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18个哥伦比亚派萨多代家庭中的注意力缺陷/多动障碍及其共病情况

Attention-deficit/hyperactivity disorder and comorbidities in 18 Paisa Colombian multigenerational families.

作者信息

Palacio Juan D, Castellanos F Xavier, Pineda David A, Lopera Francisco, Arcos-Burgos Mauricio, Quiroz Yakeel T, Henao Gloria C, Puerta Isabel C, Ramírez Dora L, Rapoport Judith L, Bailey-Wilson Joan, Berg Kate, Muenke Maximilian

机构信息

Neurosciences Group, University of Antioquia, Medellín, Colombia.

出版信息

J Am Acad Child Adolesc Psychiatry. 2004 Dec;43(12):1506-15. doi: 10.1097/01.chi.0000142279.79805.dc.

DOI:10.1097/01.chi.0000142279.79805.dc
PMID:15564820
Abstract

OBJECTIVE

Eighteen extended multigenerational families were recruited from the genetically isolated Paisa community in Colombia to conduct genetic studies of attention-deficit/hyperactivity disorder (ADHD). This report describes the inclusion strategy and clinical features of participants to facilitate comparisons with other data sets.

METHOD

Families were selected through a fixed-sampling scheme beginning with child probands referred for clinical evaluation for ADHD. Direct structured psychiatric interviews were conducted with 433 informative individuals, including 92 children aged 4 to 11, 57 adolescents aged 12 to 17, and 284 adults. Best estimate ADHD diagnoses were established for each informative pedigree member.

RESULTS

These families contained a high proportion of individuals affected with ADHD (32.8%), which was highly comorbid with conduct disorder (50%; odds ratio 11.5, 95% confidence interval = 6.4-20.9), oppositional defiant disorder (25.4%; odds ratio 2.7, confidence interval = 1.5-4.8), and associated conditions including nicotine dependence and alcohol abuse and/or dependence.

CONCLUSIONS

ADHD in these extended Paisa families is highly comorbid with conduct and oppositional defiant disorders. This pattern of comorbidity, as well as the large dense pedigrees of the sample, suggests that it will be particularly useful for molecular genetic studies that are currently under way.

摘要

目的

从哥伦比亚基因隔离的派萨社区招募了18个多代大家庭,以进行注意力缺陷多动障碍(ADHD)的遗传学研究。本报告描述了参与者的纳入策略和临床特征,以便与其他数据集进行比较。

方法

通过固定抽样方案选择家庭,从因ADHD接受临床评估的儿童先证者开始。对433名信息提供者进行了直接结构化精神科访谈,包括92名4至11岁的儿童、57名12至17岁的青少年和284名成年人。为每个信息丰富的家系成员确定了最佳估计ADHD诊断。

结果

这些家庭中受ADHD影响的个体比例很高(32.8%),与品行障碍(50%;优势比11.5,95%置信区间=6.4-20.9)、对立违抗障碍(25.4%;优势比2.7,置信区间=1.5-4.8)以及包括尼古丁依赖和酒精滥用和/或依赖在内的相关病症高度共病。

结论

这些派萨大家庭中的ADHD与品行障碍和对立违抗障碍高度共病。这种共病模式以及样本中庞大密集的家系表明,它对于目前正在进行的分子遗传学研究将特别有用。

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