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Therapeutic effects and complications of simplified pericardial devascularization for patients with portal hypertension. 门静脉高压症患者简化心包血管切断术的治疗效果和并发症。
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-08-15 eCollection Date: 2015-01-01
Hongwei Lu, Sida Liu, Yafei Zhang, Hao Shang, Hong Ji, Yiming Li

Objectives: To evaluate the therapeutic effects and complications of simplified pericardial devascularization for patients with portal hypertension.

Methods: By means of prospective study, 212 patients who underwent simplified pericardial devascularization (Group A) and 309 patients who underwent traditional pericardial devascularization (Group B) were followed up from 2003' to 2011'. Results were performed with the general condition of the patients and the incidence of complications to assess the value of the two operating methods.

Results: The operating time was 1.0-3.83 hours (mean 1.94 ± 0.32 hours) in Group A versus 1.67-4.50 hours (mean 2.86 ± 0.40 hours) in Group B. The amount of bleeding, postoperative hospital stay and hospitalization expenses were 110-500 ml (mean 224.81 ± 78.44 ml), 7-22 days (mean 10.41 ± 4.01 days) and 15700-27500 yuan with an average of 19300 ± 1600 yuan in Group A and 200-700 ml (mean 423.50 ± 85.19 ml), 9-32 days (mean 14.76 ± 4.52 days) and 18700-44500 yuan with an average of 23400 ± 2200 yuan in Group B. In September 2012', successful follow-up was completed for 438 patients, of which, 181 underwent the simplified devascularization with 31 patients lost (follow-up rate 85.4%). Meanwhile, 257 patients in Group B were followed up completely and 52 patients were lost (follow-up rate 83.2%). The follow-up time ranged from 1 to 9.5 years and the average time was 5.03 ± 2.13 years. The mortality, rebleeding rate, rate of hepatic encephalopathy, rate of ascites and the incidence of gastric fistula and (or) esophageal fistula were 6.1%, 6.1%, 1.7%, 8.3% and 0 in Group A versus 14.0%, 15.2%, 4.3%, 17.7% and 3.1% in Group B.

Conclusions: The final results suggested that simplified pericardial devascularization performed more effectively and conveniently than the traditional method, depending on the mitigated operative wound and the shortened operation time. We concluded that simplified pericardial devascularization was better in treatment of portal hypertension compared than the traditional method.

目的评估简化心包血管扩张术对门静脉高压症患者的治疗效果和并发症:通过前瞻性研究,对 2003 年至 2011 年接受简化心包血管扩张术的 212 例患者(A 组)和接受传统心包血管扩张术的 309 例患者(B 组)进行随访。结果与患者的一般情况和并发症的发生率进行比较,以评估两种手术方法的价值:A组手术时间为1.0-3.83小时(平均1.94±0.32小时),B组为1.67-4.50小时(平均2.86±0.40小时);A组出血量、术后住院时间和住院费用分别为110-500毫升(平均224.81±78.44毫升)、7-22天(平均10.41±4.01天)和15700-27500元,平均19300±1600元;B组出血量、术后住院时间和住院费用分别为200-700毫升(平均423.2012年9月',成功完成了438例患者的随访,其中181例患者接受了简化去血管术,31例患者失访(随访率85.4%)。同时,对 B 组的 257 名患者进行了完整的随访,52 名患者失访(随访率为 83.2%)。随访时间从 1 年到 9.5 年不等,平均为 5.03±2.13 年。A组的死亡率、再出血率、肝性脑病率、腹水率和胃瘘及(或)食管瘘发生率分别为6.1%、6.1%、1.7%、8.3%和0,而B组分别为14.0%、15.2%、4.3%、17.7%和3.1%:最终结果表明,简化心包血管置换术比传统方法更有效、更方便,这取决于手术伤口的减轻和手术时间的缩短。我们认为,简化心包血管置换术治疗门静脉高压症的效果优于传统方法。
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引用次数: 0
Investigation of relationship of visceral body fat and inflammatory markers with metabolic syndrome and its components among apparently healthy individuals. 内脏脂肪和炎症标志物与代谢综合征及其组成部分之间关系的调查。
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-08-15 eCollection Date: 2015-01-01
Yasemin Turker, Davut Baltaci, Yasin Turker, Serkan Ozturk, Cemil Isik Sonmez, Mehmet Harun Deler, Yunus Cem Sariguzel, Feyza Sariguzel, Handan Ankarali

Metabolic syndrome is a cluster of disorders and great risk for cardiovascular diseases. We aimed to investigate association between severity of metabolic syndrome (MetS) and anthropometric measurements, and to evaluate correlation of MetS and its components with metabolic deterioration and inflammatory indexes. The cross-sectional study enrolled 1474 patients with obesity and overweight. The patients were grouped as MetS and Non-MetS, and were sub-grouped as group 1 (three criteria), 2 (four criteria) and 3 (≥ five criteria) according to NCEP ATP III. Mean age was 38.7 ± 11.9 years and BMI was 35.1 ± 6.3 kg/m(2). Lipid profile, anthropometric and blood pressure measurements, liver function tests, bioelectric impedance body fat compositions, insulin resistance and HbA1c, and spot urinary albumin-creatinine ratio were significantly different between groups of MetS and Non-MetS. Age, lipid profile, bioelectric impedance fat analyses, BMI, blood pressure values, glucose, insulin resistance, uric acid and hs-CRP levels were significantly different between groups of MetS component groups. ROC analysis revealed that hs-CRP was found to be more predictive for severity of metabolic syndrome components 3 and 4 (P=0.030); uric acid and visceral fat were more actual to predict severity of metabolic syndrome between 3 and 5 MetS components, (P=0.006) and uric acid was detected as more actual to predict severity of MetS between 4 and 5 components (P=0.023). In conclusion, uric acid, hs-CRP and visceral body fat composition were useful to predict to severity of MetS in primary care.

代谢综合征是一组疾病,是心血管疾病的高危因素。我们旨在研究代谢综合征(MetS)的严重程度与人体测量值之间的关系,并评估代谢综合征及其组成部分与代谢恶化和炎症指数之间的相关性。这项横断面研究共纳入了 1474 名肥胖和超重患者。根据 NCEP ATP III 将患者分为 MetS 和非 MetS 两组,并将其细分为 1 组(3 项标准)、2 组(4 项标准)和 3 组(≥ 5 项标准)。平均年龄为 38.7 ± 11.9 岁,体重指数为 35.1 ± 6.3 kg/m(2)。血脂概况、人体测量和血压测量、肝功能检测、生物电阻抗体脂构成、胰岛素抵抗和 HbA1c 以及定点尿白蛋白-肌酐比值在 MetS 组和非 MetS 组之间存在显著差异。MetS 组与非 MetS 组之间在年龄、血脂概况、生物电阻抗脂肪分析、体重指数、血压值、血糖、胰岛素抵抗、尿酸和 hs-CRP 水平方面存在明显差异。ROC 分析显示,hs-CRP 对代谢综合征第 3 和第 4 部分的严重程度更有预测作用(P=0.030);尿酸和内脏脂肪对代谢综合征第 3 和第 5 部分的严重程度更有预测作用(P=0.006);尿酸对代谢综合征第 4 和第 5 部分的严重程度更有预测作用(P=0.023)。总之,尿酸、hs-CRP和内脏脂肪组成有助于预测初级保健中 MetS 的严重程度。
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引用次数: 0
Decreased mean platelet volume is associated with the developing stage of fetoplacental unit in spontaneous abortion. 自然流产时平均血小板体积减少与胎胎盘单位发育阶段有关。
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Mustafa Kaplanoglu, Tuncay Yuce, Mehmet Bulbul

Aim: The aim was to evaluate the place of mean platelet volume (MPV) in predicting spontaneous miscarriage and to identify any differences in its values following miscarriage after biochemical and clinical pregnancy.

Material and method: We retrospectively evaluated the data of 305 spontaneous miscarriages and 168 control subjects. The miscarriage subjects were evaluated in two groups: miscarriage after biochemical pregnancy (n=79) (BA group) and miscarriage after clinical pregnancy (n=226) (CA group). Demographic and laboratory data of all subjects were statistically compared.

Results: No statistically significant difference was found between the miscarriage and control subjects in terms of demographic data and Hb, Htc, WBC, and Plt values. The mean platelet volume (MPV) value in the miscarriage group (8.99±1.47 fl) was statistically significantly lower than in the control group (9.66±1.64 fl) (P<0.001). A statistically significant difference was present between the BA, CA and control group, with the lowest MPV value in the BA group (8.64±1.34 fl, 9.11±1.49 fl, and 9.66±1.64 fl, respectively) (P<0.001).

Discussion: MPV was significantly lower in patients with miscarriage than the control group, and this was correlated with the gestational stage when the miscarriage occurred.

目的:目的是评估平均血小板体积(MPV)在预测自然流产中的地位,并确定生化和临床妊娠后流产后其值的差异。材料与方法:回顾性分析305例自然流产患者和168例对照患者的资料。将流产受试者分为两组:生化妊娠后流产(n=79) (BA组)和临床妊娠后流产(n=226) (CA组)。对所有受试者的人口学和实验室数据进行统计学比较。结果:流产组与对照组的人口统计学数据及Hb、Htc、WBC、Plt值均无统计学差异。流产组平均血小板体积(MPV)值(8.99±1.47 fl)低于对照组(9.66±1.64 fl),差异有统计学意义(p讨论:流产患者血小板体积(MPV)明显低于对照组,且与流产发生时的妊娠期有关。
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引用次数: 0
XRCC1 Arg399Gln polymorphism is not associated with breast cancer in Chinese. 中国人乳腺癌与XRCC1 Arg399Gln多态性无关
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Shuren Guo, Xiaohuan Mao, Liang Ming

Background: A number of studies have been conducted to explore the association of XRCC1 polymorphisms with Breast cancer (BC) risk in Asians, but the results have been inconsistent. We therefore performed the present meta-analysis to explore the relationship in detail.

Materials and methods: Reported studies were searched from 1990 to October 15, 2014 in PubMed and Wan fang Med Online. We performed a meta-analysis of 13 published case-control studies fitting our eligibility criteria. These studies involved XRCC1 Arg399Gln polymorphisms in 4984 BC cases and 5744 controls in dominant (ArgArg vs. GlnGln+ArgGln), recessive (ArgGln+ArgArg vs. GlnGln), and co-dominant (ArgArg vs. GlnGln) inheritance models. The total odds Ratio (OR) and 95% CI were calculated and analyzed by Review Manager 5.2 and STATE 12.

Results: Overall, significantly increased BC risk was observed in any genetic model (dominant model: odds ration [OR] = 1.31, 95% confidence interval [CI] = [1.08, 1.58]; recessive model: OR = 0.63, 95% CI = [0.50, 0.81]; codominant model: OR = 2.52, 95% CI: [1.38, 4.60]) when all eligible studies were pooled into the meta-analysis. In further stratified analyses, no association was found between Arg399Gln polymorphism and BC risk in Chinese fewer than three hereditary models.

Conclusions: Our results suggest that the XRCC1 Arg399Gln polymorphism may be associated with increased Breast cancer risk among Asians, except Chinese population.

背景:已经进行了许多研究来探索XRCC1多态性与亚洲人乳腺癌(BC)风险的关系,但结果并不一致。因此,我们进行了本荟萃分析来详细探讨这种关系。材料和方法:检索PubMed和万方医学在线1990年至2014年10月15日所报道的研究。我们对符合我们入选标准的13项已发表的病例对照研究进行了荟萃分析。这些研究涉及4984例BC病例和5744例对照中显性(ArgArg vs. GlnGln+ArgGln)、隐性(ArgGln+ArgArg vs. GlnGln)和共显性(ArgArg vs. GlnGln)遗传模型的XRCC1 Arg399Gln多态性。通过Review Manager 5.2和STATE 12计算和分析总优势比(OR)和95% CI。结果:总体而言,在任何遗传模型中都观察到BC风险显著增加(优势模型:优势比[OR] = 1.31, 95%可信区间[CI] = [1.08, 1.58];隐性模型:OR = 0.63, 95% CI = [0.50, 0.81];共优势模型:OR = 2.52, 95% CI:[1.38, 4.60]),将所有符合条件的研究纳入meta分析。在进一步的分层分析中,在少于三个遗传模型的中国人中,没有发现Arg399Gln多态性与BC风险之间的关联。结论:我们的研究结果表明,XRCC1 Arg399Gln多态性可能与亚洲人乳腺癌风险增加有关,中国人群除外。
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引用次数: 0
Folic acid in combination with adult neural stem cells for the treatment of spinal cord injury in rats. 叶酸联合成体神经干细胞治疗大鼠脊髓损伤。
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Chen Zhang, Lin Shen

Purpose: To observe the therapeutic effect of folic acid in combination with adult neural stem cells on spinal cord injury and to investigate the possible mechanism.

Methods: A total of 120 Wistar rats were randomly assigned to six groups: normal, model, sham-surgery, folic acid injection, adult neural stem cell transplantation, and combination (folic acid injection + adult neural stem cells transplantation) groups. Morphology of neural stem cells was observed by inverted microscopy. Expression of CD105, CD45, CD44, and CD29 were detected by flow cytometry; expression of neuron-specific enolase and glial fibrillary acidic protein were determined by immunofluorescence. Motor coordination and integration capabilities were assessed using BBB scores; Morphology of spinal cord tissues was observed by hematoxylin-eosin staining and 5-bromodeoxyuridine immunohistochemistry. GDNF, BDNF and NT-3 expression in spinal cord tissues were determined by ELISA; while expression of the apoptosis-related proteins BCL-2, Bax and caspase-3 was detected using western blotting.

Results: Flow cytometry showed that the isolated cells were positive for CD44 and CD29 and negative for CD105 and CD45. Combination treatment significantly improved the behavior of model rats with spinal cord injury, attenuated inflammatory reaction of spinal cord tissues, restored injured nerve cells, and increased expression of GDNF, BDNF and NT-3 in spinal cord tissues, up regulated BCL-2 expression, and down regulated Bax and caspase-3 expression.

Conclusions: Folic acid in combination with adult neural stem cells significantly improved nerve function and plays a key role in maintaining microenvironment homeostasis in the neurons of rats with spinal cord injury.

目的:观察叶酸联合成体神经干细胞治疗脊髓损伤的疗效,并探讨其可能的机制。方法:将120只Wistar大鼠随机分为正常组、模型组、假手术组、叶酸注射组、成体神经干细胞移植组、叶酸注射组+成体神经干细胞移植组6组。倒置显微镜观察神经干细胞形态。流式细胞术检测CD105、CD45、CD44、CD29的表达;免疫荧光法检测神经元特异性烯醇化酶和胶质原纤维酸性蛋白的表达。采用BBB评分评估运动协调和整合能力;采用苏木精-伊红染色和5-溴脱氧尿苷免疫组化观察脊髓组织形态。ELISA法检测脊髓组织中GDNF、BDNF、NT-3的表达;western blotting检测凋亡相关蛋白BCL-2、Bax和caspase-3的表达。结果:流式细胞术显示分离细胞CD44、CD29阳性,CD105、CD45阴性。联合治疗可显著改善脊髓损伤模型大鼠行为,减轻脊髓组织炎症反应,恢复损伤神经细胞,脊髓组织中GDNF、BDNF、NT-3表达增加,上调BCL-2表达,下调Bax、caspase-3表达。结论:叶酸联合成体神经干细胞可显著改善脊髓损伤大鼠神经功能,并在维持神经元微环境稳态中起关键作用。
{"title":"Folic acid in combination with adult neural stem cells for the treatment of spinal cord injury in rats.","authors":"Chen Zhang,&nbsp;Lin Shen","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Purpose: </strong>To observe the therapeutic effect of folic acid in combination with adult neural stem cells on spinal cord injury and to investigate the possible mechanism.</p><p><strong>Methods: </strong>A total of 120 Wistar rats were randomly assigned to six groups: normal, model, sham-surgery, folic acid injection, adult neural stem cell transplantation, and combination (folic acid injection + adult neural stem cells transplantation) groups. Morphology of neural stem cells was observed by inverted microscopy. Expression of CD105, CD45, CD44, and CD29 were detected by flow cytometry; expression of neuron-specific enolase and glial fibrillary acidic protein were determined by immunofluorescence. Motor coordination and integration capabilities were assessed using BBB scores; Morphology of spinal cord tissues was observed by hematoxylin-eosin staining and 5-bromodeoxyuridine immunohistochemistry. GDNF, BDNF and NT-3 expression in spinal cord tissues were determined by ELISA; while expression of the apoptosis-related proteins BCL-2, Bax and caspase-3 was detected using western blotting.</p><p><strong>Results: </strong>Flow cytometry showed that the isolated cells were positive for CD44 and CD29 and negative for CD105 and CD45. Combination treatment significantly improved the behavior of model rats with spinal cord injury, attenuated inflammatory reaction of spinal cord tissues, restored injured nerve cells, and increased expression of GDNF, BDNF and NT-3 in spinal cord tissues, up regulated BCL-2 expression, and down regulated Bax and caspase-3 expression.</p><p><strong>Conclusions: </strong>Folic acid in combination with adult neural stem cells significantly improved nerve function and plays a key role in maintaining microenvironment homeostasis in the neurons of rats with spinal cord injury.</p>","PeriodicalId":13892,"journal":{"name":"International journal of clinical and experimental medicine","volume":"8 7","pages":"10471-80"},"PeriodicalIF":0.1,"publicationDate":"2015-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565220/pdf/ijcem0008-10471.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34183645","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Promising potency of retinoic acid-poly(ethylene glycol)-thiol gold nanoparticle conjugates for cervical cancer treatment. 维甲酸-聚乙二醇-硫醇金纳米颗粒偶联物治疗宫颈癌的前景看好。
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Li Ye, Qian Song

We investigated the effect of synthesized retinoic acid-poly(ethylene glycol)-thiol gold nanoparticle conjugates on cervical carcinoma cells. Cervical cancer is the major cause of deaths for the women of reproductive age in the developing countries. Compared to retinoic acid, the nanoparticle conjugates exhibited better activity against cervical carcinoma. Selective delivery of gold nanoparticle conjugates to estrogen receptor positive cervical cancer cells with 6-fold enhanced drug potency was observed. Transfer of gold nanoparticles was found to be dominated by estrogen ligand and receptor. It appeared that retinoic acid nanoparticle conjugates were selectively taken and retained by the estrogen receptor alpha present in the plasma membrane. Thus IC50 values for RA-PEG-SH were significantly improvedon nanoparticle ligation. Cells on treatment with RA-PEG-SH-AuNPsshowed growth inhibition at 12 and 24 h after incubation. The IC50 for RA in RA-PEG-SH-AuNPs after 12 and 24 h were 3 and 1 μM, respectively. Thus, the use of RA nanoparticle conjugates can be a better strategy for cervical carcinoma treatment.

研究了合成的维甲酸-聚乙二醇-硫醇金纳米颗粒偶联物对宫颈癌细胞的作用。宫颈癌是发展中国家育龄妇女死亡的主要原因。与维甲酸相比,纳米粒子缀合物对宫颈癌具有更好的活性。观察到金纳米颗粒偶联物选择性递送至雌激素受体阳性宫颈癌细胞,其药物效力增强6倍。发现金纳米颗粒的转移受雌激素配体和受体的支配。维甲酸纳米颗粒缀合物似乎被存在于质膜中的雌激素受体α选择性地摄取和保留。因此,纳米颗粒连接显著提高了RA-PEG-SH的IC50值。用ra - peg - sh - aunps处理的细胞在孵育后12和24小时表现出生长抑制。RA- peg - sh - aunps在12 h和24 h的IC50分别为3 μM和1 μM。因此,使用RA纳米颗粒偶联物可能是宫颈癌治疗的更好策略。
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引用次数: 0
Neutrophil-lymphocyte ratio in systemic lupus erythematosus disease: a retrospective study. 系统性红斑狼疮中性粒细胞-淋巴细胞比率的回顾性研究。
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Lixiu Li, Yuncheng Xia, Chunmei Chen, Ping Cheng, Canhui Peng

Background: Systemic lupus erythematosus (SLE) is a chronic autoimmune disease. Lupus nephritis (LN) is an important cause of morbidity and even mortality in patients with SLE. Some evidences suggest that neutrophil-lymphocyte ratio (NLR) associated with different inflammatory malignancies, ischemic injury and cardiovascular disease. Few scholars have investigated the relationship between NLR and SLE. This study aims to evaluate the role of NLR in SLE without nephritis and LN patients.

Methods: A total of 228 subjects were participated in this study. 79 diagnosed with SLE in patients group and 149 healthy age-and sex-matched in control group. In patient team, 20 of them were diagnosed with LN.

Results: The SLE without nephritis group showed significantly higher NLR than control group (control=2.00±0.76, SLE=4.26±3.38, P<0.001), and the NLR values of the patients with LN were higher than those of the patients without LN (SLE=4.26±3.38, LN=7.21±6.01, P<0.001). Receiver-operating characteristics analysis (ROC) of NLR to predict SLE showed that the area under the curve (AUC) was 0.757. The cutoff value using the ROC curve was 3.13 (sensitivity, 0.574; specificity, 0.926; 95% confidence interval (CI), 0.668-0.845; P<0.001). While ROC analysis of NLR to predict LN showed that the AUC was 0.828). Logistic regression analysis showed that SLE without nephritis and LN were independently related to NLR.

Conclusion: NLR is independently associated with SLE, and it may be a promising marker that reflects renal involvement in patients with SLE.

背景:系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病。狼疮性肾炎(LN)是SLE患者发病甚至死亡的重要原因。一些证据表明,中性粒细胞-淋巴细胞比率(NLR)与不同的炎性恶性肿瘤、缺血性损伤和心血管疾病有关。很少有学者研究NLR与SLE的关系。本研究旨在评估NLR在SLE无肾炎和LN患者中的作用。方法:共228名受试者参与本研究。患者组有79例SLE患者,对照组有149例年龄和性别匹配的健康人。在患者组中,其中20人被诊断为LN。结果:SLE无肾炎组NLR明显高于对照组(对照组=2.00±0.76,SLE=4.26±3.38)。结论:NLR与SLE独立相关,可能是反映SLE患者肾脏受累的有希望的标志物。
{"title":"Neutrophil-lymphocyte ratio in systemic lupus erythematosus disease: a retrospective study.","authors":"Lixiu Li,&nbsp;Yuncheng Xia,&nbsp;Chunmei Chen,&nbsp;Ping Cheng,&nbsp;Canhui Peng","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Background: </strong>Systemic lupus erythematosus (SLE) is a chronic autoimmune disease. Lupus nephritis (LN) is an important cause of morbidity and even mortality in patients with SLE. Some evidences suggest that neutrophil-lymphocyte ratio (NLR) associated with different inflammatory malignancies, ischemic injury and cardiovascular disease. Few scholars have investigated the relationship between NLR and SLE. This study aims to evaluate the role of NLR in SLE without nephritis and LN patients.</p><p><strong>Methods: </strong>A total of 228 subjects were participated in this study. 79 diagnosed with SLE in patients group and 149 healthy age-and sex-matched in control group. In patient team, 20 of them were diagnosed with LN.</p><p><strong>Results: </strong>The SLE without nephritis group showed significantly higher NLR than control group (control=2.00±0.76, SLE=4.26±3.38, P<0.001), and the NLR values of the patients with LN were higher than those of the patients without LN (SLE=4.26±3.38, LN=7.21±6.01, P<0.001). Receiver-operating characteristics analysis (ROC) of NLR to predict SLE showed that the area under the curve (AUC) was 0.757. The cutoff value using the ROC curve was 3.13 (sensitivity, 0.574; specificity, 0.926; 95% confidence interval (CI), 0.668-0.845; P<0.001). While ROC analysis of NLR to predict LN showed that the AUC was 0.828). Logistic regression analysis showed that SLE without nephritis and LN were independently related to NLR.</p><p><strong>Conclusion: </strong>NLR is independently associated with SLE, and it may be a promising marker that reflects renal involvement in patients with SLE.</p>","PeriodicalId":13892,"journal":{"name":"International journal of clinical and experimental medicine","volume":"8 7","pages":"11026-31"},"PeriodicalIF":0.1,"publicationDate":"2015-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565283/pdf/ijcem0008-11026.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34183652","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Rapid prototyping for tissue-engineered bone scaffold by 3D printing and biocompatibility study. 组织工程骨支架的3D打印快速成型及生物相容性研究。
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Hui-Yu He, Jia-Yu Zhang, Xue Mi, Yang Hu, Xiao-Yu Gu

The prototyping of tissue-engineered bone scaffold (calcined goat spongy bone-biphasic ceramic composite/PVA gel) by 3D printing was performed, and the biocompatibility of the fabricated bone scaffold was studied. Pre-designed STL file was imported into the GXYZ303010-XYLE 3D printing system, and the tissue-engineered bone scaffold was fabricated by 3D printing using gel extrusion. Rabbit bone marrow stromal cells (BMSCs) were cultured in vitro and then inoculated to the sterilized bone scaffold obtained by 3D printing. The growth of rabbit BMSCs on the bone scaffold was observed under the scanning electron microscope (SEM). The effect of the tissue-engineered bone scaffold on the proliferation and differentiation of rabbit BMSCs using MTT assay. Universal testing machine was adopted to test the tensile strength of the bone scaffold. The leachate of the bone scaffold was prepared and injected into the New Zealand rabbits. Cytotoxicity test, acute toxicity test, pyrogenic test and intracutaneous stimulation test were performed to assess the biocompatibility of the bone scaffold. Bone scaffold manufactured by 3D printing had uniform pore size with the porosity of about 68.3%. The pores were well interconnected, and the bone scaffold showed excellent mechanical property. Rabbit BMSCs grew and proliferated on the surface of the bone scaffold after adherence. MTT assay indicated that the proliferation and differentiation of rabbit BMSCs on the bone scaffold did not differ significantly from that of the cells in the control. In vivo experiments proved that the bone scaffold fabricated by 3D printing had no acute toxicity, pyrogenic reaction or stimulation. Bone scaffold manufactured by 3D printing allows the rabbit BMSCs to adhere, grow and proliferate and exhibits excellent biomechanical property and high biocompatibility. 3D printing has a good application prospect in the prototyping of tissue-engineered bone scaffold.

采用3D打印技术制备了组织工程骨支架(煅烧山羊海绵骨-双相陶瓷复合材料/PVA凝胶),并对其生物相容性进行了研究。将预先设计好的STL文件导入GXYZ303010-XYLE 3D打印系统,采用凝胶挤出技术3D打印制备组织工程骨支架。体外培养兔骨髓基质细胞(BMSCs),并将其接种于3D打印获得的无菌骨支架上。扫描电镜下观察骨髓间充质干细胞在骨支架上的生长情况。MTT法观察组织工程骨支架对兔骨髓间充质干细胞增殖分化的影响。采用万能试验机对骨支架的抗拉强度进行测试。制备骨支架的渗滤液并注射到新西兰兔体内。采用细胞毒性试验、急性毒性试验、热原试验和皮内刺激试验评价骨支架的生物相容性。3D打印制备的骨支架孔径均匀,孔隙率约为68.3%。孔隙连通良好,骨支架具有良好的力学性能。兔骨髓间充质干细胞贴壁后在骨支架表面生长增殖。MTT实验表明,兔骨髓间充质干细胞在骨支架上的增殖和分化与对照细胞无明显差异。体内实验证明,3D打印制备的骨支架无急性毒性、无热原反应、无刺激。3D打印制备的骨支架能够使兔骨髓间充质干细胞粘附、生长和增殖,具有优异的生物力学性能和较高的生物相容性。3D打印在组织工程骨支架的原型制作中具有良好的应用前景。
{"title":"Rapid prototyping for tissue-engineered bone scaffold by 3D printing and biocompatibility study.","authors":"Hui-Yu He,&nbsp;Jia-Yu Zhang,&nbsp;Xue Mi,&nbsp;Yang Hu,&nbsp;Xiao-Yu Gu","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>The prototyping of tissue-engineered bone scaffold (calcined goat spongy bone-biphasic ceramic composite/PVA gel) by 3D printing was performed, and the biocompatibility of the fabricated bone scaffold was studied. Pre-designed STL file was imported into the GXYZ303010-XYLE 3D printing system, and the tissue-engineered bone scaffold was fabricated by 3D printing using gel extrusion. Rabbit bone marrow stromal cells (BMSCs) were cultured in vitro and then inoculated to the sterilized bone scaffold obtained by 3D printing. The growth of rabbit BMSCs on the bone scaffold was observed under the scanning electron microscope (SEM). The effect of the tissue-engineered bone scaffold on the proliferation and differentiation of rabbit BMSCs using MTT assay. Universal testing machine was adopted to test the tensile strength of the bone scaffold. The leachate of the bone scaffold was prepared and injected into the New Zealand rabbits. Cytotoxicity test, acute toxicity test, pyrogenic test and intracutaneous stimulation test were performed to assess the biocompatibility of the bone scaffold. Bone scaffold manufactured by 3D printing had uniform pore size with the porosity of about 68.3%. The pores were well interconnected, and the bone scaffold showed excellent mechanical property. Rabbit BMSCs grew and proliferated on the surface of the bone scaffold after adherence. MTT assay indicated that the proliferation and differentiation of rabbit BMSCs on the bone scaffold did not differ significantly from that of the cells in the control. In vivo experiments proved that the bone scaffold fabricated by 3D printing had no acute toxicity, pyrogenic reaction or stimulation. Bone scaffold manufactured by 3D printing allows the rabbit BMSCs to adhere, grow and proliferate and exhibits excellent biomechanical property and high biocompatibility. 3D printing has a good application prospect in the prototyping of tissue-engineered bone scaffold. </p>","PeriodicalId":13892,"journal":{"name":"International journal of clinical and experimental medicine","volume":"8 7","pages":"11777-85"},"PeriodicalIF":0.1,"publicationDate":"2015-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565401/pdf/ijcem0008-11777.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34013955","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
LMNA gene single nucleotide polymorphisms in dilated cardiomyopathy of Han children. 汉族儿童扩张型心肌病的LMNA基因单核苷酸多态性。
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Li-Jian Xie, Ting-Ting Xiao, Min Huang, Jie Shen

Objective: To investigate whether LMNA gene mutation is associated with dilated cardiomyopathy (DCM) in Chinese Han Race children.

Methods: DNA was isolated from 78 patients with DCM and 100 healthy Chinese children who served as controls. 12 exons in the functional regions and the adjacent part of introns of the LMNA gene were amplified with polymerase chain reactions (PCR) and the PCR products were sequenced with DNA sequencer. We compared the DNA sequence with Blast software online PubMed website. The differences of allele and genotype between the groups were detected by χ(2) test.

Results: No disease-causing mutation in LMNA gene was found in all DCM patients. Three nonsense single nucleotide polymorphisms (SNPs) were identified. ① The first is c.1908C>T (H566H, rs4641) which was located at exon 10 of LMNA gene. It was found in 29 DCM cases and 15 control subjects. Compared to healthy controls, the frequency of TT and TC genotypes, and the C allele were significantly increased in DCM patients (P<0.05). ② The second was c.861C>T (A287A, rs5380) which was located at exon 5 of LMNA gene. It was found in 9 DCM cases and 2 control subjects. The frequency of TC genotype was significantly increased in DCM patients (P<0.05). ③ The third was c.1338C>T (D446D, rs5058) which located at exon 7 of LMNA gene. It was found in 8 DCM cases and 3 control subjects. The frequency of TC genotype was significantly increased in DCM patients (P<0.05).

Conclusion: The SNP of LMNA gene may be associated with the susceptivity of DCM in Chinese Han children.

目的:探讨中国汉族儿童LMNA基因突变与扩张型心肌病(DCM)的相关性。方法:从78例DCM患者和100例健康中国儿童中分离DNA作为对照。利用聚合酶链式反应(PCR)扩增出LMNA基因功能区外显子及邻近内含子的12个外显子,并用DNA测序仪对PCR产物进行测序。我们将DNA序列与PubMed网站上的Blast软件进行了比较。采用χ(2)检验检测各组间等位基因和基因型的差异。结果:所有DCM患者均未发现致病性LMNA基因突变。鉴定出3个无义单核苷酸多态性(snp)。①c.1908C>T (H566H, rs4641)位于LMNA基因外显子10;DCM患者29例,对照组15例。与健康对照组相比,DCM患者位于LMNA基因外显子5的PT (A287A, rs5380)的TT、TC基因型和C等位基因的频率显著增加。DCM病例9例,对照组2例。在DCM患者中,位于LMNA基因外显子7的PT (D446D, rs5058)基因型频率显著升高。DCM患者8例,对照组3例。结论:LMNA基因SNP可能与中国汉族儿童DCM的易感性有关。
{"title":"LMNA gene single nucleotide polymorphisms in dilated cardiomyopathy of Han children.","authors":"Li-Jian Xie,&nbsp;Ting-Ting Xiao,&nbsp;Min Huang,&nbsp;Jie Shen","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Objective: </strong>To investigate whether LMNA gene mutation is associated with dilated cardiomyopathy (DCM) in Chinese Han Race children.</p><p><strong>Methods: </strong>DNA was isolated from 78 patients with DCM and 100 healthy Chinese children who served as controls. 12 exons in the functional regions and the adjacent part of introns of the LMNA gene were amplified with polymerase chain reactions (PCR) and the PCR products were sequenced with DNA sequencer. We compared the DNA sequence with Blast software online PubMed website. The differences of allele and genotype between the groups were detected by χ(2) test.</p><p><strong>Results: </strong>No disease-causing mutation in LMNA gene was found in all DCM patients. Three nonsense single nucleotide polymorphisms (SNPs) were identified. ① The first is c.1908C>T (H566H, rs4641) which was located at exon 10 of LMNA gene. It was found in 29 DCM cases and 15 control subjects. Compared to healthy controls, the frequency of TT and TC genotypes, and the C allele were significantly increased in DCM patients (P<0.05). ② The second was c.861C>T (A287A, rs5380) which was located at exon 5 of LMNA gene. It was found in 9 DCM cases and 2 control subjects. The frequency of TC genotype was significantly increased in DCM patients (P<0.05). ③ The third was c.1338C>T (D446D, rs5058) which located at exon 7 of LMNA gene. It was found in 8 DCM cases and 3 control subjects. The frequency of TC genotype was significantly increased in DCM patients (P<0.05).</p><p><strong>Conclusion: </strong>The SNP of LMNA gene may be associated with the susceptivity of DCM in Chinese Han children.</p>","PeriodicalId":13892,"journal":{"name":"International journal of clinical and experimental medicine","volume":"8 7","pages":"11230-4"},"PeriodicalIF":0.1,"publicationDate":"2015-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4565312/pdf/ijcem0008-11230.pdf","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"34079627","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
In-hospital clinical outcomes of elderly patients (≥60 years) undergoing primary percutaneous coronary intervention. 老年患者(≥60岁)初次经皮冠状动脉介入治疗的住院临床结果
IF 0.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2015-07-15 eCollection Date: 2015-01-01
Ya-Min Su, Xing-Xing Cai, Hai-Hua Geng, Hong-Zhuan Sheng, Meng-Kan Fan, Min Pan

Elderly patients are at high risk of mortality when they present with ST-elevation myocardial infarction (STEMI). However, the clinical outcomes of this sub-group undergoing primary percutaneous coronary intervention (PPCI) have not been well established, despite recent advances in both devices and techniques. In the present retrospective cohort study from a Chinese single center, we assessed the clinical outcomes and predictors of mortality in elderly patients (≥60 years) underwent with PPCI. The primary endpoints were immediate angiographic success and in-hospital procedural success. The secondary endpoints were all-cause death in hospital. Between January 2011 and December 2013, a total of 184 consecutive patients with acute STEMI underwent PPCI were enrolled. 116 (63.04%) patients were in the elderly group. Despite the difference in lesion complexity between groups, the immediate angiographic success rate was similar (93.97% in the elderly group, and 94.12% in the non-elderly group, P=0.966). The procedural success rate were not significantly different between the two groups (90.52% in the elderly group, and 94.12% in the non-elderly group, P=0.389). However, in-hospital mortality was statistically higher in elderly group than in the non-elderly group (8.62% Vs 1.47%, P=0.048). The major causes of death were cardiac shock and malignant arrhythmias (ventricular tachycardia and fibrillation). Our results indicate that PPCI in the elderly is feasible and has a high likelihood of immediate angiographic and procedural success.

老年患者st段抬高型心肌梗死(STEMI)的死亡风险较高。然而,尽管最近设备和技术都取得了进展,但该亚组接受原发性经皮冠状动脉介入治疗(PPCI)的临床结果尚未得到很好的确定。在目前来自中国单中心的回顾性队列研究中,我们评估了接受PPCI的老年患者(≥60岁)的临床结局和死亡率预测因素。主要终点为即时血管造影成功和院内手术成功。次要终点为院内全因死亡。2011年1月至2013年12月,共有184例急性STEMI患者连续接受PPCI。老年组116例(63.04%)。尽管两组间病变复杂程度不同,但即刻血管造影成功率相似(老年组93.97%,非老年组94.12%,P=0.966)。两组手术成功率差异无统计学意义(老年组90.52%,非老年组94.12%,P=0.389)。老年组住院死亡率高于非老年组(8.62% Vs 1.47%, P=0.048)。死亡的主要原因是心源性休克和恶性心律失常(室性心动过速和纤颤)。我们的结果表明,老年人PPCI是可行的,并且有很高的可能性立即血管造影和手术成功。
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International journal of clinical and experimental medicine
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