W Wasan Al-Bassam, B D H Al Khayali, S T Hamad, W Noor Ali, A Haider Hassan
{"title":"8-Hydroxy-2'-Deoxiguanosine (8-OHdG) as a reliable biomarker for rheumatoid arthritis.","authors":"W Wasan Al-Bassam, B D H Al Khayali, S T Hamad, W Noor Ali, A Haider Hassan","doi":"","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Rheumatoid arthritis (RA) is a chronic, autoimmune, destructive inflammatory synovitis that ultimately affects metabolic function, the vascular system, and systemic bone. Many researchers have demonstrated that free radicals induce oxidative stress and are involved in several disease conditions. It was observed that a physiological equilibrium between oxidants and antioxidants is being disrupted by oxidative stress. Free radicals are molecules, ions, or atoms with unpaired electrons. These elements tend to be stabilized. For stabilization, they attack other molecules to get electrons. In the cells, this behavior can cause mutations or even cellular death. This study aimed to evaluate the oxidative stress marker 8-Hydroxy-2-Deoxiguanosine (8-OHdG) as a biomarker for Iraqi RA patients.</p><p><strong>Materials and methods: </strong>The estimation of the plasma level of this marker was achieved in human RA patients using ELISA. The current study included 132 adult individuals who were diagnosed as RA patients with joint complications, while the remaining 66 were healthy and served as controls. Blood plasma levels of 8-OHdG were estimated using a commercial ELISA kit. The resultant solution was washed after being incubated, and then a conjugate enzyme was added; finally, the results were read using an ELISA reader at 450nm.</p><p><strong>Results: </strong>A significant increase in plasma concentration of 8- OHdG was detected in the disease group. The most significant increase in this biomarker (p = 0.001) appeared in RA patients in comparison with the healthy subjects. The significant increase of inflammatory and oxidative biomarkers highlighted in this study might point to a relationship between these biomarkers and the pathogenesis and progression of rheumatoid arthritis in adult subjects.</p><p><strong>Conclusion: </strong>This study suggests the role of 8-OHdG as an early diagnostic marker of RA. Because 8-OHdG is a strong indicator of oxidative stress-related DNA damage, this result may have significant clinical implications.</p>","PeriodicalId":39388,"journal":{"name":"Medical Journal of Malaysia","volume":"81 5","pages":"634-638"},"PeriodicalIF":0.0000,"publicationDate":"2026-09-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medical Journal of Malaysia","FirstCategoryId":"1085","ListUrlMain":"","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"Medicine","Score":null,"Total":0}
引用次数: 0
Abstract
Introduction: Rheumatoid arthritis (RA) is a chronic, autoimmune, destructive inflammatory synovitis that ultimately affects metabolic function, the vascular system, and systemic bone. Many researchers have demonstrated that free radicals induce oxidative stress and are involved in several disease conditions. It was observed that a physiological equilibrium between oxidants and antioxidants is being disrupted by oxidative stress. Free radicals are molecules, ions, or atoms with unpaired electrons. These elements tend to be stabilized. For stabilization, they attack other molecules to get electrons. In the cells, this behavior can cause mutations or even cellular death. This study aimed to evaluate the oxidative stress marker 8-Hydroxy-2-Deoxiguanosine (8-OHdG) as a biomarker for Iraqi RA patients.
Materials and methods: The estimation of the plasma level of this marker was achieved in human RA patients using ELISA. The current study included 132 adult individuals who were diagnosed as RA patients with joint complications, while the remaining 66 were healthy and served as controls. Blood plasma levels of 8-OHdG were estimated using a commercial ELISA kit. The resultant solution was washed after being incubated, and then a conjugate enzyme was added; finally, the results were read using an ELISA reader at 450nm.
Results: A significant increase in plasma concentration of 8- OHdG was detected in the disease group. The most significant increase in this biomarker (p = 0.001) appeared in RA patients in comparison with the healthy subjects. The significant increase of inflammatory and oxidative biomarkers highlighted in this study might point to a relationship between these biomarkers and the pathogenesis and progression of rheumatoid arthritis in adult subjects.
Conclusion: This study suggests the role of 8-OHdG as an early diagnostic marker of RA. Because 8-OHdG is a strong indicator of oxidative stress-related DNA damage, this result may have significant clinical implications.
期刊介绍:
Published since 1890 this journal originated as the Journal of the Straits Medical Association. With the formation of the Malaysian Medical Association (MMA), the Journal became the official organ, supervised by an editorial board. Some of the early Hon. Editors were Mr. H.M. McGladdery (1960 - 1964), Dr. A.A. Sandosham (1965 - 1977), Prof. Paul C.Y. Chen (1977 - 1987). It is a scientific journal, published quarterly and can be found in medical libraries in many parts of the world. The Journal also enjoys the status of being listed in the Index Medicus, the internationally accepted reference index of medical journals. The editorial columns often reflect the Association''s views and attitudes towards medical problems in the country. The MJM aims to be a peer reviewed scientific journal of the highest quality. We want to ensure that whatever data is published is true and any opinion expressed important to medical science. We believe being Malaysian is our unique niche; our priority will be for scientific knowledge about diseases found in Malaysia and for the practice of medicine in Malaysia. The MJM will archive knowledge about the changing pattern of human diseases and our endeavours to overcome them. It will also document how medicine develops as a profession in the nation. We will communicate and co-operate with other scientific journals in Malaysia. We seek articles that are of educational value to doctors. We will consider all unsolicited articles submitted to the journal and will commission distinguished Malaysians to write relevant review articles. We want to help doctors make better decisions and be good at judging the value of scientific data. We want to help doctors write better, to be articulate and precise.