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Commentary: “Exposure to ambient air pollution-does it affect semen quality and the level of reproductive hormones?” by Michał Radwan, Joanna Jurewicz, Kinga Polańska, Wojciech Sobala, Paweł Radwan, Michał Bochenek and Wojciech Hanke 评论:"Michał Radwan、Joanna Jurewicz、Kinga Polańska、Wojciech Sobala、Paweł Radwan、Michał Bochenek 和 Wojciech Hanke 撰写的《暴露于环境空气污染中--会影响精液质量和生殖激素水平吗?
IF 1.7 4区 医学 Q2 ANTHROPOLOGY Pub Date : 2024-09-09 DOI: 10.1080/03014460.2024.2397130
L. M. Schell
Published in Annals of Human Biology (Vol. 51, No. 1, 2024)
发表于《人类生物学年鉴》(第 51 卷第 1 期,2024 年)
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引用次数: 0
Underweight in young Japanese women over time: a longitudinal retrospective study of the change in body mass index from ages 6 to 20 years 日本年轻女性长期体重不足的情况:对 6 至 20 岁体重指数变化的纵向回顾研究
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-04-29 DOI: 10.1080/03014460.2024.2345393
Yuka Nagashima, Mikako Inokuchi, Yasunori Sato, Tomonobu Hasegawa
The high prevalence of underweight in young women has become a serious health problem in Japan. When and how young women reach a low body mass index (BMI) has not been clarified.To clarify the char...
在日本,年轻女性体重不足的高发率已成为一个严重的健康问题。年轻女性何时以及如何达到低体重指数(BMI)尚未明确。
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引用次数: 0
MTHFR and MTRR gene polymorphisms in patients with chronic hepatitis B virus infections in Zigong, Sichuan Province 四川省自贡市慢性乙型肝炎病毒感染患者的 MTHFR 和 MTRR 基因多态性
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-04-18 DOI: 10.1080/03014460.2024.2330926
Shunhua Qiu, Lifen Jin, Dan Yang, Dewen Zhang
Chronic hepatitis B virus (HBV) infection is a severe disease affecting the physical and economic well-being of patients. The relationship between polymorphisms in the MTHFR gene and disease progre...
慢性乙型肝炎病毒(HBV)感染是一种严重影响患者身体和经济福祉的疾病。MTHFR基因的多态性与疾病进展之间的关系是研究的重点。
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引用次数: 0
Causal relationship of genetically predicted particulate matter 2.5 level with Alzheimer’s disease and the mediating effect of dehydroepiandrosterone sulphate 遗传预测颗粒物 2.5 水平与阿尔茨海默病的因果关系以及硫酸脱氢表雄酮的中介效应
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-04-18 DOI: 10.1080/03014460.2024.2337731
Zehan Huang, Guodong He, Shuo Sun, Yuqing Huang
The causal association between particulate matter 2.5 (PM2.5) and Alzheimer’s disease (AD) remains inconclusive, and the mediators of the association have yet to be explored.We aimed to assess the ...
颗粒物2.5(PM2.5)与阿尔茨海默病(AD)之间的因果关系尚无定论,其中介因素也有待探索。
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引用次数: 0
Total daily energy expenditure and elevated water turnover in a small-scale semi-nomadic pastoralist society from Northern Kenya 肯尼亚北部一个小规模半游牧社会的每日总能量消耗和较高的水周转率
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-03-04 DOI: 10.1080/03014460.2024.2310724
Amanda McGrosky, Zane S. Swanson, Rebecca Rimbach, Hilary Bethancourt, Emmanuel Ndiema, Rosemary Nzunza, David R. Braun, Asher Y. Rosinger, Herman Pontzer
Pastoralists live in challenging environments, which may be accompanied by unique activity, energy, and water requirements.Few studies have examined whether the demands of pastoralism contribute to...
牧民生活在充满挑战的环境中,对活动、能量和水的需求可能与众不同。
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引用次数: 0
To be or not to be bitter? The knowns, and unknowns, of the genetics of phenylthiocarbamide perception. 苦还是不苦?苯硫甲酰胺感知遗传学的已知与未知。
IF 1.2 4区 医学 Q2 ANTHROPOLOGY Pub Date : 2024-02-01 Epub Date: 2024-08-15 DOI: 10.1080/03014460.2024.2379900
Davide Risso, Dennis Drayna
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引用次数: 0
Relationship between dietary inflammation index and frailty in patients with osteoarthritis. 骨关节炎患者饮食炎症指数与虚弱之间的关系。
IF 1.2 4区 医学 Q2 ANTHROPOLOGY Pub Date : 2024-02-01 Epub Date: 2024-07-09 DOI: 10.1080/03014460.2024.2369274
Feng Zhao, Fang Pan, Jian Li

Background: Osteoarthritis (OA) is a common chronic joint disease that significantly affects an individual's quality-of-life and frailty has become one of the common complications in OA patients as the disease progresses. The relationship between dietary patterns is not clear.

Methods: All participants are from the National Health and Nutrition Examination Survey (NHANES) and have been diagnosed with OA. The dietary inflammation index (DII) is calculated based on the dietary intake reported by the participants. Logistic regression analysis is used to investigate the relationship between DII and frailty. Restricted cubic splines are utilised to explore their nonlinear relationship. Mediation analysis is conducted to explore the role of inflammation in this relationship.

Results: A total of 2,530 OA patients were included in the study, with an average age of 64.46 (12.67) years. After adjusting for covariates, for each one standard deviation increase in DII, the risk of frailty increased by 15% (OR = 1.15, 95% CI = 1.03-1.28). Compared to patients with DII < -1, patients with DII > 1 had a significantly higher risk of frailty (OR = 1.50, 95% CI = 1.05-2.14).

Conclusions: The findings of this study indicate a positive association between DII and the risk of frailty in OA patients. These results underscore the potential impact of dietary interventions in improving the quality-of-life for OA patients.

背景:骨关节炎(OA)是一种常见的慢性关节疾病,严重影响患者的生活质量,随着病情的发展,虚弱已成为OA患者常见的并发症之一。饮食模式之间的关系尚不清楚:所有参与者均来自美国国家健康与营养调查(NHANES),并已被确诊为 OA。根据参与者报告的饮食摄入量计算饮食炎症指数(DII)。逻辑回归分析用于研究 DII 与虚弱之间的关系。利用限制性三次样条来探讨两者之间的非线性关系。进行中介分析以探讨炎症在这一关系中的作用:研究共纳入 2,530 名 OA 患者,平均年龄为 64.46 (12.67) 岁。在对协变量进行调整后,DII每增加一个标准差,虚弱的风险就会增加15%(OR = 1.15,95% CI = 1.03-1.28)。与 DII < -1 的患者相比,DII > 1 的患者发生虚弱的风险明显更高(OR = 1.50,95% CI = 1.05-2.14):本研究结果表明,DII 与 OA 患者的虚弱风险呈正相关。这些结果强调了饮食干预对改善 OA 患者生活质量的潜在影响。
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引用次数: 0
Worldwide distribution of genetic factors related to severity of COVID-19 infection. 与 COVID-19 感染严重程度有关的遗传因素在全球的分布情况。
IF 1.2 4区 医学 Q2 ANTHROPOLOGY Pub Date : 2024-02-01 Epub Date: 2024-07-16 DOI: 10.1080/03014460.2024.2366248
María Esther Esteban, Débora Pino, Alicia Romero-Lorca, Apolonia Novillo, María Gaibar, José A Riancho, Augusto Rojas-Martínez, Carlos Flores, Pablo Lapunzina, Ángel Carracedo, Georgios Athanasiadis, Ana Fernández-Santander

Background: Genome-wide association studies of COVID-19 severity have been carried out mostly on European or East Asian populations with small representation of other world regions. Here we explore the worldwide distribution and linkage disequilibrium (LD) patterns of genetic variants previously associated with COVID-19 severity.

Methods: We followed up the results of a large Spanish genome-wide meta-analysis on 26 populations from the 1000 Genomes Project by calculating allele frequencies and LD scores of the nine most significant SNPs. We also used the entire set of summary statistics to compute polygenic risk scores (PRSs) and carried out comparisons at the population and continental level.

Results: We observed the strongest differences among continental regions for the five top SNPs in chromosome 3. European, American, and South Asian populations showed similar LD patterns. Average PRSs in South Asian and American populations were consistently higher than those observed in Europeans. While PRS distributions were similar among South Asians, the American populations showed striking differences among them.

Conclusions: Considering the caveats of PRS transferability across ethnicities, our analysis showed that American populations present the highest genetic risk score, hence potentially higher propensity, for COVID-19 severity. Independent validation is warranted with additional summary statistics and phenotype data.

背景:有关 COVID-19 严重程度的全基因组关联研究大多在欧洲或东亚人群中进行,在世界其他地区的代表性较小。在此,我们探讨了以前与 COVID-19 严重程度相关的遗传变异的全球分布和连锁不平衡(LD)模式:方法:我们通过计算 9 个最重要 SNP 的等位基因频率和 LD 分值,对西班牙 1000 基因组计划(1000 Genomes Project)中 26 个人群的大型全基因组荟萃分析结果进行了跟进。我们还利用整套汇总统计数据计算了多基因风险评分(PRS),并在人群和大洲层面进行了比较:结果:我们观察到,在 3 号染色体的五个顶级 SNPs 上,各大洲之间的差异最大。欧洲、美洲和南亚人群表现出相似的 LD 模式。南亚和美洲人群的平均 PRS 始终高于欧洲人。南亚人的 PRS 分布相似,而美洲人的 PRS 分布则存在显著差异:考虑到 PRS 在不同种族间的可转移性的注意事项,我们的分析表明,美国人的遗传风险得分最高,因此 COVID-19 严重性的倾向性也可能较高。我们有必要利用更多的汇总统计和表型数据进行独立验证。
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引用次数: 0
Forensic parameters and population analysis of 21 autosomal STR loci in the Wuhu Han population from Anhui Province, East China. 华东安徽芜湖汉族人群 21 个常染色体 STR 位点的法医参数和人群分析。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-02-01 Epub Date: 2024-01-22 DOI: 10.1080/03014460.2023.2298470
Yanyan Yang, Qianqian Li, Xinrui Yang, Ziwei Zhang, Yongliang Hu, Yue Zhang, Fang He

Background: At present, there are no available genetic data on the AGCU EX22 Kit from the Wuhu Han population.

Aim: This study investigates the applicability of the AGCU EX22 kit, designed for the Chinese population for forensic analysis and population genetics of the Wuhu Han population.

Subjects and methods: Bloodstains from 1565 unrelated healthy individuals in Wuhu city, Anhui Province, were collected for analysis. The AGCU EX22 kit was used for amplification, and capillary electrophoresis was used to separate the amplification products. Allele frequencies and forensic parameters were determined. The Wuhu Han population was compared to 10 reference populations through genetic distance, a phylogenetic neighbor-joining tree and principal component analysis.

Results: In total, 281 alleles and 1187 genotypes were observed. No significant deviations from Hardy-Weinberg equilibrium at any locus were found after Bonferroni's correction. The 21 autosomal short tandem repeat (STR) genetic markers exhibited high informativeness and polymorphism. The cumulative power of discrimination and power of exclusion were 0.999999999999999999999999913380 and 0.999999996752339, respectively. Population comparisons revealed a genetic affinity between Wuhu Han and southern Han populations, except for the Guangdong Han population, which aligned with the traditional geographical division in China.

Conclusion: The AGCU EX22 Kit, containing 21 STR loci, is suitable for forensic application and population genetics studies in the Wuhu Han population.

背景:目的:本研究调查了专为中国人口设计的 AGCU EX22 试剂盒在芜湖汉族人口法医分析和人口遗传学中的适用性:采集安徽省芜湖市 1565 名无血缘关系健康人的血迹进行分析。采用 AGCU EX22 试剂盒进行扩增,毛细管电泳分离扩增产物。测定了等位基因频率和法证参数。通过遗传距离、系统发育邻接树和主成分分析,将芜湖汉族人群与 10 个参考人群进行比较:共观察到 281 个等位基因和 1187 个基因型。经 Bonferroni 校正后,未发现任何基因位点明显偏离 Hardy-Weinberg 平衡。21 个常染色体短串联重复(STR)遗传标记表现出较高的信息量和多态性。累积鉴别力和排除力分别为 0.9999999999999999999999913380 和 0.999999996752339。种群比较显示,除广东汉族种群外,芜湖汉族与南方汉族种群之间存在遗传亲缘关系,这与中国传统的地理分区一致:结论:包含 21 个 STR 位点的 AGCU EX22 套件适用于芜湖汉族人口的法医应用和人口遗传学研究。
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引用次数: 0
Genetic polymorphism analysis and forensic application evaluation of 57 insertion/deletion polymorphisms from Yi ethnic group in Yunnan. 云南彝族 57 个插入/缺失多态性的遗传多态性分析和法医应用评估。
IF 1.7 4区 医学 Q3 Medicine Pub Date : 2024-02-01 Epub Date: 2024-01-22 DOI: 10.1080/03014460.2023.2294743
Kuo Zeng, Dong Zhao

Background: As a new kind of diallelic genetic marker, insertion/deletion (InDel) polymorphisms have recently been used in forensic science. However, there are relatively few studies on the forensic evaluation of InDel genetic polymorphisms from different populations.

Aim: The aim of the present work is to assess the genetic polymorphism and forensic applicability of 57 InDels from the Yi ethnic group and explore the genetic background of this group.

Subjects and methods: A total sample of 122 unrelated individuals of Yi group from the Yunnan province were genotyped by the AGCU indel 60 Kit. Multiplex population genetic analyses on the same 57 InDels were carried out among the Yunnan Yi group and 29 reference populations.

Results: The average allele frequency of these loci in the Yi ethnic group was 0.485. Heterozygosity, polymorphism information content, and the power of discrimination were 0.477, 0.362, and 0.612, respectively. The combined power of discrimination and the combined power of exclusion reached to 0.99999999999999999669 and 0.999962965, respectively. The results showed that 57 InDels polymorphisms have high genetic polymorphisms in the Yi ethnic group.

Conclusions: The 57 InDels could be used for forensic individual identification, paternity testing, and intercontinental population discrimination, with the potential for use in biogeographic ancestry inference.

背景:插入/缺失(InDel)多态性作为一种新的二联遗传标记,最近已被用于法医学。目的:本研究旨在评估彝族群体中 57 个 InDel 基因多态性和法医学适用性,并探索该群体的遗传背景:采用AGCU indel 60试剂盒对云南彝族122名无血缘关系的个体进行了基因分型。在云南彝族群体和 29 个参考群体中对相同的 57 个 InDels 位点进行了多重群体遗传分析:结果:这些位点在彝族群体中的平均等位基因频率为 0.485。杂合度、多态性信息含量和鉴别力分别为 0.477、0.362 和 0.612。综合辨别力和综合排除力分别达到 0.999999999999999669 和 0.999962965。结果表明,57 个 InDels 多态性在彝族中具有较高的遗传多态性:结论:57 个 InDels 可用于法医鉴定、亲子鉴定和洲际人群鉴别,并有可能用于生物地理祖先推断。
{"title":"Genetic polymorphism analysis and forensic application evaluation of 57 insertion/deletion polymorphisms from Yi ethnic group in Yunnan.","authors":"Kuo Zeng, Dong Zhao","doi":"10.1080/03014460.2023.2294743","DOIUrl":"10.1080/03014460.2023.2294743","url":null,"abstract":"<p><strong>Background: </strong>As a new kind of diallelic genetic marker, insertion/deletion (InDel) polymorphisms have recently been used in forensic science. However, there are relatively few studies on the forensic evaluation of InDel genetic polymorphisms from different populations.</p><p><strong>Aim: </strong>The aim of the present work is to assess the genetic polymorphism and forensic applicability of 57 InDels from the Yi ethnic group and explore the genetic background of this group.</p><p><strong>Subjects and methods: </strong>A total sample of 122 unrelated individuals of Yi group from the Yunnan province were genotyped by the AGCU indel 60 Kit. Multiplex population genetic analyses on the same 57 InDels were carried out among the Yunnan Yi group and 29 reference populations.</p><p><strong>Results: </strong>The average allele frequency of these loci in the Yi ethnic group was 0.485. Heterozygosity, polymorphism information content, and the power of discrimination were 0.477, 0.362, and 0.612, respectively. The combined power of discrimination and the combined power of exclusion reached to 0.99999999999999999669 and 0.999962965, respectively. The results showed that 57 InDels polymorphisms have high genetic polymorphisms in the Yi ethnic group.</p><p><strong>Conclusions: </strong>The 57 InDels could be used for forensic individual identification, paternity testing, and intercontinental population discrimination, with the potential for use in biogeographic ancestry inference.</p>","PeriodicalId":50765,"journal":{"name":"Annals of Human Biology","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2024-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139514158","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Annals of Human Biology
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