Please use this identifier to cite or link to this item: http://dl.umsu.ac.ir/handle/Hannan/29451
Title: Adiponectin Gene Polymorphisms and Acute Respiratory Distress Syndrome Susceptibility and Mortality
Authors: Ahasic, Amy M.;Zhao, Yang;Su, Li;Sheu, Chau-Chyun;Thompson, B. Taylor;Christiani, David C.
subject: Biology;Genetics;Human genetics;Genetic association studies;Population genetics;Genetic polymorphism;Genetics of disease;Medicine;Clinical Immunology;Immune system;Cytokines;Critical care and emergency medicine;Respiratory failure;Endocrinology;Endocrine physiology;Epidemiology;Genetic epidemiology;Nutrition;Obesity
Year: 2014
Publisher: Public Library of Science
Description: Rationale: Adiponectin is an anti-inflammatory adipokine that is the most abundant gene product of adipose tissue. Lower levels have been observed in obesity, insulin resistance, and in critical illness. However, elevated levels early in acute respiratory failure have been associated with mortality. Polymorphisms in adiponectin-related genes (ADIPOQ, ADIPOR1, ADIPOR2) have been examined for relationships with obesity, insulin resistance and diabetes, cardiovascular disease, and to circulating adipokine levels, but many gaps in knowledge remain. The current study aims to assess the association between potentially functional polymorphisms in adiponectin-related genes with acute respiratory distress syndrome (ARDS) risk and mortality. Methods: Consecutive patients with risk factors for ARDS admitted to the ICU were enrolled and followed prospectively for development of ARDS. ARDS cases were followed through day 60 for all-cause mortality. 2067 patients were successfully genotyped using the Illumina CVD BeadChip high-density platform. Of these, 567 patients developed ARDS. Forty-four single nucleotide polymorphisms (SNPs) on ADIPOQ, ADIPOR1 and ADIPOR2 were successfully genotyped. Of these, 9 SNPs were hypothesized to be functional based on their location (promoter, exon, or 3′ untranslated region). These 9 SNPs were analyzed for association with ARDS case status and mortality among ARDS cases. Results: After multivariable analysis and adjustment for multiple comparisons, no SNPs were significantly associated with ARDS case status. Among ARDS cases, homozygotes for the minor allele of rs2082940 (ADIPOQ) had increased mortality (hazard ratio 2.61, 95% confidence interval 1.36–5.00, p = 0.0039) after adjustment for significant covariates. The significance of this association persisted after adjustment for multiple comparisons (FDR_q = 0.029). Conclusions: A common and potentially functional polymorphism in ADIPOQ may impact survival in ARDS. Further studies are required to replicate these results and to correlate genotype with circulating adiponectin levels.
URI: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3929660/pdf/
http://nrs.harvard.edu/urn-3:HUL.InstRepos:11879767
Standard no: Ahasic, Amy M., Yang Zhao, Li Su, Chau-Chyun Sheu, B. Taylor Thompson, and David C. Christiani. 2014. “Adiponectin Gene Polymorphisms and Acute Respiratory Distress Syndrome Susceptibility and Mortality.” PLoS ONE 9 (2): e89170. doi:10.1371/journal.pone.0089170. http://dx.doi.org/10.1371/journal.pone.0089170.
1932-6203
Appears in Collections:HMS Scholarly Articles

Files in This Item:
Click on the URI links for accessing contents.


Items in HannanDL are protected by copyright, with all rights reserved, unless otherwise indicated.