Mendelian randomization study of height and risk of colorectal cancer.

Int J Epidemiol
Authors
Keywords
Abstract

BACKGROUND: For men and women, taller height is associated with increased risk of all cancers combined. For colorectal cancer (CRC), it is unclear whether the differential association of height by sex is real or is due to confounding or bias inherent in observational studies. We performed a Mendelian randomization study to examine the association between height and CRC risk.

METHODS: To minimize confounding and bias, we derived a weighted genetic risk score predicting height (using 696 genetic variants associated with height) in 10,226 CRC cases and 10,286 controls. Logistic regression was used to estimate odds ratios (OR) and 95% confidence intervals (95% CI) for associations between height, genetically predicted height and CRC.

RESULTS: Using conventional methods, increased height (per 10-cm increment) was associated with increased CRC risk (OR = 1.08, 95% CI = 1.02-1.15). In sex-specific analyses, height was associated with CRC risk for women (OR = 1.15, 95% CI = 1.05-1.26), but not men (OR = 0.98, 95% CI = 0.92-1.05). Consistent with these results, carrying greater numbers of (weighted) height-increasing alleles (per 1-unit increase) was associated with higher CRC risk for women and men combined (OR = 1.07, 95% CI = 1.01-1.14) and for women (OR = 1.09, 95% CI =  .01-1.19). There was weaker evidence of an association for men (OR = 1.05, 95% CI = 0.96-1.15).

CONCLUSION: We provide evidence for a causal association between height and CRC for women. The CRC-height association for men remains unclear and warrants further investigation in other large studies.

Year of Publication
2015
Journal
Int J Epidemiol
Volume
44
Issue
2
Pages
662-72
Date Published
2015 Apr
ISSN
1464-3685
URL
DOI
10.1093/ije/dyv082
PubMed ID
25997436
PubMed Central ID
PMC4481609
Links
Grant list
R01 CA059045 / CA / NCI NIH HHS / United States
P01 CA 087969 / CA / NCI NIH HHS / United States
HHSN271201100004C / PHS HHS / United States
HHSN268201100001C / PHS HHS / United States
R01 CA076366 / CA / NCI NIH HHS / United States
U24 CA074783 / CA / NCI NIH HHS / United States
P50 CA 127003 / CA / NCI NIH HHS / United States
U01CA137088 / CA / NCI NIH HHS / United States
R01 137178 / PHS HHS / United States
R25 CA094880 / CA / NCI NIH HHS / United States
R01 CA151993 / CA / NCI NIH HHS / United States
U01 CA137088 / CA / NCI NIH HHS / United States
U24 CA074794 / CA / NCI NIH HHS / United States
RFA # CA-95-011 / CA / NCI NIH HHS / United States
R01 CA 151993 / CA / NCI NIH HHS / United States
K05 CA154337 / CA / NCI NIH HHS / United States
HHSN268201100003C / PHS HHS / United States
U24 CA097735 / CA / NCI NIH HHS / United States
U01 CA074794 / CA / NCI NIH HHS / United States
P30 CA008748 / CA / NCI NIH HHS / United States
NIH GEI U01 HG 004438 / HG / NHGRI NIH HHS / United States
HHSN268201100004C / PHS HHS / United States
Intramural NIH HHS / United States
R01CA137178 / CA / NCI NIH HHS / United States
R01 CA48998 / CA / NCI NIH HHS / United States
Canadian Institutes of Health Research / Canada
U01 CA122839 / CA / NCI NIH HHS / United States
UM1 CA167552 / CA / NCI NIH HHS / United States
NIH U01 HG004446 / HG / NHGRI NIH HHS / United States
U01 CA097735 / CA / NCI NIH HHS / United States
R01 CA042182 / CA / NCI NIH HHS / United States
UM1 CA167551 / CA / NCI NIH HHS / United States
HHSN268201100046C / PHS HHS / United States
S10 OD020069 / OD / NIH HHS / United States
U01 CA074783 / CA / NCI NIH HHS / United States
P01CA 055075 / CA / NCI NIH HHS / United States
Z01 CP 010200 / CP / NCI NIH HHS / United States
HHSN268201100002C / PHS HHS / United States