Tatsuya Takeshita

Dr. Tatsuya Takeshita


Research Focus & Metrics

Academic Career Length

33Years (1994-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 September 1994 in Human Genetics
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Journal Article
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TTTatsuya Takeshita
Tatsuya Takeshita
KMKanehisa Morimoto
Kanehisa Morimoto
XMXiaoQuang Mao
XiaoQuang Mao
THTomoko Hashimoto
Tomoko Hashimoto
JFJun-Ichi Furuyama
Jun-Ichi Furuyama

1 January 2012 in Journal of Epidemiology
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Journal Article
Open access
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HMHideo Matsuura
Hideo Matsuura
KMKanae Mure
Kanae Mure
NNNobuhiro Nishio
Nobuhiro Nishio
NKNaomi Kitano
Naomi Kitano
NNNaoko Nagai
Naoko Nagai
TTTatsuya Takeshita
Tatsuya Takeshita
Japan's largest platform for academic e-journals: J-STAGE is a full text database for reviewed academic papers published by Japanese societies

1 February 2000 in Cancer Letters
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Journal Article
Closed access
TTTatsuya Takeshita
Tatsuya Takeshita
XYXing Yang
Xing Yang
YIYoshiki Inoue
Yoshiki Inoue
SSShigeaki Sato
Shigeaki Sato
KMKanehisa Morimoto
Kanehisa Morimoto

1 February 2004 in Journal of Dental Research
Verified
Journal Article
Closed access
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NNN. Nishida
N. Nishida
MTM. Tanaka
M. Tanaka
NHN. Hayashi
N. Hayashi
HNH. Nagata
H. Nagata
TTTatsuya Takeshita
Tatsuya Takeshita
SSS. Shizukuishi
S. Shizukuishi
There is little information regarding the association between alcohol consumption and periodontitis risk. We assessed whether alcohol consumption and ALDH2 genotypes were associated with periodontitis. Subjects’ lifestyle was examined by a self-administered questionnaire, and the percentage of pocket depths ≥ 3.5 mm was used as a periodontal parameter. ALDH2 genotypes were determined with the use of a PCR/RFLP method. Multiple logistic analyses showed that alcohol consumption was significantly associated with periodontitis, and its odds ratio was 1.98. There was no significant relationship between periodontal status and ALDH2 genotypes. However, ALDH2*1/*2 subjects who consumed ≥ 33 g/day of alcohol had a significantly greater percentage of pocket depths ≥ 3.5 mm than those whose daily consumption was lower, while there was no significant difference in periodontal status associated with alcohol consumption in ALDH2*1/*1 subjects. Our results suggest that alcohol consumption may be a risk indicator for periodontitis in ALDH2*1/*2 subjects who consume larger amounts of alcohol.

1 July 2013 in Nutrition
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Journal Article
Closed access
KMKanae Mure
Kanae Mure
SMShinya Maeda
Shinya Maeda
CMChizu Mukoubayashi
Chizu Mukoubayashi
KMKouichi Mugitani
Kouichi Mugitani
MIMasataka Iwane
Masataka Iwane
TTTatsuya Takeshita
Tatsuya Takeshita

1 May 1996 in Environmental Health Perspectives
Verified
Journal Article
Open access
KMK Morimoto
K Morimoto
TTTatsuya Takeshita
Tatsuya Takeshita
Excessive drinking of alcohol is now widely known to be one of the major lifestyle choices that ca effect health. Among the various effects of alcohol drinking, cytogenetic and other genotoxic effects are of major concern from the viewpoint of prevention of alcohol-related diseases. Alcohol is first metabolized to acetaldehyde, which directly causes various types of chromosomal DNA lesions and alcohol-related diseases, and is then further detoxified to the much less toxic metabolite acetate. About 50% of Oriental people are deficient in the aldehyde-dehydrogenase 2 isozyme (ALDH2) that can most efficiently detoxify acetaldehyde. We have performed a series of experiments to investigate how the genetic deficiency in ALDH2 affects the behavioral pattern for alcohol drinking and the sensitivity of peripheral lymphocytes to the induction of chromosome alterations by exposure to alcohol and alcohol-related chemicals. We found great effects of the ALDH2 genotypes on alcohol sensitivity and alcohol-drinking behavior. We also show that lymphocytes from habitual drinkers with the deficient ALDH2 enzyme had significantly higher frequencies of sister chromatid exchanges than those from ALDH2-proficient individuals.