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Light and Shadow of Na-Glucose Cotransporter 2 Inhibitors in the Treatment of Diabetes Mellitus: Points for Improvement Based on Our Clinical Experience Na-Glucose Cotransporter 2 抑制剂在糖尿病治疗中的光与影:基于临床经验的改进要点
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2024-01-25 DOI: 10.1155/2024/3937927
Akihiro Sonoda, Toshio Shimada, Kohei Saito, Rieko Kosugi, Yoshitaka Taguchi, Tatsuhide Inoue
We analyzed the effect of Na-glucose cotransporter 2 inhibitors (SGLT2-I) in diabetic patients visiting our hospital. The study included 236 patients treated with SGLT2-I alone or with codiabetic drugs for at least two years. We analyzed overtime changes in glycosylated hemoglobin A1c (HbA1c) in the patients by repeated analyses of variance (ANOVA) and evaluated the therapeutic effect. HbA1c levels decreased significantly in the first six months after treatment. Afterward, they leveled off and increased slightly over the next two years. Six months after treatment, the mean (SD) of HbA1c was 8.19 (1.46) %; the mean difference dropped by 0.91%, and HbA1c in mild DM2 did not drop by below 8.0%. Overall, there was only a slight improvement. We performed multivariate logistic regression analysis using a model with or without improvement as the objective variable and several explanatory variables. Na and Hct were significant factors. They increased considerably over six months and then leveled off. eGFR significantly reduced in the hyperfiltration group six months after treatment. The annual decline rate in eGFR was also faster, even in the nonhyperfiltration group than in the healthy subjects, which may be a characteristic of renal clearance in SGLT2-I treatment. In conclusion, SGLT2-I is an excellent antidiabetic, nephroprotective agent to eliminate hyperfiltration, but unfortunately, SGLT2-I alone does not have enough power to reduce blood glucose levels. SGLT2-I, with insulin or insulin secretagogues, enhances insulin resistance, induces hyperinsulinemia, and exacerbates type 2 DM. In contrast, SGLT2-I, with noninsulin antidiabetic agents and a low-carbohydrate diet, may bring better results.
我们分析了 Na 葡萄糖共转运体 2 抑制剂(SGLT2-I)对本院就诊糖尿病患者的影响。研究包括 236 名接受 SGLT2-I 单独治疗或与同种糖尿病药物一起治疗至少两年的患者。我们通过重复方差分析(ANOVA)分析了患者糖化血红蛋白A1c(HbA1c)的超时变化,并评估了治疗效果。治疗后的前六个月,HbA1c 水平明显下降。之后,HbA1c 水平趋于平稳,并在接下来的两年中略有上升。治疗 6 个月后,HbA1c 的平均值(标度)为 8.19 (1.46) %;平均值下降了 0.91%,轻度 DM2 患者的 HbA1c 降幅未低于 8.0%。总体而言,只有轻微改善。我们使用以是否有改善为目标变量的模型和几个解释变量进行了多变量逻辑回归分析。Na 和 Hct 是重要因素。治疗六个月后,高滤过组的 eGFR 显著下降。即使在非高滤过组,eGFR 的年下降率也比健康受试者快,这可能是 SGLT2-I 治疗中肾脏清除率的一个特征。总之,SGLT2-I 是一种消除高滤过的优良抗糖尿病肾保护剂,但遗憾的是,单靠 SGLT2-I 并不足以降低血糖水平。SGLT2-I 与胰岛素或胰岛素促泌剂一起使用时,会增强胰岛素抵抗,诱发高胰岛素血症,加重 2 型糖尿病。相比之下,SGLT2-I 配合非胰岛素抗糖尿病药物和低碳水化合物饮食可能会带来更好的效果。
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引用次数: 0
Whether Detection of Gene Mutations Could Identify Low- or High-Risk Papillary Thyroid Microcarcinoma? Data from 393 Cases Using the Next-Generation Sequencing 检测基因突变能否识别低危或高危甲状腺乳头状微癌?使用新一代测序技术分析393例病例的数据
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2024-01-16 DOI: 10.1155/2024/2470721
Lei Jin, Liang Zhou, Jian-Biao Wang, Li Tao, Xiao-Xiao Lu, Na Yan, Qian-Ming Chen, Li-Ping Cao, Lei Xie
<i>Objective</i>. The objective of this study is to explore the utilization of next-generation sequencing (NGS) technology in evaluating the likelihood of identifying individuals with papillary thyroid microcarcinoma (PTMC ≤10 mm) who are at high or low risk. <i>Design</i>. NGS was used to analyze 393 formalin-fixed, paraffin-embedded tissues of PTC tumors, all of which were smaller than 15 mm. <i>Results</i>. The study found that bilateralism, multifocality, intrathyroidal spread, and extrathyroidal extension were present in 84 (21.4%), 153 (38.9%), 16 (4.1%), and 54 (13.7%) cases, respectively. Metastasis of cervical lymph nodes was identified in 226 (57.5%) cases and 96 (24.4%) cases with CLNM >5. Out of the total number of cases studied, 8 cases (2.3%) showed signs of tumor recurrence, all of which were localized and regional. Genetic alterations were detected in 342 cases (87.0%), with 336 cases revealing single mutations and 6 cases manifesting compound mutations. 332 cases (84.5%) had BRAF<sup>V600E</sup> mutation, 2 cases had KRAS<sup>Q61K</sup> mutation, 2 cases had NRAS<sup>Q61R</sup> mutation, 8 cases had RET/PTC1 rearrangement, 3 cases had RET/PTC3 rearrangement, and 1 case had TERT promoter mutation. Additionally, six individuals harbored concurrent mutations in two genes. These mutations were of various types and combinations: BRAF<sup>V600E</sup> and NRAS<sup>Q61R</sup> (<i>n</i> = 2), BRAF<sup>V600E</sup> and RET/PTC3 (<i>n</i> = 2), BRAF<sup>V600E</sup> and RET/PTC1 (<i>n</i> = 1), and BRAF<sup>V600E</sup> and TERT promoter (<i>n</i> = 1). The subsequent analysis did not uncover a significant distinction in the incidence of gene mutation or fusion between the cN0 and cN1 patient cohorts. The presence of BRAF<sup>V600E</sup> mutation and CLNM incidence rates were found to be positively correlated with larger tumor size in PTMC. Our data showed that gene mutations did not appear to have much to do with high-risk papillary thyroid microcarcinoma (PTMC). However, when we looked at tumor size, we found that if the tumor was at least 5 millimeters in size, there was a higher chance of it being at high risk for PTM (<span><svg height="9.2729pt" style="vertical-align:-0.6370001pt" version="1.1" viewbox="-0.0498162 -8.6359 19.289 9.2729" width="19.289pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink"><g transform="matrix(.013,0,0,-0.013,0,0)"></path></g><g transform="matrix(.013,0,0,-0.013,11.658,0)"></path></g></svg><span></span><span><svg height="9.2729pt" style="vertical-align:-0.6370001pt" version="1.1" viewbox="22.8711838 -8.6359 28.182 9.2729" width="28.182pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink"><g transform="matrix(.013,0,0,-0.013,22.921,0)"></path></g><g transform="matrix(.013,0,0,-0.013,29.161,0)"></path></g><g transform="matrix(.013,0,0,-0.013,32.125,0)"><use xlink:href="#g113-49"></use></g><g transform="matrix(.013,0,0,-0.013,38.365,0)"><use xlink:href=
研究目的本研究旨在探讨如何利用下一代测序(NGS)技术评估识别甲状腺乳头状微癌(PTMC ≤10 mm)高危或低危患者的可能性。设计。使用 NGS 分析 393 例福尔马林固定、石蜡包埋的 PTC 肿瘤组织,所有肿瘤均小于 15 毫米。结果研究发现,分别有 84 例(21.4%)、153 例(38.9%)、16 例(4.1%)和 54 例(13.7%)存在双侧性、多灶性、甲状腺内扩散和甲状腺外延伸。226例(57.5%)和96例(24.4%)CLNM >5发现有颈淋巴结转移。在所有研究病例中,有 8 例(2.3%)出现肿瘤复发迹象,均为局部和区域性复发。342个病例(87.0%)检测到基因突变,其中336个病例显示单突变,6个病例显示复合突变。332例(84.5%)有BRAFV600E突变,2例有KRASQ61K突变,2例有NRASQ61R突变,8例有RET/PTC1重排,3例有RET/PTC3重排,1例有TERT启动子突变。此外,有 6 人同时携带两个基因的突变。这些突变的类型和组合多种多样:BRAFV600E和NRASQ61R(2例)、BRAFV600E和RET/PTC3(2例)、BRAFV600E和RET/PTC1(1例)以及BRAFV600E和TERT启动子(1例)。随后的分析并未发现 cN0 和 cN1 患者群在基因突变或融合发生率上有明显差异。在PTMC中,BRAFV600E基因突变的存在和CLNM发病率与肿瘤大小呈正相关。我们的数据显示,基因突变与高风险甲状腺乳头状微癌(PTMC)似乎没有太大关系。然而,当我们研究肿瘤大小时,我们发现如果肿瘤大小至少为5毫米,那么它成为PTM高风险的几率就会更高(几率比(OR)=2.55,95%置信区间(CI):1.57-4.14)。BRAFV600E 基因突变与晚期临床病理特征无显著相关性,但与肿瘤直径较大密切相关(OR = 4.92,95% 置信区间:2.40-10.07)。结论在临床实践中,BRAFV600E突变并不能一直作为区分高风险PTMC或预测肿瘤进展的有效生物标志物。肿瘤大小与其侵袭性特征有显著相关性。应将直径≤5 毫米的 PTMC 作为一个独特的亚群加以区分并进行专门治疗。
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引用次数: 0
Machine Learning for Predicting Distant Metastasis of Medullary Thyroid Carcinoma Using the SEER Database 利用 SEER 数据库预测甲状腺髓样癌远处转移的机器学习方法
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2023-12-30 DOI: 10.1155/2023/9965578
Zhen-Tian Guo, Kun Tian, Xi-Yuan Xie, Yu-Hang Zhang, De-Bao Fang
Objectives. We aimed to establish an effective machine learning (ML) model for predicting the risk of distant metastasis (DM) in medullary thyroid carcinoma (MTC). Methods. Demographic data of MTC patients were extracted from the Surveillance, Epidemiology, and End Results (SEER) database of the National Institutes of Health between 2004 and 2015 to develop six ML algorithm models. Models were evaluated based on accuracy, precision, recall rate, F1-score, and area under the receiver operating characteristic curve (AUC). The association between clinicopathological characteristics and target variables was interpreted. Analyses were performed using traditional logistic regression (LR). Results. In total, 2049 patients were included and 138 developed DM. Multivariable LR showed that age, sex, tumor size, extrathyroidal extension, and lymph node metastasis were predictive features for DM in MTC. Among the six ML models, the random forest (RF) had the best predictability in assessing the risk of DM in MTC, with an accuracy, precision, recall rate, F1-score, and AUC higher than those of the traditional binary LR model. Conclusion. RF was superior to traditional LR in predicting the risk of DM in MTC and can provide a valuable reference for clinicians in decision-making.
研究目的我们旨在建立一个有效的机器学习(ML)模型,用于预测甲状腺髓样癌(MTC)的远处转移(DM)风险。方法我们从美国国立卫生研究院的监测、流行病学和最终结果(SEER)数据库中提取了2004年至2015年间MTC患者的人口统计学数据,开发了六种ML算法模型。根据准确率、精确度、召回率、F1-分数和接收者工作特征曲线下面积(AUC)对模型进行了评估。对临床病理特征与目标变量之间的关联进行了解释。使用传统的逻辑回归(LR)进行分析。结果共纳入 2049 例患者,其中 138 例发展为 DM。多变量LR显示,年龄、性别、肿瘤大小、甲状腺外扩展和淋巴结转移是MTC中DM的预测特征。在六个ML模型中,随机森林(RF)在评估MTC中DM的风险方面具有最佳预测能力,其准确率、精确度、召回率、F1-分数和AUC均高于传统的二元LR模型。结论在预测 MTC 中的 DM 风险方面,RF 优于传统的 LR,可为临床医生的决策提供有价值的参考。
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引用次数: 0
Effects of a Novel Glucokinase Activator, Dorzagliatin, on Glycemic Control and Glucose Fluctuation in Drug-Naïve Patients with Type 2 Diabetes Mellitus 新型葡萄糖激酶激活剂多扎格拉汀对药物过敏的 2 型糖尿病患者血糖控制和血糖波动的影响
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2023-12-27 DOI: 10.1155/2023/4996057
Yuming Wang, Xiaofei Su, Wenli Zhang, Yunting Zhou, Xiao Zhou, Wei Yang, Huiqin Li, Jianhua Ma
Aim. The prevalence rate of type 2 diabetes mellitus (T2DM) has been increasing and a large proportion of patients still do not achieve adequate or sustainable glycemic control on the basis of previous hypoglycemic treatment. In this present study, we explored whether dorzagliatin, a novel glucokinase activator (GKA), could improve glycemic control and lessen glucose fluctuation in drug-naïve patients with T2DM. Methods. A self-comparative observational study of 25 drug-naïve patients with T2DM (aged 18–75 years and HbA1c of 7.5%–11.0%) treated with dorzagliatin 75 mg twice daily for 52 weeks. Before and after dorzagliatin intervention, the serum levels of hemoglobin A1c (HbA1c), insulin, and C-peptide were measured repeatedly during fasting and after a mixed meal. The continuous glucose monitoring (CGM) device was also used to obtain 24-hour glucose profiles and assess the changes in glycemic variability parameters. Results. After 52 weeks of treatment with dorzagliatin, a numerally greater reduction in HbA1c of 1.03% from the baseline was observed in patients with T2DM, accompanied by significant improvement in insulin resistance and insulin secretion. Moreover, the standard deviation of blood glucose (SDBG) and the mean amplitude of glycemic excursion (MAGE) derived from CGM data were significantly decreased after dorzagliatin therapy. The 24-h glucose variation profile showed that study patients had obviously lower mean glucose levels during the postprandial period from the baseline to week 52, an effect also demonstrated by the significant decrease in the incremental area under glucose concentration versus time curve for 2 h (iAUC0–2 h) after meals. Conclusions. This study suggests that dorzagliatin therapy could effectively improve glycemic control and glucose fluctuation in drug-naïve patients with T2DM.
目的2 型糖尿病(T2DM)的发病率不断上升,但仍有很大一部分患者在既往接受降糖治疗的基础上,血糖控制不佳或无法持续。在本研究中,我们探讨了新型葡萄糖激酶激活剂(GKA)多扎格列汀能否改善药物治疗无效的 T2DM 患者的血糖控制并减少血糖波动。研究方法对 25 名 T2DM 药物治疗无效患者(年龄在 18-75 岁之间,HbA1c 在 7.5%-11.0% 之间)进行了一项自我比较观察研究,这些患者接受了连续 52 周、每天两次、每次 75 毫克的多扎格列汀治疗。在多沙格列汀干预前后,分别在空腹和混合餐后反复测量血红蛋白 A1c (HbA1c)、胰岛素和 C 肽的血清水平。此外,还使用连续血糖监测(CGM)设备获取 24 小时血糖曲线,并评估血糖变异性参数的变化。研究结果使用多扎格雷丁治疗 52 周后,T2DM 患者的 HbA1c 比基线值降低了 1.03%,同时胰岛素抵抗和胰岛素分泌也得到了显著改善。此外,根据 CGM 数据得出的血糖标准偏差(SDBG)和血糖偏移平均幅度(MAGE)在多扎格列汀治疗后也显著下降。24 小时血糖变化曲线显示,从基线到第 52 周,研究患者餐后期间的平均血糖水平明显降低,餐后 2 小时血糖浓度随时间变化曲线下的增量面积(iAUC0-2 h)显著减少也证明了这一点。结论本研究表明,多扎格雷汀疗法可有效改善药物治疗无效的 T2DM 患者的血糖控制和血糖波动。
{"title":"Effects of a Novel Glucokinase Activator, Dorzagliatin, on Glycemic Control and Glucose Fluctuation in Drug-Naïve Patients with Type 2 Diabetes Mellitus","authors":"Yuming Wang, Xiaofei Su, Wenli Zhang, Yunting Zhou, Xiao Zhou, Wei Yang, Huiqin Li, Jianhua Ma","doi":"10.1155/2023/4996057","DOIUrl":"https://doi.org/10.1155/2023/4996057","url":null,"abstract":"<i>Aim</i>. The prevalence rate of type 2 diabetes mellitus (T2DM) has been increasing and a large proportion of patients still do not achieve adequate or sustainable glycemic control on the basis of previous hypoglycemic treatment. In this present study, we explored whether dorzagliatin, a novel glucokinase activator (GKA), could improve glycemic control and lessen glucose fluctuation in drug-naïve patients with T2DM. <i>Methods</i>. A self-comparative observational study of 25 drug-naïve patients with T2DM (aged 18–75 years and HbA1c of 7.5%–11.0%) treated with dorzagliatin 75 mg twice daily for 52 weeks. Before and after dorzagliatin intervention, the serum levels of hemoglobin A1c (HbA1c), insulin, and C-peptide were measured repeatedly during fasting and after a mixed meal. The continuous glucose monitoring (CGM) device was also used to obtain 24-hour glucose profiles and assess the changes in glycemic variability parameters. <i>Results</i>. After 52 weeks of treatment with dorzagliatin, a numerally greater reduction in HbA1c of 1.03% from the baseline was observed in patients with T2DM, accompanied by significant improvement in insulin resistance and insulin secretion. Moreover, the standard deviation of blood glucose (SDBG) and the mean amplitude of glycemic excursion (MAGE) derived from CGM data were significantly decreased after dorzagliatin therapy. The 24-h glucose variation profile showed that study patients had obviously lower mean glucose levels during the postprandial period from the baseline to week 52, an effect also demonstrated by the significant decrease in the incremental area under glucose concentration versus time curve for 2 h (iAUC0–2 h) after meals. <i>Conclusions</i>. This study suggests that dorzagliatin therapy could effectively improve glycemic control and glucose fluctuation in drug-naïve patients with T2DM.","PeriodicalId":13966,"journal":{"name":"International Journal of Endocrinology","volume":"31 1","pages":""},"PeriodicalIF":2.8,"publicationDate":"2023-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139057233","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Expression and Clinical Significance of Plasma miR-223 in Patients with Diabetic Nephropathy 糖尿病肾病患者血浆 miR-223 的表达及其临床意义
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2023-12-27 DOI: 10.1155/2023/9663320
Xingrong Guo, Meiying Huang, Dawei Yang, Zuojie Luo
<i>Background</i>. MicroRNA-223 (miR-223) is associated with diabetes and kidney diseases and serves as a novel marker for diagnosing diabetic kidney disease (DKD). This study was conducted to investigate the plasma expression of miR-223 and its clinical significance in type 2 diabetes (T2DM) and diabetic nephropathy (DN) patients. <i>Methods</i>. In this research, 20 patients with T2DM and DN, 19 patients with T2DM, and 17 healthy volunteers were finally enrolled. miR-223 expression was detected by quantitative real-time PCR (qPCR), and the diagnostic value of miR-223 in DN was further analyzed. <i>Results</i>. miR-223 was downregulated in the DN group compared to that in the T2DM group (<span><svg height="8.8423pt" style="vertical-align:-0.2064009pt" version="1.1" viewbox="-0.0498162 -8.6359 19.289 8.8423" width="19.289pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink"><g transform="matrix(.013,0,0,-0.013,0,0)"></path></g><g transform="matrix(.013,0,0,-0.013,11.658,0)"></path></g></svg><span></span><span><svg height="8.8423pt" style="vertical-align:-0.2064009pt" version="1.1" viewbox="22.8711838 -8.6359 28.182 8.8423" width="28.182pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink"><g transform="matrix(.013,0,0,-0.013,22.921,0)"></path></g><g transform="matrix(.013,0,0,-0.013,29.161,0)"></path></g><g transform="matrix(.013,0,0,-0.013,32.125,0)"><use xlink:href="#g113-49"></use></g><g transform="matrix(.013,0,0,-0.013,38.365,0)"></path></g><g transform="matrix(.013,0,0,-0.013,44.605,0)"></path></g></svg>)</span></span> and the control group (<span><svg height="9.2729pt" style="vertical-align:-0.6370001pt" version="1.1" viewbox="-0.0498162 -8.6359 19.289 9.2729" width="19.289pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink"><g transform="matrix(.013,0,0,-0.013,0,0)"><use xlink:href="#g113-81"></use></g><g transform="matrix(.013,0,0,-0.013,11.658,0)"></path></g></svg><span></span><span><svg height="9.2729pt" style="vertical-align:-0.6370001pt" version="1.1" viewbox="22.8711838 -8.6359 28.182 9.2729" width="28.182pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink"><g transform="matrix(.013,0,0,-0.013,22.921,0)"><use xlink:href="#g113-49"></use></g><g transform="matrix(.013,0,0,-0.013,29.161,0)"><use xlink:href="#g113-47"></use></g><g transform="matrix(.013,0,0,-0.013,32.125,0)"><use xlink:href="#g113-49"></use></g><g transform="matrix(.013,0,0,-0.013,38.365,0)"><use xlink:href="#g113-49"></use></g><g transform="matrix(.013,0,0,-0.013,44.605,0)"><use xlink:href="#g113-50"></use></g></svg>).</span></span> Pearson’s correlation analysis showed a negative correlation of miR-223 levels with an albumin-creatinine ratio (ACR) (<i>r</i> = −0.481; <span><svg height="8.8423pt" style="vertical-align:-0.2064009pt" version="1.1" viewbox="-0.0498162 -8.6359 19.289 8.8423" width="19.289pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http:
背景。微RNA-223(miR-223)与糖尿病和肾脏疾病有关,是诊断糖尿病肾病(DKD)的新型标志物。本研究旨在探讨 2 型糖尿病(T2DM)和糖尿病肾病(DN)患者血浆中 miR-223 的表达及其临床意义。研究方法采用实时定量 PCR(qPCR)技术检测 miR-223 的表达,并进一步分析 miR-223 在 DN 中的诊断价值。结果发现,与 T2DM 组()和对照组()相比,DN 组 miR-223 表达下调。皮尔逊相关分析显示,miR-223 水平与白蛋白-肌酐比值(ACR)(r = -0.481;)、尿β2-微球蛋白(β2-MG)(r = -0.494;)、尿α1-微球蛋白(α1-MG)(r = -0.537;)、肌酐(Cr)(r = -0.664;)、胱抑素 C(Cyc-C)(r = -0.553;)和糖化血红蛋白(HbA1c)(r = -0.761;)。二元回归分析结果表明,miR-223、ACR、Cr 和 α1-MG 是 DN 的风险因素(OR:2.019、1.166、1.031 和 1.031;均为)。此外,miR-223 对 DN 具有良好的诊断价值(AUC:0.752;灵敏度:0.722;特异性:0.842)(以 2.5 作为诊断临界点)。结论:miR-223 在 DN 患者中低表达,评估 miR-223 可能是诊断 DN 的一种好方法。
{"title":"Expression and Clinical Significance of Plasma miR-223 in Patients with Diabetic Nephropathy","authors":"Xingrong Guo, Meiying Huang, Dawei Yang, Zuojie Luo","doi":"10.1155/2023/9663320","DOIUrl":"https://doi.org/10.1155/2023/9663320","url":null,"abstract":"&lt;i&gt;Background&lt;/i&gt;. MicroRNA-223 (miR-223) is associated with diabetes and kidney diseases and serves as a novel marker for diagnosing diabetic kidney disease (DKD). This study was conducted to investigate the plasma expression of miR-223 and its clinical significance in type 2 diabetes (T2DM) and diabetic nephropathy (DN) patients. &lt;i&gt;Methods&lt;/i&gt;. In this research, 20 patients with T2DM and DN, 19 patients with T2DM, and 17 healthy volunteers were finally enrolled. miR-223 expression was detected by quantitative real-time PCR (qPCR), and the diagnostic value of miR-223 in DN was further analyzed. &lt;i&gt;Results&lt;/i&gt;. miR-223 was downregulated in the DN group compared to that in the T2DM group (&lt;span&gt;&lt;svg height=\"8.8423pt\" style=\"vertical-align:-0.2064009pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.6359 19.289 8.8423\" width=\"19.289pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,0,0)\"&gt;&lt;/path&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,11.658,0)\"&gt;&lt;/path&gt;&lt;/g&gt;&lt;/svg&gt;&lt;span&gt;&lt;/span&gt;&lt;span&gt;&lt;svg height=\"8.8423pt\" style=\"vertical-align:-0.2064009pt\" version=\"1.1\" viewbox=\"22.8711838 -8.6359 28.182 8.8423\" width=\"28.182pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,22.921,0)\"&gt;&lt;/path&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,29.161,0)\"&gt;&lt;/path&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,32.125,0)\"&gt;&lt;use xlink:href=\"#g113-49\"&gt;&lt;/use&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,38.365,0)\"&gt;&lt;/path&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,44.605,0)\"&gt;&lt;/path&gt;&lt;/g&gt;&lt;/svg&gt;)&lt;/span&gt;&lt;/span&gt; and the control group (&lt;span&gt;&lt;svg height=\"9.2729pt\" style=\"vertical-align:-0.6370001pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.6359 19.289 9.2729\" width=\"19.289pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,0,0)\"&gt;&lt;use xlink:href=\"#g113-81\"&gt;&lt;/use&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,11.658,0)\"&gt;&lt;/path&gt;&lt;/g&gt;&lt;/svg&gt;&lt;span&gt;&lt;/span&gt;&lt;span&gt;&lt;svg height=\"9.2729pt\" style=\"vertical-align:-0.6370001pt\" version=\"1.1\" viewbox=\"22.8711838 -8.6359 28.182 9.2729\" width=\"28.182pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http://www.w3.org/1999/xlink\"&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,22.921,0)\"&gt;&lt;use xlink:href=\"#g113-49\"&gt;&lt;/use&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,29.161,0)\"&gt;&lt;use xlink:href=\"#g113-47\"&gt;&lt;/use&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,32.125,0)\"&gt;&lt;use xlink:href=\"#g113-49\"&gt;&lt;/use&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,38.365,0)\"&gt;&lt;use xlink:href=\"#g113-49\"&gt;&lt;/use&gt;&lt;/g&gt;&lt;g transform=\"matrix(.013,0,0,-0.013,44.605,0)\"&gt;&lt;use xlink:href=\"#g113-50\"&gt;&lt;/use&gt;&lt;/g&gt;&lt;/svg&gt;).&lt;/span&gt;&lt;/span&gt; Pearson’s correlation analysis showed a negative correlation of miR-223 levels with an albumin-creatinine ratio (ACR) (&lt;i&gt;r&lt;/i&gt; = −0.481; &lt;span&gt;&lt;svg height=\"8.8423pt\" style=\"vertical-align:-0.2064009pt\" version=\"1.1\" viewbox=\"-0.0498162 -8.6359 19.289 8.8423\" width=\"19.289pt\" xmlns=\"http://www.w3.org/2000/svg\" xmlns:xlink=\"http:","PeriodicalId":13966,"journal":{"name":"International Journal of Endocrinology","volume":"8 1","pages":""},"PeriodicalIF":2.8,"publicationDate":"2023-12-27","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139057285","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Current Status of Metabolic Compliance and Risk of Cardiovascular Disease in Patients with Type 2 Diabetes in the Zhuang Population in China 中国壮族 2 型糖尿病患者的代谢顺应性和心血管疾病风险现状
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2023-12-22 DOI: 10.1155/2023/1057121
Danqing Xu, Xia Dai, Qiong Yang, Xueying Li, Ying Xiao, Qiuhong Huang, undefined Qingqing Lou
Introduction. This study aimed to investigate the blood glucose, blood pressure, and blood lipid status in Zhuang patients with T2DM and to analyze the correlation between compliance with metabolic monitoring and cardiovascular risk factors. Methods. A total of 1975 Zhuang patients with T2DM were evaluated in four Class III Grade A hospitals in three prefecture-level cities in the Guangxi Zhuang Autonomous Region between January and August 2022. Laboratory indicators, lifestyle, and demographic characteristics were collected. Results. The compliance rates for blood glucose, blood pressure, and blood lipids were 26.08%, 45.77%, and 30.58%, respectively, and only 5.06% of the patients reached the standard in all three indices. The compliance rates for blood glucose, blood pressure, and blood lipids in the CVD group were 32.92%, 21.74%, and 9.94%, respectively. In the CVD group, the usage rates of hypoglycemic, antihypertensive, and lipid-lowering drugs were 77.54%, 3.17%, and 4.11%, respectively. Binary logistic regression analysis showed that older age (OR = 1.033, 95% CI [1.016, 1.050]), female (OR = 0.402, 95% CI [0.260, 0.621]), smoke (OR = 1.994, 95% CI [1.361, 2.922]), blood pressure noncompliance + use of antihypertensive drugs (OR = 0.348, 95% CI [0.230, 0.527]), and blood lipid noncompliance + use of lipid-lowering drugs (OR = 0.244, 95% CI [0.142, 0.417]) were risk factors for CVDs, and moderate-intensity exercise (OR = 0.439, 95% CI [0.300,0.640]) was protective against CVD. Conclusions. Older age, female, smoke, blood lipid levels, and blood pressure noncompliance were risk factors for CVD while moderate-intensity exercise was observed to be protective.
简介本研究旨在调查壮族 T2DM 患者的血糖、血压和血脂状况,并分析代谢监测依从性与心血管危险因素之间的相关性。研究方法2022 年 1 月至 8 月期间,广西壮族自治区三个地级市的四家三级甲等医院共对 1975 名壮族 T2DM 患者进行了评估。收集了实验室指标、生活方式和人口统计学特征。结果显示血糖、血压和血脂的达标率分别为 26.08%、45.77% 和 30.58%,三项指标均达标的患者仅占 5.06%。心血管疾病组的血糖、血压和血脂达标率分别为 32.92%、21.74% 和 9.94%。在心血管疾病组中,降糖药、降压药和降脂药的使用率分别为 77.54%、3.17% 和 4.11%。二元逻辑回归分析显示,年龄较大(OR = 1.033,95% CI [1.016,1.050])、女性(OR = 0.402,95% CI [0.260,0.621])、吸烟(OR = 1.994,95% CI [1.361,2.922])、血压不达标+使用降压药(OR = 0.348,95% CI [0.230,0.527])和血脂不达标+使用降脂药(OR = 0.244,95% CI [0.142,0.417])是心血管疾病的危险因素,而中等强度运动(OR = 0.439,95% CI [0.300,0.640])对心血管疾病有保护作用。结论高龄、女性、吸烟、血脂水平和血压不达标是心血管疾病的危险因素,而中等强度的运动对心血管疾病有保护作用。
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引用次数: 0
Adrenal Vein Sampling in the Management of Primary Aldosteronism: The Added Value of Intraprocedural Cortisol Assessment 肾上腺静脉取样在原发性醛固酮增多症治疗中的应用:术中皮质醇评估的附加价值
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2023-12-21 DOI: 10.1155/2023/5563881
Inês Manique, Sara Amaral, Alexandra Matias, Bruno Bouça, Salomé Serranito, João Torres, Olga Gutu, Tiago Bilhim, Élia Coimbra, Isaura Rodrigues, Conceição Godinho, Luísa Cortez, José Silva-Nunes
<i>Introduction</i>. Primary aldosteronism is the most common cause of secondary hypertension. Adrenal vein sampling is the gold standard for subtyping primary aldosteronism. However, this procedure is technically challenging and often has a low success rate. Our center is one of the very few performing this technique in our country with an increasing experience. <i>Objective</i>. The aim of this study was to evaluate the role of the cortisol intraprocedural assay in improving the performance of adrenal vein sampling. <i>Design</i>. We enrolled all of the patients with primary aldosteronism that underwent adrenal vein sampling from February 2016 to April 2023. The cortisol intraprocedural assay was introduced in October 2021. <i>Methods</i>. We enrolled a total of 50 adrenal vein samplings performed on 43 patients with the diagnosis of primary aldosteronism. In this sample, 19 patients and 24 patients underwent adrenal vein sampling before and after intraprocedural cortisol measurement, respectively. The procedure was repeated in seven patients (one before and six after intraprocedural cortisol measurement), given the unsuccess of the first exam. Selectivity of the adrenal vein sampling was assumed if the serum cortisol concentration from the adrenal vein was at least five times higher than that of the inferior vena cava. Lateralization was assumed if the aldosterone to cortisol ratio of one adrenal vein was at least four times the aldosterone to cortisol ratio of the contralateral side. <i>Results</i>. The mean age of the patients that underwent adrenal vein sampling (<i>N</i> = 43) was 55.2 ± 8.9 years, and 53.5% (<i>n</i> = 23) were female. The mean interval between the diagnosis of hypertension and the diagnosis of primary aldosteronism was 9.8 years (±9.9). At diagnosis, 62.8% of the patients (<i>n</i> = 27) had hypokalemia (mean value of 3 mmol/L (±0.34)), 88.4% (<i>n</i> = 38) had adrenal abnormalities on preprocedural CT scan, and 67.4% (<i>n</i> = 29) described as unilateral nodules. There were no statistically significant differences in the patients’ baseline characteristics between the two groups (before and after intraprocedural cortisol measurement). Before intraprocedural cortisol measurement, adrenal vein sampling selectivity was achieved in 35% (<i>n</i> = 7) patients. Selectivity increased to 100% (30/30) after intraprocedural cortisol measurement (<span><svg height="11.7782pt" style="vertical-align:-3.42938pt" version="1.1" viewbox="-0.0498162 -8.34882 18.973 11.7782" width="18.973pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink"><g transform="matrix(.013,0,0,-0.013,0,0)"></path></g><g transform="matrix(.013,0,0,-0.013,11.342,0)"></path></g></svg><span></span><span><svg height="11.7782pt" style="vertical-align:-3.42938pt" version="1.1" viewbox="22.555183800000002 -8.34882 28.184 11.7782" width="28.184pt" xmlns="http://www.w3.org/2000/svg" xmlns:xlink="http://www.w3.org/1999/xlink"><g transform="ma
简介原发性醛固酮增多症是继发性高血压最常见的病因。肾上腺静脉取样是对原发性醛固酮增多症进行分型的金标准。然而,这项手术在技术上具有挑战性,而且成功率往往很低。我们中心是我国为数不多的开展此项技术的中心之一,经验也在不断增加。研究目的本研究旨在评估皮质醇术中测定在提高肾上腺静脉采样成功率方面的作用。设计。我们招募了 2016 年 2 月至 2023 年 4 月期间接受肾上腺静脉取样的所有原发性醛固酮增多症患者。皮质醇术中测定于 2021 年 10 月引入。方法。我们共对 43 名确诊为原发性醛固酮增多症的患者进行了 50 次肾上腺静脉采样。在这些样本中,19 名患者和 24 名患者分别在术中皮质醇测定之前和之后进行了肾上腺静脉取样。由于第一次检查不成功,有 7 名患者(1 名患者在术中皮质醇测量前,6 名患者在术中皮质醇测量后)重复了这一过程。如果肾上腺静脉的血清皮质醇浓度比下腔静脉的高至少五倍,则认为肾上腺静脉采样具有选择性。如果一侧肾上腺静脉的醛固酮与皮质醇之比至少是对侧肾上腺静脉的醛固酮与皮质醇之比四倍,则假定肾上腺静脉采样具有侧向性。结果接受肾上腺静脉采样的患者(43 人)的平均年龄为 55.2 ± 8.9 岁,53.5%(23 人)为女性。从确诊高血压到确诊原发性醛固酮增多症的平均间隔时间为 9.8 年(±9.9)。确诊时,62.8% 的患者(n = 27)患有低钾血症(平均值为 3 mmol/L (±0.34)),88.4% 的患者(n = 38)在手术前 CT 扫描中发现肾上腺异常,67.4% 的患者(n = 29)描述为单侧结节。两组患者的基线特征(术前和术中皮质醇测量前后)差异无统计学意义。在术中皮质醇测量前,35%(7 人)的患者肾上腺静脉采样选择性达标。在术中测量皮质醇后,选择性增加到 100%(30/30)()。除一名患者拒绝外,所有侧切患者均接受了单侧肾上腺切除术,术后醛固酮与肾素比值恢复正常。结论在原发性醛固酮增多症的亚型鉴定中缺乏有效的替代方法,这凸显了提高肾上腺静脉取样成功率的必要性。在这项研究中,术中皮质醇测量的选择性达到了 100%。尤其是在成功率较低的中心,应考虑将其添加到这一手术方案中。
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引用次数: 0
GLP1R rs3765467 Polymorphism Is Associated with the Risk of Early Onset Type 2 Diabetes GLP1R rs3765467 多态性与早发二型糖尿病的风险有关
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2023-12-14 DOI: 10.1155/2023/8729242
Yunyun Fang, Jingjing Zhang, Linlin Ji, Chaoyu Zhu, Yuanyuan Xiao, Qingge Gao, Wenjing Song, Li Wei
Objective. To investigate the relationship between glucagon-like peptide-1 receptor gene polymorphisms and susceptibility to early onset type 2 diabetes. Methods. Samples from 316 type 2 diabetes patients with early onset type 2 diabetes (n = 137) and late-onset type 2 diabetes (n = 179) and 145 nondiabetic individuals were analyzed. Multiplex PCR combined with resequencing Hi-Reseq technology was used to detect single nucleotide polymorphisms of the glucagon-like peptide-1 receptor gene, and the allele frequency, genotype distribution, and clinical parameters were analyzed between each diabetes subgroup and the control group. Results. Sixteen single nucleotide polymorphisms were identified in the exonic region of the glucagon-like peptide-1 receptor gene according to the minor allele frequency (MAF > 0.05) in the participants. Among these, the glucagon-like peptide-1 receptor rs3765467 (G⟶A) mutation was statistically associated with early onset type 2 diabetes. Compared with that of the GG carriers, carriers of genotype AA at rs3765467 had a decreased risk of early onset type 2 diabetes after adjusting for sex and body mass index. In the dominant model, the frequencies of the rs3765467 AA + GA genotype were significantly decreased in the early onset type 2 diabetes group, and carriers of genotype AA + GA at rs3765467 had a decreased risk of early onset type 2 diabetes after adjusting for sex and body mass index. Moreover, fasting C peptide levels were significantly higher in GA + AA genotype carriers than those in GG genotype carriers. Conclusion. The glucagon-like peptide 1 receptor rs3765467 polymorphism was significantly associated with age at type 2 diabetes diagnosis and thus may be used as a marker to screen and detect individuals at risk of developing early onset type 2 diabetes.
目标。探讨胰高血糖素样肽-1受体基因多态性与早发型2型糖尿病易感性的关系。方法。分析了316例2型糖尿病合并早发型2型糖尿病(n = 137)和晚发型2型糖尿病(n = 179)以及145例非糖尿病患者的样本。采用多重PCR联合重测序Hi-Reseq技术检测胰高血糖素样肽-1受体基因的单核苷酸多态性,并分析各糖尿病亚组与对照组之间的等位基因频率、基因型分布及临床参数。结果。根据次要等位基因频率(MAF > 0.05),在参与者的胰高血糖素样肽-1受体基因外显子区鉴定出16个单核苷酸多态性。其中,胰高血糖素样肽-1受体rs3765467 (G / A)突变与早发型2型糖尿病有统计学相关性。与GG携带者相比,rs3765467位点AA基因型携带者在调整性别和体重指数后患早发性2型糖尿病的风险降低。在优势模型中,rs3765467 AA + GA基因型的频率在早发性2型糖尿病组中显著降低,在调整性别和体重指数后,rs3765467基因型AA + GA的携带者患早发性2型糖尿病的风险降低。GA + AA基因型携带者的空腹C肽水平显著高于GG基因型携带者。结论。胰高血糖素样肽1受体rs3765467多态性与2型糖尿病诊断年龄显著相关,因此可作为筛查和检测早发性2型糖尿病高危人群的标志物。
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引用次数: 0
Factors Influencing a Favorable Outcome for RFA of Huge Benign Thyroid Nodules: Preliminary Results and Short-Term Evaluation 影响巨大良性甲状腺结节射频消融术良好疗效的因素:初步结果和短期评估
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2023-12-14 DOI: 10.1155/2023/9021903
Chun-Hua Chiu, Sheng-Dean Luo, Pi-Ling Chiang, An-Ni Lin, Cheng-Kang Wang, Chen-Kai Chou, Shun-Yu Chi, Meng-Hsiang Chen, Wei-Che Lin
Objective. This study aimed to investigate potentially favorable factors influencing the therapeutic success of radiofrequency ablation (RFA) of huge benign thyroid nodules (BTNs) (volume >100 ml) and to evaluate the feasibility of RFA as an alternative treatment modality for patients unable or unwilling to undergo surgery. Methods. This retrospective study evaluated a total of 868 patients, of which 22 patients had huge BTNs who underwent ultrasound-guided moving shot RFA treatment between May 2017 and January 2022. The huge BTNs were categorized into two groups according to a post-RFA treatment volume reduction ratio (VRR) of >80% and <80% at 6 months. Factors influencing these huge BTNs were reviewed, analyzed, and correlated with treatment effectiveness between the two groups. Results. The factors influencing an effective VRR included huge BTNs located on the left side (OR 7.875, p = 0.03), predominant solid/spongiform nodules (OR 7.875, p = 0.03), and higher initial ablation rate (IAR) (p = 0.028). Multivariable logistic regression revealed predominant solid/spongiform nodule and the higher IAR were associated with the advanced VRR. Conclusion. RFA was effective at decreasing the volume of huge BTNs with an acceptable complication rate. The BTN characteristics correlated with a better VRR at the 6-month short-term follow-up were predominant solid/spongiform BTNs and those with the first time ablation treatment initial ablation rate. Nevertheless, regarding the higher regrowth rate of these groups of patients who may need to be treated more times, RFA can only be a feasible alternative treatment modality for patients unable or unwilling to undergo operation.
目标。本研究旨在探讨影响巨大良性甲状腺结节(体积100 ml)射频消融(RFA)治疗成功的潜在有利因素,并评估射频消融作为不能或不愿接受手术治疗的患者的替代治疗方式的可行性。方法。本回顾性研究共评估了868例患者,其中22例巨大BTNs患者在2017年5月至2022年1月期间接受了超声引导的移动射击RFA治疗。根据rfa后治疗体积缩小率(VRR)为>80%和<80%, 6个月时将巨大的btn分为两组。我们对影响这些巨大BTNs的因素进行了回顾、分析,并将其与两组间的治疗效果相关联。结果。影响VRR有效的因素包括位于左侧的巨大BTNs (OR 7.875, p = 0.03),主要的实体/海海绵状结节(OR 7.875, p = 0.03)和较高的初始消融率(IAR) (p = 0.028)。多变量logistic回归显示主要为实体/海绵状结节,较高的IAR与晚期VRR相关。结论。RFA可有效减少巨大btn的体积,并发症发生率可接受。在6个月的短期随访中,与VRR较好相关的BTN特征主要是实体/海海绵状BTN和首次消融治疗的初始消融率。然而,考虑到这类患者的再生率较高,可能需要更多的治疗次数,RFA只能作为不能或不愿接受手术的患者的一种可行的替代治疗方式。
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引用次数: 0
Action Mechanisms of Metformin Combined with Exenatide and Metformin Only in the Treatment of PCOS in Obese Patients 二甲双胍联合艾塞那肽与仅使用二甲双胍治疗肥胖患者多囊卵巢综合征的作用机制
IF 2.8 4区 医学 Q3 ENDOCRINOLOGY & METABOLISM Pub Date : 2023-12-14 DOI: 10.1155/2023/4288004
Jingwen Gan, Jie Chen, Rui-lin Ma, Yan Deng, Xue-song Ding, Shi-yang Zhu, Ai-jun Sun
Background. Polycystic ovary syndrome (PCOS) is the most common endocrine disease in women of reproductive age, whose clinical characteristics are hyperandrogenism (HA), ovulatory dysfunction, and polycystic ovary, often accompanied by insulin resistance (IR) and metabolic abnormalities. Glucagon-like peptide (GLP)-1 receptor agonists (GLP-1Ra), such as exenatide, can bind to specific receptors on tissues such as the ovaries to improve the clinical phenotype of PCOS, while insulin-sensitizing agents, such as metformin, can also benefit to metabolic abnormalities in PCOS. Liquid chromatography-mass spectrometry (LC/MS) metabolomics revealed differences between the mechanisms of exenatide and metformin treatment of PCOS to some extent. Methods. In this study, 50 obese subjects with PCOS were randomly divided into the exenatide combined with metformin group (COM group, n = 28) and the metformin group (MF group, n = 22) for 12-week treatment. Before and after, serum samples were subjected to LC/MS analysis. Results. After treatment, there were 153 named differential metabolites in the COM group and 99 in the MF group. Most phosphatidylcholines (PC) and deoxycholic acid 3-glucuronide (DA3G) were significantly upregulated, while most glycerophosphoethanolamine (PE-NMe2), glycerophosphocholine (GPC), and threonine were downregulated in both groups. Only the decrease of neuromedin B, glutamate, and glutamyl groups and the increase of chenodeoxycholic acid sulfate docosadienoate (22: 2n6), and prostaglandin E2 have been observed in the COM group. In addition, salicylic acid and spisulosine increased and decanoylcarnitine decreased in the MF group. Both groups were enriched in glycerophospholipid, choline, and sphingolipid metabolism, while the COM group was especially superior in the glutamine and glutamate, bile secretion, and amino acid metabolism. Conclusion. Compared with metformin alone in the treatment of PCOS, the differential metabolites of the exenatide combined with metformin group are more extensive. The COM group may act on the hypothalamic-pituitary-gonadal axis (HPO) and its bypass, regulate multiple metabolism pathways such as phospholipids, amino acids, fatty acids, carnitine, bile acids, and glucose directly or indirectly in obese PCOS patients.
背景。多囊卵巢综合征(Polycystic ovarian syndrome, PCOS)是育龄妇女最常见的内分泌疾病,其临床特征为雄激素分泌过多(hyperandrogenism, HA)、排卵功能障碍、多囊卵巢,常伴有胰岛素抵抗(insulin resistance, IR)和代谢异常。胰高血糖素样肽(GLP)-1受体激动剂(GLP- 1ra)如艾塞那肽可与卵巢等组织上的特异性受体结合,改善PCOS的临床表型,而胰岛素增敏剂如二甲双胍也可有益于PCOS的代谢异常。液相色谱-质谱(LC/MS)代谢组学分析显示艾塞那肽与二甲双胍治疗PCOS的作用机制存在一定差异。方法。本研究将50例肥胖多囊卵巢综合征患者随机分为艾塞那肽联合二甲双胍组(COM组,n = 28)和二甲双胍组(MF组,n = 22),治疗12周。前后血清样品进行LC/MS分析。结果。治疗后,COM组有153个命名的差异代谢物,MF组有99个。两组中大部分磷脂酰胆碱(PC)和脱氧胆酸3-葡糖苷(DA3G)均显著上调,而大部分甘油磷酸乙醇胺(PE-NMe2)、甘油磷酸胆碱(GPC)和苏氨酸均下调。COM组仅神经素B、谷氨酸、谷氨酰基降低,硫酸鹅去氧胆酸(22:22 . 6)、前列腺素E2升高。此外,MF组水杨酸和葡聚糖含量升高,十二烷基肉碱含量降低。两组的甘油磷脂、胆碱和鞘脂代谢均丰富,而COM组在谷氨酰胺和谷氨酸、胆汁分泌和氨基酸代谢方面尤为突出。结论。与单用二甲双胍治疗PCOS相比,艾塞那肽联合二甲双胍组差异代谢物更广泛。COM组可能作用于下丘脑-垂体-性腺轴(HPO)及其旁路,直接或间接调节肥胖PCOS患者的磷脂、氨基酸、脂肪酸、肉碱、胆汁酸、葡萄糖等多种代谢途径。
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International Journal of Endocrinology
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