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Metabolic factors and the risk of colorectal cancer by KRAS and BRAF mutation status

Myte, Robin (författare)
Umeå universitet,Onkologi,Umea Univ, Dept Radiat Sci, Oncol, SE-90187 Umea, Sweden
Gylling, Björn, 1978- (författare)
Umeå universitet,Patologi,Umea Univ, Dept Med Biosci, Pathol, Umea, Sweden
Häggström, Jenny, 1980- (författare)
Umeå universitet,Statistik,Umea Univ, Umea Sch Business & Econ, Dept Stat, Umea, Sweden
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Häggström, Christel (författare)
Uppsala universitet,Umeå universitet,Enheten för biobanksforskning,Department of Surgical Sciences, Uppsala University, Uppsala, Sweden.,Endokrinkirurgi,Umea Univ, Dept Biobank Res, Umea, Sweden
Zingmark, Carl, 1975- (författare)
Umeå universitet,Patologi,Umea Univ, Dept Med Biosci, Pathol, Umea, Sweden
Löfgren Burström, Anna (författare)
Umeå universitet,Patologi,Umea Univ, Dept Med Biosci, Pathol, Umea, Sweden
Palmqvist, Richard (författare)
Umeå universitet,Patologi,Umea Univ, Dept Med Biosci, Pathol, Umea, Sweden
van Guelpen, Bethany (författare)
Umeå universitet,Onkologi,Wallenberg centrum för molekylär medicin vid Umeå universitet (WCMM),Umea Univ, Dept Radiat Sci, Oncol, SE-90187 Umea, Sweden;Umea Univ, Wallenberg Ctr Mol Med, Umea, Sweden
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 (creator_code:org_t)
2019-01-24
2019
Engelska.
Ingår i: International Journal of Cancer. - : John Wiley & Sons. - 0020-7136 .- 1097-0215. ; 145:2, s. 327-337
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Factors related to energy metabolism and the metabolic syndrome, such as higher body mass index (BMI), blood glucose, or blood lipids, and blood pressure, are associated with an increased risk of colorectal cancer (CRC). However, CRC is a heterogeneous disease, developing through distinct pathways with differences in molecular characteristics and prognosis, and possibly also in risk factors. For subtypes defined by KRAS and BRAF mutation status, BMI is the only metabolic factor previously studied, with inconsistent findings. We investigated whether associations between BMI, blood glucose, blood lipids, and blood pressure and CRC risk differed by tumor KRAS and BRAF mutation status in 117,687 participants from two population-based cohorts within the Northern Sweden Health and Disease Study (NSHDS). Hazard ratios (HRs) for overall CRC and CRC subtypes by metabolic factors were estimated with Cox proportional hazards regression, using multiple imputation to handle missing exposure and tumor data. During a median follow-up of 15.6 years, we acquired 1,250 prospective CRC cases, of which 766 cases had complete baseline and molecular tumor data. Consistent with previous evidence, higher BMI, total cholesterol, triglyceride levels, and blood pressure were associated with an increased risk of overall CRC (HRs per 1 standard deviation increase: 1.07 to 1.12). These associations were similar regardless of CRC subtype by KRAS and BRAF mutation status (all pheterogeneity > 0.05). The same was true for subtypes based on microsatellite instability status. Poor metabolic health may therefore be a universal mechanism for colorectal cancer, acting across multiple developmental pathways.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Cancer och onkologi (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Cancer and Oncology (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Hälsovetenskap -- Näringslära (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Health Sciences -- Nutrition and Dietetics (hsv//eng)

Nyckelord

BRAF
KRAS
colorectal cancer
metabolic factors
microsatellite instability
risk factors

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