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Rheumatoid arthritis is an autoimmune disorder, and genetic factors strongly contribute to a genetic predisposition to developing the disease. This study evaluated the genetic and molecular indicators of some Iraqi patients with rheumatoid arthritis. The study included (100) patients with rheumatoid arthritis with (100) healthy individuals who attended Al-Hussain General Teaching Hospital, Department of Arthritis and Joints Centre, al Blood Bank in Baghdad for the period from the beginning of January 2022 until the end of March 2022. The patients were diagnosed under the supervision of medical committees specialized in joint diseases. The human leukocyte antigen is one of the essential genetic factors in regulating the immune response, as these antigens contribute to the susceptibility to disease. Human leukocyte antigen (HLA) class II (Class-II- HLA-DR, -DQ) was genotyped using lymphocytotoxicity assay and PCR-SSP method. The results showed that there was a significant increase in the recurrence of human leukocyte antigens (DR4 R53) in rheumatoid arthritis patients compared to the healthy ones, as well as an increase in the recurrence of human leukocyte antigens (HLA-DQ3) with a significant difference in rheumatoid arthritis patients compared to the healthy ones. Regarding HLA-DRB1 and -DQB1 alleles, it was found that there was a significant increase in the frequency of HLA-DRB1*04 (01-22, not 0415) compared to healthy controls, while the percentage of HLA-DRB1*0701 alleles was less frequent in patients compared to healthy controls. Moreover, the frequency of HLADQB1*03(02,07) alleles was high in the patients compared to the healthy ones, while HLA-DQB1*0303 showed a highly significant difference in the healthy group compared to the patients. Keywords: Rheumatoid arthritis, genetic factors, HLA-DRB1, -DQB1 alleles, PCR.
Rheumatoid arthritis is an autoimmune disorder, and genetic factors strongly contribute to a genetic predisposition to developing the disease. This study evaluated the genetic and molecular indicators of some Iraqi patients with rheumatoid arthritis. The study included (100) patients with rheumatoid arthritis with (100) healthy individuals who attended Al-Hussain General Teaching Hospital, Department of Arthritis and Joints Centre, al Blood Bank in Baghdad for the period from the beginning of January 2022 until the end of March 2022. The patients were diagnosed under the supervision of medical committees specialized in joint diseases. The human leukocyte antigen is one of the essential genetic factors in regulating the immune response, as these antigens contribute to the susceptibility to disease. Human leukocyte antigen (HLA) class II (Class-II- HLA-DR, -DQ) was genotyped using lymphocytotoxicity assay and PCR-SSP method. The results showed that there was a significant increase in the recurrence of human leukocyte antigens (DR4 R53) in rheumatoid arthritis patients compared to the healthy ones, as well as an increase in the recurrence of human leukocyte antigens (HLA-DQ3) with a significant difference in rheumatoid arthritis patients compared to the healthy ones. Regarding HLA-DRB1 and -DQB1 alleles, it was found that there was a significant increase in the frequency of HLA-DRB1*04 (01-22, not 0415) compared to healthy controls, while the percentage of HLA-DRB1*0701 alleles was less frequent in patients compared to healthy controls. Moreover, the frequency of HLADQB1*03(02,07) alleles was high in the patients compared to the healthy ones, while HLA-DQB1*0303 showed a highly significant difference in the healthy group compared to the patients. Keywords: Rheumatoid arthritis, genetic factors, HLA-DRB1, -DQB1 alleles, PCR.
This research aims to find how three different types of mouthwashes affect the depth of artificial white spot lesions. Teeth with various depths of white spot lesions were immersed in either splat mouthwash, Biorepair mouthwash, Sensodyne mouthwash, or artificial saliva (control)twice daily for one minute for 4 weeks and 8 weeks at 37°C. After this immersion procedure, lesion depth was measured using a diagnosed pen score. A one-way analysis of variance, Dunnett T3 and Tukey's post hoc α = .05 were used to analyze the testing data. Splat mouthwash enhanced the WSL remineralization and made the lowest ΔF compared with other mouthwashes in shallow and deep enamel after 4 and 8 weeks of treatment. In the repair groups, after 4 weeks of treatment, significant recovery was observed in shallow enamel. Further improvement in shallow WSL after 8 weeks of treatment with biorepair mouthwash was observed compared to Sensodyne and the control group. Splat mouthwash is more effective than other mouthwashes in remineralizing two depths of WSLs at different time points. Keywords: DIAGNOdent pen, Shallow enamel, Deep enamel, white spot lesion.
Objective: The genetic background of HLA-B*27 in spondyloarthritis is known, and the search for another gene with similar role is ongoing. We wanted to investigate clinical presentations of HLA-B*44 patients in rheumatology practice. Methods: A cross-sectional retrospective study of 303 HLA-B*44 adult patients from the outpatient rheumatology clinic from 5/2018-5/2024. Clinical phenotype, confirmed or excluded rheumatic diagnosis, therapy used, and data on HLA A, B, and DR alleles inherited with B*44 were analyzed. Results: A female predominance of 2.79:1 was noted. A total of 150 [49.5%] patients were referred due to peripheral joint pain, 77 [25.4%] due to combined spine and peripheral joint pain or spine alone (57 [18.8%]). A total of 19 [6.3%] patients had no symptoms of the musculoskeletal system. Statistically significant peripheral joint affection was proved in females but not in males (p = 0.04). A total of 121 [40%] patients from B*44 group had established rheumatic disease, with the rest being excluded or under observation. The most common working diagnoses were polyarthritis (32 [10.5%]) and mono-oligoarthritis (14 [4.6%]). A second allele in addition to HLA B*44 showed a similar frequency to the general population. Patients with HLA B*44/44 and B*27/44 genotypes were at the most risk for having definitive rheumatic disease (>60%). Conventional synthetic disease-modifying anti-rheumatic drugs (DMARDs) were used in 38.6% of patients, non-steroidal anti-inflammatory drugs were used in 31.6% of patients, biologic DMARDs were used in 8.9% of patients, and corticosteroids were used in 7.3% of patients. Conclusions: The most common presentation in HLA-B*44 patients is peripheral joint affection. Most patients with HLA-B*27/44 and B*44/44 genotypes had definitive rheumatic disease. B*44 homozygosity or B*27/44 might be risk factors for arthritis development.
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