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抑郁症、运动障碍和偏头痛中的线粒体遗传?

Mitochondrial inheritance in depression, dysmotility and migraine?

作者信息

Burnett Brittany B, Gardner Ann, Boles Richard G

机构信息

Division of Medical Genetics and the Saban Research Institute, Childrens Hospital Los Angeles, CA 90027, USA.

出版信息

J Affect Disord. 2005 Sep;88(1):109-16. doi: 10.1016/j.jad.2005.05.009.

Abstract

BACKGROUND

Several studies have reported a high degree of association of the common conditions of depression, bowel dysmotility and migraine. Mitochondrial dysfunction and mitochondrial DNA (mtDNA) sequence variants have been linked individually to each of these three conditions, providing a plausible hypothesis for the reported association. If this hypothesis is correct, the matrilineal relatives (who all share essentially the same mtDNA sequence) of patients with mitochondrial disease secondary to inherited mtDNA mutations would be expected to have an elevated prevalence of each of these three conditions.

METHODS

Families were recruited by an advertisement posted on the United Mitochondrial Disease Foundation website and invited to participate in an on-line questionnaire if at least one member was diagnosed with mitochondrial disease by a physician. Based upon the reported family histories, families were assigned by the investigators to either the probable maternal inheritance (PMI) group (55 families) or the probable non-maternal inheritance (PnMI) group (111 families).

RESULTS

Bowel disorders, migraine and depression were reported at very high prevalence in the PMI mothers (60%, 54% and 51%, respectively), but were present at significantly lower prevalence rates among the PnMI mothers (16%, 26% and 12%; P<0.0001 for each) and the fathers of both groups (range 9-16%; P < 2 x 10(-6) for each). Similar data was obtained comparing the prevalence rates among maternal and paternal grandmothers, aunts and uncles.

LIMITATIONS

Our data was obtained from families ascertained by the presence of a severely affected individual, and may not be applicable to families lacking this proband.

CONCLUSIONS

Depression, bowel dysmotility and migraine are common manifestations in individuals with mtDNA sequence-related mitochondrial dysfunction, which supports our hypothesis that mitochondrial dysfunction is a major common factor underlying the association of these three conditions.

摘要

背景

多项研究报告称抑郁症、肠道运动障碍和偏头痛等常见病症之间存在高度关联。线粒体功能障碍和线粒体DNA(mtDNA)序列变异已分别与这三种病症中的每一种相关联,为所报告的关联提供了一个合理的假设。如果这个假设正确,那么继发于遗传性mtDNA突变的线粒体疾病患者的母系亲属(他们基本上共享相同的mtDNA序列)预计会有这三种病症中每一种的患病率升高。

方法

通过在美国线粒体疾病基金会网站上发布广告招募家庭,如果至少有一名成员被医生诊断为线粒体疾病,就邀请他们参与在线问卷。根据所报告的家族病史,研究人员将家庭分为可能的母系遗传(PMI)组(55个家庭)或可能的非母系遗传(PnMI)组(111个家庭)。

结果

PMI组母亲中肠道疾病、偏头痛和抑郁症的报告患病率非常高(分别为60%、54%和51%),但在PnMI组母亲(分别为16%、26%和12%;每种情况P<0.0001)和两组父亲中(范围为9 - 16%;每种情况P < 2×10⁻⁶)的患病率明显较低。比较外祖母、祖母、姑姑和叔叔中的患病率也获得了类似的数据。

局限性

我们的数据来自因存在严重受影响个体而确定的家庭,可能不适用于没有该先证者的家庭。

结论

抑郁症、肠道运动障碍和偏头痛是与mtDNA序列相关的线粒体功能障碍个体中的常见表现,这支持了我们的假设,即线粒体功能障碍是这三种病症关联背后的主要共同因素。

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