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Diabet Med. 2007 Jun;24(6):650-5. Epub 2007 Apr 2.

Lack of association between polymorphisms in the gene encoding protein tyrosine phosphatase 1B (PTPN1) and risk of Type 2 diabetes.

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1
Joslin Diabetes Center and Department of Medicine, Harvard Medical School, Boston, MA 02215, USA.

Abstract

AIMS:

Recently, an association of Type 2 diabetes (T2DM) with polymorphisms in PTPN1 located on chromosome 20q was reported. We attempted to replicate this finding in an ethnically homogeneous Polish population.

METHODS:

The study groups comprised 474 cases with T2DM and 411 control subjects with normal fasting glucose. All individuals were genotyped for the five previously reported PTPN1 polymorphisms using a fluorescence polarization method. HAPLO.STAT software was used to infer and compare haplotype distributions.

RESULTS:

The distributions of alleles and genotypes for the five genotyped PTPN1 polymorphisms did not differ between the T2DM cases and control subjects (lowest P = 0.6). Similarly, the frequency of the common haplotype reported to be associated with T2DM did not differ in cases and control subjects. We also failed to find such an association in Whites by performing a meta-analysis of all the available data on the association of those five SNPs with T2DM.

CONCLUSION:

This case-control study in a Polish population did not confirm the reported association between polymorphisms in PTPN1 and T2DM.

[Indexed for MEDLINE]

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