首页|期刊导航|中国卒中杂志|基于神经递质图谱的卒中后抑郁患者个体化诊疗探索——2例病例报道

基于神经递质图谱的卒中后抑郁患者个体化诊疗探索——2例病例报道OA

Exploring Individualized Diagnosis and Treatment for Post-Stroke Depression Based on Neurotransmitter Atlas:A Report of Two Cases

中文摘要英文摘要

卒中后抑郁(post-stroke depression,PSD)患者体内的5-羟色胺(5-hydroxytryptamine,5-HT)水平常显著下降,这一变化与卒中病灶对神经通路的破坏及代谢异常等因素密切相关.5-羟色胺选择性再摄取抑制剂(serotonin-selective reuptake inhibitors,SSRIs),如舍曲林,可选择性抑制突触前膜5-HT再摄取,提高突触间隙5-HT浓度,是目前抗抑郁治疗的一线药物.本病例报道2例缺血性PSD患者,通过分子影像学技术,将其病灶与受累核团映射至5-HT受体/转运体密度图谱,据此区分出突触前与突触后损伤两种亚型,结果显示2例患者分别为突触前及突触后损伤,提示不同PSD亚型可能对舍曲林抗抑郁治疗存在差异反应.本病例报道为探索PSD精准诊断分型及个体化治疗策略提供了新思路.

Post-stroke depression(PSD)patients often exhibit significantly reduced 5-hydroxytryptamine(5-HT)levels.This alteration is closely associated with stroke-induced disruption of neural pathways and metabolic abnormalities.Serotonin-selective reuptake inhibitors(SSRIs),such as sertraline,the first-line antidepressant drugs,selectively inhibit presynaptic 5-HT reuptake,thereby increasing synaptic 5-HT concentrations.This case report describes two cases of ischemic PSD.Using molecular imaging techniques,the stroke lesions and affected nuclei were mapped onto 5-HT receptor/transporter density atlases,and accordingly identified presynaptic and postsynaptic injury subtypes.The results showed that the two patients presented with presynaptic injury and postsynaptic injury,respectively,suggesting that different PSD subtypes may exhibit differential response to sertraline in antidepressant treatment.This case report provides novel insights for developing precise diagnostic subtypes and individualized treatment strategies for PSD.

张之婕;张华;卫景沛;钱勋琦;赵子珺

北京 100029 北京中医药大学第一临床医学院||北京 100029 北京中医药大学东直门医院神经内科北京 100029 北京中医药大学东直门医院神经内科北京 100029 北京中医药大学东直门医院神经内科北京 100029 北京中医药大学第一临床医学院||北京 100029 北京中医药大学东直门医院神经内科北京 100029 北京中医药大学东直门医院神经内科

医药卫生

缺血性卒中卒中后抑郁神经递质映射分子影像学病例报道

Ischemic strokePost-stroke depressionNeurotransmitter mappingMolecular imagingCase report

《中国卒中杂志》 2026 (1)

105-112,8

中央高水平中医医院临床科研业务费资助(DZMG-QNHB009)

10.3969/j.issn.1673-5765.2026.01.012

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