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.jpg): Failed to open stream: No such file or directory in C:\Inetpub\vhosts\kidney.de\httpdocs\pget.php on line 117 PLoS+One
2017 ; 12
(10
): e0186554
Nephropedia Template TP
gab.com Text
Twit Text FOAVip
Twit Text #
English Wikipedia
Effect of diacerein on renal function and inflammatory cytokines in participants
with type 2 diabetes mellitus and chronic kidney disease: A randomized controlled
trial
#MMPMID29049415
Piovesan F
; Tres GS
; Moreira LB
; Andrades ME
; Lisboa HK
; Fuchs SC
PLoS One
2017[]; 12
(10
): e0186554
PMID29049415
show ga
Diacerein seems to improve metabolic control and reduce inflammatory marker
levels in individuals with type 2 diabetes mellitus (Type 2 DM), but for
participants with chronic kidney disease (CKD) its effect is unknown. This study
aimed to evaluate the effect of diacerein vs. placebo on urinary
albumin/creatinine ratio (ACR), glomerular filtration rate (GFR), and
inflammatory cytokines in type 2 DM participants with CKD. Blood pressure (BP)
and metabolic control were secondary outcomes. This randomized,
placebo-controlled, parallel trial of adjuvant treatment of type 2 DM with
diacerein enrolled seventy-two participants with CKD, aged 30-80 years, with
glycated hemoglobin levels from 53-97 mmol/mol (7.0-11.0%), receiving
angiotensin-converting enzyme inhibitors or angiotensin receptor blockers and
antidiabetic agents. Participants randomized to diacerein or placebo were
followed-up up to 90 days. Both groups had a marked reduction in ACR, but there
was no effect on glomerular filtration rate. While the diacerein group had
reduced TNF-? levels at the 75th percentile with a borderline significance (P =
0.05), there were no changes in the IL levels at the 75th percentile. Diacerein
prevented the increase in blood glucose to the level observed in the placebo
group (P = 0.04), improving metabolic control by 74%, reducing 24-hour diastolic
BP, nighttime systolic and diastolic BP compared to the placebo group. In
conclusion, among patients with type 2 DM and CKD, diacerein does not have an
effect on ACR or GFR, but slows metabolic control deterioration and is associated
with lower nighttime systolic and diastolic blood pressure. TRIAL REGISTRATION:
Brazilian Clinical Trials Registry (Registro Brasileiro de Ensaios Clinicos;
ReBeC) U1111-1156-0255.