Ronald J Ellis, Shibangi Pal, Cristian L Achim, Erin Sundermann, David J Moore, Virawudh Soontornniyomkij, Howard Feldman
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Two participants had gross and microscopic examination and immunohistochemistry of the brain at autopsy; one was assessed clinically for Alzheimer's disease by cerebrospinal fluid (CSF) analysis of phosphorylated-Tau, Total-Tau and Aβ42. Additionally, a larger cohort of 250 autopsied individuals was evaluated for presence of amyloid plaques, Tau, and related pathologies. Three older, virally suppressed individuals with HIV who had long-term treatment with RTIs were included in analyses. Two cases demonstrated substantial cerebral amyloid deposition at autopsy. The third case met clinical criteria for AD based on a typical clinical course and CSF biomarker profile. In the larger cohort of autopsied individuals, the prevalence of cerebral amyloidosis among people with HIV (PWH) was greater for those on RTIs. Our study showed that long-term RTI therapy did not protect against Alzheimer-type brain amyloidogenesis in the context of HIV infection in these patients. 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The third case met clinical criteria for AD based on a typical clinical course and CSF biomarker profile. In the larger cohort of autopsied individuals, the prevalence of cerebral amyloidosis among people with HIV (PWH) was greater for those on RTIs. Our study showed that long-term RTI therapy did not protect against Alzheimer-type brain amyloidogenesis in the context of HIV infection in these patients. 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引用次数: 0
摘要
逆转录酶抑制剂(RTI)目前被广泛用于治疗艾滋病病毒感染,但也被认为可以通过防止淀粉样变性来预防阿尔茨海默病(AD)的发展。我们的研究评估了逆转录酶抑制剂在艾滋病病毒感染的情况下防止阿尔茨海默型脑淀粉样蛋白生成的假设。我们从艾滋病病毒神经行为研究项目(HNRP)的一项艾滋病病毒感染神经后果前瞻性研究中收集了一系列病例,这些病例接受了一系列神经心理学和神经学评估,并服用了逆转录酶抑制剂。两名参与者在尸检时对大脑进行了大体和显微镜检查以及免疫组化;一名参与者通过脑脊液(CSF)中磷酸化-Tau、总-Tau 和 Aβ42 的分析进行了阿尔茨海默病的临床评估。此外,还对 250 名尸检者进行了淀粉样蛋白斑、Tau 和相关病理的评估。分析中包括了三位年龄较大、病毒抑制但长期接受 RTIs 治疗的 HIV 感染者。其中两例在尸检时显示出大量脑淀粉样沉积。第三个病例根据典型的临床过程和脑脊液生物标志物特征,符合AD的临床标准。在更大的尸检人群中,接受RTI治疗的艾滋病病毒感染者(PWH)的脑淀粉样变性发病率更高。我们的研究表明,在这些患者感染艾滋病毒的情况下,长期RTI疗法并不能防止阿尔茨海默型脑淀粉样变性的发生。鉴于 RTIs 的已知毒性,向未感染 HIV 的阿尔茨海默氏症高危人群或患者推荐 RTIs 还为时过早。
Alzheimer-Type Cerebral Amyloidosis in the Context of HIV Infection: Implications for a Proposed New Treatment Approach.
Reverse transcriptase inhibitors (RTIs) are currently broadly prescribed for the treatment of HIV infection but are also thought to prevent Alzheimer's disease (AD) progression by protecting against amyloidosis. Our study evaluates the hypothesis that reverse transcriptase inhibitors protect against Alzheimer-type brain amyloidogenesis in the context of HIV infection. We compiled a case series of participants from a prospective study of the neurological consequences of HIV infection at the HIV Neurobehavioral Research Program (HNRP) who had serial neuropsychological and neurological assessments and were on RTIs. Two participants had gross and microscopic examination and immunohistochemistry of the brain at autopsy; one was assessed clinically for Alzheimer's disease by cerebrospinal fluid (CSF) analysis of phosphorylated-Tau, Total-Tau and Aβ42. Additionally, a larger cohort of 250 autopsied individuals was evaluated for presence of amyloid plaques, Tau, and related pathologies. Three older, virally suppressed individuals with HIV who had long-term treatment with RTIs were included in analyses. Two cases demonstrated substantial cerebral amyloid deposition at autopsy. The third case met clinical criteria for AD based on a typical clinical course and CSF biomarker profile. In the larger cohort of autopsied individuals, the prevalence of cerebral amyloidosis among people with HIV (PWH) was greater for those on RTIs. Our study showed that long-term RTI therapy did not protect against Alzheimer-type brain amyloidogenesis in the context of HIV infection in these patients. Given the known toxicities of RTIs, it is premature to recommend them to individuals at risk or with Alzheimer's disease who do not have HIV infection.