Thangiah Nithiah, Chinna Karuthan, Su Tin Tin, Jalaludin Muhammad Yazid, Al-Sadat Nabilla, Majid Hazreen Abdul
Department of Social and Preventive Medicine, Faculty of Medicine, Centre for Population Health (CePH), University of Malaya, Kuala Lumpur, Malaysia.
Faculty of Health and Medical Sciences, School of Medicine, Taylor's University, Selangor, Malaysia.
Front Public Health. 2020 Mar 17;8:69. doi: 10.3389/fpubh.2020.00069. eCollection 2020.
Cardiovascular disease (CVD) risk factors tend to cluster and progress from adolescence to young adulthood. Reliable and meaningful clustering of CVD risk factors is essential to circumvent loss of information. Tracking adverse and high-risk profiles of adolescents is hoped to curb CVD progression later in life. The study aims to investigate the clustering of biological CVD risk factor among adolescents in Malaysia and the transitions between clusters over time. The Malaysian Health and Adolescents Longitudinal Research Team study (MyHeARTs) examined school students aged 13 in 2012 and re-examined them in 2014 and 2016. In a two-stage stratified cluster sampling, 1,361 students were recruited, of which, 1,320 had complete data. In the follow-up, there were 881 and 637 students in 2014 and in 2016, respectively. Pearson's correlation coefficients were used to identify and remove highly correlated CVD risk factors. All risk factors were standardized into z-scores. The hierarchical and non-hierarchical (k-means) cluster analyses were used to classify students into high, medium and low risk clusters in each screening year. The tracking and stability of cluster transitions through cross-classification were enumerated with Pearson's inter-age correlations and percentages. Three significant clusters of high, medium and low risk groups were derived from the clustering of eight biological CVD risk factors. The transitions between risk clusters from one screening year to the other were categorized as either stagnant, improved or adverse. The number of students who had adverse transitions increased from 15.5% (13-15 year) to 19.5% (15-17 year), 13.8 to 18.2% among the girls and 19.9 to 22.8% among the boys. For girls, the number of them who remained at high risk over the two transition periods were about the same (13.6 vs. 13.8%) whereas for boys, the percentage reduced from 14.6 to 12.3%. Over time, more than 12% of adolescents remained in the high risk cluster. There were sizable adverse transitions over time as more adolescents appear to be shifting toward an increased risk of having CVD. Collaborative and constant measures should be taken by parents, school, health promotion boards and policy makers to curb the multiplicative effect of clustering CVD risk factors among adolescents.
心血管疾病(CVD)风险因素往往会聚集,并从青春期发展至青年期。可靠且有意义地对CVD风险因素进行聚类对于避免信息丢失至关重要。追踪青少年的不良和高风险特征有望抑制其日后生活中心血管疾病的发展。本研究旨在调查马来西亚青少年中生物性CVD风险因素的聚类情况以及不同聚类随时间的转变。马来西亚健康与青少年纵向研究团队(MyHeARTs)研究在2012年对13岁的在校学生进行了检查,并于2014年和2016年对他们进行了再次检查。在两阶段分层整群抽样中,招募了1361名学生,其中1320名学生有完整数据。在随访中,2014年和2016年分别有881名和637名学生。使用Pearson相关系数来识别和去除高度相关的CVD风险因素。所有风险因素均标准化为z分数。使用层次聚类分析和非层次聚类分析(k均值)将学生在每个筛查年份分为高、中、低风险组。通过交叉分类对聚类转变的追踪和稳定性进行了Pearson年龄间相关性和百分比的计算。从八个生物性CVD风险因素的聚类中得出了高、中、低风险组的三个显著聚类。从一个筛查年份到另一个筛查年份,风险聚类之间的转变被归类为停滞、改善或不良。发生不良转变的学生人数从15.5%(13 - 15岁)增加到19.5%(15 - 17岁),女孩中从13.8%增加到18.2%,男孩中从19.9%增加到22.8%。对于女孩,在两个转变期内仍处于高风险的人数大致相同(13.6%对13.8%),而对于男孩,这一比例从14.6%降至12.3%。随着时间推移,超过12%的青少年仍处于高风险聚类中。随着越来越多的青少年似乎转向患心血管疾病风险增加的状态,随着时间的推移出现了相当数量的不良转变。家长、学校、健康促进委员会和政策制定者应采取协作且持续的措施来抑制青少年中CVD风险因素聚类的倍增效应。