whites

白色
  • 文章类型: Journal Article
    未经证实:非黑色素瘤皮肤癌(NMSC)是世界上最常见的癌症类型。在传统的波斯医学(TPM)中,各种类型的气质(Mizaj)被认为是诊断,请客,预防各种疾病。本研究旨在评估NMSC患者与对照组的气质。
    UNASSIGNED:2018年在设拉子医科大学附属ShahidFaghihi医院皮肤科诊所进行了一项病例对照研究(Shiraz,伊朗)。共有110名患者,年龄≥20岁,确诊NMSC(病例组),181名没有NMSC的个体(对照组)被纳入研究。使用Mojahedi的Mizaj问卷评估两组参与者的气质。数据采用SPSS软件进行分析,P<0.05被认为具有统计学意义。
    UNASSIGNED:结果表明,干性气质个体的发展中NMSC的比值比为2.62(95CI:1.42-4.83,P=0.002)倍。此外,有慢性皮肤溃疡和其他类型癌症病史的患者的比值比分别为35.7倍(95CI:11.9-107.15,P<0.001)和5.22倍(95CI:1.43-19.06,P=0.012),分别,比对照组。
    未经评估:气质与NMSC有关,特别是干的气质类型,应该被认为是一个风险因素。
    UNASSIGNED: Non-melanoma skin cancer (NMSC) is the most common type of cancer in the world. In traditional Persian medicine (TPM), various types of temperament (Mizaj) are considered to diagnose, treat, and prevent a variety of illnesses. The present study aimed to evaluate the temperament of patients with NMSC in comparison with a control group.
    UNASSIGNED: A case-control study was conducted in 2018 at the Dermatology Clinic of Shahid Faghihi Hospital affiliated with Shiraz University of Medical Sciences (Shiraz, Iran). A total of 110 patients, aged ≥20 years with confirmed NMSC (case group), and 181 individuals without NMSC (control group) were enrolled in the study. The temperament of the participants in both groups was evaluated using Mojahedi\'s Mizaj questionnaire. The data were analyzed using SPSS software, and P<0.05 was considered statistically significant.
    UNASSIGNED: The results showed that the odds ratio of developing NMSC was 2.62 (95%CI: 1.42-4.83, P=0.002) times higher in individuals with dry temperament than other types of temperament. Moreover, the odds ratio of patients with a history of chronic skin ulcers and other types of cancer was 35.7 (95%CI: 11.9-107.15, P<0.001) and 5.22 (95%CI: 1.43-19.06, P=0.012) times higher, respectively, than the control group.
    UNASSIGNED: Temperament is associated with NMSC, particularly the dry temperament type, and should be considered a risk factor.
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  • 文章类型: Journal Article
    背景:医学案例插图长期以来一直用于医学生教育,并且经常包括人口统计学变量,例如种族,种族和性别。然而,在没有背景的情况下纳入人口统计学变量可能会强化假设和偏见。然而,没有种族,性取向,健康的社会决定因素可能会加强反映文化盲目性的隐藏课程。这项复制研究比较了种族的比例,种族,和性别与明尼苏达大学(UMN)的调查结果。这项研究旨在确定案例小插曲中人口统计学特征的表示是否取得了进展。
    方法:分析了北卡罗来纳大学(UNC)2015-2016年的病例插图,并与1996-1998年的UMN病例插图进行了比较。数据包括提及种族,种族,健康的性别和社会决定因素。
    结果:在278UNC小插曲中,在19.7%的病例中发现了白人种族,黑人占7.9%,76.6%的病例不明。在983UMN小插曲中,白种人占2.85%,黑人种族占0.41%。这些机构在描述种族的病例比例上存在显着差异(0.20;95%CI(0.15,0.25))。男性在大多数小插曲中都有代表。
    结论:比较两个医学院的病例对照结果提示,报告明确的人口统计学差异没有显著差异。研究结果表明,性别是一贯描述的人口统计学特征,男性人数过多。基于这些发现,在医学生教育中,需要更大的文化多样性,因为它与健康的社会决定因素相交。
    BACKGROUND: The medical case vignette has long been used in medical student education and frequently includes demographic variables such as race, ethnicity and gender. However, inclusion of demographic variables without context may reinforce assumptions and biases. Yet, the absence of race, sexual orientation, and social determinants of health may reinforce a hidden curriculum that reflects cultural blindness. This replication study compared proportions of race, ethnicity, and gender with University of Minnesota (UMN) findings. This study sought to determine if there has been progress in the representation of demographic characteristics in case vignettes.
    METHODS: University of North Carolina (UNC) case vignettes from 2015-2016 were analyzed and compared to UMN case vignettes from 1996-1998. Data included mentions of race, ethnicity, gender and social determinants of health.
    RESULTS: In the 278 UNC vignettes, white race was noted in 19.7% of cases, black race was in 7.9% cases, and 76.6% of cases were unspecified. In the 983 UMN vignettes, white race was recorded in 2.85% cases, and black race in 0.41% cases. The institutions were significantly different in the proportion of their cases depicting race (0.20; 95% CI (0.15, 0.25)). Males were represented in the majority of vignettes.
    CONCLUSIONS: Comparing case vignettes results from two medical schools suggests that reporting explicit demographic diversity was not significantly different. The findings illustrate that sex was the demographic characteristic consistently described, where males were over-represented. Based on these findings, greater cultural diversity as it intersects with social determinants of health is needed in medical student education.
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  • 文章类型: Journal Article
    互联网已经成为青少年生活中无处不在的核心元素。在这篇概念性论文中,我们专注于数字白人种族社会化(D-WRS),争论:(1)为了扩大WRS的概念化,(2)社交媒体可能通过扩展传统环境和创造独特的社交环境来改变WRS的过程。我们强调了社交媒体环境的独特性,因为白度的设计正常化,软弱的种族主义,社交媒体提供,和种族化的教学区,允许青少年练习种族。我们介绍了D-WRS的概念框架,并以对社交媒体与WRS过程之间的多维关系进行概念指导研究的明确需求结束。
    The Internet has become a ubiquitous central element in the lives of adolescents. In this conceptual paper, we focus on digital white racial socialization (D-WRS), arguing: (1) for an expanded conceptualization of WRS as doings, and (2) that social media may be changing processes of WRS through an extension of traditional settings and through the creation of unique social contexts. We highlight the uniqueness of social media contexts due to the designed normalization of whiteness, weak-tie racism, social media affordances, and racialized pedagogical zones allowing adolescents to practice doing race. We introduce a conceptual framework for D-WRS and end with an expressed need for conceptually guided research on the multidimensional relationship between social media and WRS processes.
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  • 文章类型: Journal Article
    全科医生(GP)是来自有健康问题的种族和移民群体的人的第一个联系点。歧视可能发生在这个卫生保健部门。很少有研究,然而,调查了一般实践中对种族和移民群体的内隐和外显偏见。这项研究,因此,调查了实习全科医生中隐性种族偏见的程度和适应移民患者的意愿,以及其中涉及的因素,为了衡量显性偏见,探索文化能力的一个维度。
    2021年,从比利时法语地区的207名受训全科医生那里收集了数据。受访者通过了内隐协会测试(IAT),一种经过验证的工具,用于衡量针对种族群体的内隐偏见。明确的愿意使护理适应多样性的态度,文化能力的一个维度,是用Hudelson量表测量的。
    绝大多数受训GP(82.6%,95%CI:0.77-0.88)对他们的群体有隐性偏好,损害了种族和移民群体。总的来说,大多数受访者认为全科医生有责任使他们的态度和做法适应移民的需求。超过50%的受训GP,然而,认为移民患者有责任适应东道国的价值观和习惯。
    这项研究发现,受训全科医生有很高到很高的内隐种族偏见,他们并不总是愿意适应移民的价值观。因此,我们建议他们意识到这种偏见,并建议使用IAT和Hudelson量表作为教育工具来解决初级保健中的种族偏见。
    General Practitioners (GPs) are the first point of contact for people from ethnic and migrant groups who have health problems. Discrimination can occur in this health care sector. Few studies, however, have investigated implicit and explicit biases in general practice against ethnic and migrant groups. This study, therefore, investigated the extent of implicit ethnic biases and willingness to adapt care to migrant patients among trainee GPs, and the factors involved therein, in order to measure explicit bias and explore a dimension of cultural competence.
    In 2021, data were collected from 207 trainee GPs in the French-speaking part of Belgium. The respondents passed an Implicit Association Test (IAT), a validated tool used to measure implicit biases against ethnic groups. An explicit attitude of willingness to adapt care to diversity, one of the dimensions of cultural competence, was measured using the Hudelson scale.
    The overwhelming majority of trainee GPs (82.6%, 95% CI: 0.77 - 0.88) had implicit preferences for their ingroup to the detriment of ethnic and migrant groups. Overall, the majority of respondents considered it the responsibility of GPs to adapt their attitudes and practices to migrants\' needs. More than 50% of trainee GPs, however, considered it the responsibility of migrant patients to adapt to the values and habits of the host country.
    This study found that the trainee GPs had high to very high levels of implicit ethnic bias and that they were not always willing to adapt care to the values of migrants. We therefore recommend that they are made aware of this bias and we recommend using the IAT and Hudelson scales as educational tools to address ethnic biases in primary care.
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  • 文章类型: Journal Article
    SARS-CoV-2,COVID-19的病原体,持续的大流行,通过丝氨酸蛋白酶引发的S蛋白激活ACE2受体进入宿主细胞,TMPRSS2。TMPRSS2基因的变化可能是人群之间疾病易感性差异的原因。因此,在本研究中,我们使用了来自393名个体的世界人群的下一代测序(NGS)数据,并使用基于单倍型的方法分析了TMPRSS2基因,该方法主要关注南亚,以研究其系统发育结构及其在全球不同人群中的单倍型共享.因此,我们对系统发育相关性的分析表明,南亚人与西欧亚人口的亲和力更紧密,宿主疾病的易感性和严重程度,特别是在TMPRSS2的背景下,将更类似于西欧亚,而不是东欧亚。这与我们先前对ACE2基因的研究相反,该研究表明南亚单倍型对西欧亚人有很强的亲和力。因此,ACE2和TMPRSS2在南亚人之间具有拮抗遗传相关性。考虑到TMPRSS2基因在SARS-CoV-2致病性中的意义,因此,COVID-19感染和强度趋势可能与表达增加直接相关,我们还测试了该基因在印度各个州人群中的SNP频率与病死率(CFR)的关系。有趣的是,我们发现rs2070788SNP(G等位基因)与印度人群的CFR之间存在显着正相关。进一步我们对rs2070788的顺式eQTL分析表明,与AG和AA基因型相比,rs2070788的GG基因型倾向于在肺中具有明显更高的TMPRSS2基因表达,从而验证了先前的观察结果,因此它可能在确定差异疾病脆弱性中起着至关重要的作用。我们相信,这些信息将有助于了解TMPRSS2变体在COVID-19易感性中的作用,并将其用作生物标志物可能有助于预测处于危险中的人群。
    SARS-CoV-2, the causative agent for COVID-19, an ongoing pandemic, engages the ACE2 receptor to enter the host cell through S protein priming by a serine protease, TMPRSS2. Variation in the TMPRSS2 gene may account for the disparity in disease susceptibility between populations. Therefore, in the present study, we have used next-generation sequencing (NGS) data of world populations from 393 individuals and analyzed the TMPRSS2 gene using a haplotype-based approach with a major focus on South Asia to study its phylogenetic structure and their haplotype sharing among various populations worldwide. Our analysis of phylogenetic relatedness showed a closer affinity of South Asians with the West Eurasian populations therefore, host disease susceptibility and severity particularly in the context of TMPRSS2 will be more akin to West Eurasian instead of East Eurasian. This is in contrast to our prior study on the ACE2 gene which shows South Asian haplotypes have a strong affinity towards West Eurasians. Thus ACE2 and TMPRSS2 have an antagonistic genetic relatedness among South Asians. Considering the significance of the TMPRSS2 gene in the SARS-CoV-2 pathogenicity, COVID-19 infection and intensity trends could be directly associated with increased expression therefore, we have also tested the SNPs frequencies of this gene among various Indian state populations with respect to the case fatality rate (CFR). Interestingly, we found a significant positive association between the rs2070788 SNP (G Allele) and the CFR among Indian populations. Further our cis eQTL analysis of rs2070788 shows that the GG genotype of the rs2070788 tends to have a significantly higher expression of TMPRSS2 gene in the lung compared to the AG and AA genotypes thus validating the previous observation and therefore it might play a vital part in determining differential disease vulnerability. We trust that this information will be useful in understanding the role of the TMPRSS2 variant in COVID-19 susceptibility and using it as a biomarker may help to predict populations at risk.
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  • 文章类型: Historical Article
    意大利半岛,横跨地中海的天然码头,自从欧洲人类占领开始以来,见证了错综复杂的人口事件。在过去的几年里,国际研究界已经发表了越来越多的来自该地区的现代和古代基因组。这种基因组观点开始揭示意大利的相关性,以了解欧洲的最后一次冰川最大(LGM)重新居住,新石器时代向西迁移的早期阶段,及其在铁器时代之后在东地中海地区和西地中海地区之间的联系作用。然而,许多悬而未决的问题仍在等待更多的数据得到充分解决。通过这次审查,我们总结了从可用的古代意大利人中出现的当前知识,通过一次重新分析它们,我们试图阐明该领域未来研究应涵盖的途径。特别是,悬而未决的问题涉及(1)Villabruna前欧洲人的命运以及LGM后的狩猎采集者在多大程度上吸收了它们的基因组成分;(2)西西里岛和撒丁岛在LGM之前的作用;(3)在何种程度上,新石器时代早期定居者中记录的遗传结构可以被描述为两个独立的迁徙;(4)在新石器时代和类似的伊朗时代的欧洲样本中明显
    The Italian Peninsula, a natural pier across the Mediterranean Sea, witnessed intricate population events since the very beginning of the human occupation in Europe. In the last few years, an increasing number of modern and ancient genomes from the area have been published by the international research community. This genomic perspective started unveiling the relevance of Italy to understand the post-Last Glacial Maximum (LGM) re-peopling of Europe, the earlier phase of the Neolithic westward migrations, and its linking role between Eastern and Western Mediterranean areas after the Iron Age. However, many open questions are still waiting for more data to be addressed in full. With this review, we summarize the current knowledge emerging from the available ancient Italian individuals and, by re-analysing them all at once, we try to shed light on the avenues future research in the area should cover. In particular, open questions concern (1) the fate of pre-Villabruna Europeans and to what extent their genomic components were absorbed by the post-LGM hunter-gatherers; (2) the role of Sicily and Sardinia before LGM; (3) to what degree the documented genetic structure within the Early Neolithic settlers can be described as two separate migrations; (4) what are the population events behind the marked presence of an Iranian Neolithic-like component in Bronze Age and Iron Age Italian and Southern European samples.
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  • 文章类型: Letter
    暂无摘要。
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  • 文章类型: Journal Article
    目的:症状性颈动脉网(CaW)患者的基线特征尚不清楚。我们调查了这种被忽视的卒中病因患者的人口统计学和脑血管危险因素。
    方法:我们确定了2014年7月至2018年12月在综合卒中中心诊断为有症状CaW的连续患者。这些患者以1:4的比例(基于年龄和NIHSS评分)进行匹配,以从当地GetWithTheGuidelines卒中数据库中创建具有非CaW病因的急性缺血性卒中(AIS)患者的对照组。
    结果:将30例有症状的CaW患者与120例非CaW病因的AIS患者进行了比较。有症状的CaW患者更可能是女性(73.3vs.44.2%;p=0.004)和黑色(86.7vs.64.2%;p=0.02)。有症状的CaWs患者的可改变的脑血管危险因素的绝对数量较少(1.7±1.1vs.2.5±1.2;p=0.002),较低的高血压发病率(43.4vs.63.3%;p=0.04),和更有利的血脂与较低的平均LDL(89.5±30.3vs.111.2±43.7mg/dL;p=0.01)和更高的平均HDL(47.9±11.3vs.与具有非CaW病因的中风相比,42.2±13.8mg/dL;p=0.01)。有症状的CaW患者更容易出现大血管闭塞(80.0vs.51.7%;p=0.005),尽管两组之间的e-ASPECTS相似(8.1±2.1vs.8.3±2.2;p=0.30)。在多变量分析中,有症状的CaW是出院时独立性的独立预测因子(OR3.72;95CI1.27-10.94).
    结论:有症状的CaWs可能存在性别和种族偏好,因为发现女性和黑人更有可能受到影响。有症状的CaW患者具有更良性的脑血管危险因素特征,证实了所提出的局部淤滞和血栓栓塞的机制。尽管LVO更常见,有症状的CaW与良好的功能结局相关,值得进一步研究。
    OBJECTIVE: The baseline characteristics of patients with symptomatic carotid web (CaW) are unclear. We investigate demographic and cerebrovascular risk factors in patients with this overlooked stroke etiology.
    METHODS: We identified consecutive patients diagnosed with symptomatic CaW at a comprehensive stroke center from July 2014-December 2018. These patients were matched at a 1:4 ratio (based on age and NIHSS scores) to create a control group of acute ischemic stroke (AIS) patients with non-CaW etiologies from the local GetWithTheGuidelines stroke database.
    RESULTS: Thirty patients with symptomatic CaW were compared to 120 AIS patients with non-CaW etiologies. Symptomatic CaW patients were more likely to be female (73.3 vs. 44.2%; p = 0.004) and black (86.7 vs. 64.2%; p = 0.02). Symptomatic CaWs patients had a fewer absolute number of modifiable cerebrovascular risk factors (1.7±1.1 vs. 2.5±1.2; p = 0.002), lower rates of hypertension (43.4 vs. 63.3%; p = 0.04), and a more favorable lipid profile with lower average LDL (89.5±30.3 vs. 111.2±43.7 mg/dL; p = 0.01) and higher average HDL (47.9±11.3 vs. 42.2±13.8 mg/dL; p = 0.01) as compared to strokes with non-CaW etiology. Symptomatic CaW patients were more likely to have a large vessel occlusion (80.0 vs. 51.7%; p = 0.005), despite similar e-ASPECTS between the groups (8.1±2.1 vs. 8.3±2.2; p = 0.30). On multivariable analysis, symptomatic CaW was an independent predictor of independence at discharge (OR 3.72; 95%CI 1.27-10.94).
    CONCLUSIONS: A gender and racial predilection of symptomatic CaWs may exist as females and blacks were were found to be more likely affected. Symptomatic CaW patients have a more benign cerebrovascular risk factor profile corroborating the proposed mechanism of local stasis and thromboembolism. Despite presenting more commonly with LVO, symptomatic CaW was associated with good functional outcome, warranting further studies.
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  • 文章类型: Letter
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  • 文章类型: Journal Article
    To describe how using a combined approach of community-based participatory research and intervention mapping principles could inform the development of a tailored complex intervention to improve management of asthma for South Asian (SA) children; Management and Interventions for Asthma (MIA) study.
    A qualitative study using interviews, focus groups, workshops, and modified intervention mapping procedures to develop an intervention planning framework in an urban community setting in Leicester, UK. The modified form of intervention mapping (IM) included: systematic evidence synthesis; community study; families and healthcare professionals study; and development of potential collaborative intervention strategies. Participants in the community study were 63 SA community members and 12 key informants; in-depth semi-structured interviews involved 30 SA families, 14 White British (WB) families and 37 Healthcare Professionals (HCPs) treating SA children living with asthma; prioritisation workshops involved 145 SA, 6 WB and 37 HCP participants; 30 participants in finalisation workshops.
    Two key principles were utilised throughout the development of the intervention; community-based participatory research (CBPR) principles and intervention mapping (IM) procedures. The CBPR approach allowed close engagement with stakeholders and generated valuable knowledge to inform intervention development. It accounted for diverse perceptions and experiences with regard to asthma and recognised the priorities of patients and their families/caregivers for service improvement. The \'ACT on Asthma\' programme was devised, comprising four arms of an intervention strategy: education and training, clinical support, advice centre and raising awareness, to be co-ordinated by a central team.
    The modified IM principles utilised in this study were systematic and informed by theory. The combined IM and participatory approach could be considered when tailoring interventions for other clinical problems within diverse communities. The IM approach to intervention development was however resource intensive. Working in meaningful collaboration with minority communities requires specific resources and a culturally competent methodology.
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