cardiometabolic disease

心血管代谢疾病
  • 文章类型: Journal Article
    代谢健康肥胖(MHO)的人有患心脏代谢疾病的风险。我们调查了MHO的患病率以及影响其转变为代谢不健康状态(MUS)的因素。这项研究是作为Kerman冠状动脉疾病危险因素研究(KERCADRS)的一部分进行的。从2014年到2018年,评估了9997人。MHO参与者的肥胖和代谢状态在他们最初参与研究5年后被重新检查。在347MHO中,238人在随访中被访问。29人(12.2%)有代谢不健康的正常体重(MUNW),169名(71.0%)患有代谢不健康肥胖(MUO),其他人有健康的代谢状态。年龄,总胆固醇,舒张压和甘油三酯(TG)变量,基线血清TG水平与5年内发生MUS的风险显著增加相关(p<.05)。预测发展为MUS的TG水平最佳切点为107mg/dL,灵敏度为62.1%,特异性为77.5%(AUC=0.734,p<.001)。在5年内,很高比例的MHO人进入MUS。高于107mg/dL的TG水平可以帮助识别发展为MUS的风险较高的人。
    People with metabolically healthy obesity (MHO) are at risk of developing cardiometabolic diseases. We investigated the prevalence of MHO and factors influencing its transition into a metabolically unhealthy state (MUS). This study was conducted as part of the Kerman Coronary Artery Disease Risk Factor Study (KERCADRS). From 2014 to 2018, 9997 people were evaluated. The obesity and metabolic status of the MHO participants were re-examined after 5 years of their initial participation in the study. Out of 347 MHO, 238 individuals were accessed at follow-up. Twenty-nine (12.2%) had metabolic unhealthy normal weight (MUNW), 169 (71.0%) had metabolic unhealthy obesity (MUO), and the others had healthy metabolic state. Among age, total cholesterol, diastolic blood pressure and triglyceride (TG) variables, the baseline serum TG level was associated with a significant increase in the risk of developing MUS during 5 years (p <.05). The TG level optimal cut-off point for predicting the development into MUS was 107 mg/dL with 62.1% sensitivity and 77.5% specificity (AUC = 0.734, p <.001). A high percentage of MHO people transit into MUS during 5 years. A TG level higher than 107 mg/dL can help to identify people at a higher risk of developing into MUS.
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  • 文章类型: Journal Article
    背景:久坐行为(SB)对心脏代谢疾病(CMD)风险有害,这可以从年轻的成年开始。为了在年轻人中设计有效的SB-CMD干预措施,重要的是要了解哪些特定环境的久坐行为(CS-SB)对CMD风险最有害,与CS-SB共存的生活方式行为,以及CS-SB的社会生态预测因子。方法这项纵向观察研究将招募500名大学生(18-24岁)。将进行两次实验室访问,相隔12个月,其中复合CMD风险评分(例如,动脉僵硬度,代谢和炎症生物标志物,心率变异性,和身体成分)将被计算,并进行问卷调查,以测量生活方式行为和社会生态模型的不同水平。每次访问后,总SB(activPAL)和CS-SB(电视,交通运输,学术/职业,休闲电脑,\“其他\”;生态瞬时评估)将在七天内进行测量。讨论假设某些CS-SB将显示与CMD风险的更强关联,与T-SB相比,即使考虑到共存的生活方式行为。预计一系列的个体内,个体间,物理环境和社会生态因素将预测CS-SB。这项研究的结果将支持基于证据的发展,多层次干预以降低SB为目标,减轻CBYA的CMD风险。
    UNASSIGNED: Sedentary behavior (SB) is detrimental to cardiometabolic disease (CMD) risk, which can begin in young adulthood. To devise effective SB-CMD interventions in young adults, it is important to understand which context-specific sedentary behaviors (CS-SB) are most detrimental for CMD risk, the lifestyle behaviors that co-exist with CS-SBs, and the socioecological predictors of CS-SB.
    UNASSIGNED: This longitudinal observational study will recruit 500 college-aged (18-24 years) individuals. Two laboratory visits will occur, spaced 12 months apart, where a composite CMD risk score (e.g., arterial stiffness, metabolic and inflammatory biomarkers, heart rate variability, and body composition) will be calculated, and questionnaires to measure lifestyle behaviors and different levels of the socioecological model will be administered. After each visit, total SB (activPAL) and CS-SB (television, transportation, academic/ occupational, leisure computer, \"other\"; ecological momentary assessment) will be measured across seven days.
    UNASSIGNED: It is hypothesized that certain CS-SB will show stronger associations with CMD risk, compared to T-SB, even after accounting for coexisting lifestyle behaviors. It is expected that a range of intra-individual, inter-individual, and physical environment socioecological factors will predict CS-SB. The findings from this study will support the development of an evidence-based, multi-level intervention to target SB reduction and mitigate CMD risk in CBYA.
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  • 文章类型: Journal Article
    在过去的几年里,人们对睡眠持续时间和质量之间的联系的兴趣激增,睡眠障碍,主要是阻塞性睡眠呼吸暂停(OSA)和维生素D。越来越多的证据支持维生素D在维持和调节最佳睡眠中的新作用。此外,OSA与血清维生素D水平下降之间存在显着联系,随着睡眠呼吸暂停的严重程度恶化,这种情况似乎会加剧。维生素D状态也可能作为介质或为OSA和心脏代谢疾病之间的关联提供解释。但是目前这方面的研究还不够。研究表明,补充维生素D可以优化睡眠质量,提供更多维生素D水平不足与睡眠障碍之间联系的证据。然而,目前尚不清楚低血清维生素D水平是否是OSA发展的一个促成因素,或者OSA是否会导致个体维生素D缺乏.因此,各种研究都在努力研究OSA与维生素D缺乏之间的复杂关系。在儿童和青少年中,虽然数据有限,睡眠障碍和维生素D水平之间似乎也有联系。因此,本综述的目的是全面概述目前关于维生素D与成人和儿童睡眠障碍之间关联的证据.
    Over the past few years, there has been a surge in interest regarding the connection between sleep duration and quality, sleep disorders, mainly Obstructive sleep apnoea (OSA) and Vitamin D. There is growing evidence to support a new role of Vitamin D in the maintenance and regulation of optimal sleep. Furthermore, a notable link has been identified between OSA and a decrease in serum Vitamin D levels, which appears to intensify as the severity of sleep apnea worsens. Vitamin D status could also potentially serve as a mediator or provide an explanation for the association between OSA and cardiometabolic morbidity, but the current state of research in this area is inadequate. Studies have indicated that the supplementation of Vitamin D can optimize sleep quality, presenting more proof of the connection between insufficient vitamin D levels and sleep disorders. However, it is unclear whether low serum Vitamin D levels are a contributing factor to OSA development or if OSA predisposes individuals to Vitamin D deficiency. As a result, various studies have endeavored to examine the complex relationship between OSA and Vitamin D deficiency. In children and adolescents, while data is limited, there seems also to be a link between sleep disorders and Vitamin D levels. Therefore, the objective of this review is to provide a comprehensive overview of the current evidence on the association between Vitamin D and sleep disorders in both adults and children.
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  • 文章类型: Journal Article
    子宫内环境在塑造生命过程中的慢性疾病风险中起着至关重要的作用。我们前瞻性评估了有与没有产前严重急性呼吸道综合症冠状病毒2感染的母亲所生的幼儿的心脏代谢结果。子宫内严重急性呼吸综合征冠状病毒2暴露的儿童左心室质量较高,与母体免疫学指标改变有关。
    The intrauterine environment plays a critical role in shaping chronic disease risk over the life course. We prospectively evaluated cardiometabolic outcomes in toddlers born to mothers with versus without prenatal severe acute respiratory syndrome coronavirus 2 infection. Children with in utero severe acute respiratory syndrome coronavirus 2 exposure had higher left ventricular mass in association with altered maternal immunologic indices.
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  • 文章类型: Journal Article
    背景:在美国,癌症人群的有效生存期延长已引起人们对该人群心脏代谢疾病发病率和死亡率上升风险的极大关注.这种增加的风险强调了迫切需要研究癌症幸存者的有效药物干预措施。值得注意的是,二甲双胍,一种具有多效性的众所周知的代谢调节剂,已显示出对糖尿病个体心脏代谢紊乱的保护作用。尽管有这些有希望的迹象,支持其改善癌症幸存者心脏代谢结局的证据仍然很少.
    方法:使用美国国家健康和营养调查(NHANES)登记的全国代表性癌症幸存者样本,建立了一个前瞻性队列。从2003年到2018年。结果来自患者访谈,体检,以及截至2019年的公共访问相关死亡率档案。氧化平衡评分用于评估参与者的氧化应激水平。评估二甲双胍使用与心脏代谢疾病风险和相关死亡率之间的相关性。通过Cox比例风险模型进行心脏代谢死亡率的生存分析,使用logistic回归模型对心脏代谢疾病结局进行横断面分析.进行相互作用分析以探讨二甲双胍的具体药理机制。
    结果:在3995名癌症幸存者中(加权人群,21,671,061,加权平均数[SE]年龄,62.62[0.33]岁;2119[53.04%]女性;2727[68.26%]非西班牙裔白人),448报告了二甲双胍的使用情况。在长达17年的随访期间(中位数,6.42年),有记录的1233人死亡,包括481例心脏代谢疾病死亡.多变量模型表明,使用二甲双胍与全因风险较低相关(风险比[HR],0.62;95%置信区间[CI],0.47-0.81)和心脏代谢(HR,0.65;95%CI,0.44-0.97)死亡率与非二甲双胍使用者相比。二甲双胍的使用也与总心血管疾病的风险较低相关(比值比[OR],0.41;95%CI,0.28-0.59),stroke(OR,0.44;95%CI,0.26-0.74),高血压(OR,0.27;95%CI,0.14-0.52),和冠心病(或,0.41;95%CI,0.21-0.78)。在四个被确定为心脏代谢高风险组的特定癌症人群中,观察到的逆关联在亚组分析中是一致的。相互作用分析表明,与不使用二甲双胍相比,使用二甲双胍可能会抵消氧化应激。
    结论:在这项涉及美国癌症幸存者全国代表性人群的队列研究中,二甲双胍的使用与心脏代谢疾病的风险降低显著相关,全因死亡率,和心脏代谢死亡率。
    BACKGROUND: In the USA, the prolonged effective survival of cancer population has brought significant attention to the rising risk of cardiometabolic morbidity and mortality in this population. This heightened risk underscores the urgent need for research into effective pharmacological interventions for cancer survivors. Notably, metformin, a well-known metabolic regulator with pleiotropic effects, has shown protective effects against cardiometabolic disorders in diabetic individuals. Despite these promising indications, evidence supporting its efficacy in improving cardiometabolic outcomes in cancer survivors remains scarce.
    METHODS: A prospective cohort was established using a nationally representative sample of cancer survivors enrolled in the US National Health and Nutrition Examination Survey (NHANES), spanning 2003 to 2018. Outcomes were derived from patient interviews, physical examinations, and public-access linked mortality archives up to 2019. The Oxidative Balance Score was utilized to assess participants\' levels of oxidative stress. To evaluate the correlations between metformin use and the risk of cardiometabolic diseases and related mortality, survival analysis of cardiometabolic mortality was performed by Cox proportional hazards model, and cross-sectional analysis of cardiometabolic diseases outcomes was performed using logistic regression models. Interaction analyses were conducted to explore the specific pharmacological mechanism of metformin.
    RESULTS: Among 3995 cancer survivors (weighted population, 21,671,061, weighted mean [SE] age, 62.62 [0.33] years; 2119 [53.04%] females; 2727 [68.26%] Non-Hispanic White individuals), 448 reported metformin usage. During the follow-up period of up to 17 years (median, 6.42 years), there were 1233 recorded deaths, including 481 deaths from cardiometabolic causes. Multivariable models indicated that metformin use was associated with a lower risk of all-cause (hazard ratio [HR], 0.62; 95% confidence interval [CI], 0.47-0.81) and cardiometabolic (HR, 0.65; 95% CI, 0.44-0.97) mortality compared with metformin nonusers. Metformin use was also correlated with a lower risk of total cardiovascular disease (odds ratio [OR], 0.41; 95% CI, 0.28-0.59), stroke (OR, 0.44; 95% CI, 0.26-0.74), hypertension (OR, 0.27; 95% CI, 0.14-0.52), and coronary heart disease (OR, 0.41; 95% CI, 0.21-0.78). The observed inverse associations were consistent across subgroup analyses in four specific cancer populations identified as cardiometabolic high-risk groups. Interaction analyses suggested that metformin use as compared to non-use may counter-balance oxidative stress.
    CONCLUSIONS: In this cohort study involving a nationally representative population of US cancer survivors, metformin use was significantly correlated with a lower risk of cardiometabolic diseases, all-cause mortality, and cardiometabolic mortality.
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  • 文章类型: Journal Article
    多囊卵巢综合征(PCOS)是一种全球常见的内分泌疾病,临床表现包括生殖,新陈代谢,和内分泌元素。然而,对PCOS的评估和管理仍然不一致,许多妇女未经诊断和治疗。我们现在也了解到,PCOS的管理应该贯穿女性的整个生命周期,因为该综合征的许多因素在绝经后仍然存在。传统上,管理侧重于高雄激素血症和月经少发的治疗。PCOS女性常有血脂异常,高血压,肥胖,代谢综合征,荷尔蒙异常可能会恶化,因此心血管疾病发病率和死亡率的风险更高,绝经后风险增加。在用激素疗法治疗时,特别是联合口服避孕药,可以改善心血管危险因素,管理计划应包括对这些因素的具体诊断和管理,如果存在,因为对动脉粥样硬化性心血管疾病(ASCVD)的风险有很大的贡献。鉴于综合症的复杂性,最佳管理通常需要多学科的方法,包括脂质和心脏代谢专家,以提供咨询和支持生活方式的改变以及药物治疗,以解决所有生殖,内分泌,和心脏代谢异常。
    Polycystic ovary syndrome (PCOS) is a common endocrinopathy worldwide with a heterogeneous clinical presentation including reproductive, metabolic, and endocrine elements. However, the assessment and management of PCOS remains inconsistent, with many women undiagnosed and untreated. We now also understand that the management of PCOS should extend throughout a woman\'s lifespan as many elements of the syndrome persist after menopause. Management has traditionally focused on the treatment of hyperandrogenism and oligomenorrhea. Women with PCOS often have dyslipidemia, hypertension, obesity, and metabolic syndrome, which may be worsened by the hormonal abnormalities, and are therefore at higher risk for cardiovascular disease morbidity and mortality, a risk that increases after menopause. While treatment with hormonal therapy, in particular combined oral contraceptives, may improve cardiovascular risk factors, management plans should incorporate specific diagnosis and management of these factors, if present, because of the strong contribution to the risk for atherosclerotic cardiovascular disease (ASCVD). Given the complexities of the syndrome, optimal management often requires a multi-disciplinary approach including the lipid and cardiometabolic specialist to provide counseling and support for lifestyle modification along with pharmacologic therapy as indicated to address the full range of any reproductive, endocrine, and cardiometabolic abnormalities.
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  • 文章类型: Journal Article
    MFGE8是一种主要的外泌体(EV)蛋白,在动物研究中已知可介导2型糖尿病(T2DM)中的炎症和动脉粥样硬化。该蛋白在肥胖中的病理生理作用,T2DM,心血管疾病在人类中的研究较少。早些时候,我们报道了MFGE8基因中罕见的亚裔印度人口特异性错义变体(rs371227978;Arg148His),该基因与循环Mfge8和T2DM增加有关。我们进一步研究了Mfge8在其他亚洲印第安人(n=4897),欧洲人和其他来自英国生物银行(UKBB)(n=455,808)和美国(n=1150)的多种族队列中与T2DM风险的作用。我们还评估了斑马鱼(ZF)中富含Mfge8的人类EV对心脏代谢器官系统的影响。Arg148His变异体的大多数个体携带者不仅具有高循环Mfge8,而且与葡萄糖呈正相关(r=0.42;p=4.9×10-04),而在亚洲印第安人中,非携带者显示Mfge8与葡萄糖呈负相关(r=-0.38;p=0.001)。在非南亚种族中,相同的变体是单态的。即使没有变体,在其他非南亚种族中,血清Mfge8与血糖显着相关(r=0.47;p=2.2×10-13)。由于Mfge8是EV标记,作为一项探索性研究,我们测试了富含Mfge8的人类电动汽车对ZF幼虫的暴露情况。ZF幼虫对胰岛素敏感器官表现出快速作用,发展为脂肪肝疾病,有或没有高脂饮食(HFD)的情况下,心脏肥大并表现出多余的生长,肌肉结构较差。相比之下,对照组鱼仅在HFD喂养后才出现脂肪肝和心脏肥大。动物研究支持Mfge8在肥胖中的作用,胰岛素抵抗,和动脉粥样硬化,目前的研究表明,循环Mfge8可能成为预测人类T2DM和心血管疾病风险的潜在标志物.
    MFGE8 is a major exosome (EV) protein known to mediate inflammation and atherosclerosis in type 2 diabetes mellitus (T2DM) in animal studies. The pathophysiological role of this protein in obesity, T2DM, and cardiovascular disease is less investigated in humans. Earlier we reported a rare Asian Indian population-specific missense variant (rs371227978; Arg148His) in the MFGE8 gene associated with increased circulating Mfge8 and T2DM. We have further investigated the role of Mfge8 with T2DM risk in additional Asian Indians (n = 4897) and Europeans and other multiethnic cohorts from UK Biobank (UKBB) (n = 455,808) and the US (n = 1150). We also evaluated the exposure of Mfge8-enriched human EVs in zebrafish (ZF) for their impact on cardiometabolic organ system. Most individual carriers of Arg148His variant not only had high circulating Mfge8 but also revealed a positive significant correlation with glucose (r = 0.42; p = 4.9 × 10-04), while the non-carriers showed a negative correlation of Mfge8 with glucose (r = -0.38; p = 0.001) in Asian Indians. The same variant was monomorphic in non-South Asian ethnicities. Even without the variant, serum Mfge8 correlated significantly with blood glucose in other non-South Asian ethnicities (r = 0.47; p = 2.2 × 10-13). Since Mfge8 is an EV marker, we tested the exposure of Mfge8-enriched human EVs to ZF larvae as an exploratory study. The ZF larvae showed rapid effects on insulin-sensitive organs, developing fatty liver disease, heart hypertrophy and exhibiting redundant growth with poor muscular architecture with and without the high-fat diet (HFD). In contrast, the control group fishes developed fatty liver disease and heart hypertrophy only after the HFD feeding. Backed with strong support from animal studies on the role of Mfge8 in obesity, insulin resistance, and atherosclerosis, the current research suggests that circulating Mfge8 may become a potential marker for predicting the risk of T2DM and cardiovascular disease in humans.
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  • 文章类型: Journal Article
    背景:地中海饮食与几种心脏代谢疾病的风险降低有关。科学文献中缺乏对地中海饮食的明确定义以及互联网上营养错误信息的增加表明,寻求基于网络的地中海饮食信息的消费者可能会感到困惑。
    目的:我们在有影响力的社交媒体平台上对有关地中海饮食的信息进行了社交媒体内容分析,TikTok,检查关于饮食的公共话语,并确定潜在的错误信息领域。然后,我们在健康促进的背景下分析了这些发现,以确定使用TikTok促进地中海饮食健康生活的潜在挑战和机遇。
    方法:下载并定性检查了搜索#mediterraneandiet标签后首次出现的202个TikTok帖子。岗位特点和特点,海报信息,并在各个帖子中提取和合成了参与度指标。根据海报报告的凭证,将职位分为由卫生专业人员创建的职位和由非卫生专业人员创建的职位。除了整个样本的描述性统计之外,我们使用卡方检验比较了专业人士和非专业人士为内容创建的帖子。
    结果:TikTok帖子的内容各不相同,但是,由卫生专业人员与非专业人员开发的帖子更有可能提供地中海饮食的定义(16/106,15.1%vs2/96,2.1%;P=.001),使用科学引用来支持索赔(26/106,24.5%vs0/96,0%;P<.001),并讨论特定营养素(33/106,31.1%vs6/96,6.3%;P<.001)和与饮食相关的疾病(27/106,25.5%vs5/96,5.2%;P<.001)与非健康专业人员创建的职位相比。
    结论:社交媒体有望成为推广地中海饮食的场所,但是在这项研究中发现的信息的可变性突出表明,在开发使用新媒体结构的地中海饮食干预措施时,需要对饮食及其成分进行明确的定义。
    BACKGROUND: The Mediterranean diet has been linked to reduced risk for several cardiometabolic diseases. The lack of a clear definition of the Mediterranean diet in the scientific literature and the documented proliferation of nutrition misinformation on the internet suggest the potential for confusion among consumers seeking web-based Mediterranean diet information.
    OBJECTIVE: We conducted a social media content analysis of information about the Mediterranean diet on the influential social media platform, TikTok, to examine public discourse about the diet and identify potential areas of misinformation. We then analyzed these findings in the context of health promotion to identify potential challenges and opportunities for the use of TikTok in promoting the Mediterranean diet for healthy living.
    METHODS: The first-appearing 202 TikTok posts that resulted from a search of the hashtag #mediterraneandiet were downloaded and qualitatively examined. Post features and characteristics, poster information, and engagement metrics were extracted and synthesized across posts. Posts were categorized as those created by health professionals and those created by nonhealth professionals based on poster-reported credentials. In addition to descriptive statistics of the entire sample, we compared posts created by professionals and nonprofessionals for content using chi-square tests.
    RESULTS: TikTok posts varied in content, but posts that were developed by health professionals versus nonprofessionals were more likely to offer a definition of the Mediterranean diet (16/106, 15.1% vs 2/96, 2.1%; P=.001), use scientific citations to support claims (26/106, 24.5% vs 0/96, 0%; P<.001), and discuss specific nutrients (33/106, 31.1% vs 6/96, 6.3%; P<.001) and diseases related to the diet (27/106, 25.5% vs 5/96, 5.2%; P<.001) compared to posts created by nonhealth professionals.
    CONCLUSIONS: Social media holds promise as a venue to promote the Mediterranean diet, but the variability in information found in this study highlights the need to create clear definitions about the diet and its components when developing Mediterranean diet interventions that use new media structures.
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  • 文章类型: Journal Article
    背景:肠道代谢产物三甲胺-N-氧化物(TMAO)的升高与心血管和代谢疾病有关。TMAO水平升高是否反映了早期的机械参与或不断发展的疾病的后遗症,尚待阐明。这项研究的目的是进一步探索这些潜在的关联。
    方法:我们研究了TMAO的循环水平与其前体底物之间的关系,饮食因素,健康BMI(18.530,n=27)和代谢综合征(MetS;≥3ATPIII报告标准,n=39)。
    结果:出乎意料的是,血浆[TMAO]在组间没有实质性变化(平均值为3-4μM;p>0.05),尽管肉碱在MetS参与者中升高。MetS组肠道微生物多样性和Firmicutes也显著降低(p<0.05)。对不同参数的探索性分析揭示了循环[TMAO]和海鲜摄入量之间的显着相关性(p=0.007),肠道微生物多样性(p=0.017-0.048),和血浆[三甲胺](TMA;p=0.001)。与人体测量参数或心脏代谢疾病风险无明显关联。组内和组间[TMAO]的大多数差异仍无法解释。
    结论:数据表明循环[TMAO]可能与海鲜摄入量显著相关,健康和早期疾病表型的TMA底物水平和肠道微生物多样性。然而,平均浓度保持<5µM,几乎没有证据表明TMAO和心脏代谢疾病风险之间存在联系。这些观察结果表明,循环TMAO可能不会在机制上参与心脏代谢疾病的发展。后来的升高可能是现存疾病的有害后遗症。
    BACKGROUND: Elevations in the gut metabolite trimethylamine-N-oxide (TMAO) have been linked to cardiovascular and metabolic diseases. Whether elevated TMAO levels reflect early mechanistic involvement or a sequela of evolving disease awaits elucidation. The purpose of this study was to further explore these potential associations.
    METHODS: We investigated relationships between circulating levels of TMAO and its pre-cursor substrates, dietary factors, gut microbiome profiles and disease risk in individuals with a Healthy BMI (18.5 < BMI < 25, n = 41) or key precursor states for cardiometabolic disease: Overweight (25 < BMI < 30 kg/m2, n = 33), Obese (BMI > 30, n = 27) and Metabolic Syndrome (MetS; ≥ 3 ATPIII report criteria, n = 39).
    RESULTS: Unexpectedly, plasma [TMAO] did not vary substantially between groups (means of 3-4 µM; p > 0.05), although carnitine was elevated in participants with MetS. Gut microbial diversity and Firmicutes were also significantly reduced in the MetS group (p < 0.05). Exploratory analysis across diverse parameters reveals significant correlations between circulating [TMAO] and seafood intake (p = 0.007), gut microbial diversity (p = 0.017-0.048), and plasma [trimethylamine] (TMA; p = 0.001). No associations were evident with anthropometric parameters or cardiometabolic disease risk. Most variance in [TMAO] within and between groups remained unexplained.
    CONCLUSIONS: Data indicate that circulating [TMAO] may be significantly linked to seafood intake, levels of TMA substrate and gut microbial diversity across healthy and early disease phenotypes. However, mean concentrations remain < 5 µM, with little evidence of links between TMAO and cardiometabolic disease risk. These observations suggest circulating TMAO may not participate mechanistically in cardiometabolic disease development, with later elevations likely a detrimental sequela of extant disease.
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  • 文章类型: Journal Article
    背景:非裔美国妇女(AAW)患有与压力相关的心脏代谢(CM)疾病(包括肥胖)的高风险,心脏病,和糖尿病。先前的干预措施缺乏对文化上细微的压力现象的关注(女超人模式[SWS],语境压力,和网络压力),它们与不健康的饮食和久坐的行为呈正相关。
    目的:和谐研究旨在测试一种文化定制的基于正念的压力管理干预措施,以解决SWS,语境压力,网络压力是坚持健康运动和饮食目标的潜在障碍。这项研究将帮助AAW利用他们的优势,通过加强积极的重新评估来促进心脏代谢健康。自我调节,和自我效能感作为对抗慢性应激诱导的生物行为发病率和死亡风险的保护因素。
    方法:这种双臂,随机对照试验将测试两组的效果,在线干预。和谐1包括文化定制的锻炼和营养教育。和谐2包括基于正念的减压,锻炼,营养教育。我们的目标是招募200名年龄≥18岁的有CM风险的AAW。
    结果:主要结果(活动记录和类胡萝卜素水平)和次要结果(身体组成,炎症标志物,葡萄糖代谢,和压力)正在基线和4-,8-,干预后12个月。意向治疗,数据分析方法将用于测试主要结果的群体差异。
    结论:这项研究是第一个解决AAW中文化上细微的压力现象的研究(SWS,网络应力,和情境化压力)使用文化定制的压力管理,锻炼,和营养教育方法,以降低AAW中的生物行为CM风险。定量和定性结果将为AAW的可扩展和可持续的CM风险降低计划的开发提供信息。
    背景:根据NIH资助的临床试验信息传播政策,多个PI注册了临床试验(标识符:NCT04705779)并在ClinicalTrials.gov中报告了汇总结果,在规定的时间内。
    BACKGROUND: African American Women (AAW) are at high risk for stress-related cardiometabolic (CM) conditions including obesity, heart disease, and diabetes. Prior interventions lack attention to culturally-nuanced stress phenomena (Superwoman Schema [SWS], contextualized stress, and network stress), which are positively and significantly associated with unhealthy eating and sedentary behavior.
    OBJECTIVE: The HARMONY Study is designed to test a culturally tailored mindfulness-based stress management intervention to address SWS, contextualized stress, and network stress as potential barriers to adherence to healthy exercise and eating goals. The study will help AAW build on their strengths to promote cardiometabolic health by enhancing positive reappraisal, self-regulation, and self-efficacy as protective factors against chronic stress-inducing biobehavioral morbidity and mortality risk.
    METHODS: This two-arm, randomized-controlled trial will test the effects of two group-based, online interventions. HARMONY 1 includes culturally-tailored exercise and nutrition education. HARMONY 2 includes mindfulness-based stress reduction, exercise, and nutrition education. We aim to recruit 200 AAW ≥ 18 years old with CM risk.
    RESULTS: Primary outcomes (actigraphy and carotenoid levels) and secondary outcomes (body composition, inflammatory markers, glucose metabolism, and stress) are being collected at baseline and 4-, 8-, and 12-months post-intervention. Intent-to-treat, data analytic approaches will be used to test group differences for the primary outcomes.
    CONCLUSIONS: This study is the first to address culturally-nuanced stress phenomena in AAW (SWS, network stress, and contextualized stress) using culturally-tailored stress management, exercise, and nutrition educational approaches to reduce biobehavioral CM risk among AAW. Quantitative and qualitative results will inform the development of scalable and sustainable CM risk-reduction programming for AAW.
    BACKGROUND: The Multiple PIs registered the clinical trial (Identifier: NCT04705779) and reporting of summary results in ClinicalTrials.gov in accordance with the NIH Policy on the Dissemination of NIH-Funded Clinical Trial Information, within the required timelines.
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