Tyrberg Erika, Hagberg Lars, Andersson Lars-Magnus, Nilsson Staffan, Yilmaz Aylin, Mellgren Åsa, Blennow Kaj, Zetterberg Henrik, Gisslén Magnus
Department of Infectious Diseases, Institute of Biomedicine, The Sahlgrenska Academy at the University of Gothenburg, Gothenburg, Sweden.
Department of Infectious Diseases, Sahlgrenska University Hospital, Gothenburg, Sweden.
Brain Commun. 2022 Oct 15;4(6):fcac259. doi: 10.1093/braincomms/fcac259. eCollection 2022.
Effective antiretroviral therapy has radically changed the course of the HIV pandemic. However, despite efficient therapy, milder forms of neurocognitive symptoms are still present in people living with HIV. Plasma homocysteine is a marker of vitamin B deficiency and has been associated with cognitive impairment. People living with HIV have higher homocysteine concentrations than HIV-negative controls, and we have previously found an association between plasma homocysteine concentration and CSF concentration of neurofilament light protein, a sensitive marker for ongoing neuronal injury in HIV. This prompted us to perform this randomized controlled trial, to evaluate the effect of vitamin B supplementation on neuronal injury in a cohort of people living with HIV on stable antiretroviral therapy. At the Department of Infectious Diseases at Sahlgrenska University Hospital in Gothenburg, Sweden, 124 virally suppressed people living with HIV were screened to determine eligibility for this study. Sixty-one fulfilled the inclusion criteria by having plasma homocysteine levels at or above 12 μmol/l. They were randomized (1:1) to either active treatment (with cyanocobalamin 0.5 mg, folic acid 0.8 mg and pyridoxine 3.0 mg) q.d. or to a control arm with a cross over to active treatment after 12 months. Cognitive function was measured repeatedly during the trial, which ran for 24 months. We found a significant correlation between plasma neurofilament light protein and plasma homocysteine at screening ( = 124, = 0.35, < 0.0001). Plasma homocysteine levels decreased by 35% from a geometric mean of 15.7 μmol/l (95% confidence interval 14.7-16.7) to 10.3 μmol/l (95% confidence interval 9.3-11.3) in the active treatment arm between baseline and Month 12. No significant change was detected in the control arm during the same time period [geometric mean 15.2 (95% confidence interval 14.3-16.2) versus geometric mean 16.5 μmol/l (95% confidence interval 14.7-18.6)]. A significant difference in change in plasma homocysteine levels was seen between arms at 12 months [-40% (95% confidence interval -48 to -30%), < 0.001]. However, no difference between arms was seen in either plasma neurofilament light protein levels [-6.5% (-20 to 9%), = 0.39], or cognitive measures [-0.08 (-0.33 to 0.17), = 0.53]. Our results do not support a vitamin B-dependent cause of the correlation between neurofilament light protein and homocysteine. Additional studies are needed to further elucidate this matter.
有效的抗逆转录病毒疗法已从根本上改变了艾滋病疫情的发展进程。然而,尽管治疗有效,但感染艾滋病毒的人仍存在较轻微形式的神经认知症状。血浆同型半胱氨酸是维生素B缺乏的一个标志物,且与认知障碍有关。感染艾滋病毒的人血浆同型半胱氨酸浓度高于未感染艾滋病毒的对照组,我们之前还发现血浆同型半胱氨酸浓度与神经丝轻链蛋白的脑脊液浓度之间存在关联,神经丝轻链蛋白是艾滋病毒中正在发生的神经元损伤的一个敏感标志物。这促使我们开展这项随机对照试验,以评估补充维生素B对接受稳定抗逆转录病毒治疗的一组艾滋病毒感染者神经元损伤的影响。在瑞典哥德堡的萨尔格伦斯卡大学医院传染病科,对124名病毒得到抑制的艾滋病毒感染者进行了筛查,以确定其是否符合本研究的条件。61人因血浆同型半胱氨酸水平等于或高于12 μmol/l而符合纳入标准。他们被随机(1:1)分为每日接受活性治疗组(服用0.5 mg氰钴胺、0.8 mg叶酸和3.0 mg吡哆醇)或对照组,对照组在12个月后交叉接受活性治疗。在为期24个月的试验期间,对认知功能进行了多次测量。我们发现在筛查时血浆神经丝轻链蛋白与血浆同型半胱氨酸之间存在显著相关性(n = 124,r = 0.35,P < 0.0001)。在活性治疗组中,血浆同型半胱氨酸水平从基线时的几何平均值15.7 μmol/l(95%置信区间14.7 - 16.7)降至第12个月时的10.3 μmol/l(95%置信区间9.3 - 11.3),下降了35%。在同一时间段内,对照组未检测到显著变化[几何平均值15.2(95%置信区间14.3 - 16.2)与几何平均值16.5 μmol/l(95%置信区间14.7 - 18.6)]。在12个月时,两组之间血浆同型半胱氨酸水平变化存在显著差异[-40%(95%置信区间 - 48至 - 30%),P < 0.001]。然而,在血浆神经丝轻链蛋白水平[-6.5%(-20至9%),P = 0.39]或认知指标[-0.08(-0.33至0.17),P = 0.53]方面,两组之间均未发现差异。我们的结果不支持维生素B是神经丝轻链蛋白与同型半胱氨酸之间相关性的原因。需要进一步的研究来进一步阐明这一问题。