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Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes
MJ. Machiela, Q. Lan, SL. Slager, RC. Vermeulen, LR. Teras, NJ. Camp, JR. Cerhan, JJ. Spinelli, SS. Wang, A. Nieters, J. Vijai, M. Yeager, Z. Wang, H. Ghesquières, J. McKay, L. Conde, PI. de Bakker, DG. Cox, L. Burdett, A. Monnereau, CR. Flowers,...
Jazyk angličtina Země Anglie, Velká Británie
Typ dokumentu časopisecké články, Research Support, N.I.H., Extramural, Research Support, N.I.H., Intramural, práce podpořená grantem, Research Support, U.S. Gov't, Non-P.H.S., Research Support, U.S. Gov't, P.H.S.
NLK
Free Medical Journals
od 1996 do Před 1 rokem
Open Access Digital Library
od 1996-01-01
PubMed
27008888
DOI
10.1093/hmg/ddw027
Knihovny.cz E-zdroje
- MeSH
- B-buněčný lymfom genetika patologie MeSH
- dospělí MeSH
- genetická predispozice k nemoci * MeSH
- genetické asociační studie metody MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- prospektivní studie MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- telomery patologie MeSH
- věkové faktory MeSH
- Check Tag
- dospělí MeSH
- lidé středního věku MeSH
- lidé MeSH
- mladiství MeSH
- mužské pohlaví MeSH
- senioři nad 80 let MeSH
- senioři MeSH
- ženské pohlaví MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
- Research Support, N.I.H., Extramural MeSH
- Research Support, N.I.H., Intramural MeSH
- Research Support, U.S. Gov't, Non-P.H.S. MeSH
- Research Support, U.S. Gov't, P.H.S. MeSH
Evidence from a small number of studies suggests that longer telomere length measured in peripheral leukocytes is associated with an increased risk of non-Hodgkin lymphoma (NHL). However, these studies may be biased by reverse causation, confounded by unmeasured environmental exposures and might miss time points for which prospective telomere measurement would best reveal a relationship between telomere length and NHL risk. We performed an analysis of genetically inferred telomere length and NHL risk in a study of 10 102 NHL cases of the four most common B-cell histologic types and 9562 controls using a genetic risk score (GRS) comprising nine telomere length-associated single-nucleotide polymorphisms. This approach uses existing genotype data and estimates telomere length by weighing the number of telomere length-associated variant alleles an individual carries with the published change in kb of telomere length. The analysis of the telomere length GRS resulted in an association between longer telomere length and increased NHL risk [four B-cell histologic types combined; odds ratio (OR) = 1.49, 95% CI 1.22-1.82,P-value = 8.5 × 10(-5)]. Subtype-specific analyses indicated that chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) was the principal NHL subtype contributing to this association (OR = 2.60, 95% CI 1.93-3.51,P-value = 4.0 × 10(-10)). Significant interactions were observed across strata of sex for CLL/SLL and marginal zone lymphoma subtypes as well as age for the follicular lymphoma subtype. Our results indicate that a genetic background that favors longer telomere length may increase NHL risk, particularly risk of CLL/SLL, and are consistent with earlier studies relating longer telomere length with increased NHL risk.
Centre for Big Data Research in Health University of New South Wales Sydney NSW Australia
Centre Heni Becquerel Université de Rouen Rouen France
Chronic Disease Prevention Unit National Institute for Health and Welfare Helsinki Finland
Danish Cancer Society Research Center Copenhagen Denmark
Department of Biomedical Science and
Department of Biostatistics University of Alabama at Birmingham Birmingham AL USA
Department of Biostatistics Yale School of Public Health New Haven CT USA
Department of Environmental Health Sciences and
Department of Epidemiology Department of Biostatistics Harvard School of Public Health Boston MA USA
Department of Epidemiology German Institute for Human Nutrition Potsdam Germany
Department of Epidemiology MD Anderson Cancer Center Houston TX USA
Department of Epidemiology MRC PHE Centre for Environment and Health School of Public Health and
Department of Family Medicine and Public Health Sciences Wayne State University Detroit MI USA
Department of Health Sciences Research
Department of Health Sciences University of York York UK
Department of Health Studies University of Chicago Chicago IL USA
Department of Immunology Genetics and Pathology Uppsala University Uppsala Sweden
Department of Internal Medicine Carver College of Medicine The University of Iowa Iowa City IA USA
Department of Internal Medicine University of Utah School of Medicine Salt Lake City UT USA
Department of Medical Biosciences Umeå University Umeå Sweden
Department of Medicine Solna Karolinska Institutet Karolinska University Hospital Stockholm Sweden
Department of Pathology City of Hope National Medical Center Duarte CA USA
Department of Statistics Dongguk University Seoul Republic of Korea
Division of Cancer Epidemiology and Genetics National Cancer Institute Bethesda MD USA
Division of Cancer Epidemiology German Cancer Research Center Heidelberg Baden Württemberg Germany
Division of Cancer Etiology City of Hope Beckman Research Institute Duarte CA USA
Division of Endocrinology Diabetes and Metabolism The Ohio State University Columbus OH USA
Division of Public Health Sciences Fred Hutchinson Cancer Research Center Seattle WA USA
Epidemiology Research Program American Cancer Society Atlanta GA USA
Hematology Unit Ospedale Oncologico di Riferimento Regionale A Businco Cagliari Italy
INSERM U1052 Cancer Research Center of Lyon Centre Léon Bérard Lyon France
International Agency for Research on Cancer Lyon France
Lymphoid Malignancies Unit Henri Mondor Hospital and University Paris Est Créteil France
Ontario Health Study Toronto ON Canada
School of Nursing and Human Sciences Dublin City University Dublin Ireland
School of Public Health Imperial College London London UK
The Tisch Cancer Institute and
Winship Cancer Institute Emory University School of Medicine Atlanta GA USA
Citace poskytuje Crossref.org
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- $a Genetically predicted longer telomere length is associated with increased risk of B-cell lymphoma subtypes / $c MJ. Machiela, Q. Lan, SL. Slager, RC. Vermeulen, LR. Teras, NJ. Camp, JR. Cerhan, JJ. Spinelli, SS. Wang, A. Nieters, J. Vijai, M. Yeager, Z. Wang, H. Ghesquières, J. McKay, L. Conde, PI. de Bakker, DG. Cox, L. Burdett, A. Monnereau, CR. Flowers, AJ. De Roos, AR. Brooks-Wilson, GG. Giles, M. Melbye, J. Gu, RD. Jackson, E. Kane, MP. Purdue, CM. Vajdic, D. Albanes, RS. Kelly, M. Zucca, KA. Bertrand, A. Zeleniuch-Jacquotte, C. Lawrence, A. Hutchinson, D. Zhi, TM. Habermann, BK. Link, AJ. Novak, A. Dogan, YW. Asmann, M. Liebow, CA. Thompson, SM. Ansell, TE. Witzig, H. Tilly, C. Haioun, TJ. Molina, H. Hjalgrim, B. Glimelius, HO. Adami, G. Roos, PM. Bracci, J. Riby, MT. Smith, EA. Holly, W. Cozen, P. Hartge, LM. Morton, RK. Severson, LF. Tinker, KE. North, N. Becker, Y. Benavente, P. Boffetta, P. Brennan, L. Foretova, M. Maynadie, A. Staines, T. Lightfoot, S. Crouch, A. Smith, E. Roman, WR. Diver, K. Offit, A. Zelenetz, RJ. Klein, DJ. Villano, T. Zheng, Y. Zhang, TR. Holford, J. Turner, MC. Southey, J. Clavel, J. Virtamo, S. Weinstein, E. Riboli, P. Vineis, R. Kaaks, H. Boeing, A. Tjønneland, E. Angelucci, S. Di Lollo, M. Rais, I. De Vivo, E. Giovannucci, P. Kraft, J. Huang, B. Ma, Y. Ye, BC. Chiu, L. Liang, JH. Park, CC. Chung, DD. Weisenburger, JF. Fraumeni, G. Salles, M. Glenn, L. Cannon-Albright, K. Curtin, X. Wu, KE. Smedby, S. de Sanjose, CF. Skibola, SI. Berndt, BM. Birmann, SJ. Chanock, N. Rothman,
- 520 9_
- $a Evidence from a small number of studies suggests that longer telomere length measured in peripheral leukocytes is associated with an increased risk of non-Hodgkin lymphoma (NHL). However, these studies may be biased by reverse causation, confounded by unmeasured environmental exposures and might miss time points for which prospective telomere measurement would best reveal a relationship between telomere length and NHL risk. We performed an analysis of genetically inferred telomere length and NHL risk in a study of 10 102 NHL cases of the four most common B-cell histologic types and 9562 controls using a genetic risk score (GRS) comprising nine telomere length-associated single-nucleotide polymorphisms. This approach uses existing genotype data and estimates telomere length by weighing the number of telomere length-associated variant alleles an individual carries with the published change in kb of telomere length. The analysis of the telomere length GRS resulted in an association between longer telomere length and increased NHL risk [four B-cell histologic types combined; odds ratio (OR) = 1.49, 95% CI 1.22-1.82,P-value = 8.5 × 10(-5)]. Subtype-specific analyses indicated that chronic lymphocytic leukemia or small lymphocytic lymphoma (CLL/SLL) was the principal NHL subtype contributing to this association (OR = 2.60, 95% CI 1.93-3.51,P-value = 4.0 × 10(-10)). Significant interactions were observed across strata of sex for CLL/SLL and marginal zone lymphoma subtypes as well as age for the follicular lymphoma subtype. Our results indicate that a genetic background that favors longer telomere length may increase NHL risk, particularly risk of CLL/SLL, and are consistent with earlier studies relating longer telomere length with increased NHL risk.
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- 700 1_
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