Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
1-2
pubmed:dateCreated
2001-6-28
pubmed:abstractText
There is increasing evidence that in human obesity, particularly the abdominal phenotype, the activity of the hypothalamic-pituitary-adrenal (HPA) axis is disregulated. At least two distinct alterations have been reported: one is characterized by several neuroendocrine abnormalities and hyperresponsiveness of the HPA axis to different neuropeptides, the other is characterized by elevated cortisol traffic and probably by supranormal cortisol production. The 11beta-hydroxysteroid dehydrogenase (11beta-HSD) enzymes interconvert cortisol and cortisone in human. Two different isoforms have been identified. A possible modification of the activity of the enzyme 11beta-HSD1 in subjects with abdominal obesity has been described in the literature. We decided to test the hypothesis that mutated isoforms of type 11beta-HSD1 protein could be responsible for alterations of cortisol metabolism in patients with abdominal obesity. A mutational screening of the whole coding sequence and exon-flanking regions of the 11B-HSD1 gene has been performed in 8 patients. The main results of our study are the exclusion of a common association of 11beta-HSD1 mutations to obesity and the identification of two novel allelic variants for the gene 11beta-HSD1 in the Italian population, not previously described in any database.
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:chemical
pubmed:status
MEDLINE
pubmed:issn
0743-5800
pubmed:author
pubmed:issnType
Print
pubmed:volume
27
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
47-61
pubmed:dateRevised
2011-11-17
pubmed:meshHeading
pubmed-meshheading:11428721-11-beta-Hydroxysteroid Dehydrogenases, pubmed-meshheading:11428721-Abdomen, pubmed-meshheading:11428721-Adrenocorticotropic Hormone, pubmed-meshheading:11428721-Adult, pubmed-meshheading:11428721-Amino Acid Sequence, pubmed-meshheading:11428721-Blood Glucose, pubmed-meshheading:11428721-Body Mass Index, pubmed-meshheading:11428721-DNA Mutational Analysis, pubmed-meshheading:11428721-Exons, pubmed-meshheading:11428721-Female, pubmed-meshheading:11428721-Humans, pubmed-meshheading:11428721-Hydrocortisone, pubmed-meshheading:11428721-Hydroxysteroid Dehydrogenases, pubmed-meshheading:11428721-Insulin, pubmed-meshheading:11428721-Middle Aged, pubmed-meshheading:11428721-Molecular Sequence Data, pubmed-meshheading:11428721-Mutation, pubmed-meshheading:11428721-Obesity, pubmed-meshheading:11428721-Phenotype, pubmed-meshheading:11428721-Polymerase Chain Reaction, pubmed-meshheading:11428721-Pregnancy, pubmed-meshheading:11428721-Reverse Transcriptase Polymerase Chain Reaction, pubmed-meshheading:11428721-Sequence Analysis, DNA, pubmed-meshheading:11428721-Uterus
pubmed:articleTitle
Lack of mutations of type 1 11beta-hydroxysteroid dehydrogenase gene in patients with abdominal obesity.
pubmed:affiliation
Institute of Histology and General Embriology, Bologna, Italy. betty@alma.unibo.it
pubmed:publicationType
Journal Article, Research Support, Non-U.S. Gov't