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1.
Journal of Chinese Physician ; (12): 1197-1199, 2009.
Article in Chinese | WPRIM | ID: wpr-392804

ABSTRACT

Objective To study the characteristics of plasma adiponectin levels exhibiting in gestation women and newborns, as well as the relationships between adiponectin levels and fetal birth weight. Methods Totally 98 subjects have been considered in this study, in-cluding venous blood samples of 36 healthy non-pregnant women (control group), 31 uncomplicated pregnant women (pregnancies group) and the cord blood samples taken at delivery of their singleton infants born at term (newborns group). The concentrations of adiponectin and insulin were determined by radioimmunoassay technique. And SPSS was used for statistical analyses. Results The adiponectin level in women of late period of gestation (WLPG) (11.10±5.72)g/ml was lower than that of other two groups, and the newborns average cord plasma level of adiponectin was (30.71±12.77) g/ml significantly higher than that of the control group (16.52±6.87) g/ml. The adipone-ctin level for WLPG was correlated with FINS and HOMA-IR (r = -0.411, -0.393, P <0.05). The adiponectin level in cord plasma was positively correlated with birth weight(r = 0.416, P < 0.05). The adiponectin level in WLPG was correlated neither with the adiponec-tin level nor body weights of their newborns. Conclusions The average cord plasma adiponectin level of newboms is significantly higher than that of the control group and WLPG. It is positively correlated with birth weight, which suggests that adiponectin may be involved in reg-ulating fetal growth. The adiponectin level in WLPG is correlated neither with the adiponectin level nor body weights of their newborns.

2.
China Pharmacy ; (12)2001.
Article in Chinese | WPRIM | ID: wpr-523858

ABSTRACT

OBJECTIVE:To evaluate the therapeutic effect of compound glycyrrhizin on atopic dermatitis(AD)in chil?dren.METHODS:60cases of AD were randomly divided into trial group and control group.Trial group(36cases)orally received compound glycyrrhizin tablets and control group(24cases)cyproheptadine tablets.Eloson cream was topically applied to both groups.The treatment course was8weeks with an interval of1week for both groups.RESULTS:The curative rate and total effective rate were52.8%and94.4%for trial group and12.5%and62.5%for control group respectively.The differences were significant between2groups(P

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