6
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Short‐term biological variation and Reference change values of urinary 8‐oxo‐7,8‐dihydro‐2'‐deoxyguanosine and 8‐oxo‐7,8‐dihydroguanosine

      research-article

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Aim

          The DNA and RNA oxidative damage products urinary 8‐oxo‐7,8‐dihydro‐2'‐deoxyguanosine (8‐odGsn) and 8‐oxo‐7,8‐dihydroguanosine (8‐oGsn) have potential use in clinical practice. However, biological variation (BV) and reference change values (RCVs) have not been established. The aim of this study was to establish the short‐term between‐subject BV(CV G) , within‐subject BV(CV I), and RCVs for urinary 8‐odGsn and 8‐oGsn.

          Methods

          First‐morning midstream urine specimens were collected from 20 apparently healthy subjects(ten males and ten females) on five consecutive days. 8‐odGsn and 8‐oGsn were measured using LC‐MS/MS, while urine creatinine (U‐Cr) was also measured to correct their results. A two‐level nested ANOVA was used to estimate the CV I and CV G.

          Results

          The values of CV G for 8‐odGsn, 8‐odGsn/U‐Cr, 8‐oGsn, and 8‐oGsn/U‐Cr were 31.2%, 39.6%, 35.3%, and 28.8%, respectively, while CV I for them were 40.5%, 9.0%, 33.5%, and 12.1%, respectively. The RCVs for 8‐odGsn, 8‐odGsn/U‐Cr, 8‐oGsn, and 8‐oGsn/U‐Cr were 112.5%, 26.7%, 93.7%, and 36.5%, respectively.

          Conclusion

          BV and RCVs were firstly established for 8‐oxo‐dGsn and 8‐oGsn, and can be used in clinical practice.

          Abstract

          The DNA and RNA oxidative damage products urinary 8‐oxo‐7,8‐dihydro‐2'‐deoxyguanosine (8‐odGsn) and 8‐oxo‐7,8‐dihydroguanosine (8‐oGsn) have potential use in clinical practice. However, biological variation (BV) and reference change values (RCVs) have not been established. The aim of this study was to establish the short term between‐subject BV(CV G) , within‐subject BV(CV I) and RCVs for urinary 8‐odGsn and 8‐oGsn. First‐morning midstream urine specimens were collected from 20 apparently healthy subjects(ten males and ten females) on five consecutive days. 8‐odGsn and 8‐oGsn were measured using LC‐MS/MS, while urine creatinine (U‐Cr) was also measured to correct their results. A two‐level nested ANOVA was used to estimate the CV I and CV G. The values of CV Gfor 8‐odGsn, 8‐odGsn/U‐Cr, 8‐oGsn, and 8‐oGsn/U‐Cr were 31.2%, 39.6%, 35.3%, and 28.8%, respectively, while CV I for them were 40.5%, 9.0%, 33.5%, and 12.1%, respectively. The RCVs for 8‐odGsn, 8‐odGsn/U‐Cr, 8‐oGsn, and 8‐oGsn/U‐Cr were 112.5%, 26.7%, 93.7%, and 36.5%, respectively. BV and RCVs were firstly established for 8‐oxo‐dGsn and 8‐oGsn, and can be used in clinical practice.

          Related collections

          Most cited references25

          • Record: found
          • Abstract: found
          • Article: not found

          The Biological Variation Data Critical Appraisal Checklist: A Standard for Evaluating Studies on Biological Variation.

          Concern has been raised about the quality of available biological variation (BV) estimates and the effect of their application in clinical practice. A European Federation of Clinical Chemistry and Laboratory Medicine Task and Finish Group has addressed this issue. The aim of this report is to (a) describe the Biological Variation Data Critical Appraisal Checklist (BIVAC), which verifies whether publications have included all essential elements that may impact the veracity of associated BV estimates, (b) use the BIVAC to critically appraise existing BV publications on enzymes, lipids, kidney, and diabetes-related measurands, and (c) apply metaanalysis to deliver a global within-subject BV (CVI) estimate for alanine aminotransferase (ALT).
            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Reference change values.

            Reference change values (RCV) provide objective tools for assessment of the significance of differences in serial results from an individual. The concept is simple and the calculation easy, since all laboratories know their analytical imprecision (CV(A)) and estimates of within-subject biological variation (CV(I)) are available for a large number of quantities. Generally, CV(I) are constant over time, geography, methodology and in health and chronic stable disease. The formula is RCV=2(1/2) · Z · (CV(A)(2) + CV(I)(2))(1/2), where Z is the number of standard deviations appropriate to the probability. Correct interpretation of the semantics describing the clinical use of RCV is vital for selection of the Z-score. Many quantities of clinically importance exist for which good estimates of RCV are unavailable. Derivation of CV(I) may be difficult for such quantities: flair and imagination are required in selecting populations with chronic but stable disease on whom CV(I) can be determined. RCV can be used for delta-checking and auto-verification and laboratory information management systems (LIMS) can be adapted to do this. Recently, log-normal transformation to obtain unidirectional RCV has been used. Gaps in knowledge of RCV still require filling since the need for measures of change is clearly expressed in guidelines.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Age-dependent increases in the oxidative damage of DNA, RNA, and their metabolites in normal and senescence-accelerated mice analyzed by LC-MS/MS: urinary 8-oxoguanosine as a novel biomarker of aging.

              A sensitive and accurate isotope-diluted LC-MS/MS method was developed for determination of 8-oxo-7,8-dihydro-2'-deoxyguanosine (8-oxo-dGsn), derived from DNA, and 8-oxo-7,8-dihydroguanosine (8-oxo-Gsn), derived from RNA, in various tissue specimens obtained from normal SAMR1 and senescence-accelerated SAMP8 mice. An age-dependent accumulation of oxidative DNA and RNA damage was observed in all the organs examined, namely, the brain, liver, lungs, heart, kidneys, and testes. Among these, the brain samples exhibited the highest values for DNA damage. These age-related increases in the 8-oxoguanine content in DNA and RNA occurred more rapidly in SAMP8 than in SAMR1 mice. Age-related increases in the contents of 8-oxo-dGsn and 8-oxo-Gsn were also observed in the plasma and urine; however, the ratios of 8-oxo-Gsn to 8-oxo-dGsn in these samples were considerably higher (6 to 13) compared with the values for the samples derived from other tissues (roughly 1), indicating that measurement of 8-oxo-Gsn in urine could be a novel means of evaluating the aging process. Copyright © 2012 Elsevier Inc. All rights reserved.
                Bookmark

                Author and article information

                Contributors
                caoyongtong92@sina.com
                lingqiubj@163.com
                Journal
                J Clin Lab Anal
                J Clin Lab Anal
                10.1002/(ISSN)1098-2825
                JCLA
                Journal of Clinical Laboratory Analysis
                John Wiley and Sons Inc. (Hoboken )
                0887-8013
                1098-2825
                22 August 2020
                December 2020
                : 34
                : 12 ( doiID: 10.1002/jcla.v34.12 )
                : e23522
                Affiliations
                [ 1 ] Department of Clinical Laboratory China‐Japan Friendship Hospital Beijing China
                [ 2 ] Department of Clinical Laboratory Peking Union Medical College Hospital Peking Union Medical College & Chinese Academy of Medical Sciences Beijing China
                Author notes
                [*] [* ] Correspondence

                Ling Qiu, Department of Clinical Laboratory, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences, No. 1 Shuaifu Yuan, Dongcheng District, Beijing 100730, China.

                Email: lingqiubj@ 123456163.com

                Yongtong Cao, Department of Clinical Laboratory, China‐Japan Friendship Hospital, Beijing 100730, China.

                Email: caoyongtong92@ 123456sina.com

                Author information
                https://orcid.org/0000-0003-2688-3203
                https://orcid.org/0000-0002-0734-8144
                Article
                JCLA23522
                10.1002/jcla.23522
                7755802
                32827234
                12d0badd-1943-412a-b4f4-f701734c7686
                © 2020 The Authors. Journal of Clinical Laboratory Analysis Published by Wiley Periodicals LLC

                This is an open access article under the terms of the http://creativecommons.org/licenses/by-nc/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited and is not used for commercial purposes.

                History
                : 11 May 2020
                : 16 July 2020
                : 20 July 2020
                Page count
                Figures: 2, Tables: 2, Pages: 6, Words: 4444
                Categories
                Research Article
                Research Articles
                Custom metadata
                2.0
                December 2020
                Converter:WILEY_ML3GV2_TO_JATSPMC version:5.9.6 mode:remove_FC converted:22.12.2020

                Clinical chemistry
                8‐oxo‐7,8‐dihydro‐2'‐deoxyguanosine,8‐oxo‐7,8‐dihydroguanosine,biological variation,oxidative damage biomarkers,reference change values

                Comments

                Comment on this article