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Type 2 diabetes mellitus, blood cholesterol, triglyceride and colorectal cancer risk in Lynch syndrome.
Dashti, S Ghazaleh; Li, Wing Yan; Buchanan, Daniel D; Clendenning, Mark; Rosty, Christophe; Winship, Ingrid M; Macrae, Finlay A; Giles, Graham G; Hardikar, Sheetal; Hua, Xinwei; Thibodeau, Stephen N; Figueiredo, Jane C; Casey, Graham; Haile, Robert W; Gallinger, Steven; Le Marchand, Loïc; Newcomb, Polly A; Potter, John D; Lindor, Noralane M; Hopper, John L; Jenkins, Mark A; Win, Aung Ko.
Affiliation
  • Dashti SG; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Li WY; Victorian Comprehensive Cancer Centre, University of Melbourne Centre for Cancer Research, Melbourne, VIC, 3000, Australia.
  • Buchanan DD; Cancer Epidemiology and Intelligence Division, Cancer Council Victoria, Melbourne, VIC, 3004, Australia.
  • Clendenning M; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Rosty C; Victorian Comprehensive Cancer Centre, University of Melbourne Centre for Cancer Research, Melbourne, VIC, 3000, Australia.
  • Winship IM; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Macrae FA; Victorian Comprehensive Cancer Centre, University of Melbourne Centre for Cancer Research, Melbourne, VIC, 3000, Australia.
  • Giles GG; Genetic Medicine, Royal Melbourne Hospital, Parkville, VIC, 3050, Australia.
  • Hardikar S; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Hua X; Victorian Comprehensive Cancer Centre, University of Melbourne Centre for Cancer Research, Melbourne, VIC, 3000, Australia.
  • Thibodeau SN; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Figueiredo JC; Victorian Comprehensive Cancer Centre, University of Melbourne Centre for Cancer Research, Melbourne, VIC, 3000, Australia.
  • Casey G; Colorectal Oncogenomics Group, Department of Clinical Pathology, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Haile RW; Envoi Specialist Pathologists, Brisbane, QLD, 4059, Australia.
  • Gallinger S; Faculty of Medicine, University of Queensland, Brisbane, QLD, 4006, Australia.
  • Le Marchand L; Genetic Medicine, Royal Melbourne Hospital, Parkville, VIC, 3050, Australia.
  • Newcomb PA; Department of Medicine, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Potter JD; Genetic Medicine, Royal Melbourne Hospital, Parkville, VIC, 3050, Australia.
  • Lindor NM; Department of Medicine, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Hopper JL; Colorectal Medicine and Genetics, Royal Melbourne Hospital, Parkville, VIC, 3050, Australia.
  • Jenkins MA; Centre for Epidemiology and Biostatistics, Melbourne School of Population and Global Health, The University of Melbourne, Parkville, VIC, 3010, Australia.
  • Win AK; Cancer Epidemiology and Intelligence Division, Cancer Council Victoria, Melbourne, VIC, 3004, Australia.
Br J Cancer ; 121(10): 869-876, 2019 11.
Article in En | MEDLINE | ID: mdl-31551580
ABSTRACT

BACKGROUND:

Type 2 diabetes mellitus and high total cholesterol and triglycerides are known to be associated with increased colorectal cancer risk for the general population. These associations are unknown for people with a germline DNA mismatch repair gene mutation (Lynch syndrome), who are at high risk of colorectal cancer.

METHODS:

This study included 2023 (56.4% female) carriers with a mismatch repair gene mutation (737 in MLH1, 928 in MSH2, 230 in MSH6, 106 in PMS2, 22 in EPCAM) recruited by the Colon Cancer Family Registry between 1998 and 2012. Weighted Cox regression was used to estimate the hazard ratios (HR) and 95% confidence intervals (CI) for the associations between self-reported type 2 diabetes, high cholesterol, triglyceride and colorectal cancer risk.

RESULTS:

Overall, 802 carriers were diagnosed with colorectal cancer at a median age of 42 years. A higher risk of colorectal cancer was observed in those with self-reported type-2 diabetes (HR 1.92; 95% CI, 1.03-3.58) and high cholesterol (HR 1.76; CI 1.23-2.52) compared with those without these conditions. There was no evidence of high triglyceride being associated with colorectal cancer risk.

CONCLUSION:

For people with Lynch syndrome, self-reported type-2 diabetes mellitus and high cholesterol were associated with increased colorectal cancer risk.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Colorectal Neoplasms, Hereditary Nonpolyposis / Genetic Predisposition to Disease / Diabetes Mellitus, Type 2 Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Br J Cancer Year: 2019 Type: Article Affiliation country: Australia

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Colorectal Neoplasms / Colorectal Neoplasms, Hereditary Nonpolyposis / Genetic Predisposition to Disease / Diabetes Mellitus, Type 2 Type of study: Etiology_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Aged / Aged80 / Female / Humans / Male / Middle aged Language: En Journal: Br J Cancer Year: 2019 Type: Article Affiliation country: Australia