scholarly journals Dapagliflozin, metformin, monotherapy or both in patients with metabolic syndrome

2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Lan Cheng ◽  
Qianyu Fu ◽  
Longhua Zhou ◽  
Yuqin Fan ◽  
Fenfen Liu ◽  
...  

AbstractThe present study evaluated the effects of dapagliflozin, a SGLT2 inhibitor, or dapagliflozin plus metformin versus metformin monotherapy in patients with metabolic syndrome. This study included patients who admitted in Jiangxi Provincial People’s Hospital from January 1, 2017 to December 31, 2019 and were diagnosed with metabolic syndrome. A total of 248 participants were randomly assigned to divide into three groups: dapagliflozin group; metformin group; dapagliflozin in combined with metformin group. Dapagliflozin group and metformin group were associated with similar improvements in components of metabolic syndrome. Relative to dapagliflozin or metformin monotherapy, dapagliflozin combined with metformin provided greater improvements in components of metabolic syndrome. So did HOMA-IR scores, fasting plasma insulin and inflammatory indicators (hsCRP, PMN/HDL-C and Monocytes/HDL-C). Dapagliflozin improved all components of metabolic syndrome in patients with metabolic syndrome. Furthermore, dapagliflozin combined with metformin showed more meaningful improvements in any of components of metabolic syndrome than dapagliflozin or metformin monotherapy.

2011 ◽  
Vol 18 (4) ◽  
pp. 291-297 ◽  
Author(s):  
Hideyuki Kanda ◽  
Peiyu Wang ◽  
Tomonori Okamura ◽  
GaoWa Wuyun ◽  
HePing Wu ◽  
...  

Metabolism ◽  
1998 ◽  
Vol 47 (5) ◽  
pp. 535-540 ◽  
Author(s):  
M. Carantoni ◽  
G. Zuliani ◽  
S. Volpato ◽  
E. Palmieri ◽  
A. Mezzetti ◽  
...  

Angiology ◽  
2005 ◽  
Vol 56 (3) ◽  
pp. 249-251 ◽  
Author(s):  
Rishi Sukhija ◽  
Wilbert S. Aronow ◽  
Devraj Nayak ◽  
Chul Ahn ◽  
Melvin B. Weiss

1995 ◽  
Vol 268 (1) ◽  
pp. E1-E5 ◽  
Author(s):  
A. Quinones Galvan ◽  
A. Natali ◽  
S. Baldi ◽  
S. Frascerra ◽  
G. Sanna ◽  
...  

Although hyperuricemia is a frequent finding in insulin-resistant states, insulin's effect on renal uric acid (UA) handling is not known. In 20 healthy volunteers, diastolic blood pressure, body weight, and fasting plasma insulin were positively (and age was negatively) related to fasting plasma UA concentrations, together accounting for 53% of their variability. During an insulin clamp, urine flow was lower than during fasting conditions (1.01 +/- 0.12 vs. 1.56 +/- 0.32 ml/min, P = 0.04), whereas creatinine clearance was unchanged (129 +/- 7 and 131 +/- 9 ml/min, P = not significant). Hyperinsulinemia did not alter serum UA concentrations (303 +/- 13 vs. 304 +/- 12 microM) but caused a significant decrease in urinary UA excretion [whether expressed as absolute excretion rate (1.66 +/- 0.21 vs. 2.12 +/- 0.23 mumol/min, P = 0.03), clearance rate (5.6 +/- 0.8 vs. 7.3 +/- 0.8 ml/min, P = 0.03), or fractional excretion (4.48 +/- 0.80 ml/min vs. 6.06 +/- 0.64%, P < 0.03)]. Hyperinsulinemia was also associated with a 30% (P < 0.001) fall in urine Na excretion. Fractional UA excretion was related to Na fractional excretion under basal conditions (r = 0.59, P < 0.01) and during the insulin period (r = 0.53, P < 0.02). Furthermore, the insulin-induced changes in fractional UA and Na excretion correlated with one another (r = 0.66, P < 0.001). Physiological hyperinsulinemia acutely reduces urinary UA and Na excretion in a coupled fashion.


PLoS ONE ◽  
2015 ◽  
Vol 10 (6) ◽  
pp. e0127389 ◽  
Author(s):  
Yan Yan Chen ◽  
Jin Ping Wang ◽  
Ya Yun Jiang ◽  
Hui Li ◽  
Ying Hua Hu ◽  
...  

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