Overweight modifies the longitudinal association between uric acid and some components of the metabolic syndrome: The Tromso Study

被引:43
作者
Norvik, Jon V. [1 ,3 ,6 ]
Storhaug, Hilde M. [1 ]
Ytrehus, Kirsti [1 ,3 ]
Jenssen, Trond G. [1 ,4 ]
Zykova, Svetlana N. [1 ,5 ]
Eriksen, Bjorn O. [1 ,2 ]
Solbu, Marit D. [1 ,2 ]
机构
[1] UiT Arctic Univ Norway, Metab & Renal Res Grp, N-9037 Tromso, Norway
[2] Univ Hosp North Norway, Nephrol Sect, N-9038 Tromso, Norway
[3] UiT Arctic Univ Norway, Dept Med Biol, N-9037 Tromso, Norway
[4] Oslo Univ Hosp, Rikshosp, Dept Transplant Med, N-0424 Oslo, Norway
[5] Univ Hosp North Norway, Ctr Clin Res & Educ, N-9038 Tromso, Norway
[6] Northern Norway Reg Hlth Author, N-8038 Bodo, Norway
来源
BMC CARDIOVASCULAR DISORDERS | 2016年 / 16卷
关键词
Metabolic syndrome; Uric acid; Cardiovascular risk; Overweight; Obesity; Hypertension; Prospective; Cohort; Longitudinal; Insulin resistance; FOLLOW-UP; CARDIOVASCULAR-DISEASE; GENERAL-POPULATION; INSULIN-RESISTANCE; PREVALENCE; RISK; HYPERURICEMIA; ADIPONECTIN; HEALTH; HYPERTENSION;
D O I
10.1186/s12872-016-0265-8
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background: Elevated uric acid (UA) is associated with the presence of the metabolic syndrome (MetS). In a prospective cohort study, we assessed whether baseline and longitudinal change in UA were risk factors for development of MetS and its individual components. Methods: We included 3087 women and 2996 men who had UA measured in the population based Tromso Study 1994-95. The participants were stratified according to body mass index (BMI). Endpoints were MetS and each component of the syndrome after 7 years, according to the revised National Cholesterol Education Program's Adult Treatment Panel III (NCEP-ATP III) definition. Results: Multiple logistic regression analyses showed that higher baseline UA was associated with higher odds of developing elevated blood pressure in overweight subjects (BMI = 25 kg/m(2), odds ratio [OR] per 59 mu mol/L UA increase 1.44, 95 % confidence interval [CI] = 1.17-1.77, P = 0.001), but not in normal-weight subjects (BMI < 25 kg/m(2), P for interaction = 0.04). Overweight also modified the association between baseline UA and the development of elevated fasting glucose (P for interaction = 0.01). UA was a predictor of MetS in all subjects (OR per 59 mu mol/L UA increase 1.29, 95 % CI 1.18-1.41, P < 0.001). Furthermore, longitudinal UA change was independently associated with the development of MetS in all subjects (OR per 59 mu mol/L UA increase over 7 years 1.28, 95 % CI 1.16-1.42, P < 0.001). Conclusion: Increased levels of baseline UA independently predicted development of elevated blood pressure and higher fasting glycemia in the overweight, but not the normal-weight subjects. Baseline UA and longitudinal increase in UA over 7 years was associated with the development of MetS in all subjects. Whether increased UA should be treated differently in normal-weight and overweight persons needs further study.
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页数:9
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