NOD2/CARD15 gene mutations in patients with gouty arthritis

Nucleotide binding and oligomerization domains/caspase recruitment domain-containing protein 15 (NOD2/CARD15) is a cytoplasmic molecule controlling apoptosis and inflammatory processes by recognizing some microbial components. We aimed to identify the frequencies of NOD2/CARD15 gene mutations in pa...

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Main Authors: Ahmet Karaarslan, Senol Kobak, Afig Berdeli
Format: Article
Language:English
Published: Association of Basic Medical Sciences of Federation of Bosnia and Herzegovina 2016-11-01
Series:Biomolecules & Biomedicine
Subjects:
Online Access:https://www.bjbms.org/ojs/index.php/bjbms/article/view/1339
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author Ahmet Karaarslan
Senol Kobak
Afig Berdeli
author_facet Ahmet Karaarslan
Senol Kobak
Afig Berdeli
author_sort Ahmet Karaarslan
collection DOAJ
description Nucleotide binding and oligomerization domains/caspase recruitment domain-containing protein 15 (NOD2/CARD15) is a cytoplasmic molecule controlling apoptosis and inflammatory processes by recognizing some microbial components. We aimed to identify the frequencies of NOD2/CARD15 gene mutations in patients with gouty arthritis and to determine their possible correlation with the disease phenotype. The study included 93 patients with gouty arthritis and 51 healthy controls matched for age, gender, and ethnicity. The NOD2/CARD15 R702W and G908R gene mutations were explored by the polymerase chain reaction restriction fragment length polymorphism method while the 3020insC mutation was analyzed by DNA sequencing. The mean patient age was 54.2 ± 14.2 years and mean duration of the disease was 3.1 ± 2.9 years. The first metatarsophalangeal and finger joint involvements were detected in 72 (77.4%) and 18 (19.5%) patients, respectively. Ankle arthritis and knee arthritis were detected in 43 (46.2%) and 20 (21.5%) patients, respectively. In total, 4 (9%) heterozygous mutations were detected in the G908R and R702W genes, while no mutation was detected in the 3020insC gene. Compared to the control group, there were no significant differences in all three DNA regions (G908R, R702W, and 3020insC; p = 0.452, p = 0.583, and p = 0.350, respectively). No correlation between the NOD2/CARD15 variants and clinical or laboratory findings (p > 0.05) was found. The frequencies of the NOD2/CARD15 gene mutations in the patients were similar to healthy control group. No association between clinical or laboratory findings and the NOD2/CARD15 gene mutations was observed.
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spelling doaj.art-365e46f5c1ef47f78aaffdc7c0f203b52024-03-15T14:31:51ZengAssociation of Basic Medical Sciences of Federation of Bosnia and HerzegovinaBiomolecules & Biomedicine2831-08962831-090X2016-11-0116410.17305/bjbms.2016.1339121NOD2/CARD15 gene mutations in patients with gouty arthritisAhmet Karaarslan0Senol Kobak1Afig Berdeli2Department of Orthopedics, Faculty of Medicine, Sifa University, Izmir, TurkeyDepartment of Rheumatology, Faculty of Medicine, Sifa University, Izmir, TurkeyDepartment of Genetics and Molecular Medicine, Faculty of Medicine, Ege University, Izmir, Turkey Nucleotide binding and oligomerization domains/caspase recruitment domain-containing protein 15 (NOD2/CARD15) is a cytoplasmic molecule controlling apoptosis and inflammatory processes by recognizing some microbial components. We aimed to identify the frequencies of NOD2/CARD15 gene mutations in patients with gouty arthritis and to determine their possible correlation with the disease phenotype. The study included 93 patients with gouty arthritis and 51 healthy controls matched for age, gender, and ethnicity. The NOD2/CARD15 R702W and G908R gene mutations were explored by the polymerase chain reaction restriction fragment length polymorphism method while the 3020insC mutation was analyzed by DNA sequencing. The mean patient age was 54.2 ± 14.2 years and mean duration of the disease was 3.1 ± 2.9 years. The first metatarsophalangeal and finger joint involvements were detected in 72 (77.4%) and 18 (19.5%) patients, respectively. Ankle arthritis and knee arthritis were detected in 43 (46.2%) and 20 (21.5%) patients, respectively. In total, 4 (9%) heterozygous mutations were detected in the G908R and R702W genes, while no mutation was detected in the 3020insC gene. Compared to the control group, there were no significant differences in all three DNA regions (G908R, R702W, and 3020insC; p = 0.452, p = 0.583, and p = 0.350, respectively). No correlation between the NOD2/CARD15 variants and clinical or laboratory findings (p > 0.05) was found. The frequencies of the NOD2/CARD15 gene mutations in the patients were similar to healthy control group. No association between clinical or laboratory findings and the NOD2/CARD15 gene mutations was observed. https://www.bjbms.org/ojs/index.php/bjbms/article/view/1339Gouty arthritisnucleotide binding and oligomerization domains/caspase recruitment domain-containing protein 15 gene mutationsprevalence
spellingShingle Ahmet Karaarslan
Senol Kobak
Afig Berdeli
NOD2/CARD15 gene mutations in patients with gouty arthritis
Biomolecules & Biomedicine
Gouty arthritis
nucleotide binding and oligomerization domains/caspase recruitment domain-containing protein 15 gene mutations
prevalence
title NOD2/CARD15 gene mutations in patients with gouty arthritis
title_full NOD2/CARD15 gene mutations in patients with gouty arthritis
title_fullStr NOD2/CARD15 gene mutations in patients with gouty arthritis
title_full_unstemmed NOD2/CARD15 gene mutations in patients with gouty arthritis
title_short NOD2/CARD15 gene mutations in patients with gouty arthritis
title_sort nod2 card15 gene mutations in patients with gouty arthritis
topic Gouty arthritis
nucleotide binding and oligomerization domains/caspase recruitment domain-containing protein 15 gene mutations
prevalence
url https://www.bjbms.org/ojs/index.php/bjbms/article/view/1339
work_keys_str_mv AT ahmetkaraarslan nod2card15genemutationsinpatientswithgoutyarthritis
AT senolkobak nod2card15genemutationsinpatientswithgoutyarthritis
AT afigberdeli nod2card15genemutationsinpatientswithgoutyarthritis