S141 A novel dimethylarginine dimethylaminohydrolase 1 (DDAH1) genetic variant associated with lower asymmetric dimethylarginine (ADMA) levels predicts accelerated lung function decline and mortality in idiopathic pulmonary fibrosis
| Autor: | EA Renzoni, Harpreet K Lota, AU Wells, Cjw Stock, JM Leiper |
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| Rok vydání: | 2018 |
| Předmět: |
medicine.medical_specialty
Proportional hazards model business.industry respiratory system medicine.disease Gastroenterology respiratory tract diseases Pulmonary function testing Minor allele frequency FEV1/FVC ratio Idiopathic pulmonary fibrosis chemistry.chemical_compound chemistry Internal medicine Cohort medicine Asymmetric dimethylarginine business Survival analysis |
| Zdroj: | Guilt by association: ILD genetics and co-morbidities. |
| DOI: | 10.1136/thorax-2018-212555.147 |
| Popis: | Background Increased nitric oxide (NO) and its generating enzyme, inducible nitric oxide synthase (iNOS), are observed in experimental models of idiopathic pulmonary fibrosis (IPF). Asymmetric dimethylarginine (ADMA) competitively inhibits iNOS and is hydrolysed by dimethylarginine dimethylaminohydrolase (DDAH) 1 and 2. Modulation of NO bioavailability via pharmacological/genetic knock-out of DDAH1 attenuates bleomycin-induced fibrosis in vivo. Using a candidate gene approach with an a priori hypothesis, we investigated the impact of DDAH1 variants associated with lower ADMA (thus indicative of DDAH1 over-activity) on lung function decline and survival in IPF. Methods Consecutive patients with a new diagnosis IPF were recruited from a tertiary UK ILD centre (n=70). Only Caucasian individuals were included, patients on anti-fibrotic agents were excluded. Clinical end points were: time to first FVC decline (≥10% relative change in FVC from baseline) and survival (months survived following presentation). DDAH1 tSNPs were identified in Caucasian individuals genotyped in the International HapMap Project. Those with minor allele frequency >40% in the IPF cohort and an association with lower ADMA levels in a normal cohort were selected – rs530006 and rs6576765. Survival curves and stepwise multivariate Cox proportional hazards analyses were performed. Results Baseline pulmonary function did not vary between genotypes. FVC decline differed between rs530006 genotypes (p Conclusion Minor homozygote carriage of DDAH1 variant rs530006 was associated with accelerated disease progression and mortality in IPF. These findings require validation in a larger, replicate cohort of IPF patients. Identification of aggressive disease phenotypes may allow risk stratification and earlier therapeutic intervention in IPF. |
| Databáze: | OpenAIRE |
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