Suppr超能文献

广泛性发育障碍和智力迟钝中的血小板5-羟色胺水平:诊断组差异、组内分布及行为相关性

Platelet serotonin levels in pervasive developmental disorders and mental retardation: diagnostic group differences, within-group distribution, and behavioral correlates.

作者信息

Mulder Erik J, Anderson George M, Kema Ido P, de Bildt Annelies, van Lang Natasja D J, den Boer Johan A, Minderaa Ruud B

机构信息

Child and Adolescent Psychiatry Center, University of Groningen, The Netherlands.

出版信息

J Am Acad Child Adolesc Psychiatry. 2004 Apr;43(4):491-9. doi: 10.1097/00004583-200404000-00016.

Abstract

OBJECTIVE

To investigate group differences, the within-group distributions, and the clinical correlates of platelet serotonin (5-HT) levels in pervasive developmental disorders (PDD).

METHOD

Platelet 5-HT levels were measured in Dutch children and young adults, recruited from 2001 through 2003, with PDD (autism, Asperger's, and PDD-not otherwise specified [PDD-NOS]; n = 81) or with mental retardation (MR; n = 54) but without PDD, and in normal controls (n = 60). The distribution of platelet 5-HT levels was assessed using mixture-modeling analyses. Relationships between platelet 5-HT levels and a full range of demographic, clinical, and behavioral variables were examined.

RESULTS

Group mean (+/- SD) platelet 5-HT levels (nmol/10 platelets) were significantly higher in the autistic (4.51 +/- 1.61, n = 33) and PDD-NOS (4.90 +/- 1.54, n = 43) groups compared to the MR (3.48 +/- 1.33, n = 54) or the normal control (3.58 +/- 1.08, n = 60) groups (F4,190 = 9.35, p <.001). Platelet 5-HT values in the combined PDD group showed a bimodal distribution, and an empirical cutpoint for hyperserotonemia was determined. None of the behavioral variables examined was significantly associated with platelet 5-HT levels.

CONCLUSIONS

The platelet hyperserotonemia of autism was replicated in Dutch subjects. Platelet 5-HT levels were also increased in PDD-NOS, while no elevation was seen in MR. Platelet 5-HT levels appeared to be bimodally distributed in the PDD group, with an apparent hyperserotonemic subgroup.

摘要

目的

研究广泛性发育障碍(PDD)患者血小板5-羟色胺(5-HT)水平的组间差异、组内分布及其临床相关性。

方法

对2001年至2003年间招募的荷兰儿童和青年进行血小板5-HT水平检测,这些受试者包括患有PDD(自闭症、阿斯伯格综合征和未特定的PDD [PDD-NOS];n = 81)或智力障碍(MR;n = 54)但无PDD的患者,以及正常对照组(n = 60)。采用混合模型分析评估血小板5-HT水平的分布。研究血小板5-HT水平与一系列人口统计学、临床和行为变量之间的关系。

结果

与MR组(3.48 +/- 1.33,n = 54)或正常对照组(3.58 +/- 1.08,n = 60)相比,自闭症组(4.51 +/- 1.61,n = 33)和PDD-NOS组(4.90 +/- 1.54,n = 43)的组平均(+/- SD)血小板5-HT水平(nmol/10个血小板)显著更高(F4,190 = 9.35,p <.001)。合并的PDD组血小板5-HT值呈双峰分布,并确定了高血清素血症的经验切点。所检查的行为变量均与血小板5-HT水平无显著相关性。

结论

荷兰受试者中重现了自闭症患者的血小板高血清素血症。PDD-NOS患者的血小板5-HT水平也升高,而MR患者未见升高。PDD组血小板5-HT水平似乎呈双峰分布,存在一个明显的高血清素血症亚组。

文献AI研究员

20分钟写一篇综述,助力文献阅读效率提升50倍。

立即体验

用中文搜PubMed

大模型驱动的PubMed中文搜索引擎

马上搜索

文档翻译

学术文献翻译模型,支持多种主流文档格式。

立即体验