Ethnic Groups

民族
  • 文章类型: Journal Article
    文化和饮食习惯,不同种族之间差异很大,对饮酒行为有重大影响。这项研究旨在检查饮酒模式和原因是否因种族而异,并为寻求减少酒精摄入量的多民族地区提供有用的见解。
    我们招募了过量饮酒者,并通过问卷调查收集了多种族社会中的饮酒方式和动机。多元线性回归用于评估不同种族之间饮酒特征的变化。
    我们通过便利抽样(研究中使用的一种非概率抽样技术,研究人员根据参与者的可及性和接近性为研究选择参与者或单位)招募了1287名参与者,其中439名过度饮酒者符合资格。439名参与者的平均年龄为38岁,92.9%是男性,36.0%是汉族,以彝族为主的少数民族占64.0%。大多数参与者已婚(75.9%)和体力劳动(58.1%)。少数民族一次饮酒比汉族多(47.3比41.8g/次),而饮酒频率较低。对于少数民族和汉族参与者来说,67%和42%的人不习惯与食物一起饮用,分别。同辈压力和营造良好的氛围是少数民族和汉族最常见的饮酒原因,分别。
    我们发现少数民族和汉族在饮酒模式和原因上存在很大差异,归因于他们的文化和习俗。研究结果强调了饮酒习惯和动机在种族融合和人口移民背景下探索酒精控制教育策略的重要性。
    UNASSIGNED: Culture and eating habits, which vary greatly across different ethnic groups, have a substantial impact on drinking behavior. This study aimed to examine whether the drinking patterns and reasons differ by ethnic groups, and provide useful insights for multi-ethnic areas that seek to cut down alcohol intake.
    UNASSIGNED: We recruited excessive drinkers and collected the drinking patterns and motivations by questionnaire in a multi-ethnic society. Multiple linear regressions were used to evaluate the variations in drinking characteristics among different ethnic groups.
    UNASSIGNED: We recruited 1287 participants through convenience sampling (a non-probability sampling technique used in research where the researcher selects participants or units for a study based on their accessibility and proximity), among whom 439 excessive drinkers were eligible. The mean age was 38 years for the 439 participants, 92.9% were men, 36.0% were Han, and 64.0% were minorities mainly composed of the Yi. The majority of the participants were married (75.9%) and did physical work (58.1%). Ethnic minorities consumed more alcohol on a single occasion than Han people did (47.3 vs 41.8g/session) while drinking less frequently. For the minority and Han participants, 67% and 42% were not used to drinking with food, respectively. Peer pressure and fostering a good atmosphere were the most common drinking reasons for the minority and Han, respectively.
    UNASSIGNED: We found substantial differences in drinking patterns and reasons between ethnic minorities and Han ethnicity, attributable to their culture and customs. Findings highlight the importance of drinking habits and motivations in exploring alcohol control education strategies in the context of ethnic integration and population immigration.
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  • 文章类型: Journal Article
    人乳寡糖,包括游离的寡糖和糖缀合物,在新生儿健康和发育中发挥关键作用。已经记录了来自不同种族的牛奶的游离寡糖的变化。在这项研究中,从汉族那里收集人乳,Hui,和中国西北部的藏族人口,使用在线高效液相色谱-串联质谱法系统地比较了这三个种族之间N/O-糖的差异。在检测到的63个N-聚糖中,35表示出三个平易近族之间的显著差别(p<0.05)。在检测到的70个O-聚糖中,4种中性O-聚糖和6种酸性O-聚糖在三个种族之间表现出显著差异(p<0.05),首次报道了六种酸性O-聚糖。总的来说,汉族人群的牛奶N/O糖基化程度高于回族或藏族。这种趋势对于主要的唾液酸化N/O-聚糖尤其明显。除了硫酸化的O-聚糖,在藏族母亲的牛奶中,其他类型的N/O-聚糖在所有种族中的比例相似.了解人乳中N/O-聚糖的组成有助于研究聚糖的结构-功能关系。
    Human milk oligosaccharides, including free oligosaccharides and glycoconjugates, exert a key role in neonatal health and development. Changes in free oligosaccharides of milk from different ethnic groups have been documented. In this study, human milk was collected from Han, Hui, and Tibetan populations in northwest China, and differences in N/O-glycome among these three ethnic groups were systematically compared using online high-performance liquid chromatography-tandem mass spectrometry. Among the 63 detected N-glycans, 35 showed significant differences between the three ethnic groups (p < 0.05). Among the 70 detected O-glycans, four neutral O-glycans and six acidic O-glycans exhibited significant differences among the three ethnic groups (p < 0.05), with six acidic O-glycans reported for the first time. Overall, the extent of milk N/O-glycosylation was higher in the Han population than in the Hui or Tibetan groups. This trend was particularly pronounced for the main sialylated N/O-glycans. Except for sulfated O-glycans, which were higher in the milk from Tibetan mothers, the other types of N/O-glycans were present in similar proportions across all ethnic groups. Understanding the composition of N/O-glycans in human milk can help research on the structure-function relationship of glycans.
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  • 文章类型: Journal Article
    背景:对2型糖尿病(T2DM)患者中慢性肾脏病(CKD)自然史的种族差异的认识可能为解决住院和死亡率差异的临床策略提供依据。新西兰欧洲人(NZE)在25年期间CKDII-V阶段的风险,毛利人和帕西菲卡,奥克兰的T2DM,新西兰(NZ)进行了比较。
    方法:作为奥克兰的初级保健审计计划,糖尿病护理支持服务与国家注册数据库相关联.排除了已有CKDII-V的患者。为了平衡潜在的混杂因素,我们应用了锥形匹配方法。分别在毛利人和NZE之间以及Pasifika和NZE之间建立了“准试验”匹配的队列。通过加权Cox回归模型研究了1994-2018年CKD任何阶段和每个阶段的种族人群风险差异。
    结果:开发任何CKD的HR,毛利人(n=2215)与NZE(n=2028)的CKDII-V期为1.18(95%CI0.99至1.41),1.10(95%CI0.91至1.32),1.70(95%CI1.19至2.43),3.93(95%CI2.16至7.14),和3.74(95%CI1.74至8.05),分别。与NZE(n=2474)相比,开发任何CKD的HR,Pasifika(n=3101)的CKDII-V期为1.31(95%CI1.09至1.57),1.26(95%CI1.05至1.52),1.71(95%CI1.14至2.57),3.75(95%CI1.40至10.05),和4.96(95%CI1.56至15.75),分别。
    结论:在新西兰T2DM患者中,CKD进展至各阶段(尤其是V期)的风险存在显著的种族差异.这些差异背后的机制研究,以及需要识别生物标志物来预测早期发作的肾脏病变,是有保证的。
    Insights into ethnic differences in the natural history of chronic kidney disease (CKD) among people with type 2 diabetes mellitus (T2DM) might inform clinical strategies to address disparities in hospitalization and mortality. Risks of CKD II-V stages over a 25-year period between New Zealand Europeans (NZEs), Māori and Pasifika, and with T2DM in Auckland, New Zealand (NZ) were compared.
    As a primary care audit program in Auckland, the Diabetes Care Support Service was linked with national registration databases. People with existing CKD II-V were ruled out. To balance potential confounders, we applied a tapered matching method . \'Quasi-trial\'-matched cohorts were set up separately between Māori and NZE and between Pasifika and NZE. Ethnic population differences in risk of any and each stage of CKD over 1994-2018 were examined by weighted Cox regression model.
    The HRs for developing any CKD, CKD stages II-V for Māori (n=2215) versus NZE (n=2028) were 1.18 (95% CI 0.99 to 1.41), 1.10 (95% CI 0.91 to 1.32), 1.70 (95% CI 1.19 to 2.43), 3.93 (95% CI 2.16 to 7.14), and 3.74 (95% CI 1.74 to 8.05), respectively. Compared with NZE (n=2474), the HRs for developing any CKD, CKD stages II-V for Pasifika (n=3101) were 1.31 (95% CI 1.09 to 1.57), 1.26 (95% CI 1.05 to 1.52), 1.71 (95% CI 1.14 to 2.57), 3.75 (95% CI 1.40 to 10.05), and 4.96 (95% CI 1.56 to 15.75), respectively.
    Among people with T2DM in NZ, significant ethnic differences exist in the risk of progressing to each stage of CKD (stage V in particular). Mechanism studies underlying these differences, as well as the need for identification of biomarkers to predict the early onset renal lesion, are warranted.
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  • 文章类型: Journal Article
    重要性:癌症患者种族/族裔死亡率差异的潜在原因仍然知之甚少,特别是关于获得护理的作用。参与者:超过500万患者的主要诊断为肺,乳房,前列腺,结肠/直肠,胰腺,子房,或肝癌在2004-2014年,从国家癌症数据库中确定。Cox比例风险模型用于估计与种族/民族相关的总死亡率的风险比(HR)和95%置信区间(CI)。和获得护理相关因素(即,社会经济地位[SES],保险,治疗设施,和居住类型)为每个癌症。结果:在7种癌症中观察到了总死亡率的种族/族裔差异。与非西班牙裔(NH)白人患者相比,NH-black乳腺患者(HR=1.27,95%CI:1.26至1.29),卵巢(HR=1.20,95%CI:1.17至1.23),前列腺(HR=1.31,95%CI:1.30至1.33),结直肠癌(HR=1.11,95%CI:1.10至1.12)或胰腺癌(HR=1.03,95%CI:1.02至1.05)死亡率显著升高,而亚洲人(13-31%)和西班牙裔(13-19%)对所有癌症的死亡率较低。在获得护理相关因素的所有阶层中都观察到种族/种族差异,并受这些因素的影响。NH-black和NH-white差异在SES高或有私人保险的患者中最为明显,而西班牙裔/亚裔与NH-白种人的差异在SES较低或无/低保险的患者中更为明显。结论和相关性:主要癌症的种族/种族死亡率差异存在于获得不同护理水平的所有患者群体中。SES或保险对死亡率差异的影响遵循种族/族裔少数群体与NH白人的不同模式。影响:我们的研究强调需要针对种族/民族的策略来减少主要癌症的死亡率差异。
    Importance: The reasons underlying racial/ethnic mortality disparities for cancer patients remain poorly understood, especially regarding the role of access to care. Participants: Over five million patients with a primary diagnosis of lung, breast, prostate, colon/rectum, pancreas, ovary, or liver cancer during 2004-2014, were identified from the National Cancer Database. Cox proportional hazards models were applied to estimate hazard ratios (HR) and 95% confidence intervals (CI) for total mortality associated with race/ethnicity, and access to care related factors (i.e., socioeconomic status [SES], insurance, treating facility, and residential type) for each cancer. Results: Racial/ethnic disparities in total mortality were observed across seven cancers. Compared with non-Hispanic (NH)-white patients, NH-black patients with breast (HR = 1.27, 95% CI: 1.26 to 1.29), ovarian (HR = 1.20, 95% CI: 1.17 to 1.23), prostate (HR = 1.31, 95% CI: 1.30 to 1.33), colorectal (HR = 1.11, 95% CI: 1.10 to 1.12) or pancreatic (HR = 1.03, 95% CI: 1.02 to 1.05) cancers had significantly elevated mortality, while Asians (13-31%) and Hispanics (13-19%) had lower mortality for all cancers. Racial/ethnic disparities were observed across all strata of access to care related factors and modified by those factors. NH-black and NH-white disparities were most evident among patients with high SES or those with private insurance, while Hispanic/Asian versus NH-white disparities were more evident among patients with low SES or those with no/poor insurance. Conclusions and Relevance: Racial/ethnic mortality disparities for major cancers exist across all patient groups with different access to care levels. The influence of SES or insurance on mortality disparity follows different patterns for racial/ethnic minorities versus NH-whites. Impact: Our study highlights the need for racial/ethnic-specific strategies to reduce the mortality disparities for major cancers.
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  • 文章类型: Journal Article
    人乳低聚糖(HMO)因其对婴儿健康的积极作用而受到越来越多的关注。对包括多个异构结构的复杂HMO进行绝对定量的高通量方法很重要,但非常具有挑战性。由于高度潜水员的性质和来自不同个体的HMO含量差异很大。在这里,我们在负离子模式下使用UPLC-MS-MRM在短短15分钟内准确定量23个复杂的HMO。所选择的寡糖是其天然形式,包括中性和唾液酸化,岩藻糖基化和非岩藻糖基化,直链和支链,以及分泌者和刘易斯表型指标。该方法经过充分验证,具有良好的灵敏度,然后将恢复和再现性应用于来自五个不同种族的251名中国母亲的大人群定量调查(汉族,庄,Hui,蒙古族和藏族)因其分泌者的身份和刘易斯表型而生活在不同的地理区域。
    Human milk oligosaccharides (HMOs) have attracted increasing attention due to the emerging evidence of their positive roles for infant\'s health. A high-throughput method for absolute quantitation of the complex HMOs including multiple isomeric structures is important but very challenging, due to the highly divers nature and wide variation in content of HMOs from different individuals. Here we used UPLC-MS-MRM in the negative-ion mode for accurate quantitation of 23 complex HMOs in just 15 min. The selected oligosaccharides are in their native forms and include neutral and sialylated, fucosylated and non-fucosylated, linear and branched, and secretor and Lewis phenotype indicators. The well validated method with good sensitivity, recovery and reproducibility was then applied to a large population quantitative survey of 251 Chinese mothers from five different ethnic groups (Han, Zhuang, Hui, Mongolian and Tibetan) living in different geographical regions for their secretor\'s status and Lewis phenotypes.
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  • 文章类型: Journal Article
    人类肠道菌群已被提议作为宿主代谢中的多功能器官,对营养获取有影响,免疫反应,和消化健康。斋月期间的禁食可能会通过饮食行为的变化来改变肠道微生物群的组成,最终影响肠道中各种代谢物的含量。这里,我们使用基于液相色谱-质谱的代谢组学研究了中国人和巴基斯坦人在斋月禁食前后的粪便代谢物组成。主成分分析显示,种族之间以及禁食前后样本之间的代谢物分布有明显的分离。斋月后,中国和巴基斯坦组的各种粪便代谢物含量存在显着差异。特别是,L-组氨酸,lycofawcine,中国人群斋月后虫草素浓度较高,而巴基斯坦集团富含马钱子碱。KEGG分析表明与嘌呤代谢有关的代谢物,2-氧代羧酸代谢,和赖氨酸降解在禁食前的总受试者群体中显著富集禁食后比较。几个细菌类群与每个种族特有的特定代谢产物显着相关,这表明与斋月禁食相关的粪便代谢物谱的变化可能受到肠道微生物群相关变化的影响。粪便代谢物谱的空腹相关差异,以及分类群和代谢物之间的这些群体特异性相关性,支持我们先前的发现,即膳食组成的种族差异也会导致肠道微生物组成和多样性的变化。这种相互关联的饮食行为的景观视图,微生物群,和代谢物有助于个性化的未来发展,基于饮食的肠道相关疾病的治疗策略。
    The human gut microbiota has been proposed to serve as a multifunctional organ in host metabolism, contributing effects to nutrient acquisition, immune response, and digestive health. Fasting during Ramadan may alter the composition of gut microbiota through changes in dietary behavior, which ultimately affects the contents of various metabolites in the gut. Here, we used liquid chromatography-mass spectrometry-based metabolomics to investigate the composition of fecal metabolites in Chinese and Pakistani individuals before and after Ramadan fasting. Principal component analysis showed distinct separation of metabolite profiles among ethnic groups as well as between pre- and post-fasting samples. After Ramadan fasting, the Chinese and Pakistani groups showed significant differences in their respective contents of various fecal metabolites. In particular, L-histidine, lycofawcine, and cordycepin concentrations were higher after Ramadan fasting in the Chinese group, while brucine was enriched in the Pakistani group. The KEGG analysis suggested that metabolites related to purine metabolism, 2-oxocarboxylic acid metabolism, and lysine degradation were significantly enriched in the total subject population pre-fasting vs. post-fasting comparisons. Several bacterial taxa were significantly correlated with specific metabolites unique to each ethnic group, suggesting that changes in fecal metabolite profiles related to Ramadan fasting may be influenced by associated shifts in gut microbiota. The fasting-related differences in fecal metabolite profile, together with these group-specific correlations between taxa and metabolites, support our previous findings that ethnic differences in dietary composition also drive variation in gut microbial composition and diversity. This landscape view of interconnected dietary behaviors, microbiota, and metabolites contributes to the future development of personalized, diet-based therapeutic strategies for gut-related disorders.
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  • 文章类型: Journal Article
    背景:透明质酸(HA)是用于面部年轻化的有效真皮填充剂。本研究旨在观察HA注射液在中国患者中用于丰唇的临床疗效。
    方法:从2019年5月至2020年4月,使用“三点”注射技术对70例嘴唇丰满量表(LPS)≤3的患者进行了局部HA注射。对所有患者进行随访,观察临床疗效,LPS,不良事件,和并发症。
    结果:70例患者均获12个月随访。在治疗后6-9个月内观察到嘴唇高度的统计学显着改善(p<0.05)。随访时LFS较基线显著改善(p<0.05)。两名患者出现局部红肿,3例患者出现严重肿胀。这些不良事件通常是耐受的,并在1周内逐渐消失。其余患者未报告其他严重不良事件和并发症。
    结论:透明质酸注射液可用于中国人群的丰唇。“三点”技术很简单,安全,并且有效,不会引起严重的并发症。
    BACKGROUND: Hyaluronic acid (HA) is an effective dermal filler for facial rejuvenation. This study aimed to observe the clinical efficacy of HA injection for lip augmentation in Chinese patients.
    METHODS: From May 2019 to April 2020, 70 patients with lip fullness scale (LPS) ≤3 underwent local HA injection using the \"three-point\" injection technique. All patients were followed up to observe the clinical efficacy, LPS, adverse events, and complications.
    RESULTS: All 70 patients were followed up for 12 months. Statistically significant improvements were observed in the height of lips within 6-9 months post-treatment (p < 0.05). The LFS improved significantly at follow-up compared with baseline (p < 0.05). Local redness occurred in two patients, and serious swelling occurred in three patients. These adverse events were generally tolerated and disappeared gradually within 1 week. No other serious adverse events and complications were reported in the remaining patients.
    CONCLUSIONS: Hyaluronic acid injection can be used for lip augmentation in the Chinese population. The \"three-point\" technique is simple, safe, and effective and does not cause serious complications.
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  • 文章类型: Journal Article
    Musculoskeletal performance is a complex trait influenced by environmental and genetic factors, and it has different manifestations in different populations. Heilongjiang province, located in northern China, is a multi-ethnic region with human cultures dating back to the Paleolithic Age. The Daur, Hezhen, Ewenki, Mongolian and Manchu ethnic groups in Heilongjiang province may have strong physical fitness to a certain extent. Based on the genetic characteristics of significant correlation between some important genes and skeletal muscle function, this study selected 23 SNPs of skeletal muscle strength-related genes and analyzed the distribution of these loci and genetic diversity in the five ethnic groups. Use Haploview (version 4.1) software to calculate the chi-square and the Hardy-Weinberg equilibrium to assess the difference between the two ethnic groups. Use R (version 4.0.2) software to perform principal component analysis of different ethnic groups. Use MEGA (version 7.0) software to construct the phylogenetic tree of different ethnic groups. Use POPGENE (version 1.32) software to calculate the heterozygosity and the FST values of 23 SNPs. Use Arlequin (version 3.5.2.2) software to analyze molecular variance (AMOVA) among 31 populations. The results showed that there was haplotype diversity of VDR, angiotensin-converting enzyme, ACTN3, EPO and IGF1 genes in the five ethnic groups, and there were genetic differences in the distribution of these genes in the five ethnic groups. Among them, the average gene heterozygosity (AVE_HET) of the 23 SNPs in the five populations was 0.398. The FST values of the 23 SNPs among the five ethnic groups varied from 0.0011 to 0.0137. According to the principal component analysis, the genetic distance of Daur, Mongolian and Ewenki is relatively close. According to the phylogenetic tree, the five ethnic groups are clustered together with the Asian population. These data will enrich existing genetic information of ethnic minorities.
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  • 文章类型: Clinical Trial
    Brugada综合征(BrS)与心脏钠通道基因突变有关,SCN5A.然而,有心律失常事件的BrS患者的遗传学研究有限.我们试图比较各种临床,心电图,和根据SCN5A基因型的电生理参数,在患有首次心律失常事件的大量BrS先证者队列中。
    关于Brugada综合征心律失常事件的调查是对10个西方国家和4个亚洲国家的调查,收集678例首次发生心律失常的BrS患者。只包括先证者,和SCN5A基因型裁定。没有适当遗传数据的患者被排除在外。分析基因型与临床特征的关联。
    研究组包括392个先证者:92个(23.5%)SCN5A+(44个致病/可能致病[P/LP]和48个未知意义的变异)和300个(76.5%)SCN5A-。SCN5A错义变体和托管它们的患者相似,无论判决如何。与SCN5A-相比,P/LP患者的儿科(<16岁)比例更高(11.4%对3%,P=0.023)。与SCN5A-相比,P/LP患者中女性的比例更高(18.2%对6.3%,P=0.013)。与SCN5A-相比,P/LP先证者更可能有心源性猝死家族史(41.9%对16.8%,P<0.001)。与SCN5A-相比,P/LP患者的白人比例更高(87.5%对47%,P<0.001)。种族(赔率比,5.41[2.8-11.19],P<0.001)和心源性猝死家族史(比值比,2.73[1.28-5.82],P=0.009)是逻辑回归后与P/LP基因型相关的独立变量。
    BrS的遗传基础与性别有着复杂的关系,种族,和年龄。与SCN5A-患者相比,携带P/LP变体的前带倾向于在更年轻的年龄经历他们的第一次心律失常事件,并且发生由发烧引发的事件。此外,他们更可能是白人,并且有心源性猝死的家族史。在女性中,P/LP变异提示有症状的风险增加.应在大量前瞻性收集的国际队列中,在种族特定的基础上进一步研究这种关联。
    Brugada syndrome (BrS) is associated with mutations in the cardiac sodium channel gene, SCN5A. However, genetic studies of patients with BrS with arrhythmic events have been limited. We sought to compare various clinical, ECG, and electrophysiological parameters according to SCN5A genotype in a large cohort of BrS probands with first arrhythmic event.
    Survey on Arrhythmic Events in Brugada Syndrome is a survey of 10 Western and 4 Asian countries, gathering 678 patients with BrS with first arrhythmic event. Only probands were included, and SCN5A genotype adjudicated. Patients without appropriate genetic data were excluded. Associations of genotype with clinical features were analyzed.
    The study group comprised 392 probands: 92 (23.5%) SCN5A+(44 pathogenic/likely pathogenic [P/LP] and 48 variants of unknown significance) and 300 (76.5%) SCN5A-.SCN5A missense variants and the patients hosting them were similar regardless of adjudication. A higher proportion of patients with P/LP were pediatric (<16 years) compared with SCN5A- (11.4% versus 3%, P=0.023). The proportion of females was higher among patients with P/LP compared with SCN5A- (18.2% versus 6.3%, P=0.013). P/LP probands were more likely to have a family history of sudden cardiac death compared with SCN5A- (41.9% versus 16.8%, P<0.001). A higher proportion of patients with P/LP were White compared with SCN5A- (87.5% versus 47%, P<0.001). Ethnicity (odds ratio, 5.41 [2.8-11.19], P<0.001) and family history of sudden cardiac death (odds ratio, 2.73 [1.28-5.82], P=0.009) were independent variables associated with P/LP genotype following logistic regression.
    The genetic basis of BrS has a complex relationship with gender, ethnicity, and age. Probands hosting a P/LP variant tended to experience their first arrhythmic event at a younger age and to have events triggered by fever compared with patients with SCN5A-. In addition, they were more likely to be White and to have family history of sudden cardiac death. Among females, a P/LP variant suggests an increased risk of being symptomatic. This association should be further studied on an ethnically specific basis in large prospectively collected international cohorts.
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  • 文章类型: Journal Article
    Studies suggest that exposure to ambient air pollution during pregnancy may be associated with increased risks of birth defects (BDs), but conclusions have been inconsistent. This study describes the ethnic distribution of major BDs and examines the relationship between air pollution and BDs among different ethnic groups in Liuzhou city, China.
    Surveillance data of infants born in 114 registered hospitals in Liuzhou in 2019 were analyzed to determine the epidemiology of BDs across five major ethnic groups. Concentrations of six air pollutants (PM2.5, PM10, SO2, CO, NO2, O3) were obtained from the Liuzhou Environmental Protection Bureau. Logistic regression was used to examine the associations between ambient air pollution exposure and risk of BDs.
    Among 32,549 infants, 635 infants had BDs, yielding a prevalence of 19.5 per 1000 perinatal infants. Dong ethnic group had the highest prevalence of BDs (2.59%), followed by Yao (2.57%), Miao (2.35%), Zhuang (2.07%), and Han (1.75%). Relative to the Han ethnic group, infants from Zhuang, Miao, Yao and Dong groups had lower risks of congenital heart disease, polydactyly, and hypospadias. The Zhuang ethnic group had higher risks of severe thalassemia, cleft lip and/or palate, and syndactyls. Overall BDs were positively correlated with air pollutants PM10 (aOR =1.14, 95% CI:1.12 ~ 2.43; aOR =1.51, 95% CI:1.13 ~ 2.03 for per 10μg/mg3 increment) and CO (aOR =1.36, 95% CI:1.14 ~ 2.48; aOR =1.75, 95% CI:1.02 ~ 3.61 for every 1 mg /m3 increment) in second and third month of pregnancy. SO2 was also significantly associated with BDs in the second month before the pregnancy (aOR = 1.31; 95% CI: 1.20 ~ 3.22) and third month of pregnancy (aOR =1.75; 95% CI:1.02 ~ 3.61). Congenital heart disease, polydactyl, cleft lip and/or palate were also significantly associated with PM10, SO2 and CO exposures. However, no significant association was found between birth defects and O3, PM2.5 and NO2 exposures (P > 0.05).
    This study provides a comprehensive description of ethnic differences in BDs in Southwest China and broadens the evidence of the association between air pollution exposure during gestation and BDs.
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