M.-L. Sumelahti, A. Verkko, V. Kytö, J. O. T. Sipilä
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Amongst pwMS, male sex (adjusted hazard ratio [aHR] 1.70; 95% confidence interval [CI] 1.41–2.06), higher age at diagnosis (aHR 1.83; 95% CI 1.65–2.03 per 10-year increment) and primary progressive disease course (aHR 1.29; 95% CI 1.04–1.60) were independently associated with poorer survival. DMT use was associated with better survival (<i>p</i> < 0.0001) and better survival during follow-up (aHR 0.56; 95% CI 0.38–0.81). Compared to matched controls, median life expectancy was 8–9 years shorter in pwMS with survival diverging from controls during the first decade after diagnosis, more clearly in men than women.</p>\n </section>\n \n <section>\n \n <h3> Conclusion</h3>\n \n <p>Despite DMT use being associated with better survival, relative life expectancy of pwMS did not change over five decades in Western Finland. Male sex was an independent risk factor for death amongst pwMS, but excess mortality was higher in women. More work and methods are needed to improve survival in pwMS.</p>\n </section>\n </div>","PeriodicalId":11954,"journal":{"name":"European Journal of Neurology","volume":"31 12","pages":""},"PeriodicalIF":4.5000,"publicationDate":"2024-09-11","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ene.16480","citationCount":"0","resultStr":"{\"title\":\"Stable excess mortality in a multiple sclerosis cohort diagnosed 1970–2010\",\"authors\":\"M.-L. Sumelahti, A. Verkko, V. Kytö, J. O. T. Sipilä\",\"doi\":\"10.1111/ene.16480\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<div>\\n \\n \\n <section>\\n \\n <h3> Background and purpose</h3>\\n \\n <p>Multiple sclerosis (MS) is associated with excess mortality. The use of disease-modifying treatments (DMTs) has recently been associated with survival benefits.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Methods</h3>\\n \\n <p>A regional MS database was linked with national registries. People with MS (pwMS) diagnosed in 1971–2010 were included and followed up until the end of the year 2019. Five matched controls were acquired for every person with MS. DMTs included in the analyses were interferon and glatiramer acetate.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Results</h3>\\n \\n <p>Median follow-up time of the 1795 pwMS was 20.0 years (range 0.1–48.7 years). Survival did not differ between decades of diagnosis (<i>p</i> = 0.20). Amongst pwMS, male sex (adjusted hazard ratio [aHR] 1.70; 95% confidence interval [CI] 1.41–2.06), higher age at diagnosis (aHR 1.83; 95% CI 1.65–2.03 per 10-year increment) and primary progressive disease course (aHR 1.29; 95% CI 1.04–1.60) were independently associated with poorer survival. DMT use was associated with better survival (<i>p</i> < 0.0001) and better survival during follow-up (aHR 0.56; 95% CI 0.38–0.81). Compared to matched controls, median life expectancy was 8–9 years shorter in pwMS with survival diverging from controls during the first decade after diagnosis, more clearly in men than women.</p>\\n </section>\\n \\n <section>\\n \\n <h3> Conclusion</h3>\\n \\n <p>Despite DMT use being associated with better survival, relative life expectancy of pwMS did not change over five decades in Western Finland. Male sex was an independent risk factor for death amongst pwMS, but excess mortality was higher in women. More work and methods are needed to improve survival in pwMS.</p>\\n </section>\\n </div>\",\"PeriodicalId\":11954,\"journal\":{\"name\":\"European Journal of Neurology\",\"volume\":\"31 12\",\"pages\":\"\"},\"PeriodicalIF\":4.5000,\"publicationDate\":\"2024-09-11\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://onlinelibrary.wiley.com/doi/epdf/10.1111/ene.16480\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"European Journal of Neurology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://onlinelibrary.wiley.com/doi/10.1111/ene.16480\",\"RegionNum\":2,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q1\",\"JCRName\":\"CLINICAL NEUROLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"European Journal of Neurology","FirstCategoryId":"3","ListUrlMain":"https://onlinelibrary.wiley.com/doi/10.1111/ene.16480","RegionNum":2,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q1","JCRName":"CLINICAL NEUROLOGY","Score":null,"Total":0}
引用次数: 0
摘要
背景和目的多发性硬化症(MS)与高死亡率有关。方法将一个地区多发性硬化症数据库与国家登记处连接起来。方法将一个地区多发性硬化症数据库与国家登记处连接起来,纳入 1971-2010 年确诊的多发性硬化症患者(pwMS),并随访至 2019 年底。每名多发性硬化症患者可获得五个匹配的对照组。结果1795名多发性硬化症患者的平均随访时间为20.0年(范围为0.1-48.7年)。不同诊断年代的存活率没有差异(P = 0.20)。在 PwMS 中,男性(调整后危险比 [aHR] 1.70;95% 置信区间 [CI]1.41-2.06)、较高的诊断年龄(aHR 1.83;95% CI 1.65-2.03,每 10 年递增)和原发性进展病程(aHR 1.29;95% CI 1.04-1.60)与较差的生存率独立相关。使用 DMT 与较高的生存率(p < 0.0001)和随访期间较高的生存率(aHR 0.56; 95% CI 0.38-0.81)相关。与匹配的对照组相比,重症肌无力患者的中位预期寿命短8-9年,在确诊后的头十年中,他们的存活率与对照组存在差异,男性的差异比女性更为明显。男性是导致重症肌无力患者死亡的一个独立风险因素,但女性的死亡率更高。需要开展更多的工作和采用更多的方法来提高重症肌无力患者的存活率。
Stable excess mortality in a multiple sclerosis cohort diagnosed 1970–2010
Background and purpose
Multiple sclerosis (MS) is associated with excess mortality. The use of disease-modifying treatments (DMTs) has recently been associated with survival benefits.
Methods
A regional MS database was linked with national registries. People with MS (pwMS) diagnosed in 1971–2010 were included and followed up until the end of the year 2019. Five matched controls were acquired for every person with MS. DMTs included in the analyses were interferon and glatiramer acetate.
Results
Median follow-up time of the 1795 pwMS was 20.0 years (range 0.1–48.7 years). Survival did not differ between decades of diagnosis (p = 0.20). Amongst pwMS, male sex (adjusted hazard ratio [aHR] 1.70; 95% confidence interval [CI] 1.41–2.06), higher age at diagnosis (aHR 1.83; 95% CI 1.65–2.03 per 10-year increment) and primary progressive disease course (aHR 1.29; 95% CI 1.04–1.60) were independently associated with poorer survival. DMT use was associated with better survival (p < 0.0001) and better survival during follow-up (aHR 0.56; 95% CI 0.38–0.81). Compared to matched controls, median life expectancy was 8–9 years shorter in pwMS with survival diverging from controls during the first decade after diagnosis, more clearly in men than women.
Conclusion
Despite DMT use being associated with better survival, relative life expectancy of pwMS did not change over five decades in Western Finland. Male sex was an independent risk factor for death amongst pwMS, but excess mortality was higher in women. More work and methods are needed to improve survival in pwMS.
期刊介绍:
The European Journal of Neurology is the official journal of the European Academy of Neurology and covers all areas of clinical and basic research in neurology, including pre-clinical research of immediate translational value for new potential treatments. Emphasis is placed on major diseases of large clinical and socio-economic importance (dementia, stroke, epilepsy, headache, multiple sclerosis, movement disorders, and infectious diseases).