Your browser doesn't support javascript.
loading
Effect of dipeptidyl peptidase-4 inhibitors on tumor necrosis factor alpha levels in patients with type 2 diabetes mellitus.
Zhao, Lijia; Meng, Jie; Bai, Xueyan; Zhang, Donglei; Yang, Xingsheng; Yang, Yu; Cai, Gaojun; Liu, Xin.
Afiliação
  • Zhao L; Department of Cardiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Meng J; Department of Pathology, Beijing TongRen Hospital, Capital Medical University, Beijing, China.
  • Bai X; Department of Hemotology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Zhang D; Department of Hematology, Zhongnan Hospital, Wuhan University, Wuhan, China.
  • Yang X; Department of Cardiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Yang Y; Department of Cardiology, Beijing Tiantan Hospital, Capital Medical University, Beijing, China.
  • Cai G; Department of Cardiology, Wujin Hospital, Jiangsu University, Changzhou, Jiangsu, China. cgj982@126.com.
  • Liu X; Department of Pharmacy, Beijing Tiantan Hospital, Capital Medical University, Beijing, China. ttyydrliu@126.com.
Eur J Med Res ; 29(1): 363, 2024 Jul 12.
Article em En | MEDLINE | ID: mdl-38997754
ABSTRACT

AIMS:

Dipeptidyl peptidase-4 inhibitors (DPP-4i) served as oral antidiabetic agents for treatment of type 2 diabetes mellitus (T2DM). Although an action on glucose homeostasis was identified, no well-rounded illustration had been established on the changes of tumor necrosis factor alpha (TNF-alpha) levels during DPP-4i treatment. This study aimed to explore the anti-inflammatory effect of DPP-4i on TNF-alpha in patients with T2DM.

METHODS:

PubMed, Embase and Cochrane Library were systematically searched from inception to May 31, 2024. Randomized controlled trials exploring the impact of DPP-4i on TNF-alpha levels were identified. Risk of bias was assessed according to the Cochrane criteria. A fixed or random-effects model was selected to pool estimate on whether the heterogeneity was present. Subgroup analysis were performed to explore the potential factors that influenced heterogeneity. Related meta-analysis was conducted with the software of Revman 5.3 and STATA 12.0.

RESULTS:

Eleven trials involving 884 participants with T2DM were included. Pooled estimates suggested that DPP-4i did not significantly modulate TNF-alpha levels (WMD, - 0.70, 95% CI - 1.94 to 0.53, P = 0.26) in T2DM. DPP-4i produced a significant effect on TNF-alpha (WMD, - 4.50 pg/mL, 95% CI - 4.68 to - 4.32, P < 0.00001) when compared to placebo, and a comparable effect was demonstrated on TNF-alpha (WMD, 0.10 pg/mL, 95% CI - 0.11 to 0.30, P = 0.35) in comparison with active agents. Estimate was stable according to the sensitivity test. Subgroup analysis revealed that heterogeneity might not correlate with baseline glycated hemoglobin (HbA1c), age or treatment duration.

CONCLUSIONS:

A significant effect of DPP-4i on TNF-alpha levels was present in T2DM when compared to placebo. Administration of DPP-4i produced no significant effect on TNF-alpha in comparison with active comparators. Further studies with large samples should be performed to illustrate the impact of DPP-4i on TNF-alpha levels in T2DM. Trial registration International Prospective Register for Systematic Review (PROSPERO) number CRD42020185479.
Assuntos
Palavras-chave

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator de Necrose Tumoral alfa / Diabetes Mellitus Tipo 2 / Inibidores da Dipeptidil Peptidase IV Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Fator de Necrose Tumoral alfa / Diabetes Mellitus Tipo 2 / Inibidores da Dipeptidil Peptidase IV Idioma: En Ano de publicação: 2024 Tipo de documento: Article