Clinical Efficacy of Modified Buyang Huanwu Tang Combined with Sanrentang in Treatment of Spleen and Kidney Deficiency and Damp-heat and Blood Stasis Syndrome in Early Diabetic Nephropathy
Clinic|更新时间:2021-02-09
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Clinical Efficacy of Modified Buyang Huanwu Tang Combined with Sanrentang in Treatment of Spleen and Kidney Deficiency and Damp-heat and Blood Stasis Syndrome in Early Diabetic Nephropathy
Chinese Journal of Experimental Traditional Medical FormulaeVol. 26, Issue 5, Pages: 60-68(2020)
Ya-lan HUANG, Guo-dong HUANG, Lin-kun CAI, et al. Clinical Efficacy of Modified Buyang Huanwu Tang Combined with Sanrentang in Treatment of Spleen and Kidney Deficiency and Damp-heat and Blood Stasis Syndrome in Early Diabetic Nephropathy[J]. Chinese journal of experimental traditional medical formulae, 2020, 26(5): 60-68.
DOI:
Ya-lan HUANG, Guo-dong HUANG, Lin-kun CAI, et al. Clinical Efficacy of Modified Buyang Huanwu Tang Combined with Sanrentang in Treatment of Spleen and Kidney Deficiency and Damp-heat and Blood Stasis Syndrome in Early Diabetic Nephropathy[J]. Chinese journal of experimental traditional medical formulae, 2020, 26(5): 60-68. DOI: 10.13422/j.cnki.syfjx.20200425.
Clinical Efficacy of Modified Buyang Huanwu Tang Combined with Sanrentang in Treatment of Spleen and Kidney Deficiency and Damp-heat and Blood Stasis Syndrome in Early Diabetic Nephropathy
To observe the clinical efficacy of modified Buyang Huanwu Tang combined with Sanrentang in treating early diabetic nephropathy(DN)with deficiency of spleen and kidney
damp-heat and blood stasis syndrome and its effect on glucose and lipid metabolism
oxidative stress and inflammatory factors
in order to explore its mechanism.
Method:
2
A total of 72 early DN atients were randomly divided into control group and treatment group
with 36 cases in each group. The control group was orally treated with losartan potassium tablets(50 mg every time
once/day)
while the treatment group was treated with modified Buyang Huanwu Tang combined with Sanrentang orally in addition to the therapy of the control group(1 dose/day). Both groups were treated for 3 months. The changes in clinical efficacy and safety indicators were observed for both groups. The 24 h urine albumin excretion rate(UAER)
serum creatinine(SCr)
serum cystatin C(Cys C)
urea nitrogen (BUN)
fasting blood glucose (FBG)
2 h postprandial blood glucose (2 hPG)
glycosylated hemoglobin (HbA1c)
total cholesterol (TC)
triglyceride(TG)
low-density lipoprotein cholesterol(LDL-C)
high-density lipoprotein cholesterol(HDL-C)
malondialdehyde(MDA)
superoxide dismutase(SOD)
glutathione Peroxidase(GSH-Px)
interleukin-2(IL-2)
interleukin-4(IL-4)
interleukin-8(IL-8)
interleukin-10(IL-10)
tumor necrosis factor-
α
(TNF-
α
)of patients in two groups were observed before and after treatment.
Result:
2
The total clinical effective rate was 88.9%in therapy group
which was higher than 61.1%in control group(
P
<
0.05). After treatment
levels of UAER
SCr
Cys C and BUN were lower in both groups(
P
<
0.05)
and the levels in treatment group were all lower than those in control group(
P
<
0.05). Levels of FBG
2 hPG and HbA1c were lower in both groups(
P
<
0.05). There was no significant difference in FBG
2 hPG and HbA1c levels between two groups after treatment. The levels of HDL-C were higher in both groups(
P
<
0.05)
and the levels in treatment group were higher than that in control group(
P
<
0.05). The levels of TC
TG and LDL-C were lower in both groups(
P
<
0.05)
and the levels in treatment group were all lower than those in control group(
P
<
0.05). The level of MDA was lower in both groups(
P
<
0.05)
and the level in the treatment group was lower than that in control group(
P
<
0.05). The levels of SOD and GSH-Px were higher in both groups(
P
<
0.05)
and the levels in the treatment group were all higher than those in the control group(
P
<
0.05). Serum levels of IL-2
IL-8 and TNF-
α
were lower in both groups(
P
<
0.05)
and the levels in the treatment group were lower than those in control group(
P
<
0.05). Serum levels of IL-4 and IL-10 were higher in both groups(
P
<
0.05)
and the levels in the treatment group was higher than those in control group(
P
<
0.05).
Conclusion:
2
Modified Buyang Huanwu Tang combined with Sanrentang is effective and safe in the treatment of early DN with spleen and kidney deficiency
damp-heat and blood stasis syndrome. They can further improve renal function and lipid metabolism
inhibit oxidative stress reaction and regulate the secretion balance of inflammatory factors in early DN patients.
关键词
Keywords
references
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