Evidence map›Paper›PMID 27357501›Full record

ArticleBosnian journal of basic medical sciences2016

NOD2/CARD15 gene mutations in patients with gouty arthritis.

Ahmet Karaarslan, Senol Kobak, Afig Berdeli

Abstract read
In one paragraph

Article in Bosnian journal of basic medical sciences, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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0citing papers in PubMed
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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

3 authors.

Ahmet KaraarslanDepartment of Orthopedics, Faculty of Medicine, Sifa University, Izmir, Turkey. ahmetkaraarslan@gmail.com.
Senol Kobak
Afig Berdeli

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

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.

Indexed as

AdultAgedAnkleArthritis, GoutyDNAFemaleFingersHumansJointsKneeMaleMiddle AgedMutationNod2 Signaling Adaptor ProteinYoung AdultDNANOD2 protein, humanNod2 Signaling Adaptor Protein

Identifiers

PMID27357501
PMCPMC5136763

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