Brain metabolic signatures in patients with genetic and nongenetic amyotrophic lateral sclerosis
Pan Liu, Yongxiang Tang, Wanzhen Li, Zhen Liu, Ming Zhou, Li J, Yanchun Yuan, Liangjuan Fang, Jifeng Guo, Lu Shen, Hong Jiang, Beisha Tang, Shuo Hu, Junling Wang
Abstract
Abstract Aims To study the brain metabolic signature in Chinese amyotrophic lateral sclerosis (ALS) patients and compare the difference in brain metabolic patterns between ALS with and without genetic variants. Methods We included 146 patients with ALS and 128 healthy controls (HCs). All patients with ALS underwent genetic testing to screen for ALS related genetic variants and were then divided into genetic ( n = 22) and nongenetic ALS ( n = 93) subgroups. All participants underwent brain 18 F‐FDG‐PET scans. Group comparisons were performed using the two‐sample t ‐test model of SPM12. Results We identified a large of hypometabolic clusters in ALS patients as compared with HCs, especially in the bilateral basal ganglia, midbrain, and cerebellum. Moreover, hypometabolism in the bilateral temporal lobe, precentral gyrus and hypermetabolism in the left anterior cingulate, occipital lobe, and bilateral frontal lobe were also found in ALS patients as compared with HCs. Compared with nongenetic ALS patients, genetic ALS patients showed hypometabolism in the right postcentral gyrus, precuneus, and middle occipital gyrus. The incidence of sensory disturbance in patients with genetic ALS was higher than that in patients with nongenetic ALS (5 of 22 [22.72%] vs. 7 of 93 [7.52%], p = 0.036). Conclusions Our investigation provided unprecedented evidence of relative hypometabolism in the midbrain and cerebellum in ALS patients. Genetic ALS patients showed a specific signature of brain metabolism and a higher incidence of sensory disturbance, indicating that genetic factors may be an underlying cause affecting the brain metabolism and increasing the risk of sensory disturbance in ALS.