2
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Serum levels of tumor necrosis factor alpha in patients with IgA nephropathy are closely associated with disease severity

      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

          Background

          Tumor necrosis factor alpha (TNF-α) is considered to play an important role in the pathogenesis in IgA nephropathy (IgAN). The correlations between serum TNF-α and disease severity in patients with IgAN remain controversial.

          Methods

          Concentrations of serum TNF-α of 147 patients with IgAN and 126 healthy subjects were measured by chemiluminescence immunoassay. Correlations with clinicopathological features of patients with IgAN were evaluated.

          Results

          Serum levels of TNF-α [9.20 (7.70–10.60) pg/mL vs. 6.04 (5.11–7.23) pg/mL, P < 0.0001] were higher in patients with IgAN than that in healthy subjects. Receiver operating characteristic curve analysis revealed that TNF-α had better discrimination between patients with IgAN and healthy controls than estimated glomerular filtration rate [TNF-α: (AUC, 0.87; 95% CI, 0.83–0.91; P < 0.0001) vs. estimated glomerular filtration rate: (AUC, 0.76; 95% CI, 0.71–0.82; P < 0.0001), P = 0.007]. Multivariate linear regression analyses showed that serum levels of TNF-α were positively correlated with 24-h urine protein excretion ( r = 0.33, P = 0.04), urinary protein to serum creatinine ratio ( r = 0.33, P = 0.03), serum creatinine ( r = 0.46, P < 0.0001) and Cystatin C ( r = 0.59, P < 0.0001) in IgAN and negatively correlated with estimated glomerular filtration rate ( r = − 0.49, P < 0.0001) after adjustment for sex, systolic blood pressure and diastolic blood pressure. Patients with higher mesangial hypercellularity or tubular atrophy/interstitial fibrosis score according to Oxford classification showed higher serum levels of TNF-α.

          Conclusions

          Our data showed that serum levels of TNF-α detected by chemiluminescence immunoassay was a potential biomarker for evaluating the disease severity in IgAN.

          Electronic supplementary material

          The online version of this article (10.1186/s12882-018-1069-0) contains supplementary material, which is available to authorized users.

          Related collections

          Most cited references21

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

          Evaluation of the Chronic Kidney Disease Epidemiology Collaboration equation for estimating the glomerular filtration rate in multiple ethnicities.

          An equation from the Chronic Kidney Disease Epidemiology Collaboration (CKD-EPI) provides more accurate estimates of the glomerular filtration rate (eGFR) than that from the modification of diet in renal disease (MDRD) Study, although both include a two-level variable for race (Black and White and other). Since creatinine generation differs among ethnic groups, it is possible that a multilevel ethnic variable would allow more accurate estimates across all groups. To evaluate this, we developed an equation to calculate eGFR that includes a four-level race variable (Black, Asian, Native American and Hispanic, and White and other) using a database of 8254 patients pooled from 10 studies. This equation was then validated in 4014 patients using 17 additional studies from the United States and Europe (validation database), and in 1022 patients from China (675), Japan (248), and South Africa (99). Coefficients for the Black, Asian, and Native American and Hispanic groups resulted in 15, 5, and 1% higher levels of eGFR, respectively, compared with the White and other group. In the validation database, the two-level race equation had minimal bias in Black, Native American and Hispanic, and White and other cohorts. The four-level ethnicity equation significantly improved bias in Asians of the validation data set and in Chinese. Both equations had a large bias in Japanese and South African patients. Thus, heterogeneity in performance among the ethnic and geographic groups precludes use of the four-level race equation. The CKD-EPI two-level race equation can be used in the United States and Europe across a wide range of ethnicity.
            Bookmark
            • Record: found
            • Abstract: not found
            • Article: not found

            IgA nephropathy.

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

              Adaptive immune regulation in the gut: T cell-dependent and T cell-independent IgA synthesis.

              In mammals, the gastrointestinal tract harbors an extraordinarily dense and complex community of microorganisms. The gut microbiota provide strong selective pressure to the host to evolve adaptive immune responses required for the maintenance of local and systemic homeostasis. The continuous antigenic presence in the gut imposes a dynamic remodeling of gut-associated lymphoid tissues (GALT) and the selection of multiple layered strategies for immunoglobulin (Ig) A production. The composite and dynamic gut environment also necessitates heterogeneous, versatile, and convertible T cells, capable of inhibiting (Foxp3(+) T cells) or helping (T(FH) cells) local immune responses. In this review, we describe recent advances in our understanding of dynamic pathways that lead to IgA synthesis, in gut follicular structures and in extrafollicular sites, by T cell-dependent and T cell-independent mechanisms. We discuss the finely tuned regulatory mechanisms for IgA production and emphasize the role of mucosal IgA in the selection and maintenance of the appropriate microbial composition that is necessary for immune homeostasis.
                Bookmark

                Author and article information

                Contributors
                liguanhong91@sina.com
                ww_pumch@sina.com
                zhangxinyao9623@163.com
                huangyuan@pumch.cn
                wenyubing@hotmail.com
                lixmpumch@126.com
                86-010-69155058 , gaoruitong@gmail.com
                Journal
                BMC Nephrol
                BMC Nephrol
                BMC Nephrology
                BioMed Central (London )
                1471-2369
                14 November 2018
                14 November 2018
                2018
                : 19
                : 326
                Affiliations
                [1 ]ISNI 0000 0000 9889 6335, GRID grid.413106.1, Division of Nephrology, Department of Internal Medicine, , Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, ; NO.1, Shuaifuyuan, Dongcheng District, Beijing, 100730 China
                [2 ]ISNI 0000 0000 9889 6335, GRID grid.413106.1, Department of Clinical Laboratory, , Peking Union Medical College Hospital, Chinese Academy of Medical Sciences & Peking Union Medical College, ; Beijing, China
                Article
                1069
                10.1186/s12882-018-1069-0
                6236996
                30428849
                92826716-71c9-40a0-a7b8-f570cbe3c7e3
                © The Author(s). 2018

                Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License ( http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver ( http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.

                History
                : 11 August 2017
                : 4 October 2018
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/100007452, Wu Jieping Medical Foundation;
                Award ID: 320.6750.16023
                Categories
                Research Article
                Custom metadata
                © The Author(s) 2018

                Nephrology
                biomarkers,cytokines,tumor necrosis factor alpha,iga nephropathy
                Nephrology
                biomarkers, cytokines, tumor necrosis factor alpha, iga nephropathy

                Comments

                Comment on this article