# Calcium intake and genetic variants in the calcium sensing receptor in relation to colorectal cancer mortality: an international consortium study of 18,952 patients

**Authors:** Evertine Wesselink, William Gauderman, Sonja I. Berndt, Hermann Brenner, Daniel D. Buchanan, Peter T. Campbell, Andrew T. Chan, Jenny Chang-Claude, Michelle Cotterchoi, Marc J. Gunter, Michael Hoffmeister, Amit D. Joshi, Christina C. Newton, Rish K. Pai, Andrew J. Pellatt, Amanda I. Phipps, Mingyang Song, Caroline Y. Um, Bethany van Guelpen, Emily White, Ulrike Peters, Fränzel J. B. van Duijnhoven

PMC · DOI: 10.1038/s44276-024-00077-3 · Bjc Reports · 2024-09-02

## TL;DR

This study found that calcium intake was not linked to survival in colorectal cancer patients, but genetic variations in the calcium sensing receptor might influence the effect of calcium supplements.

## Contribution

The study is the first to explore interactions between calcium intake and CaSR gene variants in relation to colorectal cancer mortality.

## Key findings

- No association was found between calcium intake and all-cause or CRC-specific mortality.
- Genetic variants in the CaSR gene may modify the effect of supplemental calcium on mortality.
- Interactions were observed between supplemental calcium and several SNPs in the CaSR gene.

## Abstract

Research on calcium intake as well as variants in the calcium sensor receptor (CaSR) gene and their interaction in relation to CRC survival is still limited.

Data from 18,952 CRC patients, were included. Associations between primarily pre-diagnostic dietary (n = 13.085), supplemental (n = 11,837), total calcium intake (n = 5970) as well as 325 single nucleotide polymorphisms (SNPs) of the CaSR gene (n = 15,734) in relation to CRC-specific and all-cause mortality were assessed using Cox proportional hazard models. Also interactions between calcium intake and variants in the CaSR gene were assessed.

During a median follow-up of 4.8 years (IQR 2.4–8.4), 6801 deaths occurred, of which 4194 related to CRC. For all-cause mortality, no associations were observed for the highest compared to the lowest sex- and study-specific quartile of dietary (HR 1.00, 95%CI 0.92–1.09), supplemental (HR 0.97, 95%CI 0.89–1.06) and total calcium intake (HR 0.99, 95%CI 0.88–1.11). No associations with CRC-specific mortality were observed either. Interactions were observed between supplemental calcium intake and several SNPs of the CaSR gene.

Calcium intake was not associated with all-cause or CRC-specific mortality in CRC patients. The association between supplemental calcium intake and all-cause and CRC-specific mortality may be modified by genetic variants in the CaSR gene.

## Linked entities

- **Genes:** CASR (calcium sensing receptor) [NCBI Gene 846]
- **Chemicals:** calcium (PubChem CID 5460341)
- **Diseases:** colorectal cancer (MONDO:0005575)

## Full-text entities

- **Genes:** CASR (calcium sensing receptor) [NCBI Gene 846] {aka CAR, EIG8, FHH, FIH, GPRC2A, HHC}
- **Diseases:** CRC (MESH:D015179), deaths (MESH:D003643)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

1 references — full list in the complete paper: https://tomesphere.com/paper/PMC11368808/full.md

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Source: https://tomesphere.com/paper/PMC11368808