4.7 Article

Time-dependent association of total serum cholesterol and cancer incidence in a cohort of 172 210 men and women: a prospective 19-year follow-up study

Journal

ANNALS OF ONCOLOGY
Volume 20, Issue 6, Pages 1113-1120

Publisher

OXFORD UNIV PRESS
DOI: 10.1093/annonc/mdn736

Keywords

cancer incidence; prospective study; reverse causality; time dependency; total serum cholesterol

Categories

Funding

  1. Austrian National Bank [OENB-12737]
  2. National Institute on Aging Intramural Research Program
  3. NATIONAL CANCER INSTITUTE [Z01CP010181, ZIACP010181] Funding Source: NIH RePORTER
  4. NATIONAL INSTITUTE ON AGING [ZICAG000637] Funding Source: NIH RePORTER

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Background: The relationship between serum cholesterol and cancer incidence remains controversial. Patients and methods: We investigated the association of total serum cholesterol (TSC) with subsequent cancer incidence in a population-based cohort of 172 210 Austrian adults prospectively followed up for a median of 13.0 years. Cox regression, allowing for time-dependent effects, was used to estimate adjusted hazard ratios (HRs) with 95% confidence intervals (95% CIs) for the association of TSC with cancer. Results: We observed pronounced short-term associations of TSC and overall cancer incidence in both men and women. For malignancies diagnosed shortly (< 5 months) after baseline TSC measurement, the highest TSC tertile (> 235.0 mg/dl in men and > 229.0 in women) compared with the lowest tertile (< 194.0 mg/dl in men and < 190.0 in women) was associated with a significantly lower overall cancer risk [HR = 0.58 (95% CI 0.43-0.78, P-trend = 0.0001) in men, HR = 0.69 (95% CI 0.49-0.99, P-trend = 0.03) in women]. However, after roughly 5 months from baseline measurement, overall cancer risk was not significantly associated with TSC. The short-term inverse association of TSC with cancer was mainly driven by malignancies of the digestive organs and lymphoid and hematopoietic tissue. Conclusion: The short-term decrease of cancer risk seen for high levels of TSC may largely capture preclinical effects of cancer on TSC.

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