Atopic dermatitis, systemic inflammation and subsequent dementia risk

被引:1
作者
Vingeliene, Snieguole [1 ,8 ]
Hiyoshi, Ayako [1 ,2 ]
Carlberg, Michael [1 ]
Garcia-Argibay, Miguel [1 ,3 ]
Lentjes, Marleen [1 ]
Fall, Katja [1 ,4 ]
von Kobyletzki, Laura [1 ,5 ]
Montgomery, Scott [1 ,6 ,7 ]
机构
[1] Orebro Univ, Sch Med Sci, Fac Med & Hlth, Clin Epidemiol & Biostat, Orebro, Sweden
[2] Stockholm Univ, Dept Publ Hlth Sci, Stockholm, Sweden
[3] Karolinska Inst, Dept Med Epidemiol & Biostat, Stockholm, Sweden
[4] Karolinska Inst, Inst Environm Med, Integrat Epidemiol, Stockholm, Sweden
[5] Lund Univ, Dept Occupat Dermatol & Med Sci, Malmo, Sweden
[6] Karolinska Univ Hosp, Karolinska Inst, Clin Epidemiol Div, Stockholm, Sweden
[7] UCL, Dept Epidemiol & Publ Hlth, London, England
[8] Orebro Univ, Clin Epidemiol & Biostat, Campus USO,Sodra Grev Rosengatan 30, S-70182 Orebro, Sweden
来源
JEADV CLINICAL PRACTICE | 2023年 / 2卷 / 04期
基金
英国经济与社会研究理事会; 瑞典研究理事会;
关键词
atopic dermatitis; dementia; erythrocyte sedimentation rate; ALZHEIMERS-DISEASE; CHILDHOOD; ECZEMA;
D O I
10.1002/jvc2.249
中图分类号
R75 [皮肤病学与性病学];
学科分类号
100206 ;
摘要
BackgroundAtopic dermatitis is a chronic inflammatory skin disease and inflammation has been implicated in development of other chronic diseases, but few studies have examined the relationship with dementia.ObjectivesThis study examines associations of atopic dermatitis (AD) and systemic inflammation in adolescence measured using erythrocyte sedimentation rate (ESR), as well as AD diagnosed in adulthood, with dementia risk.MethodsWe used three Swedish register-based cohorts. Cohort I (N = 795,680) comprised men, born in 1951-1968, who participated in the military conscription examinations with physician-assessed AD and ESR; Cohort II (N = 1,757,600) included men and women, born in 1951-1968; and Cohort III (N = 3,988,783) included all individuals in Sweden, born in 1930-1968. We used Cox regression, estimating hazard ratios (HR), with the follow-up from 50 years of age to dementia diagnosis, date of emigration, death, or 31 December 2018, whichever occurred first. Further, we used a sibling comparison design to adjust for unmeasured confounders shared among siblings.ResultsCohort I: 1466 dementia events were accrued during follow-up of 7.8 years, with a crude rate of 21.6 [95% confidence interval (CI): 20.6, 22.8] per 100,000 person-years. Cohort II: 3549 dementia events were accrued during follow-up of 7.4 years, with a crude rate of 23.7 (95% CI: 22.9, 24.5) per 100,000 person-years. Cohort III: 120,303 dementia events were accrued during follow-up of 23.7 years, with a crude rate of 180.3 (95% CI: 179.3, 181.3) per 100,000 person-years. In multivariable analysis using Cohort I, there was no association between AD and dementia [HR 0.68 (95% CI 0.32, 1.43)], nor with moderate [HR 0.71 (95% CI: 0.46, 1.10)] or high [HR 1.23 (95% CI: 0.87, 1.75)] ESR. AD was not associated with dementia risk in Cohort II [HR 1.28 (0.97, 1.71)] or Cohort III [HR 1.01 (0.92, 1.11)].ConclusionsAD was not associated with dementia risk, neither was systemic inflammation measured by ESR in adolescence.
引用
收藏
页码:839 / 848
页数:10
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