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Darin-Mattsson, AlexanderORCID iD iconorcid.org/0000-0001-5491-1510
Publications (6 of 6) Show all publications
Yerramalla, M. S., Darin-Mattsson, A., Udeh-Momoh, C. T., Holleman, J., Kåreholt, I., Aspö, M., . . . Sindi, S. (2024). Cognitive reserve, cortisol, and Alzheimer's disease biomarkers: A memory clinic study. Alzheimer's & Dementia: Journal of the Alzheimer's Association, 20(7), 4486-4498
Open this publication in new window or tab >>Cognitive reserve, cortisol, and Alzheimer's disease biomarkers: A memory clinic study
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2024 (English)In: Alzheimer's & Dementia: Journal of the Alzheimer's Association, ISSN 1552-5260, E-ISSN 1552-5279, Vol. 20, no 7, p. 4486-4498Article in journal (Refereed) Published
Abstract [en]

INTRODUCTION: Cognitive reserve might mitigate the risk of Alzheimer's dementia among memory clinic patients. No study has examined the potential modifying role of stress on this relation. METHODS: We examined cross-sectional associations of the cognitive reserve index (CRI; education, occupational complexity, physical and leisure activities, and social health) with cognitive performance and AD-related biomarkers among 113 memory clinic patients. The longitudinal association between CRI and cognition over a 3-year follow-up was assessed. We examined whether associations were influenced by perceived stress and five measures of diurnal salivary cortisol. RESULTS: Higher CRI scores were associated with better cognition. Adjusting for cortisol measures reduced the beneficial association of CRI on cognition. A higher CRI score was associated with better working memory in individuals with higher (favorable) cortisol AM/PM ratio, but not among individuals with low cortisol AM/PM ratio. No association was found between CRI and AD-related biomarkers. DISCUSSION: Physiological stress reduces the neurocognitive benefits of cognitive reserve among memory clinic patients. Highlights: Physiological stress may reduce the neurocognitive benefits accrued from cognitively stimulating and enriching life experiences (cognitive reserve [CR]) in memory clinic patients. Cortisol awakening response modified the relation between CR and P-tau181, a marker of Alzheimer's disease (AD). Effective stress management techniques for AD and related dementia prevention are warranted.

Keywords
amyloid beta, cerebrospinal fluid biomarkers, cognitive performance, cognitive reserve, memory clinic, perceived stress, phosphorylated tau, salivary cortisol, total tau
National Category
Neurosciences Geriatrics
Identifiers
urn:nbn:se:su:diva-235608 (URN)10.1002/alz.13866 (DOI)001239197700001 ()2-s2.0-85195143468 (Scopus ID)
Available from: 2024-11-15 Created: 2024-11-15 Last updated: 2024-11-15Bibliographically approved
Harber-Aschan, L., Darin-Mattsson, A., Fratiglioni, L., Calderón-Larrañaga, A. & Dekhtyar, S. (2023). Socioeconomic differences in older adults’ unplanned hospital admissions: the role of health status and social network . Age and Ageing, 52(4), Article ID afac290.
Open this publication in new window or tab >>Socioeconomic differences in older adults’ unplanned hospital admissions: the role of health status and social network 
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2023 (English)In: Age and Ageing, ISSN 0002-0729, E-ISSN 1468-2834, Vol. 52, no 4, article id afac290Article in journal (Refereed) Published
Abstract [en]

Background: the socioeconomic distribution of unplanned hospital admissions in older adults is poorly understood. We compared associations of two life-course measures of socioeconomic status (SES) with unplanned hospital admissions while comprehensively accounting for health, and examined the role of social network in this association.

Methods: in 2,862 community-dwelling adults aged 60+ in Sweden, we derived (i) an aggregate life-course SES measure grouping individuals into Low, Middle or High SES based on a summative score, and (ii) a latent class measure that additionally identified a Mixed SES group, characterised by financial difficulties in childhood and old age. The health assessment combined measures of morbidity and functioning. The social network measure included social connections and support components. Negative binomial models estimated the change in hospital admissions over 4 years in relation to SES. Stratification and statistical interaction assessed effect modification by social network.

Results: adjusting for health and social network, unplanned hospitalisation rates were higher for the latent Low SES and Mixed SES group (incidence rate ratio [IRR] = 1.38, 95% confidence interval [CI]: 1.12–1.69, P = 0.002; IRR = 2.06, 95% CI: 1.44–2.94, P < 0.001; respectively; ref: High SES). Mixed SES was at a substantially greater risk of unplanned hospital admissions among those with poor (and not rich) social network (IRR: 2.43, 95% CI: 1.44–4.07; ref: High SES), but the statistical interaction test was non-significant (P = 0.493).

Conclusion: socioeconomic distributions of older adults’ unplanned hospitalisations were largely driven by health, although considering SES dynamics across life can reveal at-risk sub-populations. Financially disadvantaged older adults might benefit from interventions aimed at improving their social network.

Keywords
socioeconomic status, life-course, hospitalisation, older people, social network
National Category
Gerontology, specialising in Medical and Health Sciences
Identifiers
urn:nbn:se:su:diva-229522 (URN)10.1093/ageing/afac290 (DOI)001013029200009 ()37079867 (PubMedID)2-s2.0-85159964285 (Scopus ID)
Available from: 2024-05-27 Created: 2024-05-27 Last updated: 2024-05-27Bibliographically approved
Nilsen, C., Darin-Mattsson, A., Hyde, M. & Wastesson, J. W. (2022). Life-course trajectories of working conditions and successful ageing. Scandinavian Journal of Public Health, 50(5), 593-600
Open this publication in new window or tab >>Life-course trajectories of working conditions and successful ageing
2022 (English)In: Scandinavian Journal of Public Health, ISSN 1403-4948, E-ISSN 1651-1905, Vol. 50, no 5, p. 593-600Article in journal (Refereed) Published
Abstract [en]

Aims: As populations are ageing worldwide, it is important to identify strategies to promote successful ageing. We investigate how working conditions throughout working life are associated with successful ageing in later life. Methods: Data from two nationally representative longitudinal Swedish surveys were linked (n=674). In 1991, respondents were asked about their first occupation, occupations at ages 25, 30, 35, 40, 45 and 50 years and their last recorded occupation. Occupations were matched with job exposure matrices to measure working conditions at each of these time points. Random effects growth curve models were used to calculate intra-individual trajectories of working conditions. Successful ageing, operationalised using an index including social and leisure activity, cognitive and physical function and the absence of diseases, was measured at follow-up in 2014 (age 70 years and older). Multivariable ordered logistic regressions were used to assess the association between trajectories of working conditions and successful ageing. Results: Intellectually stimulating work; that is, substantive complexity, in the beginning of one's career followed by an accumulation of more intellectually stimulating work throughout working life was associated with higher levels of successful ageing. In contrast, a history of stressful, hazardous or physically demanding work was associated with lower levels of successful ageing. Conclusions: Promoting a healthy workplace, by supporting intellectually stimulating work and reducing physically demanding and stressful jobs, may contribute to successful ageing after retirement. In particular, it appears that interventions early in one's employment career could have positive, long-term effects.

Keywords
work-related stress, substantive complexity, physical working conditions, accumulation, de-accumulation, successful ageing, longitudinal
National Category
Gerontology, specialising in Medical and Health Sciences
Research subject
Psychology
Identifiers
urn:nbn:se:su:diva-195870 (URN)10.1177/14034948211013279 (DOI)000654526300001 ()34030546 (PubMedID)2-s2.0-85106443180 (Scopus ID)
Available from: 2021-08-30 Created: 2021-08-30 Last updated: 2022-08-16Bibliographically approved
Rydström, A., Darin-Mattsson, A., Kåreholt, I., Ngandu, T., Lehtisalo, J., Solomon, A., . . . Mangialasche, F. (2022). Occupational complexity and cognition in the FINGER multidomain intervention trial. Alzheimer's & Dementia: Journal of the Alzheimer's Association, 18(12), 2438-2447
Open this publication in new window or tab >>Occupational complexity and cognition in the FINGER multidomain intervention trial
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2022 (English)In: Alzheimer's & Dementia: Journal of the Alzheimer's Association, ISSN 1552-5260, E-ISSN 1552-5279, Vol. 18, no 12, p. 2438-2447Article in journal (Refereed) Published
Abstract [en]

Introduction: Lifetime exposure to occupational complexity is linked to late-life cognition, and may affect benefits of preventive interventions.

Methods: In the 2-year multidomain Finnish Geriatric Intervention Study to Prevent Cognitive Impairment and Disability (FINGER), we investigated, through post hoc analyses (N = 1026), the association of occupational complexity with cognition. Occupational complexity with data, people, and substantive complexity were classified through the Dictionary of Occupational Titles.

Results: Higher levels of occupational complexity were associated with better baseline cognition. Measures of occupational complexity had no association with intervention effects on cognition, except for occupational complexity with data, which was associated with the degree of intervention-related gains for executive function.

Discussion: In older adults at increased risk for dementia, higher occupational complexity is associated with better cognition. The cognitive benefit of the FINGER intervention did not vary significantly among participants with different levels of occupational complexity. These exploratory findings require further testing in larger studies.

Keywords
Alzheimer’s disease, cognitive decline, cognitive reserve, dementia, intelligence, multidomain intervention, occupational complexity, prevention, randomized controlled trials
National Category
Gerontology, specialising in Medical and Health Sciences
Identifiers
urn:nbn:se:su:diva-202603 (URN)10.1002/alz.12561 (DOI)000753369600001 ()35142055 (PubMedID)2-s2.0-85124570907 (Scopus ID)
Available from: 2022-03-10 Created: 2022-03-10 Last updated: 2023-03-28Bibliographically approved
Celeste, R. K., Darin-Mattsson, A., Lennartsson, C., Listl, S., Peres, M. A. & Fritzell, J. (2022). Social Mobility and Tooth Loss: A Systematic Review and Meta-analysis. Journal of Dental Research, 101(2), 143-150, Article ID 00220345211029277.
Open this publication in new window or tab >>Social Mobility and Tooth Loss: A Systematic Review and Meta-analysis
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2022 (English)In: Journal of Dental Research, ISSN 0022-0345, E-ISSN 1544-0591, Vol. 101, no 2, p. 143-150, article id 00220345211029277Article, review/survey (Refereed) Published
Abstract [en]

This study systematically reviews the evidence of the association between life course social mobility and tooth loss among middle-aged and older people. PubMed, Scopus, Embase, and Web of Science were systematically searched in addition to gray literature and contact with the authors. Data on tooth loss were collated for a 4-category social mobility variable (persistently high, upward or downward mobility, and persistently low) for studies with data on socioeconomic status (SES) before age 12 y and after age 30 y. Several study characteristics were extracted to investigate heterogeneity in a random effect meta-analysis. A total of 1,384 studies were identified and assessed for eligibility by reading titles and abstracts; 21 original articles were included, of which 18 provided sufficient data for a meta-analysis with 40 analytical data sets from 26 countries. In comparison with individuals with persistently high social mobility, the pooled odds ratios (ORs) for the other categories were as follows: upwardly mobile, OR = 1.73 (95% CI, 1.53 to 1.95); downwardly mobile, OR = 2.52 (95% CI, 2.19 to 2.90); and persistently low, OR = 3.96 (95% CI, 3.13 to 5.03). A high degree of heterogeneity was found(I2 > 78%), and subgroup analysis was performed with 17 study-level characteristics; however, none could explain heterogeneity consistently in these 3 social mobility categories. SES in childhood and adulthood is associated with tooth loss, but the high degree of heterogeneity prevented us from forming a robust conclusion on whether upwardly or downwardly mobile SES may be more detrimental. The large variability in effect size among the studies suggests that contextual factors may play an important role in explaining the difference in the effects of low SES in different life stages (PROSPERO CRD42018092427).

Keywords
socioeconomic factors, prevalence, epidemiology, social mobility, meta-analysis, dental public health
National Category
Public Health, Global Health and Social Medicine
Identifiers
urn:nbn:se:su:diva-198321 (URN)10.1177/00220345211029277 (DOI)000690412600001 ()34448425 (PubMedID)
Available from: 2021-11-08 Created: 2021-11-08 Last updated: 2025-02-20Bibliographically approved
Marseglia, A., Darin-Mattsson, A., Skoog, J., Rydén, L., Hadarsson-Bodin, T., Kern, S., . . . Skoog, I. (2021). Metabolic Syndrome Is Associated With Poor Cognition: A Population-Based Study of 70-Year-Old Adults Without Dementia. The journals of gerontology. Series A, Biological sciences and medical sciences, 76(12), 2275-2283
Open this publication in new window or tab >>Metabolic Syndrome Is Associated With Poor Cognition: A Population-Based Study of 70-Year-Old Adults Without Dementia
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2021 (English)In: The journals of gerontology. Series A, Biological sciences and medical sciences, ISSN 1079-5006, E-ISSN 1758-535X, Vol. 76, no 12, p. 2275-2283Article in journal (Refereed) Published
Abstract [en]

Background: Individual conditions of metabolic syndrome (MetS) have been related to dementia; however, their combined impact on the preclinical stage is unknown. We investigated the associations between MetS and domain-specific cognitive function as well as the role of sociodemographic, cardiovascular, and genetic factors.

Methods: Within the Gothenburg H70 Birth Cohort Study-Birth cohort 1944, 1131 dementia-free participants (aged 70 years) were examined during 2014-2016. MetS (central obesity plus at least 2 factors [reduced HD11.-cholesterol, elevated triglycerides, blood pressure, or blood glucose]) was identified according to the International Diabetes Federation criteria. Five cognitive domains (memory, attention/perceptual speed, executive function, verbal fluency, visuospatial abilities) were generated after z-standardizing raw scores from 10 neuropsychological tests. Education, heart disease, claudication (indicating peripheral atherosclerosis), and apolipoprotein genotype were ascertained by trained staff. Data were analyzed with linear regression models.

Results: Overall, 618 participants (55%) had MetS. In multiadjusted linear regressions, MetS was related to poorer performance in attention/ perceptual speed (beta -0.14 [95% CI -0.25, -0.02]), executive function (beta -0.12 [95% CI -0.23, -0.01]), and verbal fluency (beta -0.19 [95% CI -0.30, -0.08]). These associations were present only among individuals who did not carry any APOE-epsilon 4 allele or were highly educated. However, among those with MetS, high education was related to better cognitive performance. MetS together with comorbid heart disease or claudication was associated with even worse cognitive performance than each alone.

Conclusions: MetS is associated with poor attention/perceptual speed, executive function, and verbal fluency performance. Education, apolipoprotein E-epsilon 4 allele, and comorbid cardiovascular disease influenced the observed associations.

Keywords
Apolipoprotein E4, Cardiovascular disease, Education, Vascular cognitive impairment
National Category
Neurology
Identifiers
urn:nbn:se:su:diva-200895 (URN)10.1093/gerona/glab195 (DOI)000728436200024 ()34228116 (PubMedID)
Available from: 2022-01-17 Created: 2022-01-17 Last updated: 2022-03-10Bibliographically approved
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ORCID iD: ORCID iD iconorcid.org/0000-0001-5491-1510

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