Folate status, genomic DNA hypomethylation, and risk of colorectal adenoma and cancer: a case control study

2003 ◽  
Vol 124 (5) ◽  
pp. 1240-1248 ◽  
Author(s):  
Maria Pufulete ◽  
Reyad Al-Ghnaniem ◽  
Andrew J.M Leather ◽  
Paul Appleby ◽  
Sally Gout ◽  
...  
2008 ◽  
Vol 9 (4) ◽  
pp. 359-366 ◽  
Author(s):  
Lee E Moore ◽  
Ruth M Pfeiffer ◽  
Cristina Poscablo ◽  
Francisco X Real ◽  
Manolis Kogevinas ◽  
...  

2015 ◽  
Vol 22 (8) ◽  
pp. 2074-2082 ◽  
Author(s):  
Julia Mendoza- Pérez ◽  
Jian Gu ◽  
Luis A. Herrera ◽  
Nizar M. Tannir ◽  
Surena F. Matin ◽  
...  

2011 ◽  
Vol 7 (2-4) ◽  
pp. 199-203 ◽  
Author(s):  
Farah Lotfi Kashani ◽  
Dor Mohammad Kordi-Tamandani ◽  
Roya Sahranavard ◽  
Mohammad Hashemi ◽  
Farzaneh Kordi-Tamandani ◽  
...  

Glutathione S-transferases (GSTs) are major intracellular antioxidants, which, impaired in their function, are involved in the progress of schizophrenia (SCZ). The aim of this case-control study was to investigate the association between the polymorphism of glutathione S-transferases M1 (GSTM1), T1 (GSTT1), the glutathione S-transferase P1 gene (GSTP1) and SCZ. We isolated genomic DNA from peripheral blood of 93 individuals with SCZ and 99 healthy control subjects' genotypes analyzing them for GSTM1, GSTT1 and GSTP1 using polymerase chain reaction. The analysis of the gene–gene interaction between GSTs indicated that the magnitude of the association was greater for the combined AG/GSTT1 & GSTM1 genotypes (OR = 2.51; 95% CI: 1.13–5.63, P = 0.02). The AG and combined AG + GG genotypes of GSTP1 increased the risk of SCZ (OR = 1.83; 95% CI: 0.94–3.75 and OR = 1.71; 95% CI: 0.92–3.19, respectively). The genotypes of GSTT/NULL, NULL/GSTM and NULL/NULL increased the risk of SCZ (OR = 2.05; 95% CI: 0.9–4.74; OR = 2.0; 95% CI: 1.68–2.31; and OR = 1.8; 95% CI: 0.57–2.46, respectively). The present study supports previous data that suggest that impairment in the function of GSTs genes may increase the risk of SCZ.


2009 ◽  
Vol 100 (11) ◽  
pp. 1812-1816 ◽  
Author(s):  
M Akhter ◽  
M Iwasaki ◽  
T Yamaji ◽  
S Sasazuki ◽  
S Tsugane

2006 ◽  
Vol 38 (9) ◽  
pp. 668-672 ◽  
Author(s):  
Y.W. Chung ◽  
D.S. Han ◽  
Y.K. Park ◽  
B.K. Son ◽  
C.H. Paik ◽  
...  

SLEEP ◽  
2020 ◽  
Vol 43 (Supplement_1) ◽  
pp. A383-A384
Author(s):  
L Guan ◽  
L Jiao ◽  
S Malhotra

Abstract Introduction Colorectal cancer is the third most common cancer in the United States, with over half of colorectal cancers estimated to be the result of modifiable risk factors. Studies relating sleep apnea (SA) and colorectal adenoma (CRA) are limited and the findings are equivocal. The objective of this study was to examine the association between SA and risk of CRA. Methods This was a retrospective cross-sectional case-control study of data collected from 460 veterans, ages 50-79, seen in the colonoscopy clinic at the Michael E. DeBakey VA Medical Center between 2014 and 2018. Information on demographics, sleep history, and co-morbidities were obtained through lifestyle questionnaire. Self-reported SA was diagnosed by a prior sleep study. Cases consisted of 297 participants had pathologically confirmed adenoma (including 117 participants having advanced CRA with villous component or diameter of polyp > 1 cm). Controls consisted of 173 polyp-free participants. The distribution of demographics and lifestyle factors were compared between CRA and non-CRA using the Student’s t or chi-square tests. Odds ratios (OR) and 95% confidence intervals (CI) of CRA in association with CRA were calculated using univariate and multivariate unconditional logistic regression models. The confounding factors included age, sex, ethnicity, obesity, smoking status, alcohol use, hypertension, and sleep duration. Results Compared with non-SA, the multivariable OR (95% CI) for CRA was 0.92 (0.58-1.48); for non-advanced CRA was 1.14 (0.68-1.91), and for advanced CRA was 0.61 (0.32-1.17) in SA participants. Adjustment of sleep duration in the model did not change the risk estimates. Conclusion Sleep-study diagnosed SA was not associated with development of CRA in this veteran population. Further studies are needed to confirm this observation and incorporate the severity and treatment of SA, and undiagnosed SA in risk assessment. Support This research is supported in part by the Gillson Longenbaugh Foundation, and Golfers Against Cancer organization (to LJ), the Cancer Prevention Research Institute of Texas (CPRIT) (RP#140767, to LJ).


1993 ◽  
Vol 3 (1) ◽  
pp. 1-5 ◽  
Author(s):  
Ikuko Kato ◽  
Suketami Tominaga ◽  
Akira Matsuura ◽  
Yuri Yoshii ◽  
Masato Shirai ◽  
...  

2006 ◽  
Vol 63 (5) ◽  
pp. AB212
Author(s):  
Yong Woo Chung ◽  
Dong Soo Han ◽  
Yoon Kyung Park ◽  
Byoung Kwan Son ◽  
Chang Hee Paik ◽  
...  

2001 ◽  
Vol 77 (4) ◽  
pp. 247-252 ◽  
Author(s):  
Aminah Jatoi ◽  
Benedict D.T. Daly ◽  
Gertrude Kramer ◽  
Joel B. Mason

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