Jun Suhnyoung, Bido-Medina Richard, Oviedo Jairo, Miches Isidro, Llano Daniel, Tusen Luis, Stoeter Peter, Rodriguez Minelly, Sadaghiani Sepideh
Beckman Institute for Advanced Science and Technology, University of Illinois at Urbana-Champaign, Urbana, Illinois.
Department of Psychology, University of Illinois at Urbana-Champaign, Urbana, Illinois, United States.
bioRxiv. 2025 May 7:2025.03.05.641727. doi: 10.1101/2025.03.05.641727.
Systemic viral infections with neurotropic potential pose significant global health challenges. The Zika virus (ZIKV) is known for its pronounced neurotropism, with recent infectious clusters raising renewed public health concerns. While research has predominantly focused on congenital populations, growing evidence suggests that the mature central nervous system (CNS) is also vulnerable. However, no study has examined the long-term impact of ZIKV infection on the adult human brain. To address this gap, we studied a rare group of adult ZIKV patients presenting with both peripheral (Guillain-Barré Syndrome; GBS) and CNS-related neurological symptoms. We compared these patients at the chronic stage (5 to 12 months post-infection) to healthy controls and to patients with GBS of non-ZIKV etiology (total =43). Structural and functional measures included cortical thickness, white matter hyperintensities, diffusion metrics, and resting-state functional connectivity. Despite the rarity of both patient populations, power analyses indicated that our sample size could detect large group differences-effect sizes deemed reasonable given the severity of neurological symptoms in the ZIKV group. Nonetheless, our multimodal analyses yielded null results, with Bayesian statistics (where applicable) providing evidence for a lack of effects. The null findings suggest that chronic ZIKV infection in adults is not associated with brain changes of large magnitude. Importantly, this study offers detailed clinical characterization of a heavily understudied group. In light of recent ZIKV outbreaks, this characterization underscores the need to monitor, study, and provide longitudinal care to adult survivors of severe ZIKV infections.
具有嗜神经潜能的全身性病毒感染给全球健康带来了重大挑战。寨卡病毒(ZIKV)以其显著的嗜神经性而闻名,最近的感染聚集事件再次引发了公众对健康的担忧。虽然研究主要集中在先天性人群,但越来越多的证据表明,成熟的中枢神经系统(CNS)也很脆弱。然而,尚无研究考察寨卡病毒感染对成人大脑的长期影响。为了填补这一空白,我们研究了一组罕见的成年寨卡病毒患者,他们同时出现了外周(吉兰 - 巴雷综合征;GBS)和中枢神经系统相关的神经症状。我们将这些处于慢性阶段(感染后5至12个月)的患者与健康对照组以及非寨卡病毒病因的吉兰 - 巴雷综合征患者(共43人)进行了比较。结构和功能测量包括皮质厚度、白质高信号、扩散指标和静息态功能连接。尽管这两类患者都很罕见,但功效分析表明,我们的样本量能够检测到较大的组间差异——鉴于寨卡病毒组神经症状的严重程度,这样的效应量被认为是合理的。尽管如此,我们的多模态分析得出了阴性结果,贝叶斯统计(如适用)为缺乏效应提供了证据。这些阴性结果表明,成人慢性寨卡病毒感染与大脑的重大变化无关。重要的是,这项研究提供了对一个研究严重不足的群体的详细临床特征描述。鉴于最近寨卡病毒的爆发,这一特征描述强调了对严重寨卡病毒感染的成年幸存者进行监测、研究和提供长期护理的必要性。