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1.
J Cell Mol Med ; 28(16): e70028, 2024 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-39160453

RESUMO

Chronic inflammation is believed as the main culprit of the link between cardiovascular disease (CVD) and rheumatoid arthritis (RA). Interleukin-6 (IL-6) is a pro-inflammatory cytokine with a key role in RA pathophysiology and also correlates with joint destruction and disease activity. This study evaluates the association between IL-6 plasma level and cardiac biomarker NT-proBNP, HS-CRP, CVD predictor algorithms, Framingham Risk Score (FRS) and Systematic Coronary Risk Evaluation (SCORE), as well as with CXCL9 and its receptor, CXCR3 in RA patients compared to the controls. Sixty RA patients (30 early and 30 late) and 30 healthy persons were included in this study. IL-6 and NT-proBNP plasma levels were measured by the ELISA. Also, HS-CRP plasma levels were quantified using the immunoturbidimetric assay. The CVD risk was assessed by the FRS and SCORE. IL-6 plasma levels were significantly higher in the early and late RA patients compared to the controls (p < 0.001). There was a positive correlation between IL-6 with DAS-28 (p = 0.007, r = 0.346), BPS (p = 0.002, r = 0.396), BPD (p = 0.046, r = 0.259), SCORE (p < 0.001, r = 0.472), and FRS (p < 0.001, r = 0.553), and a negative association with HDL (p = 0.037, r = -0.270), in the patients. Also, IL-6 plasma level positively correlated with HS-CRP (p = 0.021, r = 0.297) and NT-proBNP (p = 0.045, r = 0.260) in the patients. Furthermore, a positive association was found between IL-6 plasma levels and CXCL9 (p = 0.002, r = 0.386), and CXCR3 (p = 0.018, r = 0.304) in the patients. Given the interesting association between IL-6 with various variables of CVD, IL-6 may be considered a biomarker for assessing the risk for future cardiovascular events in RA patients.


Assuntos
Algoritmos , Artrite Reumatoide , Biomarcadores , Proteína C-Reativa , Doenças Cardiovasculares , Interleucina-6 , Peptídeo Natriurético Encefálico , Fragmentos de Peptídeos , Humanos , Artrite Reumatoide/sangue , Artrite Reumatoide/complicações , Biomarcadores/sangue , Feminino , Masculino , Interleucina-6/sangue , Doenças Cardiovasculares/sangue , Doenças Cardiovasculares/etiologia , Pessoa de Meia-Idade , Peptídeo Natriurético Encefálico/sangue , Proteína C-Reativa/metabolismo , Fragmentos de Peptídeos/sangue , Quimiocina CXCL9/sangue , Adulto , Estudos de Casos e Controles , Idoso , Fatores de Risco , Receptores CXCR3
2.
Phytother Res ; 38(6): 2847-2859, 2024 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-38561995

RESUMO

The present systematic review and dose-response meta-analysis was conducted to synthesize existing data from randomized clinical trials (RCTs) concerning the impact of citrus flavonoids supplementation (CFS) on endothelial function. Relevant RCTs were identified through comprehensive searches of the PubMed, ISI Web of Science, and Scopus databases up to May 30, 2023. Weighted mean differences and their corresponding 95% confidence intervals (CI) were pooled utilizing a random-effects model. A total of eight eligible RCTs, comprising 596 participants, were included in the analysis. The pooled data demonstrated a statistically significant augmentation in flow-mediated vasodilation (FMD) (2.75%; 95% CI: 1.29, 4.20; I2 = 87.3%; p < 0.001) associated with CFS compared to the placebo group. Furthermore, the linear dose-response analysis indicated that each increment of 200 mg/d in CFS led to an increase of 1.09% in FMD (95% CI: 0.70, 1.48; I2 = 94.5%; p < 0.001). The findings from the nonlinear dose-response analysis also revealed a linear relationship between CFS and FMD (Pnon-linearity = 0.903, Pdose-response <0.001). Our findings suggest that CFS enhances endothelial function. However, more extensive RTCs encompassing longer intervention durations and different populations are warranted to establish more precise conclusions.


Assuntos
Citrus , Suplementos Nutricionais , Endotélio Vascular , Flavonoides , Ensaios Clínicos Controlados Aleatórios como Assunto , Vasodilatação , Humanos , Citrus/química , Flavonoides/farmacologia , Vasodilatação/efeitos dos fármacos , Endotélio Vascular/efeitos dos fármacos , Relação Dose-Resposta a Droga
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