BACKGROUND: Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection and subsequent COVID-19 has spread world-wide and become pandemic with about 7 million deaths reported so far. Interethnic variability of the disease has been described, but a significant part of the differences remain unexplained and may be attributable to genetic factors. AIM: To analyse genetic factors potentially influencing COVID-19 susceptibility and severity in European Roma minority. SUBJECTS AND METHODS: Two genetic determinants, within OAS-1 (2-prime,5-prime-oligoadenylate synthetase 1, a key protein in the defence against viral infection; it activates RNases that degrade viral RNAs; rs4767027 has been analysed) and LZTFL1 (leucine zipper transcription factor-like 1, expressed in the lung respiratory epithelium; rs35044562 has been analysed) genes were screened in a population-sample of Czech Roma (N = 302) and majority population (N = 2,559). RESULTS: For both polymorphisms, Roma subjects were more likely carriers of at least one risky allele for both rs4767027-C (p < 0.001) and rs35044562-G (p < 0.00001) polymorphism. There were only 5.3% Roma subjects without at least one risky allele in comparison with 10.1% in the majority population (p < 0.01). CONCLUSIONS: It is possible that different genetic background plays an important role in increased prevalence of COVID-19 in the Roma minority.

• Klíčová slova
• COVID-19, Roma, ethnicity, polymorphism,
• MeSH
• 2',5'-oligoadenylátsynthetasa genetika   MeSH
• COVID-19 * genetika   epidemiologie   MeSH
• dospělí MeSH
• genetická predispozice k nemoci MeSH
• jednonukleotidový polymorfismus MeSH
• lidé středního věku MeSH
• lidé MeSH
• mutace MeSH
• neandertálci * genetika   MeSH
• prevalence MeSH
• Romové * genetika   MeSH
• SARS-CoV-2 * MeSH
• senioři MeSH
• transkripční faktory genetika   MeSH
• zvířata MeSH
• Check Tag
• dospělí MeSH
• lidé středního věku MeSH
• lidé MeSH
• mužské pohlaví MeSH
• senioři MeSH
• ženské pohlaví MeSH
• zvířata MeSH
• Publikační typ
• časopisecké články MeSH
• Geografické názvy
• Česká republika epidemiologie   MeSH

Aim: The aim of the present study was to demonstrate the existence of uniform sexual dimorphism in some radioulnar contrasts between different finger ridge counts within the same hand in a large set of populations, thus confirming the universal nature of this dimorphism in humans.Subjects and methods: We analysed individual finger ridge counts (10 values on each hand) of both hands from archival sources (mainly the Brehme-Jantz database). In total, these included 4412 adults from 21 population samples covering all permanently inhabited continents and encompassing very different and geographically distant human populations. We calculated the contrasts (differences) of all pairs of ridge counts (45 per hand) and used diverse methods to assess the direction and degree of dimorphism of them across all population samples.Results: The highest sexual dimorphism was observed for nine contrasts involving the ridge count of the dermatoglyphic pattern on the radial side of the second finger of the right hand (R2r). Among these contrasts, we then found four that had the same direction of dimorphism in all 21 populations. The most dimorphic was the contrast R1rR2r - the difference between the ridge count of the radial side of the thumb and the radial side of the index finger.Discussion: Thus, these dermatoglyphic traits can be further investigated as potential markers of prenatal sex differentiation from ca. 10th week of intrauterine development. However, it will be useful to address the detailed factors and mechanisms for differences in the degree of dimorphism of these traits in different populations.

• Klíčová slova
• Dermatoglyphics, Finger Ridge Count, prenatal development, radioulnar contrasts, sex differences,
• MeSH
• dospělí MeSH
• fenotyp MeSH
• lidé MeSH
• pohlavní dimorfismus * MeSH
• prsty ruky * anatomie a histologie   MeSH
• ruka MeSH
• sexuální faktory MeSH
• těhotenství MeSH
• Check Tag
• dospělí MeSH
• lidé MeSH
• mužské pohlaví MeSH
• těhotenství MeSH
• ženské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH

BACKGROUND: Developmental instability is a component of non-genetic variation that results from random variation in developmental processes. It is considered a sensitive indicator of the physiological state of individuals. It is reflected in various ways, but in this study we focussed on its reflection in fluctuating asymmetry (FA) and morphological integration. AIM: To assess how, if at all, variations of facial morphology mirror developmental instability across childhood with respect to sex, growth rate and socioeconomic/environmental factors. SUBJECTS AND METHODS: A set of 210 three-dimensional facial models (of children aged between 6.3 and 14.3 years) originating from the FIDENTIS 3D Face Database was subjected to landmark-based methods of geometric morphometrics to quantify the degree of facial asymmetry and facial morphological integration. In addition, the association with age, sex, and socioeconomic factors was assessed. RESULTS: Our results showed a nonlinear increase of FA with age up to the age of 14 years. The pattern of sex-related variants in facial FA differed in relation to age, as girls exhibited higher values of FA than boys up to the age of 9 years. We found that a signal of modularity based on functional demands and organisation of the face is of particular importance. Here, girls exhibited higher morphological covariation among modules. During more rapid adolescence-related growth, however, covariation among modules at the asymmetrical level decreased in both sexes. CONCLUSION: We can conclude that facial morphology was shown to be strongly integrated, particularly until adolescence. This covariation can facilitate an increase of FA. In addition, the results of this study indicate there is a weak association between socioeconomic stress and facial asymmetries. In contrast, sex and growth rate are reflected in developmental instability.

• Klíčová slova
• Facial variability, developmental instability, facial integrity, facial modularity, fluctuating asymmetry,
• MeSH
• asymetrie obličeje * genetika   MeSH
• dítě MeSH
• hlava MeSH
• lidé MeSH
• mladiství MeSH
• obličej * MeSH
• socioekonomické faktory MeSH
• Check Tag
• dítě MeSH
• lidé MeSH
• mladiství MeSH
• mužské pohlaví MeSH
• ženské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH

Background: The size of sex differences in dermatoglyphic features and their inter-population differences remains a subject of debate. Combining fingers in traditional dermatoglyphic methodology and omitting finger-specific variations might be a cause for uncertainty.Aim: To compare sex differences in whorl frequencies between fingers.Subjects and methods: Using meta-analytical methods, the authors studied sex differences in frequencies of whorls (log Odd Ratios) for each finger separately, including their heterogeneities (between-samples variance). The dataset of 204 population samples was extracted from published dermatoglyphic studies.Results: Aggregated effects of sex differences were significant in all fingers, except for the left 1st finger. Sex differences were higher in the right hand and increased from radial to ulnar fingers. Apart from the right 1st and 3rd fingers, heterogeneities were small and literally zero in the right 4th finger.Conclusion: Higher sex differences in ulnar fingers and the lack of interpopulation differences all over the world in the 4th finger might be caused by a stronger influence of genetic and/or hormonal factors on dermatoglyphic development of the ulnar side of the hand. It is suggested that future studies, when applying dermatoglyphic traits as markers of prenatal environment, use traits by individual fingers or their relationships within the hand.

• Klíčová slova
• Dermatoglyphics, interpopulation differences, meta-analysis, prenatal programming, sex differences,
• MeSH
• dermatoglyfika * MeSH
• fenotyp * MeSH
• lidé MeSH
• pohlavní dimorfismus MeSH
• prsty ruky anatomie a histologie   MeSH
• Check Tag
• lidé MeSH
• mužské pohlaví MeSH
• ženské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH
• metaanalýza MeSH
• systematický přehled MeSH

BACKGROUND: Seasons affect many social, economic, and biological outcomes, particularly in low-resource settings, and some studies suggest that birth season affects child growth. AIM: To study a predictor of stunting that has received limited attention: birth season. SUBJECTS AND METHODS: This study uses cross-sectional data collected during 2008 in a low-resource society of horticulturists-foragers in the Bolivian Amazon, Tsimane'. It estimates the associations between birth months and height-for-age Z-scores (HAZ) for 562 girls and 546 boys separately, from birth until age 11 years or pre-puberty, which in this society occurs ∼13-14 years. RESULTS: Children born during the rainy season (February-May) were shorter, while children born during the end of the dry season and the start of the rainy season (August-November) were taller, both compared with their age-sex peers born during the rest of the year. The correlations of birth season with HAZ were stronger for boys than for girls. Controlling for birth season, there is some evidence of eventual partial catch-up growth, with the HAZ of girls or boys worsening until ∼ age 4-5 years, but improving thereafter. By age 6 years, many girls and boys had ceased to be stunted, irrespective of birth season. CONCLUSION: The results suggest that redressing stunting will require attention to conditions in utero, infancy and late childhood.

• Klíčová slova
• Tsimane', birth month, generalised additive model, sex differences, stunting,
• MeSH
• dítě MeSH
• indiáni Jižní Ameriky statistika a číselné údaje   MeSH
• kojenec MeSH
• lidé MeSH
• novorozenec MeSH
• porod MeSH
• poruchy růstu epidemiologie   etiologie   MeSH
• předškolní dítě MeSH
• průřezové studie MeSH
• puberta MeSH
• roční období MeSH
• tělesná výška * MeSH
• vývoj dítěte * MeSH
• Check Tag
• dítě MeSH
• kojenec MeSH
• lidé MeSH
• mužské pohlaví MeSH
• novorozenec MeSH
• předškolní dítě MeSH
• ženské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH
• Geografické názvy
• Bolívie epidemiologie   MeSH

BACKGROUND: Tetranucleotide Short Tandem Repeats (STRs) for human identification and common use in forensic cases have recently been used to address the population genetics of the North-Eastern Mediterranean area. However, to gain confidence in the inferences made using STRs, this kind of analysis should be challenged with changes in three main aspects of the data, i.e. the sizes of the samples, their distance across space and the genetic background from which they are drawn. AIM: To test the resilience of the gradients previously detected in the North-Eastern Mediterranean to the enlargement of the surveyed area and population set, using revised data. SUBJECTS AND METHODS: STR genotype profiles were obtained from a publicly available database (PopAffilietor databank) and a dataset was assembled including >7000 subjects from the Arabian Peninsula to Scandinavia, genotyped at eight loci. Spatial principal component analysis (sPCA) was applied and the frequency maps of the nine alleles which contributed most strongly to sPC1 were examined in detail. RESULTS: By far the greatest part of diversity was summarised by a single spatial principal component (sPC1), oriented along a SouthEast-to-NorthWest axis. The alleles with the top 5% squared loadings were TH01(9.3), D19S433(14), TH01(6), D19S433(15.2), FGA(20), FGA(24), D3S1358(14), FGA(21) and D2S1338(19). These results confirm a clinal pattern over the whole range for at least four loci (TH01, D19S433, FGA, D3S1358). CONCLUSIONS: Four of the eight STR loci (or even alleles) considered here can reproducibly capture continental arrangements of diversity. This would, in principle, allow for the exploitation of forensic data to clarify important aspects in the formation of local gene pools.

• Klíčová slova
• Mediterranean, Population structuring, allele frequency gradients, inbreeding, spatial PCA,
• MeSH
• frekvence genu * MeSH
• genetická variace * MeSH
• genotyp * MeSH
• mikrosatelitní repetice * MeSH
• populační genetika MeSH
• Publikační typ
• časopisecké články MeSH
• Geografické názvy
• severní Afrika MeSH
• Střední východ MeSH
• Středomoří MeSH

BACKGROUND: The study concerns the comparison of percentile curves of Czech breastfed children with Czech national references from 1991 and 2001 and WHO growth standards. Growth charts of breastfed children demonstrate different curve shapes, especially in the first months of life. Incorrect interpretation of the growth curve could lead to premature introduction of complementary foods or infant formula. AIM: The comparison of four body parameters of Czech breastfed children with currently used Czech national references and WHO standards in order to recommend that Czech paediatricians use either Czech references or WHO standards in their practice. SUBJECTS AND METHODS: Nine hundred and sixty breastfed children were included in the study of length-for-age, head circumference-for-age, weight-for-age and weight-for-length parameters. All percentile curves were compared. Values of the 50th percentile expressed in z-scores based on both Czech references and WHO standards were tested. RESULTS: The study confirmed results of previous surveys documenting that growth of breastfed children is specific. Nevertheless, percentile curves of growth parameters of Czech breastfed children are closer to Czech references than WHO standards. CONCLUSIONS: The Czech national references fulfil the needs of Czech paediatricians (with pointing to specifics of breastfed child growth) and WHO standards are suitable, especially for international comparison.

• Klíčová slova
• Czech reference, Growth charts, WHO growth standards, breastfed children,
• MeSH
• antropometrie * MeSH
• kojenec MeSH
• kojení statistika a číselné údaje   MeSH
• lidé MeSH
• novorozenec MeSH
• referenční standardy MeSH
• Světová zdravotnická organizace MeSH
• tělesná hmotnost MeSH
• tělesná výška MeSH
• vývoj dítěte * MeSH
• Check Tag
• kojenec MeSH
• lidé MeSH
• mužské pohlaví MeSH
• novorozenec MeSH
• ženské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH
• Geografické názvy
• Česká republika MeSH

BACKGROUND: The origin of Western African pastoralism, represented today by the Fulani nomads, has been a highly debated issue for the past decades, and has not yet been conclusively resolved. AIM: This study focused on Alu polymorphisms in sedentary and nomadic populations across the African Sahel to investigate patterns of diversity that can complement the existing results and contribute to resolving issues concerning the origin of West African pastoralism. SUBJECTS AND METHODS: A new dataset of 21 Alu biallelic markers covering a substantial part of the African Sahel has been analysed jointly with several published North African populations. RESULTS: Interestingly, with regard to Alu variation, the relationship of Fulani pastoralists to North Africans is not as evident as was earlier revealed by studies of uniparental loci such as mtDNA and NRY. Alu insertions point rather to an affinity of Fulani pastoralists to Eastern Africans also leading a pastoral lifestyle. CONCLUSIONS: It is suggested that contemporary Fulani pastoralists might be descendants of an ancestral Eastern African population that, while crossing the Sahara in the Holocene, admixed slightly with a population of Eurasian (as evidenced by uniparental polymorphisms) ancestry. It seems that, in the Fulani pastoralists, Alu elements reflect more ancient genetic relationships than do uniparental genetic systems.

• Klíčová slova
• African Sahel, Alu insertions, Fulani nomads, Western African pastoralism,
• MeSH
• elementy Alu genetika   MeSH
• lidé MeSH
• osoby s přechodným pobytem a migranti * MeSH
• polymorfismus genetický genetika   MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• Geografické názvy
• subsaharská Afrika MeSH

BACKGROUND: Several demographic events have been postulated to explain the contemporaneous structure of European genetic diversity. First, an initial settlement of the continent by anatomically modern humans; second, the re-settlement of northern latitudes after the Last Glacial Maximum; third, the demic diffusion of Neolithic farmers from the Near East; and, fourth, several historical events such as the Slavic migration. AIM: The aim of this study was to provide a more integrated picture of male-specific genetic relationships of Slovakia within the broader pan-European genetic landscape. SUBJECTS AND METHODS: This study analysed a new Y-chromosome data-set (156 individuals) for both SNP and STR polymorphisms in population samples from five different Slovakian localities. RESULTS: It was found that the male diversity of Slovakia is embedded in the clinal pattern of the major R1a and R1b clades extending over the continent and a similar pattern of population structure is found with Y-specific SNP or STR variation. CONCLUSION: The highly significant correlation between the results based on fast evolving STRs on one hand and slow evolving SNPs on the other hand suggests a recent timeframe for the settlement of the area.

• Klíčová slova
• Genetic structure, Slovakia, Y-SNP, Y-STR, Y-chromosome,
• MeSH
• fylogeografie MeSH
• genetická variace * MeSH
• jednonukleotidový polymorfismus * MeSH
• lidé MeSH
• lidský chromozom Y genetika   MeSH
• mikrosatelitní repetice * MeSH
• Check Tag
• lidé MeSH
• mužské pohlaví MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Geografické názvy
• Slovenská republika MeSH

BACKGROUND: No mitochondrial DNA (mtDNA) sequences from Chadic-speaking peoples have yet been reported, even though these populations inhabit a vast territory from eastern Nigeria to central Chad. This paper deals with the mtDNA sequences of four Central Chadic populations (Hide, Kotoko, Mafa and Masa) from northern Cameroon, biological samples from which were collected during anthropological research in the area of their homeland. OBJECTIVE: The main goals of this article are to report new mtDNA sequences of Chadic-speaking populations, to analyse their genetic diversity and to establish their relationships within the peri-Saharan area in respect of geography and languages. SUBJECT AND METHODS: The analyses are based on 104 mtDNA haplotypes, which can be localized into four different areas of northern Cameroon. Data collection was based on a strict geographical sampling strategy; the ethnonyms are retained here only for comparative purposes. RESULTS: None of the examined Chadic populations displays a departure from the normal mismatch distribution pattern, and the null hypothesis of the expansion event cannot be rejected. Analyses of molecular variance and F(ST) genetic distances revealed that the Chadic-speaking groups of northern Cameroon share more similarities with the populations of the Upper and Middle Nile Valley and East Africa than with populations from Central Africa. The results show geographical clustering to be more important than the correlation of linguistic affiliations with molecular genetic data. CONCLUSION: The observation that the Chadic group reveals some affinities to East Africans is extremely surprising giving the present-day geographical distance (around 2000 km) between them. These observations complement recent linguistic and archaeological findings, which consider the Chadic branch in the Afro-Asiatic phylum to be of eastern origin. A continuous, well-defined, geographic sampling strategy of the different genetic polymorphisms of the native populations of sub-Saharan Africa is further needed as the only way of understanding the differentiation of the mtDNA sequences at a micro-regional scale.

• MeSH
• DNA fingerprinting MeSH
• etnicita genetika   MeSH
• fylogeneze MeSH
• haplotypy MeSH
• lidé MeSH
• mitochondriální DNA * MeSH
• polymorfismus genetický MeSH
• populační genetika * MeSH
• sekvenční analýza DNA * MeSH
• zeměpis MeSH
• Check Tag
• lidé MeSH
• Publikační typ
• časopisecké články MeSH
• práce podpořená grantem MeSH
• Geografické názvy
• Afrika MeSH
• Názvy látek
• mitochondriální DNA * MeSH