11 research outputs found
Detectable clonal mosaicism and its relationship to aging and cancer
- Author
- Abnet C.C. (Christian C.)
- Ahlbom A. (Anders)
- Albanes D. (Demetrius)
- Aldrich M.C. (Melinda C.)
- Amos C. (Christopher)
- Amundadottir L. (Laufey)
- Andersson U. (Ulrika)
- Andrulis I.L. (Irene L.)
- Arslan A.A. (Alan A.)
- Baris D. (Dalsu)
- Barkauskas D.A. (Donald A.)
- Beane-Freeman L.E. (Laura E.)
- Berg C.D. (Christine D.)
- Berndt S.I. (Sonja I.)
- Bertazzi P.A. (Pier Alberto)
- Black A. (Amanda)
- Blot W.J. (William J.)
- Bock C.H. (Cathryn H.)
- Boutron-Ruault M.C. (Marie-Christine)
- Bracci P.M. (Paige M.)
- Brinton L.A. (Louise A.)
- Bueno-de-Mesquita H.B. (H. Bas)
- Burdett L. (Laurie)
- Buring J.E. (Julie E.)
- Butler M.A. (Mary A.)
- Canzian F. (Federico)
- Caporaso N.E. (Neil E.)
- Carreon T. (Tania)
- Chang K. (Kenneth)
- Chanock S.J. (Stephen J.)
- Chatterjee N. (Nilanjan)
- Chow W.H. (Wong-Ho)
- Chung C.C. (Charles C.)
- Consonni D. (Dario)
- Cook M.B. (Michael B.)
- Cotterchio M. (Michelle)
- Cullen M. (Michael)
- Davis F.G. (Faith G.)
- Dean M.C. (Michael C.)
- Deng X. (Xiang)
- Ding T. (Ti)
- Duell E.J. (Eric J.)
- Elena J.W. (Joanne W.)
- Epstein C.G. (Caroline G.)
- Erickson R.L. (Ralph L.)
- Fan J.H. (Jin-Hu)
- Feychting M. (Maria)
- Figueroa J.D. (Jonine D.)
- Fraumeni J.F. (Joseph F.)
- Freedman N.D. (Neal D.)
- Fuchs C.S. (Charles S.)
- Gallinger S. (Steven)
- Gao Y.T. (Yu-Tang)
- Gapstur S.M. (Susan M.)
- Garcia-Closas M. (Montserrat)
- Gaudet M.M. (Mia M.)
- Gaziano J.M. (J. Michael)
- Giles G.G. (Graham G.)
- Gillanders E.M. (Elizabeth M.)
- Giovannucci E.L. (Edward L.)
- Goggins M. (Michael)
- Goldin L. (Lynn)
- Goldstein A.M. (Alisa M.)
- Gonzalez J.R. (Juan R.)
- Gorlick R.G. (Richard G.)
- Graubard B.I. (Barry I.)
- Greene M.H. (Mark H.)
- Gross M.D. (Myron D.)
- Haiman C.A. (Christopher A.)
- Hallmans G. (Goran)
- Hankinson S.E. (Susan E.)
- Harris C.C. (Curtis C.)
- Hartge P. (Patricia)
- Hassan M. (Manal)
- Henderson B.E. (Brian E.)
- Henriksson R. (Roger)
- Hoffman-Bolton J.A. (Judith A.)
- Holly E.A. (Elizabeth A.)
- Hoover R.N. (Robert N.)
- Horner M.J. (Marie-Josephe)
- Hsing A.W. (Ann W.)
- Hu N. (Nan)
- Hunter D.J. (David J.)
- Hutchinson A. (Amy)
- Inskip P.D. (Peter D.)
- Jacobs K. (Kevin)
- Jenab M. (Mazda)
- Jiao L. (Li)
- Johansen C. (Christoffer)
- Johnson A. (Alison)
- Khaw K.T. (Kay-Tee)
- Klein A.P. (Alison P.)
- Kogevinas M. (Manolis)
- Koh W.P. (Woon-Puay)
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- Kooperberg C. (Charles)
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- Kraft P. (Peter)
- Kratz C.P. (Christian P.)
- Krogh V. (Vittorio)
- Kurtz R.C. (Robert C.)
- LaCroix A. (Andrea)
- Landgren A. (Annelie)
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- Le-Marchand L. (Loic)
- Li D. (Donghui)
- Liao L. (Linda)
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- Mendelsohn J.B. (Julie B.)
- Michaud D.S. (Dominique S.)
- Mirabello L. (Lisa)
- Moore L.E. (Lee E.)
- Olson S.H. (Sara H.)
- Patiño-García A. (Ana)
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- Peters U. (Ulrike)
- Petersen G. (Gloria)
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- Purdue M. (Mark)
- Qiao Y.L. (You-Lin)
- Rabe K.G. (Kari G.)
- Rajaraman P. (Preetha)
- Real F.X. (Francisco X.)
- Riboli E. (Elio)
- Risch H.A. (Harvey A.)
- Rodriguez-Santiago B. (Benjamin)
- Rothman N. (Nathaniel)
- Rotunno M. (Melissa)
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- Sampson J. (Joshua)
- Savage S.A. (Sharon A.)
- Schumacher F. (Fredrick)
- Schwartz A.G. (Ann G.)
- Schwartz K.L. (Kendra L.)
- Schwenn M. (Molly)
- Sesso H.D. (Howard D.)
- Severi G. (Gianluca)
- Shu X.O. (Xiao-Ou)
- Sierrasesumaga L. (Luis)
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- Silverman D.T. (Debra T.)
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- Stevens V.L. (Victoria L.)
- Stolzenberg-Solomon R.Z. (Rachael Z.)
- Stram D. (Daniel)
- Tang Z.Z. (Ze-Zhong)
- Taylor P.R. (Philip R.)
- Teras L.R. (Lauren R.)
- Thomas G. (Gilles)
- Tjonneland A. (Anne)
- Tobias G.S. (Geoffrey S.)
- Trichopoulos D. (Dimitrios)
- Tucker M. (Margaret)
- Villa O. (Olaya)
- Virtamo J. (Jarmo)
- Visvanathan K. (Kala)
- Wacholder S. (Sholom)
- Wang Z. (Zhaoming)
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- Yu K. (Kai)
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- Zeleniuch-Jacquotte A. (Anne)
- Zheng W. (Wei)
- Zhou W. (Weiyin)
- Ziegler R.G. (Regina G.)
- Publication venue
- Nature Publishing Group
- Publication date
- 01/12/2012
- Field of study
In an analysis of 31,717 cancer cases and 26,136 cancer-free controls from 13 genome-wide association studies, we observed large chromosomal abnormalities in a subset of clones in DNA obtained from blood or buccal samples. We observed mosaic abnormalities, either aneuploidy or copy-neutral loss of heterozygosity, of >2 Mb in size in autosomes of 517 individuals (0.89%), with abnormal cell proportions of between 7% and 95%. In cancer-free individuals, frequency increased with age, from 0.23% under 50 years to 1.91% between 75 and 79 years (P = 4.8 × 10(-8)). Mosaic abnormalities were more frequent in individuals with solid tumors (0.97% versus 0.74% in cancer-free individuals; odds ratio (OR) = 1.25; P = 0.016), with stronger association with cases who had DNA collected before diagnosis or treatment (OR = 1.45; P = 0.0005). Detectable mosaicism was also more common in individuals for whom DNA was collected at least 1 year before diagnosis with leukemia compared to cancer-free individuals (OR = 35.4; P = 3.8 × 10(-11)). These findings underscore the time-dependent nature of somatic events in the etiology of cancer and potentially other late-onset diseases
An evaluation of five preservation techniques and conventional freezing temperatures of -20oC and -85oC for long-term preservation of Campylobacter jejuni
- Author
- Publication venue
- 'Wiley'
- Publication date
- Field of study
Structural predictors of lung function decline in the British early COPD network (BEACON) cohort
- Author
- Publication venue
- Publication date
- 22/05/2024
- Field of study
Identifying Exemplary Teachers and Teaching: Evidence from Student Ratings1
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- B. Bolton
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- C. Orpen
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- Publication date
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- Field of study
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- A. Cope
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Detectable clonal mosaicism and its relationship to aging and cancer
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- Nature Publishing Group
- Publication date
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- Field of study
In an analysis of 31,717 cancer cases and 26,136 cancer-free controls from 13 genome-wide association studies, we observed large chromosomal abnormalities in a subset of clones in DNA obtained from blood or buccal samples. We observed mosaic abnormalities, either aneuploidy or copy-neutral loss of heterozygosity, of >2 Mb in size in autosomes of 517 individuals (0.89%), with abnormal cell proportions of between 7% and 95%. In cancer-free individuals, frequency increased with age, from 0.23% under 50 years to 1.91% between 75 and 79 years (P = 4.8 × 10(-8)). Mosaic abnormalities were more frequent in individuals with solid tumors (0.97% versus 0.74% in cancer-free individuals; odds ratio (OR) = 1.25; P = 0.016), with stronger association with cases who had DNA collected before diagnosis or treatment (OR = 1.45; P = 0.0005). Detectable mosaicism was also more common in individuals for whom DNA was collected at least 1 year before diagnosis with leukemia compared to cancer-free individuals (OR = 35.4; P = 3.8 × 10(-11)). These findings underscore the time-dependent nature of somatic events in the etiology of cancer and potentially other late-onset diseases
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- Publication date
- 01/08/2018
- Field of study
Aim Previous studies reported conflicting evidence on the effects of obesity on outcomes after gastrointestinal surgery. The aims of this study were to explore the relationship of obesity with major postoperative complications in an international cohort and to present a metaanalysis of all available prospective data. Methods This prospective, multicentre study included adults undergoing both elective and emergency gastrointestinal resection, reversal of stoma or formation of stoma. The primary end-point was 30-day major complications (Clavien–Dindo Grades III–V). A systematic search was undertaken for studies assessing the relationship between obesity and major complications after gastrointestinal surgery. Individual patient meta-analysis was used to analyse pooled results. Results This study included 2519 patients across 127 centres, of whom 560 (22.2%) were obese. Unadjusted major complication rates were lower in obese vs normal weight patients (13.0% vs 16.2%, respectively), but this did not reach statistical significance (P = 0.863) on multivariate analysis for patients having surgery for either malignant or benign conditions. Individual patient meta-analysis demonstrated that obese patients undergoing surgery formalignancy were at increased risk of major complications (OR 2.10, 95% CI 1.49–2.96, P < 0.001), whereas obese patients undergoing surgery for benign indications were at decreased risk (OR 0.59, 95% CI 0.46–0.75, P < 0.001) compared to normal weight patients. Conclusions In our international data, obesity was not found to be associated with major complications following gastrointestinal surgery. Meta-analysis of available prospective data made a novel finding of obesity being associated with different outcomes depending on whether patients were undergoing surgery for benign or malignant disease