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在阿尔茨海默病中,托吡卡胺诱发的瞳孔散大试验受载脂蛋白E ε4等位基因剂量的调节。

Pupil dilatation assay by tropicamide is modulated by apolipoprotein E epsilon 4 allele dosage in Alzheimer's disease.

作者信息

Arai H, Terajima M, Nakagawa T, Higuchi S, Mochizuki H, Sasaki H

机构信息

Department of Geriatric Medicine, Tohoku University School of Medicine, Sendai, Japan.

出版信息

Neuroreport. 1996 Mar 22;7(4):918-20. doi: 10.1097/00001756-199603220-00017.

Abstract

The mydriatic response to dilute tropicamide was studied in 25 Japanese patients with Alzheimer's disease (AD), 13 patients with non-AD neurological diseases (non-AD) and 11 normal elderly subjects (control). Although the changes in resting pupil diameter and area over baseline were significantly greater (p < 0.05) in AD patients than in non-AD patients and controls, there was considerable overlap between the three groups. The change in resting pupil area was significantly greater (p < 0.05) in AD patients homozygous for ApoE epsilon 4 than in AD patients heterozygous for or without this allele. Despite a limited sample size in the present study, our results indicate that the pupil dilation assay by tropicamide is not an effective diagnostic tool for AD, and it may be modulated by different gene dosage of ApoE epsilon 4.

摘要

对25名日本阿尔茨海默病(AD)患者、13名非AD神经疾病患者(非AD)和11名正常老年受试者(对照)研究了对稀释托吡卡胺的散瞳反应。尽管AD患者静息瞳孔直径和面积相对于基线的变化显著大于(p<0.05)非AD患者和对照,但三组之间存在相当大的重叠。ApoE ε4纯合子的AD患者静息瞳孔面积变化显著大于(p<0.05)ApoE ε4杂合子或无此等位基因的AD患者。尽管本研究样本量有限,但我们的结果表明,托吡卡胺散瞳试验不是AD的有效诊断工具,且其可能受ApoE ε4不同基因剂量的调节。

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