Lawson Health Research Institute, London, Ontario, Canada.
Department of Medical Biophysics, Western University, London, Ontario, Canada.
J Am Soc Nephrol. 2023 Jun 1;34(6):1090-1104. doi: 10.1681/ASN.0000000000000105. Epub 2023 Mar 9.
Hemodialysis (HD) results in reduced brain blood flow, and HD-related circulatory stress and regional ischemia are associated with brain injury over time. However, studies to date have not provided definitive direct evidence of acute brain injury during a HD treatment session. Using intradialytic magnetic resonance imaging (MRI) and spectroscopy to examine HD-associated changes in brain structure and neurochemistry, the authors found that multiple white (WM) tracts had diffusion imaging changes characteristic of cytotoxic edema, a consequence of ischemic insult and a precursor to fixed structural WM injury. Spectroscopy showed decreases in prefrontal N -acetyl aspartate (NAA) and choline concentrations consistent with energy deficit and perfusion anomaly. This suggests that one HD session can cause brain injury and that studies of interventions that mitigate this treatment's effects on the brain are warranted.
Hemodialysis (HD) treatment-related hemodynamic stress results in recurrent ischemic injury to organs such as the heart and brain. Short-term reduction in brain blood flow and long-term white matter changes have been reported, but the basis of HD-induced brain injury is neither well-recognized nor understood, although progressive cognitive impairment is common.
We used neurocognitive assessments, intradialytic anatomical magnetic resonance imaging, diffusion tensor imaging, and proton magnetic resonance spectroscopy to examine the nature of acute HD-associated brain injury and associated changes in brain structure and neurochemistry relevant to ischemia. Data acquired before HD and during the last 60 minutes of HD (during maximal circulatory stress) were analyzed to assess the acute effects of HD on the brain.
We studied 17 patients (mean age 63±13 years; 58.8% were male, 76.5% were White, 17.6% were Black, and 5.9% were of Indigenous ethnicity). We found intradialytic changes, including the development of multiple regions of white matter exhibiting increased fractional anisotropy with associated decreases in mean diffusivity and radial diffusivity-characteristic features of cytotoxic edema (with increase in global brain volumes). We also observed decreases in proton magnetic resonance spectroscopy-measured N -acetyl aspartate and choline concentrations during HD, indicative of regional ischemia.
This study demonstrates for the first time that significant intradialytic changes in brain tissue volume, diffusion metrics, and brain metabolite concentrations consistent with ischemic injury occur in a single dialysis session. These findings raise the possibility that HD might have long-term neurological consequences. Further study is needed to establish an association between intradialytic magnetic resonance imaging findings of brain injury and cognitive impairment and to understand the chronic effects of HD-induced brain injury.
NCT03342183 .
血液透析(HD)会导致脑血流减少,与 HD 相关的循环应激和局部缺血随时间推移与脑损伤有关。然而,迄今为止的研究并未提供 HD 治疗过程中急性脑损伤的明确直接证据。本研究使用透析内磁共振成像(MRI)和光谱检查 HD 相关的脑结构和神经化学变化,作者发现多个白质(WM)束的弥散成像变化具有细胞毒性水肿的特征,这是缺血性损伤的后果,也是固定结构 WM 损伤的前兆。光谱显示,与能量不足和灌注异常一致的前额叶 N -乙酰天冬氨酸(NAA)和胆碱浓度降低。这表明一次 HD 治疗即可导致脑损伤,有必要研究减轻这种治疗对大脑影响的干预措施。
与血液透析(HD)治疗相关的血流动力学应激会导致心脏和大脑等器官反复发生缺血性损伤。已有报道称,脑血流短期减少和长期白质变化,但 HD 引起的脑损伤的基础既未得到充分认识,也未得到充分理解,尽管进行性认知障碍很常见。
我们使用神经认知评估、透析内解剖磁共振成像、弥散张量成像和质子磁共振波谱检查来检查急性 HD 相关脑损伤的性质以及与缺血相关的脑结构和神经化学变化。分析 HD 前和 HD 最后 60 分钟(在最大循环应激期间)获得的数据,以评估 HD 对大脑的急性影响。
我们研究了 17 名患者(平均年龄 63±13 岁;58.8%为男性,76.5%为白人,17.6%为黑人,5.9%为原住民)。我们发现了透析内的变化,包括多个白质区域的发展,这些区域表现出分数各向异性增加,同时平均弥散度和放射状弥散度降低,这是细胞毒性水肿的特征(伴有全脑体积增加)。我们还观察到质子磁共振波谱测量的 N -乙酰天冬氨酸和胆碱浓度在 HD 期间降低,表明存在局部缺血。
本研究首次证明,在单次透析过程中,脑组织体积、弥散指标和脑代谢物浓度的显著透析内变化与缺血性损伤一致。这些发现提示 HD 可能有长期的神经后果。需要进一步研究以确定透析内磁共振成像脑损伤发现与认知障碍之间的关联,并了解 HD 诱导的脑损伤的慢性影响。
NCT03342183。