TY - JOUR
T1 - Clinical and genetic predictors of weight gain in patients diagnosed with breast cancer
AU - Reddy, S. M.
AU - Sadim, M.
AU - Li, J.
AU - Yi, N.
AU - Agarwal, S.
AU - Mantzoros, C. S.
AU - Kaklamani, V. G.
N1 - Funding Information:
This study was supported by grants funded by Lynn Sage Foundation (VGK), Dolores Knes Fund (VGK), National Institute of Diabetes and Digestive and Kidney Diseases grants 58785, 79929 and 81913 (CSM), Award Number 1I01CX000422-01A1 from the Clinical Science Research and Development Service of the VA Office of Research and Development (CSM).
PY - 2013/8/20
Y1 - 2013/8/20
N2 - Background: Post-diagnosis weight gain in breast cancer patients has been associated with increased cancer recurrence and mortality. Our study was designed to identify risk factors for this weight gain and create a predictive model to identify a high-risk population for targeted interventions. Methods: Chart review was conducted on 459 breast cancer patients from Northwestern Robert H. Lurie Cancer Centre to obtain weights and body mass indices (BMIs) over an 18-month period from diagnosis. We also recorded tumour characteristics, demographics, clinical factors, and treatment regimens. Blood samples were genotyped for 14 single-nucleotide polymorphisms (SNPs) in fat mass and obesity-Associated protein (FTO) and adiponectin pathway genes (ADIPOQ and ADIPOR1). Results: In all, 56% of patients had >0.5 kg m-2 increase in BMI from diagnosis to 18 months, with average BMI and weight gain of 1.9 kg m-2 and 5.1 kg, respectively. Our best predictive model was a primarily SNP-based model incorporating all 14 FTO and adiponectin pathway SNPs studied, their epistatic interactions, and age and BMI at diagnosis, with area under receiver operating characteristic curve of 0.85 for 18-month weight gain. Conclusion: We created a powerful risk prediction model that can identify breast cancer patients at high risk for weight gain.
AB - Background: Post-diagnosis weight gain in breast cancer patients has been associated with increased cancer recurrence and mortality. Our study was designed to identify risk factors for this weight gain and create a predictive model to identify a high-risk population for targeted interventions. Methods: Chart review was conducted on 459 breast cancer patients from Northwestern Robert H. Lurie Cancer Centre to obtain weights and body mass indices (BMIs) over an 18-month period from diagnosis. We also recorded tumour characteristics, demographics, clinical factors, and treatment regimens. Blood samples were genotyped for 14 single-nucleotide polymorphisms (SNPs) in fat mass and obesity-Associated protein (FTO) and adiponectin pathway genes (ADIPOQ and ADIPOR1). Results: In all, 56% of patients had >0.5 kg m-2 increase in BMI from diagnosis to 18 months, with average BMI and weight gain of 1.9 kg m-2 and 5.1 kg, respectively. Our best predictive model was a primarily SNP-based model incorporating all 14 FTO and adiponectin pathway SNPs studied, their epistatic interactions, and age and BMI at diagnosis, with area under receiver operating characteristic curve of 0.85 for 18-month weight gain. Conclusion: We created a powerful risk prediction model that can identify breast cancer patients at high risk for weight gain.
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U2 - 10.1038/bjc.2013.441
DO - 10.1038/bjc.2013.441
M3 - Article
C2 - 23922112
AN - SCOPUS:84883154966
SN - 0007-0920
VL - 109
SP - 872
EP - 881
JO - British Journal of Cancer
JF - British Journal of Cancer
IS - 4
ER -