James Alder, Chukwu Chukwuma, Tracey Farragher, Samantha Holden Smith, Rosemary Morris, John Ealing, Hisham Hamdalla, Andrew Bentley, Saba Bokhari, Debbie Freeman, Ammar Al-Chalabi, David Rog, Joyutpal Das, Amina Chaouch
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Relative deprivation was estimated using the Index of Multiple Deprivation 2019 and patients were divided into quartiles of deprivation in England. Ethnicity was sub-grouped into White, Southeast Asian, Black, and Other. Poisson's regression analysis was used to calculate the incidence rate and its interactions with deprivation and ethnicity. <i>Results</i>: 55.4% of patients were male, 95.4% were White, 57.4% were in the two most deprived quartiles, and 87.2% had died by the end of the observation period. The crude incidence rate was 2.21 cases per 100,000 (95% CI 2.00-2.40) per year. There was no difference in the adjusted incidence rates among the quartiles of deprivation, even when considering ethnicity as a confounding variable. The risk of ALS in the White population was 2.08 (95% CI 1.47-3.04) times greater than that in the non-White population. <i>Conclusion</i>: In our cohort, relative deprivation was not an independent risk factor for ALS. A stronger association between White ethnicity and ALS was noted. The reason for this association remains unclear, highlighting the need for more research in this field.</p>","PeriodicalId":72184,"journal":{"name":"Amyotrophic lateral sclerosis & frontotemporal degeneration","volume":" ","pages":"558-565"},"PeriodicalIF":2.8000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Impact of relative deprivation and ethnicity on the incidence rate of amyotrophic lateral sclerosis.\",\"authors\":\"James Alder, Chukwu Chukwuma, Tracey Farragher, Samantha Holden Smith, Rosemary Morris, John Ealing, Hisham Hamdalla, Andrew Bentley, Saba Bokhari, Debbie Freeman, Ammar Al-Chalabi, David Rog, Joyutpal Das, Amina Chaouch\",\"doi\":\"10.1080/21678421.2025.2465609\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><i>Objective</i>: This study assessed a sizable cohort of patients with amyotrophic lateral sclerosis (ALS) in a relatively deprived and ethnically diverse area in the northwest of England. We aimed to evaluate the interaction of relative deprivation and ethnicity with the incidence of ALS. <i>Methods</i>: Six hundred and ninety-three adults from Greater Manchester who were diagnosed with ALS between 1 January 2011 and 31 December 2021 were included in this study. Data were collected from electronic patient records. Relative deprivation was estimated using the Index of Multiple Deprivation 2019 and patients were divided into quartiles of deprivation in England. Ethnicity was sub-grouped into White, Southeast Asian, Black, and Other. Poisson's regression analysis was used to calculate the incidence rate and its interactions with deprivation and ethnicity. <i>Results</i>: 55.4% of patients were male, 95.4% were White, 57.4% were in the two most deprived quartiles, and 87.2% had died by the end of the observation period. The crude incidence rate was 2.21 cases per 100,000 (95% CI 2.00-2.40) per year. 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引用次数: 0
摘要
目的:本研究在英格兰西北部一个相对贫困和种族多样化的地区评估了一组相当大的肌萎缩侧索硬化(ALS)患者。我们的目的是评估相对剥夺和种族与ALS发病率的相互作用。方法:2011年1月1日至2021年12月31日期间,来自大曼彻斯特的693名被诊断为ALS的成年人被纳入本研究。数据从电子病历中收集。在英国,使用多重剥夺指数(Index of Multiple deprivation 2019)估计了相对剥夺,并将患者分为剥夺的四分位数。种族分为白人、东南亚人、黑人和其他人种。用泊松回归分析计算发病率及其与贫困和种族的相互作用。结果:55.4%的患者为男性,95.4%的患者为白人,57.4%的患者处于最贫困的两个四分位数,87.2%的患者在观察结束时死亡。粗发病率为每年2.21例/ 10万(95% CI 2.00-2.40)。即使将种族作为一个混杂变量考虑在内,剥夺四分位数的调整后发病率也没有差异。白种人患ALS的风险是非白种人的2.08倍(95% CI 1.47-3.04)。结论:在我们的队列中,相对剥夺不是ALS的独立危险因素。研究指出,白种人与ALS之间存在更强的联系。这种关联的原因尚不清楚,这突出表明需要在这一领域进行更多的研究。
Impact of relative deprivation and ethnicity on the incidence rate of amyotrophic lateral sclerosis.
Objective: This study assessed a sizable cohort of patients with amyotrophic lateral sclerosis (ALS) in a relatively deprived and ethnically diverse area in the northwest of England. We aimed to evaluate the interaction of relative deprivation and ethnicity with the incidence of ALS. Methods: Six hundred and ninety-three adults from Greater Manchester who were diagnosed with ALS between 1 January 2011 and 31 December 2021 were included in this study. Data were collected from electronic patient records. Relative deprivation was estimated using the Index of Multiple Deprivation 2019 and patients were divided into quartiles of deprivation in England. Ethnicity was sub-grouped into White, Southeast Asian, Black, and Other. Poisson's regression analysis was used to calculate the incidence rate and its interactions with deprivation and ethnicity. Results: 55.4% of patients were male, 95.4% were White, 57.4% were in the two most deprived quartiles, and 87.2% had died by the end of the observation period. The crude incidence rate was 2.21 cases per 100,000 (95% CI 2.00-2.40) per year. There was no difference in the adjusted incidence rates among the quartiles of deprivation, even when considering ethnicity as a confounding variable. The risk of ALS in the White population was 2.08 (95% CI 1.47-3.04) times greater than that in the non-White population. Conclusion: In our cohort, relative deprivation was not an independent risk factor for ALS. A stronger association between White ethnicity and ALS was noted. The reason for this association remains unclear, highlighting the need for more research in this field.