Christian Susan, Ridsdale Ross, Lin Mu, Khoury Michael
Department of Medical Genetics (Christian, Risdale) and Department of Pediatrics (Khoury), University of Alberta; Alberta SPOR Support Unit and Provincial Research Data Services (Lin), Alberta Health Services, Edmonton, Alta.
CMAJ Open. 2023 Sep 19;11(5):E820-E825. doi: 10.9778/cmajo.20220163. Print 2023 Sep-Oct.
Familial hypercholesterolemia is a common, inherited, life-threatening and treatable condition that is characterized by marked elevations of low-density lipoprotein cholesterol (LDL-C), resulting in a high risk of cardiovascular disease, but treatment starting in childhood dramatically reduces this risk. We sought to evaluate the prevalence of pediatric lipid assessments among children in Alberta.
We reviewed laboratory and administrative data from Alberta Health between Apr. 1, 2012, and Dec. 31, 2021. We evaluated 2 pediatric cohorts (children aged 2-10 yr and children aged 9-17 yr) to allow for longitudinal assessments throughout the pediatric period. We also reviewed annual frequencies of lipid assessment for all children between 2013 and 2021.
Pediatric lipid assessments were performed for 1972 (4.3%) of 46 170 children aged 2-10 years and for 8158 (19.9%) of 40 926 children aged 9-17 years. Female children (aged 2-10 yr) and those living in rural communities were significantly less likely to have a lipid assessment, compared with male children and those in nonrural communities. Among those with lipid assessments, 23 (1.2%) and 86 (1.1%) children aged 2-10 years and 9-17 years, respectively, had an LDL-C level suggestive of probable familial hypercholesterolemia (≥ 4.0 mmol/L). Statin therapy was prescribed in 16 children during the study period. The frequency of lipid assessments was relatively stable, with the exception of a decrease in 2020.
Rates of pediatric lipid assessment in Alberta are suboptimal. These findings highlight the need to increase awareness of the benefits of early diagnosis and treatment of familial hypercholesterolemia with regard to long-term health and identify and overcome barriers to diagnosis and treatment.
家族性高胆固醇血症是一种常见的、遗传性的、危及生命但可治疗的疾病,其特征是低密度脂蛋白胆固醇(LDL-C)显著升高,导致心血管疾病风险很高,但儿童期开始治疗可显著降低这种风险。我们试图评估艾伯塔省儿童进行血脂评估的患病率。
我们回顾了2012年4月1日至2021年12月31日期间艾伯塔省卫生部门的实验室和行政数据。我们评估了两个儿科队列(2至10岁儿童和9至17岁儿童),以便在整个儿童期进行纵向评估。我们还回顾了2013年至2021年期间所有儿童的年度血脂评估频率。
在46170名2至10岁儿童中,有1972名(4.3%)进行了儿科血脂评估;在40926名9至17岁儿童中,有8158名(19.9%)进行了评估。与男童和非农村社区的儿童相比,女童(2至10岁)和生活在农村社区的儿童进行血脂评估的可能性显著更低。在进行血脂评估的儿童中,2至10岁和9至17岁的儿童分别有23名(1.2%)和86名(1.1%)的LDL-C水平提示可能患有家族性高胆固醇血症(≥4.0 mmol/L)。在研究期间,有16名儿童接受了他汀类药物治疗。血脂评估频率相对稳定,2020年有所下降。
艾伯塔省儿科血脂评估率不理想。这些发现凸显了提高对家族性高胆固醇血症早期诊断和治疗对长期健康益处的认识的必要性,并识别和克服诊断及治疗的障碍。