Edmonds L K, Mosley B J, Admiraal A J, Olds R J, Romans S E, Silverstone T, Walsh A E
Department of Psychological Medicine, Dunedin School of Medicine, New Zealand.
Aust N Z J Psychiatry. 1998 Dec;32(6):823-9. doi: 10.3109/00048679809073872.
This paper outlines the methodologies used, and preliminary descriptive data collected, on a cohort of familial bipolar disorder (BPD) probands and first-degree relatives taking part in a descriptive and genetic study into familial BPD in New Zealand.
Fifty-five bipolar probands and 67 first-degree relatives were interviewed using the modified Diagnostic Interview for Genetic Studies (DIGS) and Family Interview for Genetic Studies (FIGS). Data was also collated from other sources. Blood samples were taken for DNA genomic analysis.
New Zealand families in which BPD segregates proved willing participants in this familial based genetic research. The methodologies used were acceptable. High rates of comorbidity were found in probands (27.3% met DSM-IV criteria for panic disorder/sub-threshold panic disorder; 12.7% for phobic disorder; 1.8% for obsessive-compulsive disorder; 9.1% for alcohol-related disorders and 7.3% for an eating disorder) and relatives (major depression 34.3%; panic disorder/sub-threshold panic disorder 12.0%; phobias 11.9% and alcohol-related disorders 11.9%). The polarity of index BPD illness was related to age of onset and frequency of comorbidity. Suicidal behaviour was common.
Psychiatric genetic research in New Zealand families is highly feasible. Emerging trends in the familial transmission of BPD include high rates of comorbidity, illness patterns based on polarity of index episode and frequent suicidal behaviour. Such trends will be delineated further as numbers accrue, perhaps enabling identification of more homogenous phenotypic subgroups than currently produced by diagnostic schemes.
本文概述了在新西兰对一组家族性双相情感障碍(BPD)先证者及其一级亲属进行描述性和基因研究时所采用的方法以及收集到的初步描述性数据。
使用改良的基因研究诊断访谈(DIGS)和基因研究家族访谈(FIGS)对55名双相情感障碍先证者和67名一级亲属进行了访谈。还从其他来源整理了数据。采集血样进行DNA基因组分析。
事实证明,BPD在其中进行分离的新西兰家庭愿意参与这项基于家族的基因研究。所采用的方法是可接受的。在先证者中发现了高共病率(27.3%符合DSM-IV惊恐障碍/亚阈值惊恐障碍标准;12.7%为恐惧症;1.8%为强迫症;9.1%为酒精相关障碍;7.3%为饮食失调),在亲属中也有高共病率(重度抑郁症34.3%;惊恐障碍/亚阈值惊恐障碍12.0%;恐惧症11.9%;酒精相关障碍11.9%)。索引BPD疾病的极性与发病年龄和共病频率有关。自杀行为很常见。
在新西兰家庭中进行精神疾病基因研究非常可行。BPD家族传播的新趋势包括高共病率、基于索引发作极性的疾病模式以及频繁的自杀行为。随着病例数的增加,这些趋势将得到进一步描述,或许能够识别出比目前诊断方案所产生的更为同质的表型亚组。