Rasing Ingeborg, Voigt Sabine, Koemans Emma A, de Kort Anna M, van Harten Thijs W, van Etten Ellis S, van Zwet Erik W, Stoops Erik, Francois Cindy, Kuiperij H Bea, Klijn Catharina J M, Schreuder Floris H B M, van der Weerd Louise, van Osch Matthias J P, van Walderveen Marianne A A, Verbeek Marcel M, Terwindt Gisela M, Wermer Marieke J H
Department of Neurology, Leiden University Medical Center, Leiden, The Netherlands.
Department of Radiology, Leiden University Medical Center, Leiden, The Netherlands.
Alzheimers Res Ther. 2024 Apr 23;16(1):86. doi: 10.1186/s13195-024-01457-0.
Neurofilament light chain (NFL) is a biomarker for neuroaxonal damage and glial fibrillary acidic protein (GFAP) for reactive astrocytosis. Both processes occur in cerebral amyloid angiopathy (CAA), but studies investigating the potential of NFL and GFAP as markers for CAA are lacking. We aimed to investigate NFL and GFAP as biomarkers for neuroaxonal damage and astrocytosis in CAA.
For this cross-sectional study serum and cerebrospinal fluid (CSF) samples were collected between 2010 and 2020 from controls, (pre)symptomatic Dutch-type hereditary (D-CAA) mutation-carriers and participants with sporadic CAA (sCAA) from two prospective CAA studies at two University hospitals in the Netherlands. NFL and GFAP levels were measured with Simoa-assays. The association between NFL and GFAP levels and age, cognitive performance (MoCA), CAA-related MRI markers (CAA-CSVD-burden) and Aβ40 and Aβ42 levels in CSF were assessed with linear regression adjusted for confounders. The control group was divided in age < 55 and ≥55 years to match the specific groups.
We included 187 participants: 28 presymptomatic D-CAA mutation-carriers (mean age 40 years), 29 symptomatic D-CAA participants (mean age 58 years), 59 sCAA participants (mean age 72 years), 33 controls < 55 years (mean age 42 years) and 38 controls ≥ 55 years (mean age 65 years). In presymptomatic D-CAA, only GFAP in CSF (7.710pg/mL vs. 4.410pg/mL in controls; P<.001) was increased compared to controls. In symptomatic D-CAA, both serum (NFL:26.2pg/mL vs. 12.5pg/mL; P=0.008, GFAP:130.8pg/mL vs. 123.4pg/mL; P=0.027) and CSF (NFL:16.810pg/mL vs. 7.810pg/mL; P=0.01 and GFAP:11.410pg/mL vs. 7.510pg/mL; P<.001) levels were higher than in controls and serum levels (NFL:26.2pg/mL vs. 6.7pg/mL; P=0.05 and GFAP:130.8pg/mL vs. 66.0pg/mL; P=0.004) were higher than in pre-symptomatic D-CAA. In sCAA, only NFL levels were increased compared to controls in both serum (25.6pg/mL vs. 12.5pg/mL; P=0.005) and CSF (20.010pg/mL vs 7.810pg/mL; P=0.008). All levels correlated with age. Serum NFL correlated with MoCA (P=0.008) and CAA-CSVD score (P<.001). NFL and GFAP in CSF correlated with Aβ42 levels (P=0.01/0.02).
GFAP level in CSF is an early biomarker for CAA and is increased years before symptom onset. NFL and GFAP levels in serum and CSF are biomarkers for advanced CAA.
神经丝轻链(NFL)是神经轴突损伤的生物标志物,胶质纤维酸性蛋白(GFAP)是反应性星形细胞增生的生物标志物。这两个过程都发生在脑淀粉样血管病(CAA)中,但缺乏关于NFL和GFAP作为CAA标志物潜力的研究。我们旨在研究NFL和GFAP作为CAA中神经轴突损伤和星形细胞增生的生物标志物。
在这项横断面研究中,2010年至2020年间从荷兰两家大学医院的两项前瞻性CAA研究中的对照组、(预)症状性荷兰型遗传性(D-CAA)突变携带者和散发性CAA(sCAA)参与者中收集血清和脑脊液(CSF)样本。使用Simoa检测法测量NFL和GFAP水平。通过对混杂因素进行调整的线性回归评估NFL和GFAP水平与年龄、认知表现(MoCA)、CAA相关MRI标志物(CAA-CSVD负荷)以及脑脊液中Aβ40和Aβ42水平之间的关联。将对照组分为年龄<55岁和≥55岁两组,以匹配特定组。
我们纳入了187名参与者:28名症状前D-CAA突变携带者(平均年龄40岁)、29名症状性D-CAA参与者(平均年龄58岁)、59名sCAA参与者(平均年龄72岁)、33名年龄<55岁的对照组(平均年龄42岁)和38名年龄≥55岁的对照组(平均年龄65岁)。在症状前D-CAA中,与对照组相比,仅脑脊液中的GFAP升高(7.7×10pg/mL对对照组的4.4×(10)pg/mL;P<0.001)。在症状性D-CAA中,血清(NFL:26.2pg/mL对12.5pg/mL;P = 0.008,GFAP:130.8pg/mL对123.4pg/mL;P = 0.027)和脑脊液(NFL:16.8×10pg/mL对7.8×10pg/mL;P = 0.01,GFAP:11.4×10pg/mL对7.5×10pg/mL;P<0.001)水平均高于对照组,且血清水平(NFL:26.2pg/mL对6.7pg/mL;P = 0.05,GFAP:130.8pg/mL对66.0pg/mL;P = 0.004)高于症状前D-CAA。在sCAA中,与对照组相比,血清(25.6pg/mL对12.5pg/mL;P = 0.005)和脑脊液(20.0×10pg/mL对7.8×10pg/mL;P = 0.008)中的NFL水平均升高。所有水平均与年龄相关。血清NFL与MoCA(P = 0.008)和CAA-CSVD评分(P<0.001)相关。脑脊液中的NFL和GFAP与Aβ42水平相关(P = 0.01/0.02)。
脑脊液中的GFAP水平是CAA的早期生物标志物,在症状出现前数年就会升高。血清和脑脊液中的NFL和GFAP水平是晚期CAA的生物标志物。