Vitamin D and Isoforms of its Binding Protein, Tissue Biomarkers of Inflammation, and Colorectal Cancer Risk and Survival 公开
David, Gibbs (Fall 2020)
Abstract
Colorectal cancer (CRC) is a leading cause of cancer mortality in the United States. Vitamin D may influence CRC development and progression in part via reducing inflammation, but the effect of supplemental vitamin D on inflammation in humans and whether certain individuals may particularly benefit from higher vitamin D for CRC prevention and prognosis is unclear.
In the first study, we tested the effects of supplemental vitamin D (1000 I.U./day) and/or calcium (1,200 mg/day) on two inflammation-related biomarkers of risk for CRC (COX-2 and 15-HPGD) in the rectal mucosa of 62 colorectal adenoma patients in a placebo-controlled chemoprevention trial. We found that after one year of treatment the pro-inflammatory ratio of COX-2 /15-HPGD expression in full-length crypts statistically significantly decreased 47%more in the vitamin D group than in the placebo group (95% confidence interval [CI]: 36–76%) .
In the second study, we investigated whether the association of circulating vitamin D (25[OH]D) with CRC risk differed by the missense GC-rs4588*A variant (Thr436Lys), encoding the vitamin D-binding protein-2 (DBP2) isoform, among 1,710 incident CRC cases and 1,649 matched controls nested within three prospective cohorts. Multivariable-adjusted relative risks for CRC associated with 25(OH)D concentrations considered sufficient (≥50 nmol/L), relative to deficient (<30 nmol/L), were 0.47 (95% CI: 0.33–0.67) among individuals with DBP2, and 0.88 (95% CI: 0.61–1.27) among individuals without DBP2 (Pheterogeneity = 0.01).
In the third study, we investigated whether the association of pre-diagnostic 25(OH)D with mortality among CRC patients differed by the DBP2 isoform among 1,281 CRC cases (635 deaths, 483 from CRC) in two large prospective cohorts. In the pooled analysis, multivariable-adjusted hazard ratios for CRC-specific mortality associated with deficient relative to sufficient 25(OH)D concentrations were 2.24 (95% CI: 1.44–3.49) among those with DBP2, and 0.94 (95% CI: 0.68–1.22) among those without DBP2 (Pinteraction = 0.0002).
The results of these studies indicate that vitamin D supplementation reduces CRC-promoting inflammation in the gut and that individuals with the inherited DBP2-encoding GC-rs4588*A missense variant—linked to vitamin D insufficiency—may particularly benefit from higher vitamin D exposure for CRC prevention and prognosis.
Table of Contents
CHAPTER I: Introduction and Background …………………………………………………... 6
Introduction ………………………………………………………………….................…………… 7
Background …….……………………………………………………….................………………....8
Colorectal Cancer ……………………………………………….........................………………....8
Vitamin D Metabolism …………………………………………………………..........................15
Vitamin D, Calcium, and Biomarkers of Risk for Colorectal Neoplasms……............… 22
Epidemiologic Studies of Vitamin D and Colorectal Neoplasms ………….............…… 24
Vitamin D-Binding Protein ………………………………………………….......................….. 28
Interaction Between Vitamin D and Vitamin D-Binding Protein Isoforms in
Epidemiologic Studies …………………………………………........................…………….…. 38
Summary and Rationale for the Proposed Research ……………………………......……… 42
CHAPTER II: Research Aims and Approach ……………………………….………………... 43
Specific Aims ……………………………………………………………………..................……... 44
Research Approach..………………………………………………................……………………. 45
Innovation and Significance …………………..………………….............…………………….. 49
CHAPTER III: Modulation of inflammation by vitamin D and calcium in the
morphologically normal colorectal mucosa of colorectal adenoma patients in a
randomized chemoprevention trial…………………………………………………………..…… 50
Manuscript Information…………………………………………………………...............…….... 51
Abstract……………………………………………………………………….....................…………. 52
Introduction ………………………………………………………...................…………………….. 53
Methods ……………………………………………………….....................………………………… 54
Results…………………………………………………….....................……………………………... 61
Discussion …………………………………………….....................………………………………… 64
Main Tables and Figures…………………………….................…………………………………...70
Supplementary Tables and Figures……………….............……………………………………... 78
CHAPTER IV: Association of circulating vitamin D with colorectal cancer depends
on vitamin D-binding protein isoforms: A pooled nested case-control study…….…... 86
Manuscript Information …………………………………………………………................……... 87
Abstract ……………………………………………………………………………......................…… 90
Introduction …………………………………………………………....................………………….. 91
Methods ……………………………………………………………......................…………………… 92
Results ……………………………………………………......................…………………………….. 98
Discussion …………………………………………….....................………………………………. 100
Main Tables and Figures ………………………….................…………………………………… 105
Supplementary Tables and Figures…………………..............………………………………….110
CHAPTER V: Association of pre-diagnostic vitamin D status with colorectal
cancer mortality differs by common, inherited vitamin D-binding protein
isoforms ………………………………………………………………………………………….……...115
Manuscript Information …………………………………………..............……………..……….116
Abstract ...…………………………………………………………...................………….………...119
Introduction ………………………………………………………..................………….…………120
Methods ……………………………………………………………...................………….………..121
Results ………………………………………………………………………….....................………125
Discussion ………………………………………………………………...................……….……..128
Main Tables and Figures …………………………………………................……………………132
Supplementary Tables and Figures ………………………............…………………………… 137
CHAPTER VI: Conclusions, Public Health Implications, and Future Research……. 144
REFERENCES ………………………………………………………………………...........………. 148
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