Prediagnostic Vitamin D Status and Colorectal Cancer Survival by Vitamin D Binding Protein Isoforms in US Cohorts

Author:

Kim Hanseul123ORCID,Yuan Chen4ORCID,Nguyen Long H123ORCID,Ng Kimmie4ORCID,Giovannucci Edward L56

Affiliation:

1. Clinical and Translational Epidemiology Unit, Massachusetts General Hospital and Harvard Medical School , Boston, MA 02114 , USA

2. Division of Gastroenterology, Massachusetts General Hospital and Harvard Medical School , Boston, MA 02114 , USA

3. Department of Biostatistics, Harvard T.H. Chan School of Public Health , Boston, MA 02115 , USA

4. Department of Medical Oncology, Dana-Farber Cancer Institute and Harvard Medical School , Boston, MA 02215 , USA

5. Department of Epidemiology, Harvard T.H. Chan School of Public Health , Boston, MA 02115 , USA

6. Department of Nutrition, Harvard T.H. Chan School of Public Health , Boston, MA 02115 , USA

Abstract

Abstract Context Lower 25-hydroxyvitamin D (25(OH)D) levels have consistently been associated with higher mortality among participants with colorectal cancer (CRC). Objective To investigate whether the association between 25(OH)D and CRC mortality differs according to vitamin D binding protein (also known as Gc) isoforms. Methods We examined the association between prediagnostic 25(OH)D levels and overall and CRC-specific mortality among participants with CRC within 2 prospective US cohorts. Cox proportional hazards regression was used to estimate the hazard ratios (HRs) and 95% CIs. Results 588 participants with CRC were observed until the date of death or last follow-up (2018), whichever came first. Deficient vs sufficient 25(OH)D concentrations (<30 vs ≥50 nmol/L) were associated with higher overall mortality (HR 2.06; 95% CI 1.34-3.18) but not with CRC-specific mortality (HR 1.51; 95% CI 0.75-3.07). The HRs for overall mortality comparing deficient vs sufficient concentrations were 2.43 (95% CI 1.26-4.70) for those with the Gc1-1 isoform (rs4588 CC) and 1.63 (95% CI 0.88-3.02) for those with the Gc1-2 or Gc2-2 (rs4588 CA or AA) isoform (P for interaction = .54). The HRs for CRC-specific mortality were 1.18 (95% CI 0.27-5.14) for those with the Gc1-1 isoform and 1.41 (95% CI 0.62-3.24) for those with the Gc1-2 or Gc2-2 isoform (P for interaction = .94). Conclusion In these 2 US cohorts, we found that lower 25(OH)D levels were associated with higher overall mortality, but this association did not differ by Gc isoforms.

Funder

National Institutes of Health

Publisher

The Endocrine Society

Subject

Biochemistry (medical),Clinical Biochemistry,Endocrinology,Biochemistry,Endocrinology, Diabetes and Metabolism

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