The vitamin D binding protein axis modifies disease severity in Lymphangioleiomyomatosis

Miller, Suzanne and Coveney, Claire and Johnson, Janice and Farmaki, Aliki-Eleni and Gupta, Nishant and Tobin, Martin D. and Wain, Louise V. and McCormack, Francis and Boocock, David J. and Johnson, Simon R. (2018) The vitamin D binding protein axis modifies disease severity in Lymphangioleiomyomatosis. European Respiratory Journal . ISSN 1399-3003 (In Press)

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Abstract

Background: Lymphangioleiomyomatosis (LAM) is a rare disease of women. Decline in lung function is variable making appropriate targeting of therapy difficult. We used unbiased serum proteomics to identify markers associated with outcome in LAM.

Methods: 101 women with LAM and 22 healthy controls were recruited from the National Centre for LAM (Nottingham, UK). 152 DNA and serum samples with linked lung function and outcome data were obtained from patients in the NHLBI LAM Registry (USA). Proteomic analysis was performed on a discovery cohort of 50 LAM and 20 control sera using a SCIEX SWATH mass spectrometric workflow. Protein levels were quantitated by ELISA and SNPs in GC encoding Vitamin D Binding Protein (VTDB) genotyped.

Results: Proteomic analysis showed VTDB was 2.6 fold lower in LAM than controls. Serum VTDB was lower in progressive compared with stable LAM (p=0.001) and correlated with diffusing capacity (p=0.01). Median time to death or lung transplant was reduced by 46 months in those with CC genotypes at rs4588 and 38 months in those with non-A containing haplotypes at rs7041/4588 (p=0.014 and 0.008 respectively).

Conclusions: The VTDB axis is associated with disease severity and outcome, and GC genotype could help predict transplant free survival in LAM.

Item Type: Article
Schools/Departments: University of Nottingham, UK > Faculty of Medicine and Health Sciences > School of Medicine > Division of Respiratory Medicine
Depositing User: Hatton, Mrs Kirsty
Date Deposited: 23 Aug 2018 09:43
Last Modified: 29 Jan 2020 04:30
URI: http://eprints.nottingham.ac.uk/id/eprint/53430

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