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Evaluation of the G...
Evaluation of the Genetic Association Between Adult Obesity and Neuropsychiatric Disease
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Stahel, P (författare)
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Nahmias, A (författare)
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Sud, SK (författare)
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Lee, SJ (författare)
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Pucci, A (författare)
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Yousseif, A (författare)
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Youseff, A (författare)
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Jackson, T (författare)
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Urbach, DR (författare)
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Okrainec, A (författare)
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Allard, JP (författare)
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Sockalingam, S (författare)
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Yao, T (författare)
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Barua, M (författare)
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- Jiao, H (författare)
- Karolinska Institutet
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Magi, R (författare)
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Bassett, AS (författare)
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Paterson, AD (författare)
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- Dahlman, I (författare)
- Karolinska Institutet
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Batterham, RL (författare)
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Dash, S (författare)
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(creator_code:org_t)
- 2019-09-10
- 2019
- Engelska.
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Ingår i: Diabetes. - : American Diabetes Association. - 1939-327X .- 0012-1797. ; 68:12, s. 2235-2246
- Relaterad länk:
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https://diabetes.dia...
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http://kipublication...
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https://doi.org/10.2...
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Abstract
Ämnesord
Stäng
- Extreme obesity (EO) (BMI >50 kg/m2) is frequently associated with neuropsychiatric disease (NPD). As both EO and NPD are heritable central nervous system disorders, we assessed the prevalence of protein-truncating variants (PTVs) and copy number variants (CNVs) in genes/regions previously implicated in NPD in adults with EO (n = 149) referred for weight loss/bariatric surgery. We also assessed the prevalence of CNVs in patients referred to University College London Hospital (UCLH) with EO (n = 218) and obesity (O) (BMI 35–50 kg/m2; n = 374) and a Swedish cohort of participants from the community with predominantly O (n = 161). The prevalence of variants was compared with control subjects in the Exome Aggregation Consortium/Genome Aggregation Database. In the discovery cohort (high NPD prevalence: 77%), the cumulative PTV/CNV allele frequency (AF) was 7.7% vs. 2.6% in control subjects (odds ratio [OR] 3.1 [95% CI 2–4.1]; P < 0.0001). In the UCLH EO cohort (intermediate NPD prevalence: 47%), CNV AF (1.8% vs. 0.9% in control subjects; OR 1.95 [95% CI 0.96–3.93]; P = 0.06) was lower than the discovery cohort. CNV AF was not increased in the UCLH O cohort (0.8%). No CNVs were identified in the Swedish cohort with no NPD. These findings suggest that PTV/CNVs, in genes/regions previously associated with NPD, may contribute to NPD in patients with EO.
Publikations- och innehållstyp
- ref (ämneskategori)
- art (ämneskategori)
Hitta via bibliotek
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Diabetes
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Till lärosätets databas
- Av författaren/redakt...
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Stahel, P
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Nahmias, A
-
Sud, SK
-
Lee, SJ
-
Pucci, A
-
Yousseif, A
-
visa fler...
-
Youseff, A
-
Jackson, T
-
Urbach, DR
-
Okrainec, A
-
Allard, JP
-
Sockalingam, S
-
Yao, T
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Barua, M
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Jiao, H
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Magi, R
-
Bassett, AS
-
Paterson, AD
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Dahlman, I
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Batterham, RL
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Dash, S
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visa färre...
- Artiklar i publikationen
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Diabetes
- Av lärosätet
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Karolinska Institutet