中风后情绪障碍:新发现和未来方向。

Journal of geriatric psychiatry Pub Date : 1989-01-01
R G Robinson, S E Starkstein
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引用次数: 0

摘要

我们小组和其他人之前的调查表明,中风后的抑郁不能完全用相关损伤的严重程度来解释。然而,我们一直发现,重度抑郁症的发展与左前脑损伤之间存在很强的联系。最近的研究表明,左前皮层或皮层下病变都可能导致重度抑郁症的发展,而先前存在的皮层下萎缩可能在重度抑郁症的发展中起重要的纵容作用。可能与围产期损伤有关的轻度脑室增大的患者,在左额叶皮质或左基底神经节病变后,比先前没有脑室萎缩的患者更容易发生脑卒中后重度抑郁。另一方面,中风后躁狂与右半球病变以及先前存在的皮层下萎缩密切相关,有时还与情感障碍的家族史有关。因此,脑损伤后的躁狂症可能需要两个因素的融合:右脑损伤和先前存在的皮层下萎缩或遗传易感性。PET扫描结果表明,两个脑半球对中风的生化反应可能不同。右半球中风会增加血清素受体的结合,这在左半球中风后没有发现。在左半球,血清素结合越低,抑郁症越严重。这表明右半球而不是左半球可能有能力增加未受伤区域的血清素结合,对损伤产生生化“补偿”。右半球和左半球对损伤的不同生化反应可能部分解释了为什么左半球损伤导致抑郁,而右半球损伤(在特殊情况下)导致躁狂。然而,仍有许多未解决的问题和许多重要的领域有待未来的研究。虽然神经精神病学的这一领域才刚刚开始发展,但人们希望从对脑损伤患者的情绪障碍的研究中获得的见解也可能有助于阐明非脑损伤患者的情感障碍的机制。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mood disorders following stroke: new findings and future directions.

Previous investigations by our group and others have demonstrated that poststroke depressions are not fully explained by the severity of associated impairment. We have consistently found, however, a strong association between development of major depression and left anterior brain injury. Recent studies have demonstrated that either left anterior cortical or subcortical lesions may lead to the development of major depression and that preexisting subcortical atrophy may play an important permissive role in the development of major depression. Patients with a mild degree of ventricular enlargement perhaps related to perinatal damage may be more likely to develop poststroke major depression following a lesion of the left frontal cortex or left basal ganglia than a patient without preexisting atrophy. Poststroke mania, on the other hand, is strongly associated with right hemisphere lesions as well as a preexisting subcortical atrophy and sometimes a family history of affective disorder. Thus, mania following brain injury may require the convergence of two factors: a right hemisphere brain injury and either a preexisting subcortical atrophy or a genetic vulnerability. PET scan findings have suggested that the biochemical response of the two hemispheres to stroke may be different. Right hemisphere stroke produces an increase in serotonin receptor binding, which is not found following comparable left hemisphere strokes. Within the left hemisphere, the lower the serotonin binding, the more severe the depression. This suggests that the right but not the left hemisphere may have an ability to increase serotonin binding in noninjured regions, producing a biochemical "compensation" for damage. This differential biochemical response to injury between the right and left hemisphere may partially explain why left hemisphere injury leads to depression and right hemisphere injury (in special circumstances) lead to mania. There remain, however, numerous unanswered questions and many important areas for future research. Although this area of neuropsychiatry is just beginning to develop, it is hoped that insights gained from studying mood disorders in brain-injured patients may also help to illuminate mechanisms involved in affective disorder in patients without brain injury.

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