Growth differentiation factor 15 as a potential diagnostic biomarker for rheumatoid arthritis a systematic review

被引:0
作者
Liu, X. [1 ]
Essien, A. E. [1 ]
Lu, W. [1 ]
Jin, H. [1 ]
Pan, L. [1 ]
Li, Y. [1 ,2 ]
Xiao, W. [1 ,2 ]
机构
[1] Cent South Univ, Xiangya Hosp, Dept Orthoped, Changsha, Peoples R China
[2] Cent South Univ, Xiangya Hosp, Natl Clin Res Ctr Geriatr Disorders, Changsha, Peoples R China
基金
国家重点研发计划; 中国国家自然科学基金;
关键词
MACROPHAGE INHIBITORY CYTOKINE-1; DISEASE-ACTIVITY; FACTOR-BETA; RECEPTOR; GDF15; SERUM; ARTHROPLASTY; PATHWAY; MIC-1; RISK;
D O I
10.1302/2046-3758.145.BJR-2024-0230.R2
中图分类号
Q813 [细胞工程];
学科分类号
摘要
Aims This systematic review aimed to investigate the association between growth differentiation factor 15 (GDF-15) and rheumatoid arthritis (RA) disease activity, explore the differences at the genetic level, and evaluate the value of GDF-15 in diagnosing RA. Methods A comprehensive literature search was conducted using PubMed, Web of Science, Cochrane Library, and Embase on 23 August 2023. Methodological quality was independently assessed by using the Agency for Healthcare Research and Quality scale. The primary parameters analyzed were the serum GDF-15 concentration, disease activity, and diagnostic sensitivity and specificity. Results A total of 469 documents were retrieved, and five clinical studies were ultimately included. In the included studies, GDF-15 serum levels were found to be notably greater in RA patients than in healthy individuals, and these levels exhibited a positive correlation with disease severity. Furthermore, increased GDF-15 serum levels were associated with specific gene variations in RA patients, but varied according to ethnicity. In two included studies, GDF-15 showed high diagnostic sensitivity and specificity for highly active RA, demonstrating its utility as a diagnostic biomarker of RA. Conclusion GDF-15 expression is increased in RA patients and is associated with disease activity; thus, GDF-15 is potentially an effective diagnostic biomarker for RA. However, additional high-quality studies, especially randomized controlled trials and cohort studies with follow-up data, are needed to assess the role of GDF-15 in RA.
引用
收藏
页码:389 / 397
页数:9
相关论文
共 62 条
[1]   Diagnosis and Management of Rheumatoid Arthritis A Review [J].
Aletaha, Daniel ;
Smolen, Josef S. .
JAMA-JOURNAL OF THE AMERICAN MEDICAL ASSOCIATION, 2018, 320 (13) :1360-1372
[2]   GDF15(MIC1) H6D Polymorphism Does Not Influence Cardiovascular Disease in a Latin American Population with Rheumatoid Arthritis [J].
Amaya-Amaya, Jenny ;
Rojas-Villarraga, Adriana ;
Molano-Gonzalez, Nicolas ;
Montoya-Sanchez, Laura ;
Nath, Swapan K. ;
Anaya, Juan-Manuel .
JOURNAL OF IMMUNOLOGY RESEARCH, 2015, 2015
[3]   Rheumatoid Arthritis Disease Activity Measures: American College of Rheumatology Recommendations for Use in Clinical Practice [J].
Anderson, Jaclyn ;
Caplan, Liron ;
Yazdany, Jinoos ;
Robbins, Mark L. ;
Neogi, Tuhina ;
Michaud, Kaleb ;
Saag, Kenneth G. ;
O'Dell, James R. ;
Kazi, Salahuddin .
ARTHRITIS CARE & RESEARCH, 2012, 64 (05) :640-647
[4]   Polymorphisms of the Genes Encoding CD40 and Growth Differentiation Factor 15 and in the 9p21.3 Region in Patients with Rheumatoid Arthritis and Cardiovascular Disease [J].
Arlestig, Lisbeth ;
Rantapaa-Dahlqvist, Solbritt .
JOURNAL OF RHEUMATOLOGY, 2012, 39 (05) :939-945
[5]   The TGF-β Superfamily Cytokine MIC-1/GDF15: Secretory Mechanisms Facilitate Creation of Latent Stromal Stores [J].
Bauskin, Asne R. ;
Jiang, Lele ;
Luo, X. Wei ;
Wu, Liyun ;
Brown, David A. ;
Breit, Samuel N. .
JOURNAL OF INTERFERON AND CYTOKINE RESEARCH, 2010, 30 (06) :389-397
[6]   Growth Differentiation Factor-15 Deficiency Inhibits Atherosclerosis Progression by Regulating Interleukin-6-Dependent Inflammatory Response to Vascular Injury [J].
Bonaterra, Gabriel A. ;
Zuegel, Stefanie ;
Thogersen, Joel ;
Walter, Sabrina A. ;
Haberkorn, Uwe ;
Strelau, Jens ;
Kinscherf, Ralf .
JOURNAL OF THE AMERICAN HEART ASSOCIATION, 2012, 1 (06) :e002550
[7]   MIC-1, a novel macrophage inhibitory cytokine, is a divergent member of the TGF-beta superfamily [J].
Bootcov, MR ;
Bauskin, AR ;
Valenzuela, SM ;
Moore, AG ;
Bansal, M ;
He, XY ;
Zhang, HP ;
Donnellan, M ;
Mahler, S ;
Pryor, K ;
Walsh, BJ ;
Nicholson, RC ;
Fairlie, WD ;
Por, SB ;
Robbins, JM ;
Breit, SN .
PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 1997, 94 (21) :11514-11519
[8]   The GDF15-GFRAL Pathway in Health and Metabolic Disease: Friend or Foe? [J].
Breit, Samuel N. ;
Brown, David A. ;
Tsai, Vicky Wang-Wei .
ANNUAL REVIEW OF PHYSIOLOGY, VOL 83, 2021, 83 :127-151
[9]   The TGF-β superfamily cytokine, MIC-1/GDF15: A pleotrophic cytokine with roles in inflammation, cancer and metabolism [J].
Breit, Samuel N. ;
Johnen, Heiko ;
Cook, Andrew D. ;
Tsai, Vicky W. W. ;
Mohammad, Mohammad G. ;
Kuffner, Tamara ;
Zhang, Hong Ping ;
Marquis, Christopher P. ;
Jiang, Lele ;
Lockwood, Glen ;
Lee-Ng, Michelle ;
Husaini, Yasmin ;
Wu, Liyun ;
Hamilton, John A. ;
Brown, David A. .
GROWTH FACTORS, 2011, 29 (05) :187-195
[10]   Serum macrophage inhibitory cytokine 1 in rheumatoid arthritis - A potential marker of erosive joint destruction [J].
Brown, David A. ;
Moore, John ;
Johnen, Heiko ;
Smeets, Tom J. ;
Bauskin, Asne R. ;
Kuffner, Tamara ;
Weedon, Helen ;
Milliken, Samuel T. ;
Tak, Paul P. ;
Smith, Malcolm D. ;
Breit, Samuel N. .
ARTHRITIS AND RHEUMATISM, 2007, 56 (03) :753-764