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患有精神分裂症的年轻女性一年内的骨矿物质密度变化:与药物治疗和内分泌变量的关系。

Bone mineral density changes over a year in young females with schizophrenia: relationship to medication and endocrine variables.

作者信息

Meaney A M, O'Keane V

机构信息

Department of Psychiatry, Beaumont Hospital, Dublin 9, Ireland.

出版信息

Schizophr Res. 2007 Jul;93(1-3):136-43. doi: 10.1016/j.schres.2007.01.013. Epub 2007 Apr 30.

Abstract

INTRODUCTION

Hyperprolactinaemia is associated with the use of potent dopamine-2 receptor blocking anti-psychotic agents in schizophrenia and with bone loss in the general population. Significantly higher rates of reduced bone mineral density (BMD) have been identified in young pre-menopausal females with schizophrenia receiving prolactin-raising anti-psychotics compared to those receiving prolactin-sparing anti-psychotics. This prospective study compared BMD alterations over a period of 1 year in patients maintained on either prolactin-raising (e.g. risperidone, amisulpride or depot anti-psychotics) or prolactin-sparing (olanzapine) anti-psychotics. The effects of specific interventions to improve BMD were also examined in the context of whether patients were receiving either prolactin-raising or anti-psychotics or Olanzapine.

METHODS

Pre-menopausal females (n=38) with a diagnosis of schizophrenia, who had received exclusively either prolactin-raising (n=25) or prolactin-sparing (n=13) anti-psychotics during their treatment history, had clinical, endocrine and bone marker assessments performed at baseline and every 3 months for a period of 1 year. BMD was measured by DEXA scan at baseline and at 1-year follow-up. Patients from both groups either received specific interventions (n=16) or no interventions (n=16) to improve bone density.

RESULTS

There was an overall gain in lumbar BMD values in the prolactin-sparing subgroup, compared to an overall loss in the prolactin-raising subgroup (p=0.02), for the groups that received no specific interventions to improve BMD. Within the group that received specific interventions, the subgroup receiving prolactin-sparing anti-psychotics had a significant increase in lumbar (p=0.01) and hip (p=0.01) BMD over time, whereas alterations in the prolactin-raising subgroup were not significant.

DISCUSSION

Women taking prolactin-raising anti-psychotics and not receiving specific interventions to improve bone density had evidence of ongoing bone demineralisation over a year; whereas women taking prolactin-sparing anti-psychotics had a modest overall increase in BMD. Most clinical interventions appeared to be helpful, but were significantly more effective in those taking prolactin-sparing anti-psychotics.

摘要

引言

高催乳素血症与精神分裂症患者使用强效多巴胺-2受体阻断抗精神病药物有关,且在普通人群中与骨质流失有关。与接受不升高催乳素的抗精神病药物的年轻绝经前女性精神分裂症患者相比,接受升高催乳素的抗精神病药物的患者骨矿物质密度(BMD)降低的发生率显著更高。这项前瞻性研究比较了接受升高催乳素(如利培酮、氨磺必利或长效抗精神病药物)或不升高催乳素(奥氮平)的抗精神病药物治疗的患者在1年期间的骨密度变化。还在患者接受升高催乳素或抗精神病药物或奥氮平的背景下,研究了改善骨密度的特定干预措施的效果。

方法

38名诊断为精神分裂症的绝经前女性,她们在治疗期间仅接受过升高催乳素(25名)或不升高催乳素(13名)的抗精神病药物治疗,在基线时以及为期1年的时间里每3个月进行一次临床、内分泌和骨标志物评估。在基线和1年随访时通过双能X线吸收法扫描测量骨密度。两组患者要么接受特定干预措施(16名),要么不接受干预措施(16名)以改善骨密度。

结果

对于未接受改善骨密度的特定干预措施的组,不升高催乳素亚组的腰椎骨密度值总体增加,而升高催乳素亚组总体下降(p=0.02)。在接受特定干预措施的组中,接受不升高催乳素的抗精神病药物的亚组随时间推移腰椎(p=0.01)和髋部(p=0.01)骨密度显著增加,而升高催乳素亚组的变化不显著。

讨论

服用升高催乳素的抗精神病药物且未接受改善骨密度的特定干预措施的女性,有证据表明在1年期间持续存在骨质脱矿;而服用不升高催乳素的抗精神病药物的女性骨密度总体有适度增加。大多数临床干预措施似乎有帮助,但对服用不升高催乳素的抗精神病药物的患者效果显著更明显。

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