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双相情感障碍中的遗传早现

Anticipation in bipolar affective disorder.

作者信息

McInnis M G, McMahon F J, Chase G A, Simpson S G, Ross C A, DePaulo J R

机构信息

Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine, Baltimore, MD 21287-7463.

出版信息

Am J Hum Genet. 1993 Aug;53(2):385-90.

Abstract

Anticipation refers to the increase in disease severity or decrease in age at onset in succeeding generations. This phenomenon, formerly ascribed to observation biases, correlates with the expansion of trinucleotide repeat sequences (TNRs) in some disorders. If present in bipolar affective disorder (BPAD), anticipation could provide clues to its genetic etiology. We compared age at onset and disease severity between two generations of 34 unilineal families ascertained for a genetic linkage study of BPAD. Life-table analyses showed a significant decrease in survival to first mania or depression from the first to the second generation (P < .001). Intergenerational pairwise comparisons showed both a significantly earlier age at onset (P < .001) and a significantly increased disease severity (P < .001) in the second generation. This difference was significant under each of four data-sampling schemes which excluded probands in the second generation. The second generation experienced onset 8.9-13.5 years earlier and illness 1.8-3.4 times more severe than did the first generation. In additional analyses, drug abuse, deaths of affected individuals prior to interview, decreased fertility, censoring of age at onset, and the cohort effect did not affect our results. We conclude that genetic anticipation occurs in this sample of unilineal BPAD families. These findings may implicate genes with expanding TNRs in the genetic etiology of BPAD.

摘要

遗传早现是指在连续几代人中疾病严重程度增加或发病年龄降低。这种现象以前被归因于观察偏差,在某些疾病中与三核苷酸重复序列(TNRs)的扩增相关。如果双相情感障碍(BPAD)中存在遗传早现现象,可能为其遗传病因提供线索。我们比较了为BPAD遗传连锁研究确定的34个单系家族两代人的发病年龄和疾病严重程度。寿命表分析显示,从第一代到第二代,首次出现躁狂或抑郁的生存率显著降低(P <.001)。代际成对比较显示,第二代的发病年龄显著提前(P <.001),疾病严重程度也显著增加(P <.001)。在排除第二代先证者的四种数据抽样方案中的每一种方案下,这种差异都是显著的。第二代的发病时间比第一代早8.9 - 13.5年,疾病严重程度是第一代的1.8 - 3.4倍。在额外的分析中,药物滥用、受影响个体在访谈前死亡、生育力下降、发病年龄的审查以及队列效应均未影响我们的结果。我们得出结论,在这个单系BPAD家族样本中存在遗传早现现象。这些发现可能暗示在BPAD的遗传病因中存在具有TNRs扩增的基因。

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