Source:http://linkedlifedata.com/resource/pubmed/id/20195292
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
1
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pubmed:dateCreated |
2011-1-25
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pubmed:abstractText |
The objective of this study was to determine the association of 5-HT2C (serotonin 2C receptor) and MDR1 (multidrug resistant protein) genetic polymorphisms and antipsychotic-induced metabolic abnormalities among female patients with DSM IV schizophrenia spectrum disorders. We have previously reported the associations of -759CT 5-HT2C and G2677T and C3435T MDR1 genetic polymorphisms and olanzapine/risperidone-induced weight gain in a similar sample of patients. Here, we included a total of 101 previously non-medicated female patients treated with olanzapine/risperidone over a 3-month period. The variables analyzed included fasting glucose, total cholesterol, low-density lipoprotein, high-density lipoprotein and triglyceride levels in blood, blood pressure and waist circumferences. We observed significant association of -759T 5-HT2C genetic variant and greater increase in waist circumference (P=0.03), fasting glucose level (P=0.046) and triglyceride level (P=0.045) in blood after a 3-month period. The 2677T and 3435T MDR1 genetic variants were significantly associated with the greater increase in fasting glucose level in blood when patients were using olanzapine (P<0.001 and P=0.028, respectively). Our data indicate a possible influence of -759CT 5-HT2C and MDR1 G2677T and C3435T MDR1 genetic polymorphisms on the development of metabolic abnormalities among female patients treated with olanzapine/risperidone.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:chemical |
http://linkedlifedata.com/resource/pubmed/chemical/ABCB1 protein, human,
http://linkedlifedata.com/resource/pubmed/chemical/Antipsychotic Agents,
http://linkedlifedata.com/resource/pubmed/chemical/Benzodiazepines,
http://linkedlifedata.com/resource/pubmed/chemical/Blood Glucose,
http://linkedlifedata.com/resource/pubmed/chemical/P-Glycoprotein,
http://linkedlifedata.com/resource/pubmed/chemical/Receptor, Serotonin, 5-HT2C,
http://linkedlifedata.com/resource/pubmed/chemical/Risperidone,
http://linkedlifedata.com/resource/pubmed/chemical/olanzapine
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pubmed:status |
MEDLINE
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pubmed:month |
Feb
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pubmed:issn |
1473-1150
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pubmed:author | |
pubmed:issnType |
Electronic
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pubmed:volume |
11
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
35-44
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pubmed:meshHeading |
pubmed-meshheading:20195292-Adult,
pubmed-meshheading:20195292-Antipsychotic Agents,
pubmed-meshheading:20195292-Benzodiazepines,
pubmed-meshheading:20195292-Blood Glucose,
pubmed-meshheading:20195292-Cohort Studies,
pubmed-meshheading:20195292-Female,
pubmed-meshheading:20195292-Humans,
pubmed-meshheading:20195292-Middle Aged,
pubmed-meshheading:20195292-P-Glycoprotein,
pubmed-meshheading:20195292-Polymorphism, Genetic,
pubmed-meshheading:20195292-Receptor, Serotonin, 5-HT2C,
pubmed-meshheading:20195292-Risperidone,
pubmed-meshheading:20195292-Schizophrenia,
pubmed-meshheading:20195292-Waist Circumference,
pubmed-meshheading:20195292-Young Adult
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pubmed:year |
2011
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pubmed:articleTitle |
Association study of MDR1 and 5-HT2C genetic polymorphisms and antipsychotic-induced metabolic disturbances in female patients with schizophrenia.
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pubmed:affiliation |
Department of Psychiatry, University Hospital Centre Zagreb and Zagreb School of Medicine, Zagreb, Croatia. mrojnic@gmail.com
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pubmed:publicationType |
Journal Article,
Research Support, Non-U.S. Gov't
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