Khan Rumana J, Gebreab Samson Y, Riestra Pia, Xu Ruihua, Davis Sharon K
Cardiovascular Section, Genomics of Metabolic, Cardiovascular and Inflammatory Disease Branch, Social Epidemiology Research Unit, National Human Genome Research Institute, 10 Center Drive, Room 7 N316 MSC 1644, Bethesda, MD 20892 USA.
Diabetol Metab Syndr. 2014 Dec 15;6(1):140. doi: 10.1186/1758-5996-6-140. eCollection 2014.
Metabolic syndrome (MetS) is a clustering of five metabolic risk factors including abdominal obesity, elevated blood pressure, hypertriglyceridemia, low high-density lipoprotein cholesterol (HDL-C), and impaired fasting glucose. Few studies have fully reported the strength of clustering of these risk factors in a parent-offspring relationship. This analysis describes the associations between parents and their adult offspring in regard to MetS. It also estimates the association between each risk factor in parents and the presence of MetS in their offspring.
We analyzed data for 1193 offspring (565 sons, and 628 daughters) from the Framingham Offspring Study who attended examinations 5, 6, and 7. Information about their parents was collected from examinations 13, 14 and 15 of the Framingham Original Cohort study. We used pedigree file to combine parental and offspring's data. Participants were classified as having the MetS according to the Adult Treatment Panel III criteria. Analyses were conducted separately for mothers and fathers. Logistic regression was used to estimate the associations.
After adjusting for age, education, smoking, alcohol consumption and physical activity level of offspring, no significant association was found between father's and their offspring's MetS. Mother's MetS was significantly and positively associated with their daughter's MetS (adjusted odds ratio or adj OR: 1.63; 95% confidence Interval, CI:1.02-2.61), but not with their sons' MetS. When analyzed by individual components, maternal impaired glucose (adj OR: 2.03; 95% CI: 1.02- 9.31), abdominal obesity (adj OR: 1.56; 95% CI: 0.98- 2.55) and low HDL-C (adj OR: 2.12; 95% CI: 1.36-3.32) were associated daughter's MetS. Maternal low HDL-C and raised total cholesterol showed marginal association with son's MetS. For fathers, only impaired glucose (adj OR: 4.91; 95% CI: 2.07- 11.68) was associated with their daughter's MetS.
Using the data from Framingham Heart Study, we demonstrate differential association of MetS and its components between parents and offspring. Mother's MetS was strongly related with daughter's MetS, but the association was inconsistent with son's MetS. No association was found between father's MetS and offspring's Mets. These results provide evidence that daughters with mother's MetS are in higher risk than daughters or sons with father's MetS.
代谢综合征(MetS)是包括腹型肥胖、血压升高、高甘油三酯血症、低高密度脂蛋白胆固醇(HDL-C)和空腹血糖受损在内的五种代谢危险因素的聚集。很少有研究充分报道这些危险因素在亲子关系中的聚集强度。本分析描述了父母与成年子女在代谢综合征方面的关联。它还估计了父母中每个危险因素与子女患代谢综合征之间的关联。
我们分析了来自弗雷明汉后代研究的1193名后代(565名儿子和628名女儿)的数据,这些后代参加了第5、6和7次检查。他们父母的信息是从弗雷明汉原始队列研究的第13、14和15次检查中收集的。我们使用谱系文件来合并父母和后代的数据。根据成人治疗小组III标准将参与者分类为患有代谢综合征。分别对母亲和父亲进行分析。使用逻辑回归来估计关联。
在调整后代的年龄、教育程度、吸烟、饮酒和身体活动水平后,未发现父亲与后代的代谢综合征之间存在显著关联。母亲的代谢综合征与女儿的代谢综合征显著正相关(调整后的优势比或adj OR:1.63;95%置信区间,CI:1.02 - 2.61),但与儿子的代谢综合征无关。按个体成分分析时,母亲的血糖受损(adj OR:2.03;95% CI:1.02 - 9.31)、腹型肥胖(adj OR:1.56;95% CI:0.98 - 2.55)和低HDL-C(adj OR:2.12;95% CI:1.36 - 3.32)与女儿的代谢综合征相关。母亲的低HDL-C和总胆固醇升高与儿子的代谢综合征有边缘关联。对于父亲,只有血糖受损(adj OR:4.91;95% CI:2.07 - 11.68)与女儿的代谢综合征相关。
使用弗雷明汉心脏研究的数据,我们证明了代谢综合征及其组成部分在父母与后代之间的差异关联。母亲的代谢综合征与女儿的代谢综合征密切相关,但与儿子的代谢综合征的关联不一致。未发现父亲的代谢综合征与后代的代谢综合征之间存在关联。这些结果提供了证据,表明患有母亲代谢综合征的女儿比患有父亲代谢综合征的女儿或儿子面临更高的风险。