Atopic dermatitis, systemic inflammation and subsequent dementia risk

Abstract Background Atopic 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. Objectives This study examines associations of atopic dermatitis (AD) and systemic...

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Main Authors: Snieguole Vingeliene, Ayako Hiyoshi, Michael Carlberg, Miguel Garcia‐Argibay, Marleen Lentjes, Katja Fall, Laura vonKobyletzki, Scott Montgomery
Format: Article
Language:English
Published: Wiley 2023-12-01
Series:JEADV Clinical Practice
Subjects:
Online Access:https://doi.org/10.1002/jvc2.249
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author Snieguole Vingeliene
Ayako Hiyoshi
Michael Carlberg
Miguel Garcia‐Argibay
Marleen Lentjes
Katja Fall
Laura vonKobyletzki
Scott Montgomery
author_facet Snieguole Vingeliene
Ayako Hiyoshi
Michael Carlberg
Miguel Garcia‐Argibay
Marleen Lentjes
Katja Fall
Laura vonKobyletzki
Scott Montgomery
author_sort Snieguole Vingeliene
collection DOAJ
description Abstract Background Atopic 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. Objectives This 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. Methods We 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. Results Cohort 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)]. Conclusions AD was not associated with dementia risk, neither was systemic inflammation measured by ESR in adolescence.
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spelling doaj.art-53c7b3cfeaf441b88c150a9ac3ec62a62023-12-01T10:43:27ZengWileyJEADV Clinical Practice2768-65662023-12-012483984810.1002/jvc2.249Atopic dermatitis, systemic inflammation and subsequent dementia riskSnieguole Vingeliene0Ayako Hiyoshi1Michael Carlberg2Miguel Garcia‐Argibay3Marleen Lentjes4Katja Fall5Laura vonKobyletzki6Scott Montgomery7Clinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health Örebro University Örebro SwedenClinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health Örebro University Örebro SwedenClinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health Örebro University Örebro SwedenClinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health Örebro University Örebro SwedenClinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health Örebro University Örebro SwedenClinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health Örebro University Örebro SwedenClinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health Örebro University Örebro SwedenClinical Epidemiology and Biostatistics, School of Medical Sciences, Faculty of Medicine and Health Örebro University Örebro SwedenAbstract Background Atopic 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. Objectives This 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. Methods We 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. Results Cohort 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)]. Conclusions AD was not associated with dementia risk, neither was systemic inflammation measured by ESR in adolescence.https://doi.org/10.1002/jvc2.249atopic dermatitisdementiaerythrocyte sedimentation rate
spellingShingle Snieguole Vingeliene
Ayako Hiyoshi
Michael Carlberg
Miguel Garcia‐Argibay
Marleen Lentjes
Katja Fall
Laura vonKobyletzki
Scott Montgomery
Atopic dermatitis, systemic inflammation and subsequent dementia risk
JEADV Clinical Practice
atopic dermatitis
dementia
erythrocyte sedimentation rate
title Atopic dermatitis, systemic inflammation and subsequent dementia risk
title_full Atopic dermatitis, systemic inflammation and subsequent dementia risk
title_fullStr Atopic dermatitis, systemic inflammation and subsequent dementia risk
title_full_unstemmed Atopic dermatitis, systemic inflammation and subsequent dementia risk
title_short Atopic dermatitis, systemic inflammation and subsequent dementia risk
title_sort atopic dermatitis systemic inflammation and subsequent dementia risk
topic atopic dermatitis
dementia
erythrocyte sedimentation rate
url https://doi.org/10.1002/jvc2.249
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