Measured and genetically predicted plasma YKL-40 levels and melanoma mortality. (November 2019)

• Record Type: Journal Article
• Authors: Ismail, Hafsa; Helby, Jens; Hölmich, Lisbet R.; Chakera, Annette H.; Bastholt, Lars; Klyver, Helle; Sjøgren, Pia; Schmidt, Henrik; Schöllhammer, Liv; Johansen, Julia S.; Nordestgaard, Børge G.; Bojesen, Stig E.
• Is Part Of: European journal of cancer. Volume 121(2019)
• Page Start: 74
• Page End: 84
• Publication Date: 2019-11
• Subjects: YKL-40 -- CHI3L1 rs4950928 -- Melanoma -- Survival; AJCC American Joint Committee on Cancer -- SNP single-nucleotide polymorphism -- WHO World Health Organisation -- ICD-7 and ICD-10 International Classification of Diseases edition seven and ten -- ELISA sandwich-type enzyme-linked immunoabsorbent assay -- CI confidence interval -- IL-2 interleukin-2 -- IFN-α interferon-alpha -- CCHS Copenhagen City Heart Study -- CGPS Copenhagen General Population Study; Cancer -- Periodicals; Neoplasms -- Periodicals; Cancer -- Périodiques; Cancer; Tumors; Electronic journals; Periodicals; Electronic journals; 616.994
• DOI: 10.1016/j.ejca.2019.08.025
• Languages: English
• ISSNs: 0959-8049

Abstract

Abstract: Purpose: High plasma levels of YKL-40 might be associated with mortality in patients with melanoma, and it is unknown if YKL-40 is causally related to mortality. Experimental design: We studied two cohorts: 2618 patients with melanoma from hospital clinics and 1413 general population patients with melanoma, totalling 4031 patients followed up for mortality end-points for up to 20 years. All were genotyped for CHI3L1 rs4950928, highly predictive of lifelong plasma YKL-40, and plasma YKL-40 levels were measured in 2165 patients. We tested the hypotheses that measured and genetically predicted high plasma YKL-40 are associated with increased mortality in patients with melanoma. Results: For the hospital melanoma cohort, age- and sex-adjusted hazard ratios for death in individuals with measured plasma YKL-40 in the 96–100th percentile versus 1–95th percentile and per 10-percentile increase were 1.52 (95% confidence interval, 1.07–2.16) and 1.07 (1.02–1.11), respectively, most pronounced for patients with localised melanomas. Each C-allele of the CHI3L1 rs4950928 genotype was associated with plasma YKL-40 level increases of 32% in the hospital melanoma cohort ( p = 6 × 10 −48 ) and 43% in the general population melanoma cohort ( p = 7 × 10 −13 ). Multifactorially adjusted ratios for these increases in the combined cohorts were 1.04 (1.00–1.09) observationally for measured plasma YKL-40 and 0.98 (0.86–1.12) for the genetically predicted plasma YKL-40. Conclusion: Measured, but not genetically predicted, increasing plasma YKL-40 was associated with increased mortality in patients with melanoma. Plasma YKL-40 is a marker but less likely to be a cause of increased mortality in patients with melanoma. Highlights: Increasing plasma YKL-40 was associated with reduced survival in 4031 patients with melanoma followed up for 20 years. Genetically predicted high plasma YKL-40 was not. Increasing YKL-40 measured in plasma is a marker, and less likely to be a cause, of reduced survival in patients with melanoma.