Volume 56, Issue 2 pp. 162-165

Polymorphisms in the TNFA promoter region is not associated with palmoplantar pustulosis

H. Niizeki

H. Niizeki

Department of Dermatology and Institute of Clinical Research, National Tokyo Medical Center, Tokyo, Japan

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T. Naruse

T. Naruse

Department of Molecular Lifescience, Tokai University School of Medicine, Kanagawa, Japan

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K. Hashigucci

K. Hashigucci

Department of Otolaryngology, Kitasato Institute Hospital, Tokyo, Japan

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M. Yokoyama

M. Yokoyama

Department of Otolaryngology, Kitasato Institute Hospital, Tokyo, Japan

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Y. Yamasaki

Y. Yamasaki

Department of Dermatology and Institute of Clinical Research, National Tokyo Medical Center, Tokyo, Japan

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K. Akiya

K. Akiya

Department of Internal Medicine and Institute of Clinical Research, National Tokyo Medical Center, Tokyo, Japan

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T. Tojo

T. Tojo

Department of Internal Medicine and Institute of Clinical Research, National Tokyo Medical Center, Tokyo, Japan

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T. Urushibara

T. Urushibara

Environmental Management Center, School of Pharmaceutical Sciences, Kitasato University, Tokyo, Japan

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Y. Yamazaki

Y. Yamazaki

Department of Otolaryngology, Keio University School of Medicine, Tokyo, Japan

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H. Inoko

H. Inoko

Department of Molecular Lifescience, Tokai University School of Medicine, Kanagawa, Japan

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T. Nishikawa

T. Nishikawa

Department of Dermatology, Keio University School of Medicine, Shinjuku, Tokyo, Japan

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First published: 25 December 2001
Citations: 11

Abstract

Polymorphisms of the 5′-flanking promoter/enhancer region of the TNFA gene were determined in 80 Japanese patients with pulmoplantar pustulosis (PPP). The 5′-flanking region of the TNFA gene from –1107 to –66 was amplified by polymerase chain reaction (PCR) method. Nucleotide sequencing data from the PCR products revealed that 5 single nucleotide polymorphisms at position –1031, –863, –857, –307 and –237. None of the nucleotide substitutions were significantly increased in PPP patients when compared with those in controls. To clarify the linkage among the neighboring genetic marker, we analyzed the association between the polymorphisms in the TNFA promoter region and the NcoI polymorphism in the first intron of the TNFB gene as well as HLA-DR9. The genotype at –1031C is strongly associated with TNFB1 and negatively associated with TNFB2 which is reported to be associated with PPP. These data indicate that TNFA gene centromeric to TNFB is not associated with PPP and the susceptible gene of PPP is located between TNFB and HLA-B.

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