Dravid Ameet N, Natrajan Kartik, Kulkarni Milind M, Saraf Chinmay K, Mahajan Uma S, Kore Sachin D, Rathod Niranjan M, Mahajan Umakant S, Wadia Rustom S
Department of Medicine, Ruby Hall Clinic Department of Medicine, Poona Hospital Department of Medicine, Noble Hospital Precision Diagnostics and Biosciences, Pune Department of Dermatology, Ashwini Sahakari Rugnalaya, Solapur Department of Medicine, Apex Hospital, Kolhapur GeneOmbio Technologies Private Limited, Pune, Maharashtra, India.
Medicine (Baltimore). 2018 Feb;97(8):e9969. doi: 10.1097/MD.0000000000009969.
Aim of this study was to estimate the prevalence of cerebrospinal fluid (CSF)/Plasma HIV-1 RNA discordance in virologically suppressed individuals presenting with incident neurologic symptoms.In this retrospective cohort study conducted between March 1, 2009, and March 1, 2017, HIV-1 infected adults exposed to atleast 12 months of antiretroviral therapy (ART) and having plasma viral load (VL) <1000 copies/mL (virologically suppressed) were included. Among these, individuals presenting with neurologic symptoms during follow-up were assessed for CSF/Plasma HIV-1 RNA discordance by measuring HIV-1 RNA in collected plasma and CSF samples. CSF/plasma HIV-1 RNA discordance was defined as either detectable CSF HIV-1 RNA (VL > 20 copies/mL) with an undetectable plasma RNA (complete viral suppression, VL ≤20 copies/mL) or CSF HIV-1 RNA ≥ 0.5 log10 higher than plasma RNA when plasma VL was between 20 and 1000 copies/mL (low-level viremia, LLV).Out of 1584 virologically suppressed patients, 71 (4.4%) presented with incident neurologic symptoms. Twenty out of 71 (28.2%) patients were diagnosed with CSF/Plasma HIV-1 discordance. Median plasma and CSF VL in patients with discordance was 120 [interquartile range (IQR): <20 to 332.5] and 4250 (IQR: 2550.0- 9615.0) copies/mL, respectively. All 9 individuals in which CSF HIV-1 genotypic resistance testing was done showed mutations that would compromise efficacy of prescribed ART regimen. Prevalence of CSF/plasma HIV-1 RNA discordance was higher among neurologically symptomatic patients with plasma LLV as compared with those with complete viral suppression (70% vs 11.8%, P < .001). The risk of discordance was also greater in patients who received protease inhibitor (PI) containing ART (P < .001) and those on ART regimens with central nervous system (CNS) penetration effectiveness (CPE) value <6 (P = .006).CSF/plasma HIV-1 RNA discordance indicates replication of HIV-1 that has adapted to the CNS or has developed antiretroviral drug resistance. Larger studies should be performed to study incidence of discordance in India. This will help in managing patients presenting with neurologic symptoms on suppressive ART with appropriate neuroeffective therapy.
本研究的目的是评估出现新发神经症状的病毒学抑制个体中脑脊液(CSF)/血浆HIV-1 RNA不一致的发生率。在这项于2009年3月1日至2017年3月1日进行的回顾性队列研究中,纳入了感染HIV-1且接受至少12个月抗逆转录病毒治疗(ART)、血浆病毒载量(VL)<1000拷贝/mL(病毒学抑制)的成年人。其中,对随访期间出现神经症状的个体,通过检测采集的血浆和脑脊液样本中的HIV-1 RNA,评估脑脊液/血浆HIV-1 RNA不一致情况。脑脊液/血浆HIV-1 RNA不一致定义为:血浆RNA不可检测(完全病毒抑制,VL≤20拷贝/mL)时脑脊液HIV-1 RNA可检测(VL>20拷贝/mL),或血浆VL在20至1000拷贝/mL之间(低水平病毒血症,LLV)时脑脊液HIV-1 RNA比血浆RNA高≥0.5 log10。在1584例病毒学抑制患者中,71例(4.4%)出现新发神经症状。71例患者中有20例(28.2%)被诊断为脑脊液/血浆HIV-1不一致。不一致患者的血浆和脑脊液VL中位数分别为120[四分位间距(IQR):<20至332.5]和4250(IQR:2550.0 - 9615.0)拷贝/mL。所有9例进行了脑脊液HIV-1基因型耐药检测的个体均显示出会损害所开ART方案疗效的突变。与完全病毒抑制的神经症状患者相比,血浆LLV的神经症状患者中脑脊液/血浆HIV-1 RNA不一致的发生率更高(70%对11.8%,P<0.001)。接受含蛋白酶抑制剂(PI)的ART治疗的患者(P<0.001)以及接受中枢神经系统(CNS)渗透效能(CPE)值<6的ART方案治疗的患者(P = 0.006)出现不一致的风险也更高。脑脊液/血浆HIV-1 RNA不一致表明适应中枢神经系统或产生抗逆转录病毒耐药性的HIV-1发生了复制。应开展更大规模的研究以研究印度不一致的发生率。这将有助于对接受抑制性ART治疗且出现神经症状的患者采用适当的神经有效疗法进行管理。