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Measuring paternal discrepancy and its public health consequences.测量父系差异及其对公共卫生的影响。
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Is cascade testing a sensible method of screening a population for autosomal recessive disorders?级联检测是对人群进行常染色体隐性疾病筛查的明智方法吗?
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First and second trimester antenatal screening for Down's syndrome: the results of the Serum, Urine and Ultrasound Screening Study (SURUSS).孕早期和孕中期唐氏综合征产前筛查:血清、尿液及超声筛查研究(SURUSS)结果
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Cost effectiveness analysis of different approaches of screening for familial hypercholesterolaemia.家族性高胆固醇血症不同筛查方法的成本效益分析
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Mortality in treated heterozygous familial hypercholesterolaemia: implications for clinical management. Scientific Steering Committee on behalf of the Simon Broome Register Group.经治疗的杂合子家族性高胆固醇血症患者的死亡率:对临床管理的启示。代表西蒙·布鲁姆登记组的科学指导委员会。
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Neonatal screening for hyperlipidaemia.新生儿高脂血症筛查
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Diagnosing familial hypercholesterolaemia in childhood by measuring serum cholesterol.通过测量血清胆固醇诊断儿童家族性高胆固醇血症。
Br Med J. 1977 Jun 18;1(6076):1566-8. doi: 10.1136/bmj.1.6076.1566.
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Screening of cord blood low-density-lipoprotein cholesterol in the diagnosis of familial hypercholesterolaemia: a study of 2000 infants.脐血低密度脂蛋白胆固醇筛查在家族性高胆固醇血症诊断中的应用:一项对2000名婴儿的研究。
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Maternal serum-alpha-fetoprotein measurement in antenatal screening for anencephaly and spina bifida in early pregnancy. Report of U.K. collaborative study on alpha-fetoprotein in relation to neural-tube defects.孕早期产前筛查无脑儿和脊柱裂时母体血清甲胎蛋白测定。英国甲胎蛋白与神经管缺陷相关协作研究报告。
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儿童-父母家族性高胆固醇血症筛查:基于荟萃分析的筛查策略

Child-parent screening for familial hypercholesterolaemia: screening strategy based on a meta-analysis.

作者信息

Wald David S, Bestwick Jonathan P, Wald Nicholas J

机构信息

Wolfson Institute of Preventive Medicine, Barts and the London School of Medicine and Dentistry, London EC1M 6BQ.

出版信息

BMJ. 2007 Sep 22;335(7620):599. doi: 10.1136/bmj.39300.616076.55. Epub 2007 Sep 13.

DOI:10.1136/bmj.39300.616076.55
PMID:17855284
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC1989026/
Abstract

OBJECTIVE

To develop a population screening strategy for familial hypercholesterolaemia.

DESIGN

Meta-analysis of published data on total and low density lipoprotein (LDL) cholesterol in people with and without familial hypercholesterolaemia according to age. Thirteen studies reporting on 1907 cases and 16 221 controls were used in the analysis. Included studies had at least 10 cases and controls with data on the distribution of cholesterol in affected and unaffected individuals.

MAIN OUTCOME MEASURES

Detection rates (sensitivity) for specified false positive rates (0.1%, 0.5%, and 1%) in newborns and in age groups 1-9, 10-19, 20-39, 40-59, and > or =60 years.

RESULTS

Serum cholesterol concentration discriminated best between people with and without familial hypercholesterolaemia at ages 1-9, when the detection rates with total cholesterol were 88%, 94%, and 96% for false positive rates of 0.1%, 0.5%, and 1%. The results were similar with LDL cholesterol. Screening newborns was much less effective. Once an affected child is identified, measurement of cholesterol would detect about 96% of parents with the disorder, using the simple rule that the parent with the higher serum cholesterol concentration is the affected parent.

CONCLUSIONS

The proposed strategy of screening children and parents for familial hypercholesterolaemia could have considerable impact in preventing the medical consequences of this disorder in two generations simultaneously.

摘要

目的

制定家族性高胆固醇血症的人群筛查策略。

设计

对已发表的有关家族性高胆固醇血症患者和非患者总胆固醇及低密度脂蛋白(LDL)胆固醇水平随年龄变化的数据进行荟萃分析。分析采用了13项研究,共涉及1907例病例和16221例对照。纳入研究至少有10例病例和对照,且提供了患病和未患病个体胆固醇分布的数据。

主要观察指标

新生儿以及1 - 9岁、10 - 19岁、20 - 39岁、40 - 59岁和≥60岁年龄组在特定假阳性率(0.1%、0.5%和1%)下的检出率(敏感性)。

结果

血清胆固醇浓度在1 - 9岁人群中对家族性高胆固醇血症患者和非患者的区分效果最佳,当总胆固醇的假阳性率为0.1%、0.5%和1%时,检出率分别为88%、94%和96%。LDL胆固醇的结果类似。筛查新生儿的效果要差得多。一旦确定患病儿童,按照血清胆固醇浓度较高的一方为患病父母这一简单规则,检测胆固醇可发现约96%的患病父母。

结论

所提议的对儿童和父母进行家族性高胆固醇血症筛查的策略,可能会对同时预防两代人患此病的医学后果产生重大影响。