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共病对双相情感障碍基因研究的影响:P300和眼动追踪作为疾病的生物学标志物

Implications of comorbidity for genetic studies of bipolar disorder: P300 and eye tracking as biological markers for illness.

作者信息

Blackwood D H, Sharp C W, Walker M T, Doody G A, Glabus M F, Muir W J

机构信息

Royal Edinburgh Hospital, UK.

出版信息

Br J Psychiatry Suppl. 1996 Jun(30):85-92.

PMID:8864153
Abstract

In large families with affective illness, identification of a biological variable is needed that reflects brain dysfunction at an earlier point than symptom development. Eye movement disorder, a possible vulnerability marker in schizophrenia, is less clearly associated with affective illness, although a subgroup of affective disorders shows smooth-pursuit eye movement disorder. The auditory P300 event-related potential may be a useful marker for risk to schizophrenia, but a role in bipolar illness is less certain. The distribution of these two biological variables and their association with symptoms in two multiply affected bipolar families is described. In a single, five-generation family identified for linkage studies through two bipolar I (BPI) probands, 128 members (including 20 spouses) were interviewed. The 108 related individuals had diagnoses of BPI (7), bipolar II (2), cyclothymia (3), or major depressive disorder (19). Eight others had generalised anxiety (1), minor depression (5), intermittent depression (1), or alcoholism (1). Sixty-nine subjects had no psychiatric diagnosis. P300 latency (81) and eye tracking (71) were recorded from a subgroup of relatives within the pedigree. Eye tracking was abnormal in 11 of 71 relatives (15.5%) and was bimodally distributed. In these 11 relatives, clinical diagnoses included minor depression (1), alcoholism (1) and generalised anxiety disorder (1). P300 latency was normally distributed and did not differ from controls. In a second family in which five of seven siblings have BPI illness, P300 latency and eye movement disorder were found in affected relatives and in some unaffected offspring. In these large families, clinical diagnoses of general anxiety, alcoholism and minor depression, when associated with eye tracking abnormality, may be considered alternative clinical manifestations of the same trait that in other relatives is expressed as bipolar illness.

摘要

在患有情感性疾病的大家庭中,需要确定一种生物学变量,该变量能比症状出现更早地反映脑功能障碍。眼球运动障碍是精神分裂症中一种可能的易感性标志物,与情感性疾病的关联不太明确,尽管有一小部分情感障碍患者表现出平稳跟踪眼球运动障碍。听觉P300事件相关电位可能是精神分裂症风险的一个有用标志物,但在双相情感障碍中的作用尚不确定。本文描述了这两种生物学变量在两个多例双相情感障碍患者的家庭中的分布情况及其与症状的关联。在一个通过两名双相I型(BPI)先证者确定用于连锁研究的五代单一家系中,对128名成员(包括20名配偶)进行了访谈。108名亲属被诊断为BPI(7例)、双相II型(2例)、环性心境障碍(3例)或重度抑郁症(19例)。另外8人患有广泛性焦虑症(1例)、轻度抑郁症(5例)、间歇性抑郁症(1例)或酒精中毒(1例)。69名受试者没有精神疾病诊断。从家系中的一个亲属亚组记录了P300潜伏期(81例)和眼动追踪(71例)。71名亲属中有11名(15.5%)眼动追踪异常,且呈双峰分布。在这11名亲属中,临床诊断包括轻度抑郁症(1例)、酒精中毒(1例)和广泛性焦虑症(1例)。P300潜伏期呈正态分布,与对照组无差异。在第二个家庭中,7名兄弟姐妹中有5人患有BPI疾病,在患病亲属和一些未患病后代中发现了P300潜伏期和眼球运动障碍。在这些大家庭中,当广泛性焦虑症、酒精中毒和轻度抑郁症的临床诊断与眼动追踪异常相关时,可被视为同一特质的替代临床表现,而在其他亲属中则表现为双相情感障碍。

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