Kraja Aldi T, Borecki Ingrid B, North Kari, Tang Weihong, Myers Richard H, Hopkins Paul N, Arnett Donna, Corbett Jonathan, Adelman Avril, Province Michael A
Division of Statistical Genomics, Washington University School of Medicine, Saint Louis, MO, USA.
Nutr Metab (Lond). 2006 Dec 5;3:41. doi: 10.1186/1743-7075-3-41.
We report longitudinal changes in the metabolic syndrome (MetS) in 2,458 participants from 480 families in the Family Heart Study. Participants were examined between 1994-96 (FHS-T1) and 2002-03 (FHS-T2), about 7.4 years apart. Additionally, the impact of medication on estimates of MetS prevalence, and associations of MetS with prevalent coronary heart disease (CHD) and type 2 diabetes (T2D) were studied.
Three definitions for MetS prevalence were considered. One represented the original (o) National Cholesterol Education Program (NCEP) MetS criteria. Two others considered the confounding of medications effects, respectively (m) lipid medications constituted a categorical diagnostic criterion for lipids variables, and (c) lipids and blood pressure variables were corrected with average clinical trials medications effects. Logistic regression of MetS on CHD and T2D, as well as the trend analysis of MetS by age, were performed.
MetS increased from 17.1% in FHS-T1(o) to 28.8% in FHS-T2(o); from 19.7% in FHS-T1(m) to 42.5% in FHS-T2(m); and from 18.4% in FHS-T1(c) to 33.6% in FHS-T2(c). While we observed adverse changes in all risk factors, the greatest increase was for waist circumference (25%). The percentages of MetS were about 2 to almost 3 times higher in ages 50 years and older than in younger ages. The odds of having prevalent CHD were about 2.5 times higher in the subjects classified with MetS than without.
MetS percentages increased noticeably longitudinally and cross-sectionally with older age. These conclusions were reached with and without considering medication use, but correcting risk factors for medications use affects the MetS prevalence estimates. As found in other studies, MetS was associated with increased odds for prevalent CHD.
我们报告了家庭心脏研究中480个家庭的2458名参与者代谢综合征(MetS)的纵向变化。参与者在1994 - 1996年(FHS - T1)和2002 - 2003年(FHS - T2)接受检查,间隔约7.4年。此外,还研究了药物对MetS患病率估计的影响,以及MetS与冠心病(CHD)和2型糖尿病(T2D)患病率的关联。
考虑了三种MetS患病率的定义。一种代表原始的(o)国家胆固醇教育计划(NCEP)MetS标准。另外两种分别考虑了药物效应的混杂因素,(m)脂质药物构成脂质变量的分类诊断标准,以及(c)脂质和血压变量用平均临床试验药物效应进行校正。对MetS与CHD和T2D进行逻辑回归分析,以及按年龄对MetS进行趋势分析。
MetS患病率从FHS - T1(o)时的17.1%增至FHS - T2(o)时的28.8%;从FHS - T1(m)时的19.7%增至FHS - T2(m)时的42.5%;从FHS - T1(c)时的18.4%增至FHS - T2(c)时的33.6%。虽然我们观察到所有风险因素都有不良变化,但腰围增加幅度最大(25%)。50岁及以上人群的MetS百分比比年轻人群高约2至近3倍。患有CHD的MetS分类受试者的患病几率比未分类者高约2.5倍。
无论纵向还是横向,MetS百分比都随年龄增长而显著增加。无论是否考虑药物使用情况都得出了这些结论,但校正药物使用的风险因素会影响MetS患病率估计。正如其他研究中所发现的,MetS与CHD患病率增加相关。