scholarly journals Heritability of leptin levels and the shared genetic effects on body mass index and leptin in adult Finnish twins

2001 ◽  
Vol 25 (1) ◽  
pp. 132-137 ◽  
Author(s):  
J Kaprio ◽  
J Eriksson ◽  
M Lehtovirta ◽  
M Koskenvuo ◽  
J Tuomilehto
2018 ◽  
Vol 43 (2) ◽  
pp. 207-214 ◽  
Author(s):  
Victoria Garfield ◽  
Ghazaleh Fatemifar ◽  
Caroline Dale ◽  
Melissa Smart ◽  
Yanchun Bao ◽  
...  

2008 ◽  
Vol 17 (2) ◽  
pp. 258-266 ◽  
Author(s):  
Sampo Sammalisto ◽  
Tero Hiekkalinna ◽  
Karen Schwander ◽  
Sharon Kardia ◽  
Alan B Weder ◽  
...  

NeuroImage ◽  
2019 ◽  
Vol 199 ◽  
pp. 261-272 ◽  
Author(s):  
James T. Kennedy ◽  
Serguei V. Astafiev ◽  
Semyon Golosheykin ◽  
Ozlem Korucuoglu ◽  
Andrey P. Anokhin

Endocrine ◽  
2013 ◽  
Vol 44 (3) ◽  
pp. 675-679 ◽  
Author(s):  
Jae Woong Sull ◽  
Myoungsook Lee ◽  
Sun Ha Jee

Author(s):  
Karen Hodgson ◽  
Russell A Poldrack ◽  
Joanne E Curran ◽  
Emma E Knowles ◽  
Samuel Mathias ◽  
...  

2019 ◽  
Vol 215 (01) ◽  
pp. 428-433 ◽  
Author(s):  
Francesca Solmi ◽  
Marina Carbo Mascarell ◽  
Stanley Zammit ◽  
James B. Kirkbride ◽  
Glyn Lewis

BackgroundRecent studies suggest psychotic and eating disorders can be comorbid and could have shared genetic liability. However, this comorbidity has been overlooked in the epidemiological literature.AimsTo test whether polygenic risk scores (PRS) for schizophrenia are associated with disordered eating behaviours and body mass index (BMI) in the general population.MethodUsing data from the Avon Longitudinal Study of Parents and Children and random-effects logistic and linear regression models, we investigated the association between PRS for schizophrenia and self-reported disordered eating behaviours (binge eating, purging, fasting and excessive exercise) and BMI at 14, 16 and 18 years.ResultsOf the 6920 children with available genetic data, 4473 (64.6%) and 5069 (73.3%) had at least one disordered eating and one BMI outcome measurement, respectively. An s.d. increase in PRS was associated with greater odds of having binge eating behaviours (odds ratio, 1.36; 95% CI 1.16–1.60) and lower BMI (coefficient, −0.03; 95% CI, −0.06 to −0.01).ConclusionsOur findings suggest the presence of shared genetic risk between schizophrenia and binge eating behaviours. Intermediate phenotypes such as impaired social cognition and irritability, previously shown to be positively correlated in this sample with schizophrenia PRS, could represent risk factors for both phenotypes. Shared genetic liability between binge eating and schizophrenia could also explain higher rates of metabolic syndrome in individuals with schizophrenia, as binge eating could be a mediator of this association in drug-naïve individuals. The finding of an association between greater PRS and lower BMI, although consistent with existing epidemiological and genetic literature, requires further investigation.Declaration of interestNone.


2020 ◽  
Vol 87 (9) ◽  
pp. S222
Author(s):  
Roseann Peterson ◽  
Tim Bigdeli ◽  
Bradley Todd Webb ◽  
Jonathan Flint ◽  
Kenneth Kendler

2021 ◽  
Vol 12 ◽  
Author(s):  
Danick Goulet ◽  
Jennifer O’Loughlin ◽  
Marie-Pierre Sylvestre

The strong correlation between adiposity and blood pressure (BP) might be explained in part by shared genetic risk factors. A recent study identified three nucleotide variants [rs16933812 (PAX5), rs7638110 (MRPS22), and rs9930333 (FTO)] associated with both body mass index (BMI) and systolic blood pressure (SBP) in adolescents age 12–18years. We attempted to replicate these findings in a sample of adolescents of similar age. A total of 713 adolescents were genotyped and had anthropometric indicators and blood pressure measured at age 13, 15, 17, and 24years. Using linear mixed models, we assessed associations of these variants with BMI and SBP. In our data, rs9930333 (FTO) was associated with body mass index, but not systolic blood pressure. Neither rs16933812 (PAX5) nor rs7638110 (MRPS22) were associated with body mass index or systolic blood pressure. Although, differences in phenotypic definitions and in genetic architecture across populations may explain some of the discrepancy across studies, nucleotide variant selection in the initial study may have led to false-positive results that could not be replicated.


2020 ◽  
Vol 77 (5) ◽  
pp. 503 ◽  
Author(s):  
Shahram Bahrami ◽  
Nils Eiel Steen ◽  
Alexey Shadrin ◽  
Kevin O’Connell ◽  
Oleksandr Frei ◽  
...  

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