Copyright:
© 2016, Japanese Society of Nephrology.
PY - 2016/12/1
Y1 - 2016/12/1
N2 - Background: Serum uric acid level is regulated by gender, dietary habit, genetic predisposition, and renal function, and is associated with the development of renal and cardiovascular diseases. This study prospectively investigated the association between serum uric acid levels and mortality in a community-based population. Methods: Three thousand four hundred and eighty-seven subjects regardless of the antihyperuricemic medication (45 % male; mean age 62 years old) from the Takahata town in Japan participated in this study and were followed up for 8 years (median 7.5 years). We examined the association between serum uric acid levels at baseline and the all-cause and cardiovascular mortality, respectively, in this population. Results: One hundred seventy-nine subjects died during the follow-up period, with 49 deaths attributed to cardiovascular causes. Kaplan–Meier analysis revealed that the all-cause mortality was significantly higher along with the increase in serum uric acid levels at baseline among female (Log-rank P < 0.01), but not male subjects (P = 0.97). Cox-proportional hazard model analysis with adjustment for possible confounders including age, renal function, and comorbidities revealed that hyperuricemia (uric acid ≥7.0 mg/dL) was an independent risk factor for all-cause and cardiovascular mortality, respectively, in female [hazard ratio (HR) 5.92, 95 % confidence interval (CI) 2.10–14.6 for all-cause mortality, and HR 10.7, 95 % CI 1.76–50.2 for cardiovascular mortality], but not male subjects. Conclusion: Hyperuricemia was an independent risk for all-cause and cardiovascular mortality in female, but not among the male subjects in a community-based population.
AB - Background: Serum uric acid level is regulated by gender, dietary habit, genetic predisposition, and renal function, and is associated with the development of renal and cardiovascular diseases. This study prospectively investigated the association between serum uric acid levels and mortality in a community-based population. Methods: Three thousand four hundred and eighty-seven subjects regardless of the antihyperuricemic medication (45 % male; mean age 62 years old) from the Takahata town in Japan participated in this study and were followed up for 8 years (median 7.5 years). We examined the association between serum uric acid levels at baseline and the all-cause and cardiovascular mortality, respectively, in this population. Results: One hundred seventy-nine subjects died during the follow-up period, with 49 deaths attributed to cardiovascular causes. Kaplan–Meier analysis revealed that the all-cause mortality was significantly higher along with the increase in serum uric acid levels at baseline among female (Log-rank P < 0.01), but not male subjects (P = 0.97). Cox-proportional hazard model analysis with adjustment for possible confounders including age, renal function, and comorbidities revealed that hyperuricemia (uric acid ≥7.0 mg/dL) was an independent risk factor for all-cause and cardiovascular mortality, respectively, in female [hazard ratio (HR) 5.92, 95 % confidence interval (CI) 2.10–14.6 for all-cause mortality, and HR 10.7, 95 % CI 1.76–50.2 for cardiovascular mortality], but not male subjects. Conclusion: Hyperuricemia was an independent risk for all-cause and cardiovascular mortality in female, but not among the male subjects in a community-based population.
KW - Cohort
KW - Mortality
KW - Population
KW - Uric acid
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U2 - 10.1007/s10157-016-1228-1
DO - 10.1007/s10157-016-1228-1
M3 - Article
C2 - 26779905
AN - SCOPUS:84954411140
SN - 1342-1751
VL - 20
SP - 904
EP - 909
JO - Clinical and experimental nephrology
JF - Clinical and experimental nephrology
IS - 6
ER -