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Telomere length differences between colorectal polyp subtypes: a colonoscopy-based case-control study.
Hardikar, Sheetal; Burnett-Hartman, Andrea N; Phipps, Amanda I; Upton, Melissa P; Zhu, Lee-Ching; Newcomb, Polly A.
Afiliação
  • Hardikar S; Huntsman Cancer Institute, University of Utah, 2000 Circle of Hope Dr. Room 4711, Salt Lake City, UT, 84112, USA. sheetal.hardikar@hci.utah.edu.
  • Burnett-Hartman AN; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA. sheetal.hardikar@hci.utah.edu.
  • Phipps AI; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Upton MP; Kaiser Permanente, Colorado Institute for Health Research, Denver, CO, USA.
  • Zhu LC; Public Health Sciences Division, Fred Hutchinson Cancer Research Center, Seattle, WA, USA.
  • Newcomb PA; Department of Epidemiology, School of Public Health, University of Washington, Seattle, WA, USA.
BMC Cancer ; 18(1): 513, 2018 May 02.
Article em En | MEDLINE | ID: mdl-29720120
BACKGROUND: Short telomeres have been associated with increased risk of many cancers, particularly cancers of the gastrointestinal tract including esophagus and stomach. However, the association between telomere length (TL) and colorectal cancer and its precursors, colorectal polyps, is not clear. METHODS: We investigated the relationship between TL and risk of colorectal polyp subtypes in a colonoscopy-based study in western Washington. Participants were 35-79 year-old enrollees at an integrated health care system, who underwent a colonoscopy between 1998 and 2007 (n = 190), completed a self-administered questionnaire, provided blood samples, and were distinguished as having adenomas, serrated polyps, or as polyp-free controls through a standardized pathology review. Telomere length (T) relative to a single copy gene (S) was measured in circulating leukocytes from stored buffy coat samples using quantitative polymerase chain reaction. Multivariable polytomous logistic regression was used to compare case groups with polyp-free controls and other case groups; adjusted odds ratios (OR) and 95% confidence intervals (CI) were estimated. RESULTS: TL in the shortest tertile (T/S ratio < 0.58) was associated with increased risk of adenomas and serrated polyps [OR (95%CI) were 1.77(0.81-3.88) and 2.98(1.15-7.77), respectively). When evaluated by lesion severity within each pathway, short TL was more strongly associated with advanced adenomas and sessile serrated polyps [OR (95% CI) = 1.90(0.76-4.73) and 3.82(0.86-16.86), respectively], although the associations were not statistically significant. CONCLUSIONS: Our results suggest that short TL may be associated with an increased risk of colorectal polyps in both the adenoma-carcinoma and serrated pathways. The risk was particularly notable for sessile serrated polyps, although the association was not statistically significant and sample size was limited.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pólipos do Colo / Telômero Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Pólipos do Colo / Telômero Tipo de estudo: Observational_studies / Risk_factors_studies Limite: Adult / Aged / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2018 Tipo de documento: Article