UTPAL GOSWAMI, M.D., Professor of Psychiatry & Drug de-addiction Centre, Lady Hardinge Medical College & Associated Hospital, New Delhi - 110 001.
Indian J Psychiatry. 1998 Jul;40(3):201-11.
In this study, the prognostic determinants were investigated involving bipolar patients classified into two groups-one with favourable course and outcome, and the other with clearly unfavourable prognosis, based on certain recommended criteria, with intermediate prognosis were excluded. As compared to the poor prognosis group, the good prognosis group had lower social dysfunctions, lower ratings on psychopathotogy fewer indicators of neurodysfunction in form of neurological soft signs (NSS) and tardive dyskinesia (TD). The poor prognosis group was characterized by: (i) older age at onset; (ii) more manic than depressive episodes (5:1) and (HI) lower levels of serum dopamine-β-hydroxylase activity (DBH). The association between poor prognosis bipolar disorder having neuroleptic intolerance (TD and NSS) with low serum DBH, suggests that it is genetically governed. Further research in this direction seems in order, particularly the follow up of first episode manic disorders.
在这项研究中,研究了预后决定因素,将双相情感障碍患者分为两组:一组预后良好,结局良好,另一组预后明显不良,基于某些推荐的标准,排除了预后中等的患者。与预后不良组相比,预后良好组的社会功能障碍较低,精神病学评分较低,神经功能障碍的指标(以神经软体征(NSS)和迟发性运动障碍(TD)的形式)较少。预后不良组的特点是:(i)发病年龄较大;(ii)躁狂发作多于抑郁发作(5:1);(iii)血清多巴胺-β-羟化酶活性(DBH)水平较低。预后不良的双相情感障碍与抗精神病药物不耐受(TD 和 NSS)相关,与低血清 DBH 有关,这表明它是由遗传决定的。似乎有必要在这一方向进行进一步的研究,特别是对首发躁狂障碍的随访。