scholarly journals SEX DIFFERENCES IN HERITABILITY-BY-AGE INTERACTION ON DEMENTIA RISK IN THE SWEDISH TWIN REGISTRY

2017 ◽  
Vol 1 (suppl_1) ◽  
pp. 1209-1210
Author(s):  
C. Beam ◽  
C.A. Reynolds ◽  
N.L. Pedersen ◽  
M. Gatz
2021 ◽  
Vol 12 ◽  
Author(s):  
Alice J. Kim ◽  
Alaina I. Gold ◽  
Laura Fenton ◽  
Matthew J. D. Pilgrim ◽  
Morgan Lynch ◽  
...  

Although several studies have shown small longitudinal associations between baseline loneliness and subsequent dementia risk, studies rarely test whether change in loneliness predicts dementia risk. Furthermore, as both increase with advancing age, genetic and environmental selection processes may confound the putative causal association between loneliness and dementia risk. We used a sample of 2,476 individual twins from three longitudinal twin studies of aging in the Swedish Twin Registry to test the hypothesis that greater positive change in loneliness predicts greater dementia risk. We then used a sample of 1,632 pairs of twins to evaluate the hypothesis that effects of change in loneliness on dementia risk would remain after adjusting for effects of genetic and environmental variance. Phenotypic model results suggest that mild levels of baseline loneliness predict greater dementia risk. Contrary to our hypothesis, change in loneliness did not correlate with dementia risk, regardless of whether genetic and environmental selection confounds were taken into account. Worsening loneliness with age may not confer greater dementia risk.


2021 ◽  
Vol 7 (1) ◽  
Author(s):  
Bojing Liu ◽  
Arvid Sjölander ◽  
Nancy L. Pedersen ◽  
Jonas F. Ludvigsson ◽  
Honglei Chen ◽  
...  

AbstractTo examine whether irritable bowel syndrome (IBS) was related to the future risk of Parkinson’s disease (PD), we conducted a nested case-control study in the Swedish total population including 56,564 PD cases identified from the Swedish Patient Register and 30 controls per case individually matched by sex and year of birth. Odds ratios (ORs) with 95% confidence intervals (CIs) for having a prior diagnosis of IBS were estimated using conditional logistic regression. We furthermore conducted a cohort study using the Swedish Twin Registry following 3046 IBS patients identified by self-reported abdominal symptoms and 41,179 non-IBS individuals. Through Cox proportional hazard models, we estimated hazard ratios (HRs) and 95% CIs for PD risk. In the nested case-control study, 253 (0.4%) PD cases and 5204 (0.3%) controls had a previous IBS diagnosis. IBS diagnosis was associated with a 44% higher risk of PD (OR = 1.44, 95% CI 1.27–1.63). Temporal relationship analyses showed 53% and 38% increased risk of PD more than 5 and 10 years after IBS diagnosis, respectively. In the cohort analysis based on the Swedish Twin Registry, there was no statistically significantly increased risk of PD related to IBS (HR = 1.25, 95% CI = 0.87–1.81). Our results suggest a higher risk of PD diagnosis after IBS. These results provide additional evidence supporting the importance of the gut–brain axis in PD.


1976 ◽  
Vol 25 (1) ◽  
pp. 271-275 ◽  
Author(s):  
Ulf de Faire

From January 1971 to March 1973 all twin pairs in the Swedish Twin Registry below the age of 70, who became death-discordant, were continuously recorded. A total of 205 (78%) of the surviving cotwins were examined with respect to different manifestations of ischemic heart diseases (IHD) and several “environmental” and “biometric” risk factors. Among the death-discordant pairs, the cause of death was IHD in 57 pairs and other than IHD in 148 pairs. Analyses revealed that the prevalence rate of myocardial infarction, angina pectoris, pathologic Q-wave, and ST depressions in connection with exercise, were significantly higher among the surviving cotwins whose partners had died from IHD than those whose partners had died from other causes. The same trends were seen for most of the risk factors measured both singly and in combination, although not very pronounced. The results indicate a substantial genetic influence in the development of IHD. The genetic influence is possibly transmitted not only through some of the risk factors measured, but also through other factors, still unknown.


2005 ◽  
Vol 26 (4) ◽  
pp. 439-447 ◽  
Author(s):  
Margaret Gatz ◽  
Laura Fratiglioni ◽  
Boo Johansson ◽  
Stig Berg ◽  
James A. Mortimer ◽  
...  

2009 ◽  
Vol 66 (8) ◽  
pp. 857 ◽  
Author(s):  
Kenneth S. Kendler ◽  
Charles O. Gardner ◽  
Amy Fiske ◽  
Margaret Gatz

2009 ◽  
Vol 265 (6) ◽  
pp. 717-724 ◽  
Author(s):  
J. Hansson ◽  
N. L. Pedersen ◽  
M. R. Galanti ◽  
T. Andersson ◽  
A. Ahlbom ◽  
...  

2007 ◽  
Vol 115 (3) ◽  
pp. 214-220 ◽  
Author(s):  
K. S. Kendler ◽  
M. Gatz ◽  
C. O. Gardner ◽  
N. L. Pedersen

2013 ◽  
Vol 16 (5) ◽  
pp. 977-984 ◽  
Author(s):  
Giorgio Tettamanti ◽  
Daniel Altman ◽  
Anastasia N. Iliadou ◽  
Rino Bellocco ◽  
Nancy L. Pedersen

Previous studies have found that major depression and neuroticism are positively associated with urinary incontinence (UI). However, the genetic contribution to these associations has never been investigated. In 2005, a total of 14,094 female twins born 1959–1985 in the Swedish Twin Registry participated in a comprehensive survey on common exposures and complex diseases. Structured questions provided information on UI, depressive symptoms, major depression, and neuroticism. A logistic regression model based on generalized estimating equations (GEE) was used to estimate odds ratios (ORs) with 95% confidence intervals (CIs). Environmental and genetic influences were assessed in co-twin control analyses and quantitative genetic analyses, which were also used to determine the proportion of the phenotypic correlation explained by familial factors. Major depression, depressive symptoms, and neuroticism were positively associated with all UI subtypes (overall, stress, urge, and mixed UI). In a trivariate Cholesky model with neuroticism, depressive symptoms (or depression), and UI a modest genetic correlation was found between indicators of depression and overall, or stress, UI. The majority of this correlation was independent from neuroticism. In contrast, the genetic factors shared between indicators of depression and urge or mixed UI were entirely in common with neuroticism. In conclusion, depression and neuroticism are associated with UI among premenopausal women: the associations are in part determined by genetic factors in common to the disorders.


2003 ◽  
Vol 106 (4) ◽  
pp. 594-599 ◽  
Author(s):  
Fredrik Jonsson ◽  
Alicja Wolk ◽  
Nancy L. Pedersen ◽  
Paul Lichtenstein ◽  
Paul Terry ◽  
...  

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