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Association of Vitamin D Status withMetabolic Syndrome and itsComponents in Bangladeshi UrbanWomen 孟加拉国城市妇女维生素D水平与代谢综合征及其组成部分的关系
Pub Date : 2020-01-01 DOI: 10.21767/J
Z. H. Howlader
Alzheimer's disease (AD) is a global epidemic; every 3 seconds someone in the world develops dementia. An estimated 50 million people are living with a disease that cannot be prevented, treated or cured. Without novel breakthroughs, AD is predicted to exceed 130 million by 2050. Pharmaceuticals offer minimal relief with dismal evidence of reversing neurodegeneration. Research focuses on β-amyloid plaques and tau tangles; but, in clinical trial, medications designed to sop-up toxic proteins in the brain fail to impede neural decline. Instead, plaques and tangles appear to be late-arrivers in the insidious progression of dementia. The recent explosion of comorbid metabolic pathologies (global prevalence of T2DM estimated @ 463 million) invites researchers into a deeper discussion of the bioenergetics regulating cognitive impairment and metabolic dysregulation. Age-related energy deficits, driven by peripheral insulin resistance, exacerbate Aβ/tau accumulation, increase oxidative stress and impede mitochondrial function; work by Sergi et al. and Mastroeni et al. suggest that mitochondrial dysfunction with epigenetic impairment in oxidative respiration appear to be the earliest offenders in the progression of T2DM and AD [1,2]. This case report highlights a novel, integrated intervention with a 69 year-old male dually diagnosed with T2DM and Mild Cognitive Impairment (MCI). Physiological biomarkers were measured pre/mid/post intervention; the MoCA (Montreal Cognitive Assessment) measured cognitive function, pre/post. Statistically significant results were observed in the metabolic risk biomarkers, memory was restored to normal ranges, and the HbA1c normalized out of the diabetic range @ <5.6%. Furthermore, the metabolic and cognitive improvements were sustained @ 3 months post-intervention. These promising results suggest that dietary ketogenesis restores peripheral insulin sensitivity, mitigates T2DM and improves cognition by circumventing neural starvation via the restoration of metabolic flexibility.
阿尔茨海默病(AD)是一种全球性流行病;世界上每三秒钟就有一人患上痴呆症。估计有5000万人患有无法预防、治疗或治愈的疾病。如果没有新的突破,预计到2050年,AD将超过1.3亿。药物提供的缓解效果微乎其微,而且有令人沮丧的证据表明可以逆转神经变性。研究重点是β-淀粉样蛋白斑块和tau蛋白缠结;但是,在临床试验中,旨在吸收大脑中有毒蛋白质的药物未能阻止神经衰退。相反,斑块和缠结似乎是痴呆潜伏过程中的后来者。近年来,伴随代谢疾病的激增(全球2型糖尿病患病率估计为4.63亿)促使研究人员对调节认知障碍和代谢失调的生物能量学进行了更深入的讨论。由外周胰岛素抵抗驱动的年龄相关能量不足会加剧Aβ/tau积累,增加氧化应激并阻碍线粒体功能;Sergi等人和Mastroeni等人的研究表明,氧化呼吸表观遗传损伤的线粒体功能障碍似乎是T2DM和AD进展的最早罪魁祸首[1,2]。本病例报告强调了一种新的综合干预方法,该方法治疗了一位69岁的男性,同时诊断为2型糖尿病和轻度认知障碍(MCI)。在干预前/中/后测量生理生物标志物;MoCA(蒙特利尔认知评估)测量认知功能,前后。代谢风险生物标志物的结果具有统计学意义,记忆恢复到正常范围,HbA1c正常化到糖尿病范围@ <5.6%。此外,干预后3个月,代谢和认知改善持续。这些有希望的结果表明,饮食生酮可以恢复外周胰岛素敏感性,减轻T2DM,并通过恢复代谢灵活性来避免神经饥饿,从而改善认知。
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引用次数: 0
The effects of a combined aerobic and resistance exercise programme on insulin resistance among prediabetes subjects 有氧与抗阻联合运动对糖尿病前期胰岛素抵抗的影响
Pub Date : 2019-04-10 DOI: 10.4172/2167-0943:1000247
Bander Alharbi, N. Alsubaie, T. Sahota, M. Taylor
Aim: Insulin resistance is a common health disorder that contributes to developed overt diabetes among prediabetes subjects. The aim of the study is to examine the effects of a combined programme of aerobic and resistance exercise on insulin resistance among prediabetes subjects (Pre-D) using Oral Glucose Tolerance Test (OGTT) as a tool to define the improvement in insulin resistance. Method: 20 prediabetes subjects were asked to join a supervised combined exercise program consists of 30 min of resistance exercise followed by 20 min cycling twice at moderate-intensity a week for 6 weeks. Result: a significant improvement in Blood Glucose (BG) after combination exercise at two occasions when compared to BG before exercise (Pre S1), after 1st exercise session (Post S1) and at the end of intervention trial (Post S12). Conclusion: The result of this study has shown that 6 weeks of moderate-intensity exercise combined with aerobic and resistance exercise program had significantly ameliorated insulin resistance among Pre-D.
目的:胰岛素抵抗是一种常见的健康障碍,有助于糖尿病前期受试者发展为显性糖尿病。本研究的目的是利用口服葡萄糖耐量试验(OGTT)作为确定胰岛素抵抗改善的工具,检查有氧运动和抵抗运动联合方案对前驱糖尿病受试者(Pre-D)胰岛素抵抗的影响。方法:20名前驱糖尿病受试者参加一项有监督的联合运动计划,该计划包括30分钟的阻力运动,随后20分钟的骑车,每周两次,中等强度,持续6周。结果:与运动前(S1前)、第一次运动后(S1后)和干预试验结束时(S1后)相比,两次联合运动后的血糖(BG)有显著改善。结论:本研究结果表明,6周的中等强度运动结合有氧和抗阻运动方案可显著改善Pre-D患者的胰岛素抵抗。
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引用次数: 0
The effects of (a combined exercise programme aerobic and resistance) on blood glucose and incretin hormone that could control the diabetes in type 2 diabetes. (有氧运动和抵抗运动)对血糖和促肠促胰岛素激素的影响,可以控制2型糖尿病。
Pub Date : 2019-04-02 DOI: 10.4172/2167-0943.1000246
N. Alsubaie, Bander Alharbi, T. Sahota, M. Taylor
Aim: An excessive number of calories consumed daily, in addition to a sedentary lifestyle, are the main causes of increasing Type 2 Diabetes (T2D) prevalence worldwide. Diabetes is usually accompanied by hypertension, lipid disorders, and obesity. The aim of this study is to show that the combination exercise is effective. It will compare T2D and Non-Diabetes (ND) volunteer doing combination exercise consisting of resistance and cycling. The interventions are minor and fairly short consisting of 12 episodes of exercise over 6 weeks, yet this was enough to produce measurable change and improvement. This included the re-categorization of two T2D volunteers to being ND, using normal metrics. A literature search was conducted by using electronic databases (Science direct, google scholar, Medline, Embase, Sports medicine, PubMed, CINAHL, Cochrane library, and Scopus) from April 2015 until January 2019. Results show that changes in primary and secondary outcomes are significant between the different groups. The primary outcome is HbA1c, and the secondary outcomes are weight, waist, BMI, lipid, BP, HR, lactate and body fitness. Moreover, this study focuses on the changes in incretin level in the T2D group for effects of exercise on the secretion of this hormone and compare within T2D who are using a different medication for diabetes Results: After just six weeks, there was a reduction in the HbA1c level for the T2D volunteers which is significant (P=0.000). Moreover, in ND the reduction was also significant (P=0.000). In the T2D group who are using (Metformin and SGT2-I group), their result shows elevation in GLP-1 in the assessment of the both acute and chronic effect of the programme. GLP-1 in this group was (3.9 ± 1.5) and increased to (8.4 ± 1.2), (P=0.345) after S1 and then increased more to (11.0 ± 0.8), (P=0.196) after 6 weeks of exercise. This was of interest because of the inference that incretins and exercise were linked. The crucial factor is metformin. Conclusion: In T2D and ND combination exercise has a beneficial effect on HbA1c, the improvement was higher in T2D. The anthropometric variables (weight, waist, BMI and lung capacity) improved significantly as well in T2D and ND. Exercise is also important to improve GLP-1 secretion. Despite the range of studies on incretin undertaken here, still, there is a need to compare the effect of exercise and different types of pharmacological therapy on GLP1. This study compared the effect of exercise on T2D plus medication in volunteers. It has been found that within the T2D group only Metformin and SGT2-I group was improved. Both SGLT2 inhibitors and metformin have been found to affect body weight and this may explain the improvement of GLP-1 level, suggesting an area for future investigation.
目的:每天摄入过多的卡路里,加上久坐不动的生活方式,是全球2型糖尿病(T2D)患病率上升的主要原因。糖尿病通常伴有高血压、脂质紊乱和肥胖。本研究的目的是证明这种组合运动是有效的。它将比较T2D和非糖尿病(ND)志愿者进行由阻力和骑自行车组成的组合运动。这些干预措施很小,时间也很短,在6周内只进行了12次锻炼,但这足以产生可测量的变化和改善。这包括使用正常指标将两名T2D志愿者重新分类为ND。从2015年4月至2019年1月,通过电子数据库(Science direct、google scholar、Medline、Embase、Sports medicine、PubMed、CINAHL、Cochrane library和Scopus)进行文献检索。结果显示,不同组间主要和次要结局的变化是显著的。主要终点为HbA1c,次要终点为体重、腰围、BMI、血脂、BP、HR、乳酸、体适能。此外,本研究重点关注T2D组肠促胰岛素水平的变化,以了解运动对该激素分泌的影响,并比较使用不同药物治疗糖尿病的T2D组。结果:仅六周后,T2D志愿者的HbA1c水平显著降低(P=0.000)。此外,在ND中,减少也很显著(P=0.000)。在使用二甲双胍和SGT2-I的T2D组中,他们的结果显示在评估该方案的急性和慢性效果时GLP-1升高。组GLP-1为(3.9±1.5),S1后升高至(8.4±1.2)(P=0.345), 6周后进一步升高至(11.0±0.8)(P=0.196)。这很有趣,因为人们推断胰岛素和锻炼是有联系的。关键因素是二甲双胍。结论:T2D与ND联合运动对HbA1c有有益的影响,其中T2D的改善更明显。T2D和ND的人体测量变量(体重、腰围、BMI和肺活量)也有显著改善。运动对改善GLP-1分泌也很重要。尽管这里开展了一系列关于肠促胰岛素的研究,但仍有必要比较运动和不同类型的药物治疗对GLP1的影响。这项研究比较了运动和药物对志愿者T2D的影响。我们发现在T2D组中只有Metformin和SGT2-I组有改善。SGLT2抑制剂和二甲双胍均可影响体重,这可能解释了GLP-1水平的改善,这是未来研究的一个领域。
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引用次数: 0
Acute renal failure due to anabolic steroid or creatinine supplement 合成代谢类固醇或肌酐补充引起的急性肾功能衰竭
Pub Date : 2018-08-27 DOI: 10.4172/2167-0943-c1-009
pMoayed Alhelfi, Massimo Piraccip
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引用次数: 0
COX-2 Expression in the Aorta of Obese Zucker Rats COX-2在肥胖Zucker大鼠主动脉中的表达
Pub Date : 2018-03-16 DOI: 10.4172/2167-0943.1000238
Tomoko Shimomura, I. Wakabayashi, T. Nakano, K. Goto
Objectives: Obesity is a central risk factor for atherosclerotic cardiovascular disease. The purpose of this study was to determine whether COX-2 expression is changed in the arterial wall of experimental obese animals.Methods: COX-2 expression in the aortas of 12-week-old male Zucker obese or lean rats was investigated using immunoblot and immunohistochemical analyses.Results: COX-2 expression was detected in the tunica media of the aortas of Zucker obese rats and was prominent in the perinuclear region of smooth muscle cells in the tunica media. In immunoblot analysis, the basal (non-stimulated) levels of COX-2 expression were comparable in the aortas of Zucker obese rats and Zucker lean (control) rats. COX-2 expression in response to interleukin (IL)-1β was significantly lower in the aortas of Zucker obese rats than in those of Zucker lean rats.Conclusions: The results suggest that IL-1β-induced COX-2 expression is attenuated in arteries of obese rats, and this might be involved in the obesity-induced acceleration of atherosclerosis.
目的:肥胖是动脉粥样硬化性心血管疾病的主要危险因素。本研究的目的是确定COX-2在实验性肥胖动物动脉壁中的表达是否发生改变。方法:采用免疫印迹法和免疫组织化学法检测12周龄雄性Zucker肥胖大鼠和瘦肉大鼠主动脉中COX-2的表达。结果:COX-2在Zucker肥胖大鼠主动脉的中膜中有表达,且在中膜平滑肌细胞核周区有显著表达。免疫印迹分析显示,在Zucker肥胖大鼠和Zucker瘦弱(对照)大鼠的主动脉中,COX-2的基础(非刺激)表达水平相当。COX-2在Zucker肥胖大鼠主动脉中对白细胞介素(IL)-1β的表达明显低于Zucker瘦大鼠。结论:il -1β诱导的COX-2在肥胖大鼠动脉中表达减弱,这可能与肥胖诱导的动脉粥样硬化加速有关。
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引用次数: 2
Evaluation of Glycemic, Lipid, Immune-Inflammatory and Oxidative Stress Markers in Various Clinical Stages of Type 2 Diabetic Nephropathy 2型糖尿病肾病不同临床阶段的血糖、血脂、免疫炎症和氧化应激标志物的评价
Pub Date : 2018-03-06 DOI: 10.4172/2167-0943.1000237
S. Gantala, Ramanjaneyulu Kummari, M. A. Tupurani, R. K. Galimudi, Kishore Kumar Gundapaneni, Keerthi Kupsal, N. Shyamala, S. Hanumanth, S. Guditi
Type 2 Diabetic nephropathy (DN), chronic multifactorial disorder is a devastating complication of DM and a main cause of end stage renal failure. A variety of factors like metabolic, hemodynamic, genetic and multiple pathogenic events contribute to the renal damage in type 2 DN. The present study was designed to assess blood glucose, serum lipid profiles, immune-inflammatory and oxidative stress markers in type 2 DN patients in different stages of the disease and healthy controls. Our study showed that FBS, PPG, HbA1c, TC, TG, LDL-C, ADA, CRP, MDA, NO and DNA damage were significantly high in type 2 DN patients (p<0.01) compared to controls. In stage wise comparison also FBS, PPG, HbA1c, LDL-C, CRP, MDA, NO and DNA damage showed significant difference (p<0.05). Further, a significant positive correlation was found between PLBS, LDL-C and CRP and oxidative stress markers (MDA, NO, DNA damage) suggesting that monitoring these biochemical parameters at regular intervals may reduce the stage wise progression of type 2 DN and might help in early detection, precise prognosis/therapeutic modalities.
2型糖尿病肾病(DN)是一种慢性多因素疾病,是DM的一种破坏性并发症,也是终末期肾功能衰竭的主要原因。代谢、血流动力学、遗传和多种致病事件等多种因素可导致2型DN的肾脏损害。本研究旨在评估不同阶段的2型DN患者和健康对照者的血糖、血脂、免疫炎症和氧化应激指标。我们的研究显示,与对照组相比,2型DN患者FBS、PPG、HbA1c、TC、TG、LDL-C、ADA、CRP、MDA、NO、DNA损伤显著升高(p<0.01)。分期比较FBS、PPG、HbA1c、LDL-C、CRP、MDA、NO、DNA损伤差异均有统计学意义(p<0.05)。此外,PLBS、LDL-C和CRP与氧化应激标志物(MDA、NO、DNA损伤)之间存在显著正相关,这表明定期监测这些生化参数可能会减少2型DN的分期进展,并可能有助于早期发现、精确预后/治疗模式。
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引用次数: 5
Evaluation of Dietary Habits and Lifestyle on the Prevalence of Metabolic Syndrome and Obesity in Undergraduate University Students in Cameroon: A Cross Sectional Study 饮食习惯和生活方式对喀麦隆大学生代谢综合征和肥胖症患病率的影响:一项横断面研究
Pub Date : 2018-01-26 DOI: 10.4172/2167-0943.1000236
Solange Dabou, P. Telefo, L. F. Sama
Background: Obesity and metabolic syndrome have nowadays a widespread dissemination around the world. Their prevalence is increasing in developing countries, due to modifications in dietary habits and lifestyle. Limited data exist on those issues among school going youths in Cameroon. Methods: A cross-sectional study including 203 consenting Cameroonian freshmen was conducted at the medical center of the University of Dschang. Anthropometric measurements, blood pressure, fasting blood glucose and lipid profile markers were measured using standard procedures. Metabolic syndrome was diagnosed using a harmonized definition while obesity diagnosis used BMI criterion. Dietary and lifestyle habits were recorded using a questionnaire. Results: The prevalence of obesity and metabolic syndrome were 3.94% and 11.33% respectively. We found strong associations between the prevalence of metabolic syndrome and high frequency of consumption of “Koki” (OR=9.9, 95% CI: 7.09-14.04, P=0.0000), “Achu soup” (OR=7.3, 95% CI: 4.4-12.3, P=0.0000), corn couscous (OR=5.64, 95% CI: 4.34-7.33, P=0.0000), “Ndole” (OR=2.4,95% CI: 1.9-3.05, P=0.0000). Regular consumption of green vegetables is associated with low prevalence of metabolic syndrome (OR=0.4, 95% CI: 0.2-0.3, P=0.0000). There is also a strong association between prevalence of obesity and high number of meal per day (OR=5.1, 95% CI: 3.07-8.4, P=0.0000) as well as more than 6 hours of TV watching per day (OR=4.9, 95% CI: 2.8-7.09, P=0.0000). Conclusion: Metabolic syndrome is present in young Cameroonians and is associated to certain dietary and lifestyle habits. Interventions targeting youth may therefore be multiplied with special concern on those dietary and lifestyle issues.
背景:肥胖和代谢综合征目前在世界范围内广泛传播。由于饮食习惯和生活方式的改变,它们在发展中国家的患病率正在上升。在喀麦隆的学龄青年中,关于这些问题的数据有限。方法:横断面研究,包括203名喀麦隆大一新生,同意在昌大学医学中心进行。采用标准程序测量人体测量、血压、空腹血糖和血脂指标。代谢综合征诊断采用统一定义,肥胖症诊断采用BMI标准。通过问卷调查记录饮食和生活习惯。结果:肥胖和代谢综合征患病率分别为3.94%和11.33%。我们发现代谢综合征的患病率与食用“Koki”(OR=9.9, 95% CI: 7.09-14.04, P=0.0000)、“Achu soup”(OR=7.3, 95% CI: 4.4-12.3, P=0.0000)、玉米蒸粗麦粉(OR=5.64, 95% CI: 4.34-7.33, P=0.0000)、“Ndole”(OR=2.4,95% CI: 1.9-3.05, P=0.0000)的频率密切相关。经常食用绿色蔬菜与代谢综合征患病率较低相关(OR=0.4, 95% CI: 0.2-0.3, P=0.0000)。肥胖患病率与每天大量进餐(OR=5.1, 95% CI: 3.07-8.4, P=0.0000)以及每天看电视超过6小时(OR=4.9, 95% CI: 2.8-7.09, P=0.0000)之间也有很强的关联。结论:代谢综合征存在于喀麦隆年轻人中,并与某些饮食和生活习惯有关。因此,针对青年的干预措施可能会增加,并特别关注那些饮食和生活方式问题。
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引用次数: 6
Multiple Roles of Sms2 in White and Brown Adipose Tissues from Dietinduced Obese Mice Sms2在饮食诱导肥胖小鼠白色和棕色脂肪组织中的多重作用
Pub Date : 2018-01-01 DOI: 10.4172/2167-0943.1000241
H. Hanamatsu, S. Mitsutake, S. Sakai, T. Okazaki, Ken Watanabe, Y. Igarashi, K. Yuyama
Background/Objectives: Adipose tissue (AT) has an important role in energy homeostasis. The dysfunction of AT or the hyper-accumulation of neutral lipids leads to various metabolic diseases. Recent studies indicate that sphingo lipid metabolism associates with the development of metabolic diseases. Sphingomyelin, a major sphingolipid in mammals, requires sphingomyelin synthase (SMS) for biosynthesis. Previously, we reported that Sms2 deficiency inhibited diet-induced obesity, fatty liver, and insulin resistance in mice. However, the contribution of Sms2 to obesity and insulin resistance in AT is largely unknown. In this study, we investigated whether Sms2 deficiency in ATs affects obesity and insulin resistance.Subjects/Methods: Wild-type and Sms2 knockout (KO) mice were fed a high-fat for 12 weeks. Body and AT weights, and the food intake, were recorded. The AT status and macrophage infiltration were evaluated by histological analysis. The expression levels of genes and proteins involved in adipogenesis, inflammation, energy expenditure, and fatty acid metabolism were examined.Results: In white adipose tissue (WAT) from Sms2 KO mice, the number of small adipocytes increased but the adipocyte size decreased. In epididymal WAT, Sms2 deficiency inhibited inflammation and macrophage infiltration. Moreover, adipogenesis was moderately suppressed. In subcutaneous WAT from Sms2 KO mice, the expression of genes involved in energy expenditure and browning (Ucp1, Cidea, Tbx1) was elevated. In brown adipose tissue (BAT) from Sms2 KO mice, the lipid droplet surface area was lower than that of WT mice and the expression of genes involved in fatty acid synthesis (Fasn, Scd1) decreased.Conclusion: These results demonstrate that Sms2 deficiency leads to moderate adipogenesis and inflammatory suppression in epididymal WAT, increased energy expenditure by the browning of subcutaneous WAT, and suppression of fatty acid synthesis in BAT, suggesting that these synergetic effects in ATs from Sms2 KO mice contribute to the suppression of diet-induced obesity and insulin resistance.
背景/目的:脂肪组织(AT)在能量稳态中起着重要作用。AT功能障碍或中性脂质的过度积累导致各种代谢疾病。近年来的研究表明鞘脂代谢与代谢性疾病的发生有关。鞘磷脂是哺乳动物主要的鞘脂,需要鞘磷脂合成酶(Sphingomyelin synthase, SMS)进行生物合成。先前,我们报道了Sms2缺乏抑制小鼠饮食诱导的肥胖、脂肪肝和胰岛素抵抗。然而,Sms2对AT患者肥胖和胰岛素抵抗的作用在很大程度上是未知的。在这项研究中,我们研究了ATs中Sms2缺乏是否会影响肥胖和胰岛素抵抗。对象/方法:野生型和Sms2敲除(KO)小鼠高脂喂养12周。记录体重、腹侧肌重量和食物摄入量。组织学分析AT状态及巨噬细胞浸润情况。研究人员检测了参与脂肪形成、炎症、能量消耗和脂肪酸代谢的基因和蛋白质的表达水平。结果:Sms2 KO小鼠白色脂肪组织(WAT)中,小脂肪细胞数量增加,但脂肪细胞大小减小。在附睾WAT中,Sms2缺乏抑制炎症和巨噬细胞浸润。此外,脂肪生成受到适度抑制。在Sms2 KO小鼠皮下WAT中,参与能量消耗和褐变的基因(Ucp1, Cidea, Tbx1)的表达升高。在Sms2 KO小鼠的棕色脂肪组织(BAT)中,脂滴表面积低于WT小鼠,参与脂肪酸合成的基因(Fasn, Scd1)的表达降低。结论:这些结果表明Sms2缺乏导致附睾WAT中度脂肪生成和炎症抑制,皮下WAT褐化增加能量消耗,BAT脂肪酸合成抑制,提示Sms2 KO小鼠ATs的这些协同作用有助于抑制饮食性肥胖和胰岛素抵抗。
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引用次数: 2
Impact of Shared Medical Appointment among Persons with Diabetes 糖尿病患者共享医疗预约的影响
Pub Date : 2018-01-01 DOI: 10.4172/2167-0943.1000242
Greck Bd, W. Ae, Lima En
Purpose: To determine the impact of shared medical appointments on diabetes outcomes. In addition, we hoped to identify patient characteristics that may facilitate greater improvement in A1c through management via shared medical appointments by exploring previous mode of diabetes management, mental health utilization, and service connection status. Methods: The study was a retrospective chart review of electronic health records of patients involved in a diabetes-focused shared medical appointment clinic from July 1, 2011 through December 31, 2015. Diabetes outcome measures (A1c, weight) were collected prior to enrollment in the clinic and up to 3 years after enrollment to determine impact of SMA on disease management. Data regarding service connection status and mental health enrollment was collected as a tool in hopes to characterize the types of patients best benefitting from SMA's. Results: A total of 71 patients were included in this study. Mean A1c of our study cohort decreased at years 1, 2, and 3 from original A1c at baseline. Weight did not change greatly over the three years. The decrease in A1c from baseline at years 1 and 3 (pvalue = 0.003 and 0.037, respectively) was statistically significant. The other secondary variables studied did not show any correlation. Conclusions: A shared medical appointment is an effective means to diabetes management, resulting in significant decrease in A1c that persists over time. Certain patients may specifically benefit from management in this way, although the specific characteristics of those individuals have not been identified.
目的:确定共享医疗预约对糖尿病结局的影响。此外,我们希望通过探索以往的糖尿病管理模式、心理健康利用和服务连接状况,确定患者特征,通过共享医疗预约管理来促进A1c的更大改善。方法:本研究是对2011年7月1日至2015年12月31日在一家以糖尿病为重点的共享医疗预约诊所就诊的患者的电子健康记录进行回顾性图表回顾。在临床入组前和入组后3年内收集糖尿病结局指标(A1c、体重),以确定SMA对疾病管理的影响。收集有关服务连接状态和心理健康登记的数据作为一种工具,希望能够表征从SMA中获益最多的患者类型。结果:本研究共纳入71例患者。我们研究队列的平均糖化血红蛋白在第1年、第2年和第3年从基线时的原始糖化血红蛋白下降。体重在三年内没有太大变化。第1年和第3年的A1c较基线下降(p值分别为0.003和0.037)具有统计学意义。研究的其他次要变量没有显示出任何相关性。结论:共享医疗预约是糖尿病管理的有效手段,可导致A1c显著降低并持续一段时间。某些患者可能特别受益于这种管理方式,尽管这些个体的具体特征尚未确定。
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引用次数: 0
HIV-AIDS, is not a Viral Disease; It is a Metabolic Syndrome 艾滋病不是一种病毒性疾病;这是一种代谢综合征
Pub Date : 2018-01-01 DOI: 10.4172/2167-0943.1000239
B. R. Chowdhury
In the past 3 decades, we have been living with the hypothesis that, “HIV causes AIDS.” HIV, Human Immunodeficiency Virus is considered as the causative agent of AIDS, Acquired Immunodeficiency Syndrome; wherein the body's immune system gets damaged opening doors for major infections. However, the 3 Noble prize winner prestigious scientists including Luc Montagnier (discovered HIV), Kary Mullis (invented PCR test for HIV detection), and Wangari Maathai, (renowned African environmentalist), along with thousands of other scientists and intellects worked on the other side of the coin to prove back and again that the above said theory is a misconception. Last 35 years have provided immense literature and investigation evidences to firmly conclude that HIV is not the real cause of AIDS. On the other hand, malnutrition and metabolic syndrome due to drug abuse have been pointed as the real convicts. This review article revolves around the same theory for better understanding the HIV-AIDS hypothesis to be fallacious and search for valid causes.
在过去的30年里,我们一直生活在“HIV导致艾滋病”的假设中。HIV,人类免疫缺陷病毒被认为是艾滋病,获得性免疫缺陷综合征的病原体;身体的免疫系统受损,为重大感染打开了大门。然而,三位诺贝尔奖得主,包括Luc Montagnier(发现了HIV), Kary Mullis(发明了检测HIV的PCR测试)和Wangari Maathai(著名的非洲环保主义者),以及成千上万的其他科学家和知识分子在硬币的另一面工作,一再证明上述理论是一种误解。过去的35年提供了大量的文献和调查证据,坚定地得出结论,艾滋病毒不是艾滋病的真正原因。另一方面,药物滥用引起的营养不良和代谢综合征被认为是真正的罪犯。这篇综述文章围绕着同样的理论,以更好地理解HIV-AIDS假说是错误的,并寻找有效的原因。
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引用次数: 0
期刊
Journal of metabolic syndrome
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