Assessment of genetic factors for type 2 diabetes mellitus
The purpose of the present study was to identify gene polymorphisms for reliable assessment of genetic factors for type 2 diabetes mellitus. The study population comprised 4853 unrelated Japanese individuals (2688 men, 2165 women), including 1489 subjects with type 2 diabetes mellitus (969 men, 520...
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Published in | International journal of molecular medicine Vol. 18; no. 2; pp. 299 - 308 |
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Main Authors | , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
Greece
D.A. Spandidos
01.08.2006
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Subjects | |
Online Access | Get full text |
ISSN | 1107-3756 1791-244X |
DOI | 10.3892/ijmm.18.2.299 |
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Summary: | The purpose of the present study was to identify gene polymorphisms for
reliable assessment of genetic factors for type 2 diabetes mellitus. The study
population comprised 4853 unrelated Japanese individuals (2688 men, 2165 women),
including 1489 subjects with type 2 diabetes mellitus (969 men, 520 women) and
3364 controls (1719 men, 1645 women). The genotypes for 148 polymorphisms of 124
candidate genes were determined with a method that combines polymerase chain reaction
and sequence-specific oligonucleotide probes with suspension array technology.
Sixteen polymorphisms were related (p<0.05) to the prevalence of type 2 diabetes
mellitus as determined by the chi-square test. Multivariable logistic regression
analysis with adjustment for age, sex, and the prevalence of smoking revealed
that, among these polymorphisms, the -603A↷G polymorphism of the gene for coagulation
factor III (F3) was significantly (p<0.001) associated with the prevalence
of type 2 diabetes mellitus, with the -603G allele representing a risk factor
for this condition. A stepwise forward selection procedure demonstrated that F3
genotype (GG versus AA + AG) significantly (p<0.001) and independently affected
the prevalence of type 2 diabetes mellitus. Genotype for F3 may prove reliable
for assessment of genetic factors for type 2 diabetes mellitus. Determination
of the genotype for this gene may contribute to personalized prevention of this
condition. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 1107-3756 1791-244X |
DOI: | 10.3892/ijmm.18.2.299 |