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Risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study

BACKGROUND: There are few known risk factors for renal cell carcinoma (RCC). Two small hospital-based case–control studies suggested an association between short blood telomere length (TL) and increased RCC risk. METHODS: We conducted a large population-based case–control study in two metropolitan r...

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Autores principales: Hofmann, J N, Baccarelli, A, Schwartz, K, Davis, F G, Ruterbusch, J J, Hoxha, M, McCarthy, B J, Savage, S A, Wacholder, S, Rothman, N, Graubard, B I, Colt, J S, Chow, W-H, Purdue, M P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3242602/
https://www.ncbi.nlm.nih.gov/pubmed/22033273
http://dx.doi.org/10.1038/bjc.2011.444
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author Hofmann, J N
Baccarelli, A
Schwartz, K
Davis, F G
Ruterbusch, J J
Hoxha, M
McCarthy, B J
Savage, S A
Wacholder, S
Rothman, N
Graubard, B I
Colt, J S
Chow, W-H
Purdue, M P
author_facet Hofmann, J N
Baccarelli, A
Schwartz, K
Davis, F G
Ruterbusch, J J
Hoxha, M
McCarthy, B J
Savage, S A
Wacholder, S
Rothman, N
Graubard, B I
Colt, J S
Chow, W-H
Purdue, M P
author_sort Hofmann, J N
collection PubMed
description BACKGROUND: There are few known risk factors for renal cell carcinoma (RCC). Two small hospital-based case–control studies suggested an association between short blood telomere length (TL) and increased RCC risk. METHODS: We conducted a large population-based case–control study in two metropolitan regions of the United States comparing relative TL in DNA derived from peripheral blood samples from 891 RCC cases and 894 controls. Odds ratios and 95% confidence intervals were estimated using unconditional logistic regression in both unadjusted and adjusted models. RESULTS: Median TL was 0.85 for both cases and controls (P=0.40), and no differences in RCC risk by quartiles of TL were observed. Results of analyses stratified by age, sex, race, tumour stage, and time from RCC diagnosis to blood collection were similarly null. In multivariate analyses among controls, increasing age and history of hypertension were associated with shorter TL (P<0.001 and P=0.07, respectively), and African Americans had longer TL than Caucasians (P<0.001). CONCLUSION: These data do not support the hypothesis that blood TL is associated with RCC. This population-based case–control study is, to our knowledge, the largest investigation to date of TL and RCC.
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spelling pubmed-32426022012-11-22 Risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study Hofmann, J N Baccarelli, A Schwartz, K Davis, F G Ruterbusch, J J Hoxha, M McCarthy, B J Savage, S A Wacholder, S Rothman, N Graubard, B I Colt, J S Chow, W-H Purdue, M P Br J Cancer Short Communication BACKGROUND: There are few known risk factors for renal cell carcinoma (RCC). Two small hospital-based case–control studies suggested an association between short blood telomere length (TL) and increased RCC risk. METHODS: We conducted a large population-based case–control study in two metropolitan regions of the United States comparing relative TL in DNA derived from peripheral blood samples from 891 RCC cases and 894 controls. Odds ratios and 95% confidence intervals were estimated using unconditional logistic regression in both unadjusted and adjusted models. RESULTS: Median TL was 0.85 for both cases and controls (P=0.40), and no differences in RCC risk by quartiles of TL were observed. Results of analyses stratified by age, sex, race, tumour stage, and time from RCC diagnosis to blood collection were similarly null. In multivariate analyses among controls, increasing age and history of hypertension were associated with shorter TL (P<0.001 and P=0.07, respectively), and African Americans had longer TL than Caucasians (P<0.001). CONCLUSION: These data do not support the hypothesis that blood TL is associated with RCC. This population-based case–control study is, to our knowledge, the largest investigation to date of TL and RCC. Nature Publishing Group 2011-11-22 2011-10-27 /pmc/articles/PMC3242602/ /pubmed/22033273 http://dx.doi.org/10.1038/bjc.2011.444 Text en Copyright © 2011 Cancer Research UK https://creativecommons.org/licenses/by/4.0/This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material.If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit https://creativecommons.org/licenses/by/4.0/.
spellingShingle Short Communication
Hofmann, J N
Baccarelli, A
Schwartz, K
Davis, F G
Ruterbusch, J J
Hoxha, M
McCarthy, B J
Savage, S A
Wacholder, S
Rothman, N
Graubard, B I
Colt, J S
Chow, W-H
Purdue, M P
Risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study
title Risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study
title_full Risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study
title_fullStr Risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study
title_full_unstemmed Risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study
title_short Risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study
title_sort risk of renal cell carcinoma in relation to blood telomere length in a population-based case–control study
topic Short Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3242602/
https://www.ncbi.nlm.nih.gov/pubmed/22033273
http://dx.doi.org/10.1038/bjc.2011.444
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