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The fat mass and obesity gene is linked to reduced verbal fluency in overweight and obese elderly men
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för neurovetenskap, Funktionell farmakologi.ORCID-id: 000-0002-8911-4068
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för neurovetenskap, Funktionell farmakologi.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för folkhälso- och vårdvetenskap, Geriatrik.
Uppsala universitet, Medicinska och farmaceutiska vetenskapsområdet, Medicinska fakulteten, Institutionen för neurovetenskap, Funktionell farmakologi.
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2011 (Engelska)Ingår i: Neurobiology of Aging, ISSN 0197-4580, E-ISSN 1558-1497, Vol. 32, nr 6, s. 1159.e1-1159.e5Artikel i tidskrift (Refereegranskat) Published
Abstract [en]

Humans carrying the prevalent rs9939609 A allele of the fat mass and obesity-associated (FTO) gene are more susceptible to developing obesity than noncarries. Recently, polymorphisms in the FTO gene of elderly subjects have also been linked to a reduced volume in the frontal lobe as well as increased risk for incident Alzheimer disease. However, so far there is no evidence directly linking the FTO gene to functional cognitive processes. Here we examined whether the FTO rs9939609 A allele is associated with verbal fluency performance in 355 elderly men at the age of 82 years who have no clinically apparent cognitive impairment. Retrieval of verbal memory is a good surrogate measure reflecting frontal lobe functioning. Here we found that obese and overweight but not normal weight FTO A allele carriers showed a lower performance on verbal fluency than non-carriers (homozygous for rs9939609 T allele). This effect was not observed for a measure of general cognitive performance (i.e., Mini-Mental State Examination score), thereby indicating that the FTO gene primarily affects frontal lobe-dependent cognitive processes in elderly men.

Ort, förlag, år, upplaga, sidor
2011. Vol. 32, nr 6, s. 1159.e1-1159.e5
Nationell ämneskategori
Geriatrik Neurovetenskaper
Identifikatorer
URN: urn:nbn:se:uu:diva-149331DOI: 10.1016/j.neurobiolaging.2011.02.006ISI: 000291160000017PubMedID: 21458110OAI: oai:DiVA.org:uu-149331DiVA, id: diva2:404570
Tillgänglig från: 2011-03-17 Skapad: 2011-03-17 Senast uppdaterad: 2018-01-12Bibliografiskt granskad
Ingår i avhandling
1. Obesity and Increased Susceptibility : Role of FTO and MGAT1 Genetic Variants
Öppna denna publikation i ny flik eller fönster >>Obesity and Increased Susceptibility : Role of FTO and MGAT1 Genetic Variants
2011 (Engelska)Doktorsavhandling, sammanläggning (Övrigt vetenskapligt)
Abstract [en]

Obesity is a complex and a highly individualized disease and the molecular mechanisms behind this disorder need to be better elucidated. Identification of genes and genetic variants that are involved provide opportunities to establish a genetic understanding of the disease. These findings may also provide more rational approaches to therapy, either by identifying underlying causes or point out the need for different treatments. In addition, the timing and severity of obesity may provide insights into the aetiology of obesity and also identify age-specific determinants of weight gain. Recently, genome-wide association studies have led to a rapid progress in our understanding of the genetic basis of various diseases and candidate genes for obesity have been identified. The overall aim of this thesis was to investigate the genetic impact on severity of childhood obesity and the associations between obesity and genetic variants in the fat mass and obesity associated gene, FTO, and MGAT1, the gene encoding mannosyl (α-1,3-)-glycoprotein β-1,2-N-acetyl-glucosaminyltransferase.

We show that the impact of parental body mass index (BMI) on the severity of obesity in children is strengthened as the child grows older, whereas the age at obesity onset is of limited importance.

By association studies, we show that single nucleotide polymorphisms downstream MGAT1 influence susceptibility to obesity. Moreover, these variants affect the levels of unsaturated fatty acids and desaturase indices, variables previously shown to correlate with obesity. Furthermore, one variant in the first intronic region of FTO is associated with obesity among children but not with BMI or other measures of adiposity at older ages. However, this variant shows a weight-dependent association with cognitive function among elderly men. By direct sequencing, we identified novel variants in FTO, affecting glucose homeostasis in a BMI-independent manner. Furthermore, we found gender specific effects for FTO, both regarding obesity susceptibility and related phenotypes.

Ort, förlag, år, upplaga, sidor
Uppsala: Acta Universitatis Upsaliensis, 2011. s. 68
Serie
Digital Comprehensive Summaries of Uppsala Dissertations from the Faculty of Medicine, ISSN 1651-6206 ; 658
Nyckelord
Obesity, BMI, SNP, haplotype, association study, FTO, MGAT1
Nationell ämneskategori
Farmakologi och toxikologi
Forskningsämne
Farmakologi
Identifikatorer
urn:nbn:se:uu:diva-149332 (URN)978-91-554-8039-4 (ISBN)
Disputation
2011-05-07, B22, BMC, Husargatan 3, Uppsala, 09:00 (Engelska)
Opponent
Handledare
Tillgänglig från: 2011-04-14 Skapad: 2011-03-17 Senast uppdaterad: 2018-01-12Bibliografiskt granskad

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Benedict, ChristianJacobsson, Josefin ARönnemaa, ElinaSällman Almén, MarkusBrooks, SamanthaFredriksson, RobertLannfelt, LarsKilander, LenaSchiöth, Helgi B

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Benedict, ChristianJacobsson, Josefin ARönnemaa, ElinaSällman Almén, MarkusBrooks, SamanthaFredriksson, RobertLannfelt, LarsKilander, LenaSchiöth, Helgi B
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