Heart Institute (InCor) University of Sao Paulo Medical School Hospital, Sao Paulo, Brazil.
Faculty of Sport and Health Sciences, University of Jyva ¨skyla, Finland; School of Psychology, Curtin University, Australia; School of Applied Psychology, Griffith University, Australia.
Atherosclerosis. 2018 Oct;277:464-469. doi: 10.1016/j.atherosclerosis.2018.05.036.
BACKGROUND AND AIMS: Familial hypercholesterolemia (FH) is a genetic disorder associated with high risk of early major cardiovascular events (MACE) that can impact the health related quality of life (HRQoL), however, this association is unclear. This study evaluated HRQoL in index cases (IC) and first-degree relatives (FDR) of individuals at high risk of FH undergoing genetic cascade screening. METHODS: Data collection was performed before awareness of molecular diagnosis results. Individuals were divided into four groups according to the molecular diagnosis: IC with (IC+) and without (IC-) identified mutations (n = 93 and n = 175, respectively), and affected (FDR+, n = 231) and non-affected (FDR-, n = 159) FDR of IC+. HRQoL measurements, mental (MCS) and physical component (PCS) scores were carried out with SF-12 questionnaire. Associations were tested by generalized linear models. RESULTS: The mean age was 49 ± 15 years, 42.2% were men, MACE had occurred in 30.7%. Overall, both PCS and MCS did not differ between FH and non-FH individuals, however, IC trended to have lower PCS independent of FH presence (p=0.003). Lower PCS were associated with female sex (p=0.018), lower education (p<0.001), professional inactivity (p=0.028), previous MACE occurrence (p<0.001), hypertension (p=0.016), depression (p<0.001) and obesity (p<0.001). Lower MCS were associated with female sex (p=0.009), previous MACE occurrence (p=0.034), depression (p<0.001) and smoking (p=0.009). Neither the presence of FH causing mutations nor pharmacological lipid lowering treatment was associated with HRQoL. CONCLUSIONS: HRQoL is not reduced in both IC and FDR FH individuals in comparison with their non-affected counterparts. Previous MACE and co-morbidities are associated with reduced HRQoL.
背景与目的:家族性高胆固醇血症(FH)是一种与早期重大心血管事件(MACE)风险较高相关的遗传疾病,可能会影响健康相关生活质量(HRQoL),但这种关联尚不清楚。本研究评估了正在接受遗传级联筛查的 FH 高危个体的索引病例(IC)和一级亲属(FDR)的 HRQoL。
方法:在了解分子诊断结果之前进行数据收集。根据分子诊断将个体分为四组:携带(IC+)和不携带(IC-)突变的 IC(n=93 和 n=175),以及受影响(FDR+,n=231)和未受影响(FDR-,n=159)的 IC 的 FDR。采用 SF-12 问卷进行 HRQoL 测量,包括精神(MCS)和身体成分(PCS)评分。采用广义线性模型检验相关性。
结果:平均年龄为 49±15 岁,42.2%为男性,30.7%发生过 MACE。总体而言,FH 个体与非 FH 个体的 PCS 和 MCS 均无差异,但无论 FH 状态如何,IC 的 PCS 均呈下降趋势(p=0.003)。较低的 PCS 与女性(p=0.018)、较低的教育程度(p<0.001)、非职业性(p=0.028)、既往 MACE 发生(p<0.001)、高血压(p=0.016)、抑郁(p<0.001)和肥胖(p<0.001)相关。较低的 MCS 与女性(p=0.009)、既往 MACE 发生(p=0.034)、抑郁(p<0.001)和吸烟(p=0.009)相关。FH 致病突变的存在和药物降脂治疗均与 HRQoL 无关。
结论:与未受影响的对照者相比,IC 和 FDR FH 个体的 HRQoL 并未降低。既往 MACE 和合并症与 HRQoL 降低相关。
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