Jellinger Kurt A
Institute of Clinical Neurobiology, Vienna, Austria.
Free Neuropathol. 2025 Mar 13;6:9. doi: 10.17879/freeneuropathology-2025-6135. eCollection 2025 Jan.
Patients with schizophrenia are at a higher risk of developing dementia, but the basis of cognitive impairment is a matter of discussion. Conflicting results regarding the association of schizophrenia with Alzheimer disease (AD) may partly be attributable to the inclusion of non-AD lesions, which few clinicopathological studies have considered. Therefore, a re-evaluation of an autopsy cohort of elderly schizophrenics published previously [1] was performed. Among 99 consecutive autopsy cases of patients who met the DSM-5 and ICD.10 criteria for schizophrenia (mean age 69.5 ± 8.25 years), 56 showed moderate to severe dementia. All brains were blindly examined using the current criteria for AD and looking for concomitant lesions. They were compared with the frequency of AD in an autopsy series of 1.750 aged demented individuals Four cases revealed the features of definite AD, five probable AD, and three aged 82-89 years were classified as primary age-related tauopathy (PART). Two cases were a cortical type of dementia with Lewy bodies (DLB), one Lewy body disease of brainstem type; six showed hippocampal sclerosis, 14 argyrophilic grain disease (AGD), and one progressive supranuclear palsy (PSP). Other co-pathologies were frequent lacunes in basal ganglia, moderate cerebral amyloid angiopathy, minor development anomalies in the entorhinal cortex, Fahr's disease, metastatic tumors, and acute or old cerebral infarctions (n = 4 each). Definite AD was seen in 48 % of the age-matched demented control group. In this cohort of elderly schizophrenic patients, only 7.6 % fulfilled the neuropathological criteria of definite or probable AD and 3.6 % of PART compared to 6 % to 13.7 % typical and atypical AD in the literature, whereas a considerable number of cases showed non-AD co-pathologies. This is in line with other studies showing that the frequency of AD in elderly schizophrenics may be equal to or less than in age-matched controls. Further studies are needed to elucidate the mechanisms of cognitive decline in schizophrenia.
精神分裂症患者患痴呆症的风险更高,但认知障碍的基础仍存在争议。关于精神分裂症与阿尔茨海默病(AD)关联的相互矛盾的结果,部分可能归因于纳入了非AD病变,而很少有临床病理学研究对此进行过考虑。因此,我们对先前发表的一组老年精神分裂症患者的尸检队列进行了重新评估。在99例连续符合精神分裂症DSM-5和ICD-10标准的尸检病例中(平均年龄69.5±8.25岁),56例表现为中度至重度痴呆。所有大脑均采用当前的AD标准进行盲法检查,并寻找伴随病变。将其与1750例老年痴呆患者尸检系列中AD的发生率进行比较。4例显示明确的AD特征,5例可能为AD,3例年龄在82-89岁的患者被归类为原发性年龄相关性tau病(PART)。2例为皮质型路易体痴呆(DLB),1例为脑干型路易体病;6例显示海马硬化,14例嗜银颗粒病(AGD),1例进行性核上性麻痹(PSP)。其他合并病理改变包括基底节区常见的腔隙性梗死、中度脑淀粉样血管病、内嗅皮质轻度发育异常、 Fahr病、转移性肿瘤以及急性或陈旧性脑梗死(各4例)。在年龄匹配的痴呆对照组中,48%可见明确的AD。在这组老年精神分裂症患者中,只有7.6%符合明确或可能AD的神经病理学标准,PART为3.6%,而文献中典型和非典型AD的比例为6%至13.7%,然而相当数量的病例显示存在非AD合并病理改变。这与其他研究结果一致,表明老年精神分裂症患者中AD的发生率可能等于或低于年龄匹配的对照组。需要进一步研究以阐明精神分裂症认知衰退的机制。