Complete ascertainment of dementia in the Swedish Twin Registry: the HARMONY study

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


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 ◽  
...  

Twin Research ◽  
1998 ◽  
Vol 1 (4) ◽  
pp. 212-215 ◽  
Author(s):  
Paul Lichtenstein ◽  
Bengt Källén ◽  
Max Köster

AbstractPrevious research has provided evidence for a genetic effect in monozygotic twinning, indicated by an increased risk for monozygotic women to have monozygotic offspring. However, since the biological mechanism for this trait is unknown, it is not clear if there exists a paternal inheritance. In this study we investigated twin pregnancies in offspring born in 1941–1996 to male twins in the Swedish Twin Registry and population controls born in 1926–1980. In total 4 225 331 offspring, of which 89 286 were twins, were studied. There was neither an increase in the probability for monozygotic men to have like-sexed twin offspring risk ratio (RR = 0.95; 95% CI = 0.77–1.13) nor an increase in the estimated number of monozygotic twin births. Thus, there is no evidence for a paternal effect on monozygotic twinning, suggesting that the gene(s) increasing the liability for division of the embryo are expressed in the mother and not in the fertilised egg.


2006 ◽  
Vol 3 ◽  
pp. S37
Author(s):  
Birgitta Evengard ◽  
Andreas Jacks ◽  
Nancy L. Pedersen ◽  
Patrick F. Sullivan

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