Differential expression of Vitamin D associated genes in the aorta of coronary artery disease patients with and without rheumatoid arthritis

Autor: Arne Yndestad, Pål Aukrust, Torstein Lyberg, Stein Erik Rynning, Ole Kristoffer Olstad, Jon Elling Whist, Ingvild Oma, Sven M. Almdahl, Ida Grunnan Fostad, Morten W. Fagerland, Ivana Hollan, J.K. Andersen, Øyvind Molberg
Jazyk: angličtina
Rok vydání: 2018
Předmět:
Male
rheumatoid arthritis
0301 basic medicine
Microarrays
NSAIDs
vascular pathology
Gene Expression
Organic chemistry
lcsh:Medicine
Arthritis
Cell Cycle Proteins
Vascular Medicine
Arthritis
Rheumatoid

Coronary artery disease
0302 clinical medicine
Medicine and Health Sciences
Coronary Heart Disease
Vitamin D
lcsh:Science
Aorta
Analgesics
Multidisciplinary
Nuclear Proteins
Drugs
Vitamins
Physical sciences
Chemistry
Bioassays and Physiological Analysis
Rheumatoid arthritis
language
Female
coronary artery disease
Research Article
medicine.medical_specialty
Patients
Immunology
ascending aorta
Cardiology
Norwegian
Research and Analysis Methods
Autoimmune Diseases
Chemical compounds
03 medical and health sciences
Rheumatology
Internal medicine
medicine.artery
Organic compounds
Genetics
medicine
Vitamin D and neurology
Humans
Nuclear Receptor Co-Repressor 1
RNA
Messenger

Aged
Pharmacology
030203 arthritis & rheumatology
Aryldialkylphosphatase
business.industry
Public health
lcsh:R
Biology and Life Sciences
DNA
Microarray Analysis
medicine.disease
Pain management
language.human_language
Health Care
immune system
Cross-Sectional Studies
030104 developmental biology
Clinical Immunology
lcsh:Q
Clinical Medicine
atherosclerosis
business
Rheumatism
Zdroj: 13:e0202346
PLoS ONE
PLoS ONE, Vol 13, Iss 8, p e0202346 (2018)
ISSN: 1932-6203
Popis: BACKGROUND: Vitamin D has an important role in the immune system, and has been linked to rheumatoid arthritis (RA) and coronary artery disease (CAD). The exact mechanisms by which vitamin D is involved in these processes are still unclear. Therefore, we wanted to search for differences in expression of genes involved in the vitamin D receptor (VDR) activation pathway and genes that are known to alter upon vitamin D stimulation, in the aortic adventitia of CAD patients with and without RA. METHODS: Affymetrix microarray was used to determine gene expression profile in surgical specimens from the adventitia of the ascending aorta of CAD patients with RA (n = 8) and without RA (n = 8) from the Feiring Heart Biopsy Study. RESULTS: We identified three vitamin D associated genes that were differentially expressed between RA and non-RA patients: Growth arrest and DNA-damage-inducible protein 45 alpha (GADD45A) (FC = 1.47; p = 0.006), Nuclear Receptor Co-repressor 1 (NCOR1) (FC = 1,21; p = 0.005) and paraoxonases 2 (PON2) (FC = -1.37; p = 0.01). High expression of GADD45A in RA tissues was confirmed by real-time qRT-PCR. GADD45A expression correlated with plasma levels of 1,25(OH)2D3 (rs = 0.69; p = 0.003). CONCLUSIONS: Microarray analyses revealed higher expression of GADD45A and NCOR1; and lower expression of PON2 in the aortic adventitia of RA than non-RA patients. Further studies are needed to elucidate if and how GADD45A, NCOR1 and PON2 are involved in the development of accelerated atherosclerosis in RA. In theory, some of these factors might have proatherogenic effects whereas others might reflect an underlying vascular pathology promoting atherogenesis (such as vascular stress). This study was supported by the Innlandet Hospital Trust, South-Eastern Norway Regional Health Authority, the Norwegian Women’s Public Health Association, the Norwegian Rheumatism Association, and the Norwegian Association for People with Heart and Lung Diseases.
Databáze: OpenAIRE