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Objective To investigate the roles of miR-155 and miR-23b in the differential diagnosis of idiopathic granulomatous mastitis(IGM)and breast cancer(BC).Methods A total of 32 patients with IGM(the ICM group)and 40 patients with BC(the BC group)admitted to our hospital from October 2018 to November 2021 were selected.All patients were confirmed by biopsy.In addition,33 healthy women were included as the control group.The clinical data of patients were compared.The expression levels of serum miRNAs were detected by real-time fluorescence quantitative PCR.The diagnostic value of serum miR-155 and miR-23b for IGM and BC was evaluated by receiver operating characteristic(ROC)curve.The Pearson correlation coefficient method was used to evaluate the correlation.Results There were statistically significant differences in the levels of CRP,WBC,Hb,Hct,CA19-9,CA15-3 and CA125 among the three groups(P<0.05).The expression levels of serum miR-155,miR-16-5p,miR-21-5p,miR-210-3p,miR-222-3p and miR-29c-3p in the IGM group were higher than those in the control group(P<0.001),and the expression level of serum miR-23b was lower than that in the control group(P<0.001).The expression levels of the above miRNAs of serum in the BC group were higher than those in the control group(P<0.001).The expression level of serum miR-155 in the BC group was lower than that in the IGM group(P<0.001),and the expression level of serum miR-23b was higher than that in the IGM group(P<0.001).The area under the ROC curve(AUC)for the differential diagnosis of IGM and BC by serum miR-155 and miR-23b levels were 0.722(95%CI:0.601 to 0.843)and 0.765(95%CI:0.657 to 0.874),respectively,with sensitivity of 81.00%and 77.50%,and specificity of 65.00%and 59.40%,respectively.The AUC of combined differential diagnosis was 0.869(95%CI:0.786 to 0.951),and the sensitivity and specificity were 84.10%and 92.50%,respectively.Serum miR-155 was positively correlated with WBC and CRP levels in the IGM group(P<0.05),while serum miR-23b was negatively correlated with WBC and CRP levels(P<0.05).Conclusion Serum miR-155 and miR-23b are helpful in distinguishing IGM from BC,and can be used as targets for early differential diagnosis of IGM and BC.
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To explore prescription medication regularity in the treatment of Alzheimer's disease with traditional Chinese medicine(TCM). With Alzheimer's disease or senile dementia as the subject, collecting and sorting out the journal papers in CNKI were collected as the data source to establish the literature research database of Alzheimer's disease prescriptions, and then the association rule analysis, factor analysis and systematic cluster analysis on the included TCM were conducted. Among the 113 prescriptions included in the standard, the single herb Acori Tatarinowii Rhizoma was the most common. The herbs were mainly warm and flat among four pro-perties, mainly sweet, bitter and spicy among five flavors. The drugs were mainly distributed in five internal organs, and the most commonly used drugs were deficiency tonifying drugs as well as blood activating and stasis removing drugs. In the association rule analysis, it was found that there were 6 drug pairs with the highest association strength. Eight common factors were extracted from the factor analysis, and they were classified into 6 categories in the systematic cluster analysis. The results have shown that the overall principles in treating Alzheimer's disease with modern Chinese medicine are tonifying deficiency, invigorating circulation, activating blood and dispelling phlegm.
Тема - темы
Humans , Alzheimer Disease/drug therapy , Data Mining , Drugs, Chinese Herbal/therapeutic use , Medicine, Chinese Traditional , PrescriptionsРеферат
Objective::To observe the effect of modified Dihuang Yinzi on the learning and memory ability and on the neurons in CA1 area of hippocampus of rats suffering from vascular dementia. Method::The 84 male SD rats were randomly selected to form the sham operation group of 12 rats, and the other 72 rats were chosen for the vascular dementia model by means of Bivascular occlusion, and among which 60 were chosen randomly into 6 groups of 12 rats, namely, the model group, the nimodipine group (0.011 g·kg-1), and the high, medium and low dose modified Dihuang Yinzi (4.54, 2.27, 1.14 g·kg-1) respectively. After 30 days of continuous gavage, Morris water maze was used to detect the learning and memory ability of rats, hematoxylin eosin (HE) was used to observe the morphological changes of hippocampal CA1 neurons, transmission electron microscopy was used to observe the ultrastructural changes of hippocampal CA1 neurons, TUNEL was used to detect the apoptosis level of hippocampal CA1 neurons, immunohistochemical(IHC) was used to detect the expression level of phosphatidylinositol-3(PI3K), protein kinase B (Akt), Caspase-3 in hippocampal CA1 tissues. Result::Compared with sham operation group, the escape latency of the model group was significantly prolonged, the number of times of crossing the original platform was significantly reduced (P<0.01), the neuronal morphology of hippocampal CA1 area was damaged to varying degrees, the apoptosis rate was significantly increased (P<0.01), the integral optical density and average optical density of PI3K, Akt were significantly reduced (P<0.01), and the integral optical density and average optical density of Caspase-3 were significantly reduced (P<0.01). Compared with model group, the escape latency was shortened (P<0.05, P<0.01), the number of crossing the original platform was increased (P<0.05, P<0.01), the integrated optical density and average optical density of PI3K and Akt were significantly increased (P<0.01), and the integrated optical density and average optical density of Caspase-3 were decreased in different degrees (P<0.05, P<0.01). Conclusion::Modified Dihuang Yinzi can improve the learning and memory ability of vascular dementia model rats and the damaged neurons in the hippocampal CA1 area. The potential mechanism may be related to the activation of PI3K/Akt signal transduction pathway and the inhibition of apoptosis of neurons in hippocampal CA1 area of rats.