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在接受高效抗逆转录病毒治疗的患者中,脑脊液中无法检测到HIV RNA和β-2微球蛋白并不表明艾滋病痴呆综合征处于非活动状态。

Undetectable cerebrospinal fluid HIV RNA and beta-2 microglobulin do not indicate inactive AIDS dementia complex in highly active antiretroviral therapy-treated patients.

作者信息

Cysique Lucette A, Brew Bruce J, Halman Mark, Catalan Jose, Sacktor Ned, Price Richard W, Brown Steve, Atkinson J Hampton, Clifford David B, Simpson David, Torres Gabriel, Hall Colin, Power Christopher, Marder Karen, McArthur Justin C, Symonds William, Romero Carmen

机构信息

St. Vincent's Hospital Clinical School, University of New South Wales, Darlinghurst, Sydney, Australia.

出版信息

J Acquir Immune Defic Syndr. 2005 Aug 1;39(4):426-9. doi: 10.1097/01.qai.0000165799.59322.f5.

Abstract

OBJECTIVE

To assess whether nonelevated cerebrospinal fluid (CSF) markers could delineate inactive AIDS dementia complex (ADC) in patients receiving highly active antiretroviral therapy (HAART), using neuropsychologic performance change as an indicator of ADC stability.

METHODS

We used data from the abacavir (ABC) ADC trial (n = 78) and examined the patients' neuropsychologic performance change with the Reliable Change Index according to 3 cutoff groups: (1) CSF viral load (VL) <100 copies/mL, (2) CSF beta-2 microglobulin (beta2m) <2.2 mg/L, and (3) CSF VL and CSF beta2m below cutoffs.

RESULTS

CSF marker cutoff groups did not define neuropsychologic change. Linear regression showed that only CSF VL was a weak predictor of neuropsychologic performance change.

CONCLUSION

HAART-treated ADC patients with baseline CSF markers of viral and immunologic inactivity did not necessarily have inactive ADC when followed over 12 weeks. More sensitive CSF markers to judge the activity of ADC are urgently needed, whereas the interpretation of these markers should be considered with caution in HAART-treated ADC patients.

摘要

目的

以神经心理功能变化作为艾滋病痴呆综合征(ADC)稳定性的指标,评估在接受高效抗逆转录病毒治疗(HAART)的患者中,脑脊液(CSF)标志物未升高时能否界定非活动性ADC。

方法

我们使用了阿巴卡韦(ABC)ADC试验的数据(n = 78),并根据3个临界值组,用可靠变化指数检查了患者的神经心理功能变化:(1)CSF病毒载量(VL)<100拷贝/mL,(2)CSFβ2微球蛋白(β2m)<2.2 mg/L,以及(3)CSF VL和CSFβ2m低于临界值。

结果

CSF标志物临界值组未能界定神经心理变化。线性回归显示,只有CSF VL是神经心理功能变化的弱预测指标。

结论

在接受HAART治疗的ADC患者中,在12周的随访期间,基线时CSF病毒和免疫标志物呈非活动性的患者不一定患有非活动性ADC。迫切需要更敏感的CSF标志物来判断ADC的活动性,而在接受HAART治疗的ADC患者中,对这些标志物的解读应谨慎考虑。

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