Mechri Anwar, Rouissi Khadija, Mehdi Boutheina, Khiari Geneviève, Abdelhak Sonia, Gaha Lotfi
Laboratoire de recherche Vulnérabilité aux psychoses, Service de Psychiatrie, hôpital universitaire de Monastir, Monastir, Tunisie.
Tunis Med. 2007 Nov;85(11):951-4.
The genetic transmission of bipolar disorder remained undetermined up to now, partly due to clinical and genetically heterogeneity. In Tunisia, genetic study will profit from the existence of high rates of consanguinity.
To determine the rate of consanguinity in bipolar I disorders sample and to compare the clinical characteristics and the frequency of affective disorders in first and second degree relatives of probands with and without consanguinity.
One hundred thirty subjects met DSM-IV criteria for a bipolar I disorder were recruited. Available Information was obtained from a structured clinical interview, collateral history and medical records. The family investigation allowed completion of genealogies over three generations. The comparison was based on the clinical characteristics (age of onset, numbers of affective episodes, nature and severity of the last affective episode) and the frequency of affective disorders in first and second degree relatives of probands with and without consanguinity.
the rate of consanguinity was estimated to 28,5% It was higher in patients with family history of affective disorders : 34,2% versus 20,4% (p=0,08). Bipolar I patients with consanguinity were characterised by a high frequency of affective episodes and a more severe of the last affective episode, but theses differences were not significantly. However, the frequency of affective disorders was significantly increased in first degree relatives of probands with consanguinity: 10,5% versus 6,1% (p=0,01), and in first and second degree relatives of probands with consanguinity : 4,5% versus 29% (p=0,02).
The influence of consanguinity on the clinical characteristics and the frequency of affective disorders in first and second degree relatives of bipolar patients is en favour the recessive polygenetic transmission of bipolar disorders.
双相情感障碍的遗传传递至今仍未确定,部分原因是临床和遗传异质性。在突尼斯,由于近亲结婚率高,遗传学研究将从中受益。
确定双相I型障碍样本中的近亲结婚率,并比较有血缘关系和无血缘关系的先证者一级和二级亲属的临床特征及情感障碍的发生率。
招募了130名符合双相I型障碍DSM-IV标准的受试者。通过结构化临床访谈、旁系病史和病历获取可用信息。家族调查完成了三代人的家谱。比较基于临床特征(发病年龄、情感发作次数、最后一次情感发作的性质和严重程度)以及有血缘关系和无血缘关系的先证者一级和二级亲属中情感障碍的发生率。
近亲结婚率估计为28.5%。有情感障碍家族史的患者中该比例更高:34.2%对20.4%(p = 0.08)。有血缘关系的双相I型患者的特点是情感发作频率高且最后一次情感发作更严重,但这些差异不显著。然而,有血缘关系的先证者一级亲属中情感障碍的发生率显著增加:10.5%对6.1%(p = 0.01),在有血缘关系的先证者一级和二级亲属中:4.5%对2.9%(p = 0.02)。
近亲结婚对双相情感障碍患者一级和二级亲属的临床特征及情感障碍发生率的影响支持双相情感障碍的隐性多基因传递。