glycemia

血糖
  • 文章类型: Journal Article
    肥胖或2型糖尿病患者血浆25-二羟维生素D水平降低,正如一些观察性研究报告的那样。然而,这些降低的激素水平与代谢参数之间的关联尚不清楚.无论如何,代谢综合征患者补充维生素D是标准的。尽管如此,这种补充对血糖等疾病的影响,血压,和血脂是有争议的。基于这个问题,我们对巴西的随机临床试验进行了系统评价和荟萃分析,欧洲,和美国分析了补充维生素D对肥胖或2型糖尿病患者代谢综合征参数的影响。我们的搜索产生了519篇文章,并在荟萃分析中包括12项随机对照试验。补充维生素D对分析的任何结果均无影响(空腹血糖和胰岛素血症,糖化血红蛋白,HOMA指数,收缩压和舒张压,体重,腰围,总胆固醇,LDL和HDL,和甘油三酯)。然而,亚组分析显示,每天使用维生素D至2000IU可降低参与者的空腹血糖和糖化血红蛋白.此外,干预措施仅降低了维生素D缺乏参与者的舒张压。至少两项研究显示,使用Rob2方案的偏倚风险很高。根据GRADE协议,证据质量从中等到非常低。这些结果表明,补充维生素D不能改善患者的代谢参数,血浆25-二羟维生素D水平与代谢综合征之间的关联可能不是因果关系,而是由其他混杂特征引起的。然而,无论如何,证据质量仍然很低,和更多的随机临床试验是必要的,以澄清这些关系。
    Plasma 25-dihydroxyvitamin D levels appear reduced in patients with obesity or type 2 diabetes, as reported in several observational studies. However, the association between these reduced hormone levels and metabolic parameters is unclear. In any case, vitamin D supplementation in patients with Metabolic Syndrome is standard. Still, the impacts of this supplementation on conditions such as glycemia, blood pressure, and lipidemia are debatable. Based on this question, we carried out a systematic review and meta-analysis of randomized clinical trials in Brazil, Europe, and the United States that analyzed the effects of vitamin D supplementation on Metabolic Syndrome parameters in patients with obesity or type 2 diabetes. Our search yielded 519 articles and included 12 randomized controlled trials in the meta-analysis. Vitamin D supplementation had no effect on any of the outcomes analyzed (fasting blood glucose and insulinemia, glycated hemoglobin, HOMA index, systolic and diastolic blood pressure, weight, waist circumference, total cholesterol, LDL and HDL, and triglycerides). However, subgroup analyses indicated that using vitamin D up to 2000 IU daily reduced participants\' fasting blood glucose and glycated hemoglobin. Furthermore, the intervention reduced diastolic blood pressure only in participants with vitamin D deficiency. At least two studies showed a high risk of bias using the Rob2 protocol. According to the GRADE protocol, the evidence quality varied from moderate to very low. These results indicate that vitamin D supplementation does not improve patients\' metabolic parameters and that the association between plasma 25-dihydroxyvitamin D levels and Metabolic Syndrome may not be causal but caused by other confounding characteristics. However, in any case, the quality of evidence is still low, and more randomized clinical trials are essential to clarify these relationships.
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  • 文章类型: Journal Article
    小马甲,俗称yacon,是菊科家族的一员.由于其药用和食用价值,yacon被不同的人群消费。雪莲果因其低聚果糖和菊粉含量高而独具特色,以及类黄酮,倍半萜内酯,和酚酸。根可以用来生产面粉,不易变质,可应用于各种工业产品。这篇系统的综述集中在yacon面粉对代谢参数的影响上。PubMed,科克伦,Embase,科学直接,Scopus,WebofScience,和谷歌学者数据库被咨询,在选择研究时遵循PRISMA指南。总的来说,在数据库中找到526篇文章,其中,只有28个全文符合纳入条件.在应用纳入和排除标准后,最终纳入了七项研究。结果表明,使用yacon面粉可以降低血糖,HbA1c,晚期糖基化末端,血浆脂质,身体脂肪量,体重,和腰围,改善肠道菌群和抗氧化状态。有必要进一步探索雪莲果面粉的效果,和额外的临床试验是必要的,以确定所需的最佳日消费水平,以帮助改善代谢参数。
    Smallanthus sonchifolius, popularly known as yacon, is a member of the Asteraceae family. Due to its medicinal and edible value, yacon is consumed by different populations. Yacon is unique due to its high fructo-oligosaccharide and inulin content, as well as flavonoids, sesquiterpene lactones, and phenolic acids. Roots can be used to produce flour, which is less perishable and can be applied in various industrial products. This systematic review focuses on the effects of yacon flour on metabolic parameters. PubMed, Cochrane, Embase, Science Direct, Scopus, Web of Science, and Google Scholar databases were consulted, and PRISMA guidelines were followed in the selection of the studies. In total, 526 articles were found in the databases, and of these, only 28 full texts were eligible for inclusion. After applying the inclusion and exclusion criteria, seven studies were finally included. The results showed that the use of yacon flour can reduce glycemia, HbA1c, advanced glycation ends, plasma lipids, body fat mass, body weight, and waist circumference and improve intestinal microbiota and the antioxidant status. Further exploration of the effects of yacon flour is warranted, and additional clinical trials are necessary to determine the optimal daily consumption levels required to assist in improving metabolic parameters.
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  • 文章类型: Journal Article
    背景:显然,抗性淀粉食物来源的消费,如绿色香蕉生物质,刺激短链脂肪酸肠道细菌生产者的增殖,这有助于肠道健康并降低患慢性病的风险。然而,现有的科学证据很少,没有研究对这些证据进行系统评估。
    目的:本研究的目的是分析绿色香蕉生物量对人体测量学的潜在影响,身体成分,以及人类和动物的生化和肠道变量。
    方法:Cochrane图书馆,Embase,Medline/PubMed,Scopus,和WebofScience电子数据库在2024年1月进行了搜索,以查找合格的文章。测试煮熟的去皮或未去皮的绿色香蕉对人体测量的影响的研究,生物化学,和/或肠变量包括在内。
    方法:本系统评价是根据PRISMA(系统评价和荟萃分析的首选报告项目)指南进行的。研究质量的分类和评估基于与这些研究设计相关的相关标准以及营养与饮食学会手册的质量标准清单。2001年至2021年发表的12项研究被纳入审查。
    方法:人体研究结果表明,摄入绿色香蕉生物量可以控制儿童的肠功能障碍(50-300克/天,持续5-14天或30克/天,持续8周),并显示出潜在的抗肥胖作用,抗高脂血症,和抗糖尿病(40克/天,24周)在成人的作用。在老鼠身上,生物质消耗导致潜在的抗生肥(25克/天,8周),抗高脂血症,和抗糖尿病作用(~8-30克/天,持续12周)。
    结论:食用绿色香蕉生物量似乎对肠道功能和对肥胖的潜在影响产生有益影响,血脂异常,和糖尿病。这些影响可能与由于生物质中存在3型抗性淀粉而导致的粪便短链脂肪酸浓度增加有关。
    背景:开放科学框架(OSF)(https://doi.org/10.17605/OSF)。IO/TKCWV)。
    BACKGROUND: Apparently, the consumption of resistant-starch food sources, such as green banana biomass, stimulates the proliferation of short-chain fatty acid intestinal bacteria producers, which can contribute to intestinal health and reduce the risk of chronic diseases. However, the available scientific evidence is scarce and no study has systematically evaluated such evidence.
    OBJECTIVE: The aim of this study was to analyze the potential effects of green banana biomass on anthropometry, body composition, and biochemical and intestinal variables in humans and animals.
    METHODS: The Cochrane Library, Embase, Medline/PubMed, Scopus, and Web of Science electronic databases were searched in January 2024 for eligible articles. Studies that tested the effects of cooked peeled or unpeeled green banana on anthropometric, biochemical, and/or intestinal variables were included.
    METHODS: This systematic review was conducted according to the PRISMA (Preferred Reporting Items for Systematic Reviews and Meta-Analyses) guidelines. The classification and assessment of the quality of studies were based on the relevant criteria related to the design of these studies and the quality criteria checklist of the Academy of Nutrition and Dietetics manual. Twelve studies published between 2001 and 2021 were included in the review.
    METHODS: The results of human studies indicate that the ingestion of green banana biomass controlled intestinal dysfunction (50-300 g/day for 5-14 days or 30 g/day for 8 wk) in children, and showed potential anti-obesogenic, anti-hyperlipidemic, and antidiabetic (40 g/day for 24 wk) effects in adults. In rats, biomass consumption led to potential anti-obesogenic (25 g/day for 8 wk), anti-hyperlipidemic, and antidiabetic (∼8-30 g/day for 12 wk) effects.
    CONCLUSIONS: Consumption of green banana biomass seems to exert beneficial effects on intestinal function and potential effects on obesity, dyslipidemia, and diabetes. These effects may be related to increased fecal short-chain fatty acid concentrations as a result of type 3 resistant starch present in biomass.
    BACKGROUND: Open Science Framework (OSF) (https://doi.org/10.17605/OSF.IO/TKCWV).
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  • 文章类型: Meta-Analysis
    本研究评估了比格列净的临床安全性和有效性,钠-葡萄糖协同转运蛋白2(SGLT2)抑制剂,2型糖尿病(T2DM)患者的血糖管理。
    我们检查了T2DM患者的随机对照试验,比较了20mg每日一次口服bexagliflozin与安慰剂治疗血糖的临床有效性和安全性,直至2023年5月28日,发表在ClinicalTrials.gov等数据库上,PubMed,Embase,科克伦图书馆此外,还评估了体重和收缩压(SBP)的下降以及糖化血红蛋白(HbA1c)相对于基线<7%的个体百分比.审查管理器5用于调查检索到的数据。
    我们涉及八个RCT。Bexagliflozin在降低HbA1c方面显着优于[最小二乘均差(LSMD)=-0.45,95%置信区间(CI=-0.55至-0.34,p<0.00001],空腹血浆糖(FPG)[LSMD=-1.37,95CI=-1.73至-1.00,p<0.00001],体重(LSMD=-1.77,95CI=-2.44至-1.10,p<0.00001),与安慰剂相比,SBP(LSMD=-4.11,95CI=-6.18至-2.03,p=0.0001)。bexagliflozin的安全性结果与安慰剂组一致。这项研究得出结论,bexagliflozin似乎是一种有希望的口服抗糖尿病药物,用于增强成年T2DM患者的血糖管理。
    Bexagliflozin,一种新型降血糖药,是TheracosBio开发的一种非常有效的SGLT2抑制剂,用于管理T2DM的血糖。美国食品和药物管理局(USFDA)于2023年1月20日首次批准bexagliflozin,用于作为2型糖尿病患者生活方式改变和锻炼的辅助治疗剂。所有纳入的RCTs均研究了20mgbexagliflozin对T2DM的血糖和血糖外作用的治疗效果和安全性。Bexagliflozin20mg显着降低HbA1c,FPG(血糖效应),体重,和SBP(血糖外效应)与安慰剂组相比T2DM。安全性数据显示,bexagliflozin与安慰剂组和多尿相当,尿路感染(UTI),鼻咽炎或上呼吸道感染(URTI),低血糖,恶心,和腹泻是最常见的非严重不良反应。与安慰剂组相比,Bexagliflozin20mg似乎是一种有效的SGLT2抑制剂,可以控制T2DM患者的血糖,并具有良好的血糖外作用。
    UNASSIGNED: This study assessed the clinical safety and efficacy of bexagliflozin, a sodium-glucose cotransporter 2(SGLT2) inhibitor, in managing glycemia among patients with type 2 diabetes mellitus (T2DM).
    UNASSIGNED: We examined RCTs with T2DM comparing the clinical effectiveness and safety of 20 mg once daily oral dose of bexagliflozin with placebo for managing glycemia till 28 May 2023, published on databases like ClinicalTrials.gov, PubMed, Embase, and Cochrane Library. Furthermore, reduction of body weight, fasting plasma sugarr(FPG), systolic blood pressure (SBP) and the percentage of individuals who achieved glycated hemoglobin (HbA1c) of < 7% from baseline were also evaluated. The Review Manager 5 was utilized to investigate the retrieved data.
    UNASSIGNED: We involved eight RCTs. Bexagliflozin was significantly superior in reducing HbA1c[least squares mean difference(LSMD) = -0.45,95% confidence interval (CI =-0.55 to -0.34,p < 0.00001], FPG [LSMD= -1.37, 95%CI =-1.73 to -1.00, p < 0.00001], body weight (LSMD= -1.77, 95%CI =-2.44 to-1.10, p < 0.00001), and SBP(LSMD= -4.11,95%CI = -6.18 to -2.03,p = 0.0001) in comparison to placebo. The safety outcomes of bexagliflozin were consistent with the placebo arm. This study concluded that bexagliflozin seems to be a promising oral anti-diabetic drug for enhancing glycemic management in adult patients with T2DM.
    Bexagliflozin, a novel hypoglycemic agent, is an extremely effective SGLT2 inhibitor developed by TheracosBio to manage glycemia in T2DM. The United States Food and Drug Administration (USFDA) granted first approval of bexagliflozin on 20 January 2023, for usage as an adjunctive therapy agent alongside lifestyle changes and exercise in T2DM. All included RCTs have investigated the therapeutic efficacy and safety of bexagliflozin 20 mg concerning glycemic and extra-glycemic effects in T2DM. Bexagliflozin 20 mg significantly reduces HbA1c, FPG (glycemic effect), body weight, and SBP (extra-glycemic effect) compared to the placebo arm in T2DM. Safety data show that bexagliflozin was comparable to placebo arm and polyuria, urinary tract infection (UTI), nasopharyngitis or upper respiratory tract infection (URTI), hypoglycemia, nausea, and diarrhea were the most common non-serious adverse effects. Bexagliflozin 20 mg seems to be an effective SGLT2 inhibitor compared to the placebo arm to manage glycemia in patients with T2DM along with favorable extra-glycemic effects.
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  • 文章类型: Journal Article
    代谢综合征(MetS)已成为全球重要的公共卫生问题。体重管理对于控制MetS风险因素至关重要,使能量平衡和减肥策略在营养建议中很重要。间歇性禁食(IF)已成为体重管理和降低心血管风险的饮食方法。然而,在以往的研究中,IF对心血管危险因素的影响不一致.本文旨在总结各种类型的IF对体重指数(BMI)的影响,血糖,血脂谱,还有血压,同时提供对其临床意义的见解。对干预研究和荟萃分析进行了全面搜索,并对结果进行了分析。结果表明,不同类型的IF会导致混合效应。限时进食(TRE)和隔日禁食(ADF)一致显示BMI下降,而间歇性能量限制(IER)的结果更不确定。IF对血糖和血脂的影响也是可变的,TRE和ADF通常显示出积极的结果。然而,IER的影响仍然不一致。需要更多的研究来了解IF管理代谢综合征和心血管危险因素的长期影响和最佳实施。
    Metabolic syndrome (MetS) has become a significant public health concern globally. Weight managementis crucial in controlling MetS risk factors, making energy balance and weight loss strategies important in nutrition recommendations. Intermittent fasting (IF) has gained traction as a dietary approach for weight management and cardiovascular risk reduction. However, the effects of IF on cardiovascular risk factors have been inconsistent in previous studies. This review aims to summarize the effects of various types of IF on body mass index (BMI), glycemia, lipid profile, and blood pressure, while providing insights into their clinical implications. A comprehensive search of interventional studies and meta-analyses was conducted, and the results were analyzed. The findings indicate that different types of IF lead to mixed effects. Time-restricted eating (TRE) and alternate-day fasting (ADF) consistently showed decreases in BMI, while the outcomes of intermittent energy restriction (IER) were more uncertain. The effects of IF on glycemia and lipid profile were also variable, with TRE and ADF generally showing positive results. However, the impact of IER remained inconsistent. More research is needed to understand the long-term effects and optimal implementation of IF for managing metabolic syndrome and cardiovascular risk factors.
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  • 文章类型: Journal Article
    洋地黄L.水果,也被称为猴面包树,由于其药用特性,在世界各地一直被传统地使用。据报道,各种植物部位的民族药理学用途用于水合作用,退烧药,抗寄生虫,镇咳,以及许多非洲国家的腹泻和痢疾的治疗。一些研究表明,除了这些应用之外,猴面包树有抗氧化剂,抗炎,镇痛药,和抗菌活性。猴面包树的健康益处归因于其生物活性化合物,即酚类,黄酮类化合物,原花青素,单宁,儿茶素,和类胡萝卜素。猴面包树果实也是维生素C和微量营养素的重要来源,包括锌,钾,镁,铁,钙,和蛋白质,这可以减少营养缺乏。尽管科学研究表明这种水果具有多种生物活性化合物,对健康有益,在审查有关其作用机制的信息和对临床试验探索的批判性分析方面存在差距,特别是,它们对血糖调节的影响。这项工作旨在介绍生物活性化合物的最新概况,生物活动,以及洋地黄果实对血糖的影响,强调其潜在的作用机制和对血糖调节的影响,在最近的动物和人体试验中进行了评估。
    Adansonia digitata L. fruit, also known as baobab, has been used traditionally throughout the world for its medicinal properties. Ethnopharmacological uses of various plant parts have been reported for hydration, antipyretic, antiparasitic, antitussive, and sudorific properties and also in the treatment of diarrhea and dysentery in many African countries. Several studies have revealed that in addition to these applications, baobab has antioxidant, anti-inflammatory, analgesic, and antimicrobial activities. The health benefits of baobab have been attributed to its bioactive compounds, namely phenols, flavonoids, proanthocyanins, tannins, catechins, and carotenoids. Baobab fruit is also an important source of vitamin C and micronutrients, including zinc, potassium, magnesium, iron, calcium, and protein, which may reduce nutritional deficiencies. Despite scientific studies revealing that this fruit has a wide diversity of bioactive compounds with beneficial effects on health, there is a gap in the review of information about their mechanisms of action and critical analysis of clinical trials exploring, in particular, their effect on glycemia regulation. This work aims to present a current overview of the bioactive compounds, biological activities, and effects of A. digitata fruit on blood glucose, highlighting their potential mechanisms of action and effects on glycemia regulation, evaluated in recent animal and human trials.
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  • 文章类型: Meta-Analysis
    背景:胰高血糖素样肽-1受体激动剂(GLP-1RAs)已成为2型糖尿病(T2DM)的基础治疗方法。本荟萃分析的目的是评估与其他GLP-1RA相比,司马鲁肽是否对血糖和其他心脏代谢危险因素产生更大的影响。
    方法:PubMed和CochraneLibrary数据库,连同灰色文献来源,是从2023年2月8日开始搜索的,以便头对头检索,评估司马鲁肽与其他GLP-1RAs对T2DM患者血糖和其他心脏代谢危险因素的影响的3期随机对照试验(RCTs).
    结果:我们最终汇集了总共3760名随机参与者的5个随机对照试验的数据。与其他GLP-1RAs相比,塞马鲁肽显著降低了0.44%的HbA1c水平,空腹血糖为0.48mmol/L,体重为2.53kg,体重指数为0.91kg/m2。接受司马鲁肽的受试者获得目标和最佳HbA1c的几率明显更大,同时,体重减轻>5%和10%的几率显著增加。然而,随机接受司马鲁肽治疗的受试者出现胃肠道不良事件和治疗中断的几率也显著增加.
    结论:塞马鲁肽比其他GLP-1RAs更有效,在改善血糖和其他心脏代谢危险因素方面,在T2DM患者中。
    Glucagon-like peptide-1 receptor agonists (GLP-1RAs) have emerged as a cornerstone treatment for type 2 diabetes mellitus (T2DM). The aim of the present meta-analysis was to assess whether semaglutide exerts greater effects on glycemia and other cardio-metabolic risk factors compared to other GLP-1RAs.
    PubMed and Cochrane Library databases, along with grey literature sources, were searched form inception to 8th February 2023, in order to retrieve head-to-head, phase 3 randomized controlled trials (RCTs) assessing the effect of semaglutide versus other GLP-1RAs on glycemia and other cardio-metabolic risk factors in T2DM.
    We finally pooled data from 5 RCTs in a total of 3760 randomized participants. Semaglutide compared to other GLP-1RAs provided a significantly greater reduction in HbA1c levels by 0.44 %, in fasting plasma glucose by 0.48 mmol/L, in body weight by 2.53 kg and in body mass index by 0.91 kg/m2. Subjects receiving semaglutide experienced significantly greater odds for achieving target and optimal HbA1c, along with significantly greater odds for weight loss >5 % and 10 %. However, subjects randomized to semaglutide also experienced significantly greater odds for gastrointestinal adverse events and treatment discontinuation.
    Semaglutide is more effective than rest GLP-1RAs, in terms of improvement in glycemia and other cardio-metabolic risk factors, among individuals with T2DM.
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  • 文章类型: Journal Article
    (1)背景:非传染性疾病(NCD)因其高发病率和死亡率而成为公共卫生的重要关注点。一种流行的与生活方式相关的NCD是2型糖尿病(T2D)。最近,脂肪细胞分泌的分子生物标志物,叫做脂肪因子,与T2D和肌肉功能障碍有关。然而,抗阻训练(RT)干预对T2D患者脂肪因子水平的影响尚未得到系统研究.(2)方法:遵循PRISMA指南。在PubMed/MEDLINE和WebofScience电子数据库中对研究进行了搜索。资格标准包括:(i)患有T2D的参与者;(ii)RT干预;(iii)随机对照试验;(iv)血清脂肪因子的测量。PEDro量表用于评估所选研究的方法学质量。对每个变量筛选显著差异(p≤0.05)和效应大小。(3)结果:在最初的2166条记录中,数据库搜索提取产生了14项研究纳入.纳入数据的方法学质量较高(PEDro评分中位数为6.5分)。纳入研究中分析的脂肪因子是瘦素,脂联素,visfatin,apelin,抵抗素,视黄醇结合蛋白4(RBP4),vaspin,chemerin,和门汀。RT干预(6-52周;最小有效持续时间>12周)对血清脂肪因子产生有意义的影响,(例如,瘦素)在T2D患者中的水平。(4)结论:RT可能是一种替代方案,但不是最优的,T2D中脂肪因子破坏的选项。合并(即,有氧和RT)长期训练可被认为是治疗脂肪因子水平紊乱的最佳干预措施。
    (1) Background: Non-communicable diseases (NCD) are an important concern for public health because of their high rates of morbidity and mortality. A prevalent lifestyle-linked NCD is type 2 diabetes mellitus (T2D). Recently, molecular biomarkers secreted by adipocytes, called adipokines, have been linked with T2D and muscle function disturbances. However, the effects of resistance training (RT) interventions on adipokine levels in patients with T2D have not been systematically studied. (2) Methods: The PRISMA guidelines were followed. Searches for the studies were performed in the PubMed/MEDLINE and Web of Science electronic databases. Eligibility criteria included: (i) participants with T2D; (ii) RT interventions; (iii) randomized controlled trials; and (iv) measurement of serum adipokines. The PEDro scale was used to assess the methodological quality of the selected studies. Significant differences (p ≤ 0.05) and effect size were screened for each variable. (3) Results: Of the initial 2166 records, database search extraction yielded 14 studies to be included. The methodological quality of the included data was high (median PEDro score of 6.5). Analyzed adipokines in the included studies were leptin, adiponectin, visfatin, apelin, resistin, retinol-binding protein 4 (RBP4), vaspin, chemerin, and omentin. RT interventions (6-52 weeks; minimal effective duration >12 weeks) exert a meaningful effect on serum adipokine, (e.g., leptin) levels in T2D patients. (4) Conclusions: RT may be an alternative, but not an optimal, option in adipokine disruptions in T2D. Combined (i.e., aerobic and RT) long-term training may be considered the optimal intervention for treating adipokine level disturbances.
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  • 文章类型: Meta-Analysis
    最近开发的酮(单酯或盐)补充剂可外源急剧升高血液β-羟基丁酸酯(BHB),而不会延长禁食或限制碳水化合物的时间。以前的(小规模)研究已经发现了外源性酮的降血糖作用。本研究旨在系统地回顾现有证据,并对报道外源性酮和血糖的研究进行荟萃分析。我们在2021年12月13日检索了6个电子数据库,以获得任何长度的随机和非随机试验,这些试验报告了使用外源性酮。我们在2个主要分析中计算了血液BHB和葡萄糖的原始平均差异(MD):1)与急性摄入外源性酮之前相比,以及2)急性摄入外源性酮之后与比较补充剂相比。我们使用随机效应模型汇集效应大小,并进行预先指定的亚组分析,以检查潜在解释因素的影响,包括研究人群,锻炼,血BHB,和补充类型,给药,和时间。使用Cochrane的偏倚风险工具检查偏倚风险。无法进行荟萃分析的研究进行了叙述性总结。本综述总结了43项试验,包括586名参与者。摄入后,外源性酮增加血液BHB(MD=1.73mM;95%CI:1.26,2.21mM;P<0.001),降低平均血糖(MD=-0.54mM;95%CI:-0.68,-0.40mM;P<0.001).同样,与安慰剂相比,血BHB升高(MD=1.98mM;95%CI:1.52,2.45mM;P<0.001),血糖降低(MD=-0.47mM;95%CI:-0.57,-0.36mM;P<0.001).在这两种分析中,与盐相比,酮单酯的作用明显更大(P<0.001)。现有证据表明,急性摄入外源性酮会导致血液BHB增加和血糖降低。发现长期补充酮的证据有限。
    Recently developed ketone (monoester or salt) supplements acutely elevate blood β-hydroxybutyrate (BHB) exogenously without prolonged periods of fasting or carbohydrate restriction. Previous (small-scale) studies have found a blood glucose-lowering effect of exogenous ketones. This study aimed to systematically review available evidence and conduct meta-analyses of studies reporting on exogenous ketones and blood glucose. We searched 6 electronic databases on 13 December 2021 for randomized and nonrandomized trials of any length that reported on the use of exogenous ketones. We calculated raw mean differences (MDs) in blood BHB and glucose in 2 main analyses: 1) after compared with before acute ingestion of exogenous ketones and 2) following acute ingestion of exogenous ketones compared with a comparator supplement. We pooled effect sizes using random-effects models and performed prespecified subgroup analyses to examine the effect of potential explanatory factors, including study population, exercise, blood BHB, and supplement type, dosing, and timing. Risk of bias was examined using Cochrane\'s risk-of-bias tools. Studies that could not be meta-analyzed were summarized narratively. Forty-three trials including 586 participants are summarized in this review. Following ingestion, exogenous ketones increased blood BHB (MD = 1.73 mM; 95% CI: 1.26, 2.21 mM; P < 0.001) and decreased mean blood glucose (MD = -0.54 mM; 95% CI: -0.68, -0.40 mM; P < 0.001). Similarly, when compared with placebo, blood BHB increased (MD = 1.98 mM; 95% CI: 1.52, 2.45 mM; P < 0.001) and blood glucose decreased (MD = -0.47 mM; 95% CI: -0.57, -0.36 mM; P < 0.001). Across both analyses, significantly greater effects were seen with ketone monoesters compared with salts (P < 0.001). The available evidence indicates that acute ingestion of exogenous ketones leads to increased blood BHB and decreased blood glucose. Limited evidence on prolonged ketone supplementation was found.
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  • 文章类型: Journal Article
    背景:在那里,我们综述了妊娠期糖尿病(GDM)的发病机制,它对胎儿生理的影响,和新生儿结局,以及妊娠合并GDM的产前皮质类固醇治疗(ACST)的使用。
    方法:MEDLINE和PubMed搜索在1990-2022年间进行,使用了这些主题的关键字组合。根据调查的目的,本叙述性综述确定并纳入了适当的文章.
    结果:GDM是一种与意外妊娠过程和结局相关的多因素疾病。虽然GDM对胎儿心血管和神经系统有影响,尤其是早产新生儿,在怀孕期间使用ACST必须考虑到母体和胎儿的特征。
    结论:GDM对引入ACST后的新生儿结局没有影响。ACST的使用必须根据其对发育中的胎儿的胎龄特异性影响进行个性化和考虑。
    BACKGROUND: There, we review the pathogenesis of gestational diabetes mellitus (GDM), its influence on fetal physiology, and neonatal outcomes, as well as the usage of antenatal corticosteroid therapy (ACST) in pregnancies complicated by GDM.
    METHODS: MEDLINE and PubMed search was performed for the years 1990-2022, using a combination of keywords on such topics. According to the aim of the investigation, appropriate articles were identified and included in this narrative review.
    RESULTS: GDM is a multifactorial disease related to unwanted pregnancy course and outcomes. Although GDM has an influence on the fetal cardiovascular and nervous system, especially in preterm neonates, the usage of ACST in pregnancy must be considered taking into account maternal and fetal characteristics.
    CONCLUSIONS: GDM has no influence on neonatal outcomes after ACST introduction. The ACST usage must be personalized and considered according to its gestational age-specific effects on the developing fetus.
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