Aumann Megan A, Richerson Wesley, Song Alexander K, Martin Dann, Davis L Taylor, Davis Samantha M, Milner Lauren L, Kassim Adetola A, DeBaun Michael R, Jordan Lori C, Donahue Manus J
From the Department of Neurology (M.A.A., W.R., A.K.S., M.J.D.), Department of Radiology and Radiological Sciences (D.M., L.T.D., L.C.J.), Division of Pediatric Neurology, Department of Pediatrics (S.M.D., L.L.M., L.C.J.), Division of Hematology and Oncology, Department of Medicine (A.A.K., M.R.D.), and Department of Psychiatry and Behavioral Sciences (M.J.D.), Vanderbilt University Medical Center, Nashville; Vanderbilt-Meharry Center of Excellence in Sickle Cell Disease (A.A.K., M.R.D.), Nashville; and Department of Electrical and Computer Engineering (M.J.D.), Vanderbilt University, Nashville, TN.
Neurology. 2025 Jan 14;104(1):e210191. doi: 10.1212/WNL.0000000000210191. Epub 2024 Dec 20.
Sickle cell disease (SCD) is a hemoglobinopathy resulting in hemoglobin-S production, hemolytic anemia, and elevated stroke risk. Treatments include oral hydroxyurea, blood transfusions, and hematopoietic stem cell transplantation (HSCT). Our objective was to evaluate the neurologic relevance of these therapies by characterizing how treatment-induced changes in hemoglobin (Hb) affect brain health biomarkers.
In this interventional study, adults with and without SCD underwent a 3T-MRI at Vanderbilt University Medical Center at 2 time points before and after clinically indicated transfusion or HSCT or at 2 time points without the introduction of a new Hb-altering therapy (adult controls and patients with SCD on hydroxyurea). Cerebral blood flow (CBF; mL/100 g/min) and cerebral venous blood relaxation rate (s; a marker of Hb and blood oxygen content) responses were assessed to understand how these markers of brain health vary with Hb modulation. CBF was assessed with arterial spin labeling MRI, and blood relaxation rate was assessed using T relaxation under spin tagging MRI. Measures were pairwise compared within each cohort using a 2-tailed Wilcoxon signed-rank test, and regression was applied to evaluate the parameter and Hb change relationships. The significance criterion was 2-sided < 0.05.
Adults with (n = 43; age 28.7 ± 7.7 years; 42% male) and without (n = 13; age 33.5 ± 12.2 years; 46% male) SCD were evaluated. In adults receiving hydroxyurea (n = 10), neither Hb, CBF, nor venous relaxation rate changed between time 1 (Hb = 8.6 ± 1.2 g/dL) and time 2 (Hb = 9.0 ± 1.8 g/dL) (all > 0.05). In transfusion patients (n = 19), Hb increased from 8.2 ± 1.4 g/dL to 9.3 ± 1.3 g/dL before vs after transfusion ( < 0.001), paralleling a CBF decrease of 14.2 mL/100 g/min ( < 0.001) toward control levels. The venous relaxation rate did not change after transfusion ( = 0.71). In HSCT patients (n = 14), Hb increased from 8.9 ± 1.9 g/dL to 12.9 ± 2.7 g/dL ( < 0.001) before vs after transplant, paralleling CBF decreases from 68.16 ± 20.24 to 47.43 ± 12.59 mL/100 g/min ( < 0.001) and increase in venous relaxation rate ( = 0.004). Across the Hb spectrum, a CBF decrease of 5.02 mL/100 g/min per g/dL increase in Hb was observed.
Findings demonstrate improvement in cerebral hemodynamics after transfusion and transplant therapies compared with hydroxyurea therapy; quantitative relationships should provide a framework for using these measures as trial end points to assess how new SCD therapies affect brain health.
镰状细胞病(SCD)是一种血红蛋白病,可导致血红蛋白S生成、溶血性贫血及中风风险升高。治疗方法包括口服羟基脲、输血及造血干细胞移植(HSCT)。我们的目的是通过描述治疗引起的血红蛋白(Hb)变化如何影响脑健康生物标志物,来评估这些疗法与神经学的相关性。
在这项干预性研究中,患有和未患有SCD的成年人在范德比尔特大学医学中心接受了3T磁共振成像(MRI)检查,检查在临床指示的输血或HSCT前后的2个时间点进行,或在未引入新的Hb改变疗法的2个时间点进行(成年对照组和接受羟基脲治疗的SCD患者)。评估脑血流量(CBF;毫升/100克/分钟)和脑静脉血弛豫率(秒;Hb和血氧含量的标志物)反应,以了解这些脑健康标志物如何随Hb调节而变化。使用动脉自旋标记MRI评估CBF,使用自旋标记MRI下的T弛豫评估血弛豫率。在每个队列中,使用双尾Wilcoxon符号秩检验对测量值进行成对比较,并应用回归分析来评估参数与Hb变化之间的关系。显著性标准为双侧P<0.05。
评估了患有SCD(n = 43;年龄28.7±7.7岁;42%为男性)和未患有SCD(n = 13;年龄33.5±12.2岁;46%为男性)的成年人。在接受羟基脲治疗的成年人(n = 10)中,在第1时间点(Hb = 8.6±1.2克/分升)和第2时间点(Hb = 9.0±1.8克/分升)之间,Hb、CBF和静脉弛豫率均未改变(均P>0.05)。在输血患者(n = 19)中,输血前Hb从8.2±1.4克/分升增加到9.3±1.3克/分升(P<0.001),同时CBF下降14.2毫升/100克/分钟(P<0.001),降至对照水平。输血后静脉弛豫率未改变(P = 0.71)。在HSCT患者(n = 14)中,移植前Hb从8.9±1.9克/分升增加到12.9±2.7克/分升(P<0.001),同时CBF从68.16±20.24降至47.43±12.59毫升/100克/分钟(P<0.001),静脉弛豫率增加(P = 0.004)。在整个Hb范围内,观察到Hb每增加1克/分升,CBF下降5.02毫升/100克/分钟。
研究结果表明,与羟基脲治疗相比,输血和移植治疗后脑血流动力学有所改善;定量关系应为将这些测量用作试验终点以评估新的SCD疗法如何影响脑健康提供一个框架。