Increasing risk of psychiatric morbidity after childhood onset T1DM: a population-based cohort study

Author(s):  
Dybdal D ◽  
Tolstrup JS ◽  
Sildorf SM ◽  
Boisen KA ◽  
Svensson J ◽  
...  
Diabetologia ◽  
2017 ◽  
Vol 61 (4) ◽  
pp. 831-838 ◽  
Author(s):  
Daniel Dybdal ◽  
Janne S. Tolstrup ◽  
Stine M. Sildorf ◽  
Kirsten A. Boisen ◽  
Jannet Svensson ◽  
...  

2020 ◽  
Vol 51 (8) ◽  
pp. 789-800 ◽  
Author(s):  
Natalia Mouratidou ◽  
Petter Malmborg ◽  
Michael C. Sachs ◽  
Johan Askling ◽  
Anders Ekbom ◽  
...  

Epilepsia ◽  
2019 ◽  
Vol 60 (7) ◽  
pp. 1438-1444 ◽  
Author(s):  
Christian Starck ◽  
Olli Nevalainen ◽  
Anssi Auvinen ◽  
Kai Eriksson

BMJ Open ◽  
2019 ◽  
Vol 9 (10) ◽  
pp. e032407 ◽  
Author(s):  
Valdemar Landgren ◽  
Leif Svensson ◽  
Emelie Gyllencreutz ◽  
Eva Aring ◽  
Marita Andersson Grönlund ◽  
...  

BackgroundFetal alcohol spectrum disorders (FASD) are a global health concern. To further understand FASD in adulthood is a major public health interest.ObjectiveTo describe the clinical characteristics of young adults with FASD adopted from orphanages to a socially more favourable and stable rearing environment as children.DesignProspective observational cohort studySettingWestern SwedenParticipantsA population-based cohort of 37 adoptees diagnosed with FASD in childhood.Outcome measuresAssessment consisted of clinical evaluations of social, medical, psychiatric, neuropsychological, adaptive and ophthalmological status by a physician, ophthalmologist, orthoptist and psychologist.ResultsOut of 37 adoptees with FASD, 36 (15 females) were evaluated at a median age of 22 years (range 18–28) and a mean follow-up time of 15.5 years (range 13–17). Twenty (56%) were dependent on social support. Sexual victimisation was reported by nine (26%). In 21 individuals with fetal alcohol syndrome, growth restriction in height and head circumference of approximately −1.8 SD persisted into adulthood. Of 32 examined, 22 (69%) had gross motor coordination abnormalities. High blood pressure was measured in nine (28%). Ophthalmological abnormalities were found in 29 of 30 (97%). A median IQ of 86 in childhood had declined significantly to 71 by adulthood (mean difference: 15.5; 95% CI 9.5–21.4). Psychiatric disorders were diagnosed in 88%, most commonly attention deficit hyperactivity disorder (70%). Three or more disorders were diagnosed in 48%, and 21% had attempted suicide. The median Clinical Global Impression-Severity score was 6 = ‘severely ill’.ConclusionMajor cognitive impairments, psychiatric morbidity, facial dysmorphology, growth restriction and ophthalmological abnormalities accompanies FASD in adulthood. Recognition of FASD in childhood warrants habilitation across the lifespan.


2017 ◽  
Vol 23 (4) ◽  
pp. 332-340 ◽  
Author(s):  
Mira Karrasch ◽  
Petri Tiitta ◽  
Bruce Hermann ◽  
Juho Joutsa ◽  
Shlomo Shinnar ◽  
...  

AbstractObjectives: Little is known about the very long-term cognitive outcome in patients with childhood-onset epilepsy. The aim of this unique prospective population-based cohort study was to examine cognitive outcomes in aging participants with childhood-onset epilepsy (mean onset age=5.3 years) five decades later (mean age at follow-up=56.5 years).Methods: The sample consisted of 48 participants with childhood-onset epilepsy and 48 age-matched healthy controls aged 48–63 years. Thirty-six epilepsy participants were in remission and 12 continued to have seizures. Cognitive function was examined with 11 neuropsychological tests measuring language and semantic function, episodic memory, and learning, visuomotor function, executive function, and working memory. Results: The risk of cognitive impairment was very high in participants with continuing seizures; odds ratio (OR)=11.7 (95% confidence interval [CI] (2.8, 49.6), p=.0008). They exhibited worse performances across measures of language and semantic function, and visuomotor function compared to participants with remitted epilepsy and healthy controls. In the participants with remitted epilepsy, the risk of cognitive impairment was somewhat elevated, but not statistically significant; OR=2.6 (95% CI [0.9, 7.5], p=.08).Conclusions: Our results showed that the distinction of continued versus discontinued seizures was critical for determining long-term cognitive outcome in childhood-onset epilepsy. Few participants in remission exhibited marked cognitive impairment compared to age-matched peers. However, a subgroup of participants with decades long active epilepsy, continuous seizure activity and anti-epileptic drug (AED) medication, showed clinically significant cognitive impairment and are thus in a more precarious position when entering older age. (JINS, 2017, 23, 332–340)


CMAJ Open ◽  
2020 ◽  
Vol 8 (1) ◽  
pp. E134-E141
Author(s):  
Michael Ouk ◽  
Jodi D. Edwards ◽  
Jessica Colby-Milley ◽  
Alexander Kiss ◽  
Walter Swardfager ◽  
...  

2018 ◽  
Vol 2018 (1) ◽  
Author(s):  
Stephane Buteau ◽  
Mariève Doucet ◽  
Louis-Francois Tetreault ◽  
Philippe Gamache ◽  
Michel Fournier ◽  
...  

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