A natural history comparison of SOD1-mutant patients with amyotrophic lateral sclerosis between Chinese and German populations


 Background: The gene coding the Cu/Zn superoxide dismutase (SOD1) was the first-identified causative gene of amyotrophic lateral sclerosis (ALS), and the second most common genetic cause for ALS worldwide. The promising therapeutic approaches targeting SOD1 mutations are on the road. The purpose of the present study was to compare the mutational and clinical features of Chinese and German patients with ALS carrying mutations in SOD1 gene, which will facilitate the strategy and design of SOD1-targeted trials. Methods: Demographic and clinical characteristics were collected from two longitudinal cohorts in China and Germany. Chinese and German patients carrying SOD1 mutations were compared with regard to mutational distribution, age of onset, site of onset, body mass index (BMI) at diagnosis, diagnostic delay, progression rate, and survival. Results: A total of 66 Chinese and 84 German patients with 69 distinct SOD1 mutations were identified. The most common mutation in both populations was p.His47Arg. It was found in 8 Chinese and 2 German patients and consistently showed a slow progression of disease in both countries. Across all mutations, Chinese patients showed a younger age of onset (43.9 vs 49.9 years, p=0.002), a higher proportion of young-onset cases (62.5% vs 30.7%, p<0.001) and a lower BMI at diagnosis (22.8 vs 26.0, p<0.001) compared to German patients. Although riluzole intake was less frequent in Chinese patients (28.3% vs 81.3%, p<0.001), no difference in survival between populations was observed (p=0.90). Across both cohorts, female patients had a longer diagnostic delay (15.0 vs 11.0 months, p=0.01) and a prolonged survival (248.0 vs 60.0 months, p=0.005) compared to male patients. Conclusions: Our data demonstrate the distinct mutational and clinical spectrums of SOD1-mutant patients in Asian and European populations. Clinical phenotypes seem to be primarily influenced by mutation-specific, albeit not excluding ethnicity-specific factors. Further large-scale transethnical studies are needed to clarify determinants and modifiers of SOD1 phenotypes.

Currently, there is no effective treatment for amyotrophic lateral sclerosis (ALS), despite the limited efficacy of riluzole [1] and edaravone [2]. SOD1 (coding for the Cu/ Zn superoxide dismutase) is the second most frequent genetic cause for ALS only after C9orf72 in patients with European ancestry while being the most frequent in Asian ALS populations [3]. Multiple therapeutic approaches have targeted SOD1-related ALS, including the antisense oligonucleotide tofersen with promising results in a recent phase I/II trial [4]. Given the clinical heterogeneity among different SOD1 mutations, in this study, we enrolled genetically confirmed ALS patients with SOD1 mutations from two prospectively established hospital-based cohorts from China [5] and Germany [6] to clinically characterize distinct SOD1 mutations and compare related phenotypes between Asians and Caucasians. Because of the explorative nature of this study, all results should be interpreted as hypothesis-generating only rather than confirmatory. No adjustment for multiple testing was made.
We identified 66 Chinese and 84 German ALS patients carrying a total of 69 distinct SOD1 mutations, including 61 known mutations of SOD1, 5 variants of uncertain significance, and 3 likely pathogenic variants. The most frequent mutation in both populations was p.His47Arg (8 Chinese and 2 German). All common mutations featured consistent phenotypes, including an aggressive form of ALS in p.Gly148Asp and slow-progressing forms in p.Glu41Gly, p.His47Arg and p.Asn87Ser (Additional file 1: Table S1). Interestingly, the majority of mutations in the Chinese patients were located in exon 2 while those in the German patients were in exon 4. There was a significant difference in the average age of onset between the Chinese and the German patients carrying mutations in exon 4 (37.4 vs 49.9 years, P < 0.001). The site of onset, diagnostic delay, and survival did not differ significantly among the exons (Additional file 1: Fig. S1).
Among all patients with SOD1 mutations, the median which is consistent with a previous study [6]. However, the difference was not significant after adjusting for the demographic structures of the identical general ALS populations [6] (P = 0.07). The proportion of youngonset ALS, defined as onset between 25 and 45 years, was 47.5% in the two cohorts, and was higher in China (62.5% vs 30.7%, P < 0.001). The median (IQR) body mass index (BMI) at diagnosis was significantly lower in the Chinese cohort (22.6 [20.9-24.9]) than in the German cohort (25.9 [23.1-28.7], P < 0.001); this difference remained significant (P = 0.03) after adjusting for the BMI in the identical general ALS populations (median BMI: 23.0 in Chinese and 24.5 in German) [6].
The majority of cases (94.3%) had spinal onset. There was no difference in the proportion of site of onset between two groups or between males and females. Twenty percent of patients had a pure lower motor neuron phenotype (Chinese: 17.3%, German: 25.0%, P = 0.41; Table 1). Some of these patients progressed slowly (p.His47Arg), while others showed an aggressive pattern (p.Ala5Val and p.His44Arg). Male patients had significantly shorter diagnostic delay (P = 0.01) and survival (P = 0.005) compared to females (Additional file 1: Table S2, Fig. S2).
Because of the significant relationship between diagnostic delay and early and late progression rate (see definition in Additional file 2: Supplementary Methods), only sex, age of onset, site of onset, and late progression rate were included in the multivariate Cox regression analysis, which revealed that patients with bulbar onset (hazard risk 10.31, P = 0.01) and higher late progression rate (hazard risk 2.42, P = 0.003) had a much shorter survival time (Additional file 1: Table S3, Fig. S3).
The present study has three major implications. First, this study reported for the first time distinct distributions of SOD1 mutations in Chinese (mainly in exon 2) and German patients (mainly in exon 4), and consistent phenotypes in each of the common mutations. The most common SOD1 mutations in Germany were p.Arg116Gly (26 patients) and p.Asp91Ala (11), which could be explained by the known founder effects among Caucasian populations, and a similar effect may be involved in Chinese patients carrying p.His47Arg (8 patients). The predominate mutation in North America (p.Ala5Val) [7] was rare in China (only 1 patient), albeit without the same founder haplotype [8], and absent in Germany. Second, the Chinese SOD1-mutant patients had a significantly lower age of onset and higher proportion of young-onset cases compared with the German counterparts, which may reflect a higher burden of genetic and environmental risk factors [9]. Third, the known prognostic factors BMI and  age of onset for sporadic ALS were not associated with survival in the SOD1-carrying patients, indicating the different spectrum of disease-modifying factors.
In the future, it is desirable to establish a detailed genotype-phenotype database of SOD1 mutationcarriers in different populations in order to clarify the underlying pathomechanisms and to precisely design clinical trials for SOD1-related ALS.