Journal article
A meta-analysis of individual participant data reveals an association between circulating levels of IGF-I and prostate cancer risk
- Abstract:
- The role of insulin-like growth factors (IGFs) in prostate cancer development is not fully understood. To investigate the association between circulating concentrations of IGFs (IGF-I, IGF-II, IGFBP-1, IGFBP-2, IGFBP-3) and prostate cancer risk, we pooled individual participant data from 17 prospective and two cross-sectional studies, including up to 10,554 prostate cancer cases and 13,618 control participants. Conditional logistic regression was used to estimate the odds ratios (ORs) for prostate cancer based on the study-specific fifth of each analyte. Overall, IGF-I, IGF-II, IGFBP-2, and IGFBP-3 concentrations were positively associated with prostate cancer risk (Ptrend all ≤ 0.005), and IGFBP-1 was weakly inversely associated with risk (Ptrend = 0.05). However, heterogeneity between the prospective and cross-sectional studies was evident (Pheterogeneity = 0.03), unless the analyses were restricted to prospective studies (with the exception of IGF-II, Pheterogeneity = 0.02). For prospective studies, the OR for men in the highest versus the lowest fifth of each analyte was 1.29 (95% confidence interval=1.16-1.43) for IGF-I, 0.81 (0.68- 0.96) for IGFBP-1, and 1.25 (1.12-1.40) for IGFBP-3. These associations did not differ significantly by timeto-diagnosis or tumor stage or grade. After mutual adjustment for each of the other analytes, only IGF-I remained associated with risk. Our collaborative study represents the largest pooled analysis of the relationship between prostate cancer risk and circulating concentrations of IGF-I, providing strong evidence that IGF-I is highly likely to be involved in prostate cancer development.
- Publication status:
- Published
- Peer review status:
- Peer reviewed
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(Preview, Accepted manuscript, pdf, 483.2KB, Terms of use)
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- Publisher copy:
- 10.1158/0008-5472.CAN-15-1551
Authors
- Publisher:
- American Association for Cancer Research
- Journal:
- Cancer Research More from this journal
- Volume:
- 76
- Issue:
- 8
- Pages:
- 2288–2300
- Publication date:
- 2016-02-26
- Acceptance date:
- 2015-12-22
- DOI:
- EISSN:
-
1538-7445
- ISSN:
-
0008-5472
- Keywords:
- Pubs id:
-
pubs:601697
- UUID:
-
uuid:5c694b93-8b2e-4b9e-a200-1db3081a7abc
- Local pid:
-
pubs:601697
- Source identifiers:
-
601697
- Deposit date:
-
2016-02-11
Terms of use
- Copyright holder:
- American Association for Cancer Research
- Copyright date:
- 2016
- Notes:
- © 2016 American Association for Cancer Research. This is the accepted manuscript version of the article. The final version is available online from the American Association for Cancer Research at: [10.1158/0008-5472.CAN-15-1551]
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