Increased circulating basic fibroblast growth factor levels in acute myeloid leukemia: a meta-analysis

Hematology. 2020 Dec;25(1):186-193. doi: 10.1080/16078454.2020.1766865.

Abstract

Background: Basic fibroblast growth factor (bFGF) plays an important role in the pathogenesis of acute myeloid leukemia (AML). Whether the levels of circulating bFGF are increased or not in untreated AML patients is still not clear. In order to acquire a more definite evaluation, a meta-analysis was performed.Material and methods: We searched PubMed, Embase, the Cochrane Library, China National Knowledge Infrastructure (CNKI), Wanfang, and VIP databases for possible eligible articles. Forest plot was used to present the combined effect values and 95% confidence intervals (CI) through the random-effect model. Subgroup analysis was performed based on sample size, sample type, and region. All statistical analysis was performed in STATA12.0 software.Results: After excluding the articles that did not meet the inclusion criteria, 11 studies that met the inclusion conditions were included in this meta-analysis. Overall, AML patients probably had higher circulating levels of bFGF (SMD = 1.15, 95% CI: 0.35-1.94). The results of sensitivity analysis indicated that the results were stable. Moreover, the trim and fill analysis showed that publication bias had little effect and the results were relatively robust. In addition, AML patients with N < 30 group, serum group, and Asia group (all P < 0.05) had higher circulating bFGF levels, whereas other subgroups showed no significant change.Conclusion: The results of current meta-analysis revealed that AML patients had higher circulating bFGF levels, and it was associated with sample type, sample size, and region. Considering the possible pathogenic role of bFGF in AML, drug development targeting bFGF is very promising for AML patients.

Keywords: Biological markers; acute myeloid leukemia; basic fibroblast growth factor; meta-analysis.

Publication types

  • Meta-Analysis

MeSH terms

  • Adult
  • Case-Control Studies
  • Female
  • Fibroblast Growth Factor 2 / metabolism*
  • Humans
  • Leukemia, Myeloid, Acute / blood*
  • Male
  • Middle Aged

Substances

  • Fibroblast Growth Factor 2