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1.
Homo ; 66(1): 44-59, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25435058

ABSTRACT

Short tandem repeats (STRs) of the combined DNA index system (CODIS) are probably the most employed markers for human identification purposes. STR databases generated to interpret DNA profiles are also helpful for anthropological purposes. In this work, we report admixture, population structure, and genetic relationships of Mexican Mestizos with respect to Latin American and Caribbean populations based on 13 CODIS-STRs. In addition, new STR population data were included from Tijuana, Baja California (Northwest, Mexico), which represents an interesting case of elevated genetic flow as a bordering city with the USA. Inter-population analyses included CODIS-STR data from 11 Mexican Mestizo, 12 Latin American and four Caribbean populations, in addition to European, Amerindian, and African genetic pools as ancestral references. We report allele frequencies and statistical parameters of forensic interest (PD, PE, Het, PIC, typical PI), for 15 STRs in Tijuana, Baja California. This Mexican border city was peculiar by the increase of African ancestry, and by presenting three STRs in Hardy-Weinberg disequilibrium, probably explained by recurrent gene flow. The Amerindian ancestry in Central and Southeast of Mexico was the greatest in Latin America (50.9-68.6%), only comparable with the North of Central America and Ecuador (48.8-56.4%), whereas the European ancestry was prevalent in South America (66.7-75%). The African ancestry in Mexico was the smallest (2.2-6.3%) in Latin America (≥ 2.6%), particularly regarding Brazil (21%), Honduras (62%), and the Caribbean (43.2-65.2%). CODIS-STRs allowed detecting significant population structure in Latin America based on greater presence of European, Amerindian, and African ancestries in Central/South America, Mexican Mestizos, and the Caribbean, respectively.


Subject(s)
DNA Fingerprinting , DNA/genetics , Databases, Nucleic Acid , Gene Flow/genetics , Indians, North American/genetics , Microsatellite Repeats/genetics , Black People/genetics , Caribbean Region , Central America , Gene Frequency/genetics , Humans , Latin America , Mexico , South America , White People/genetics
2.
Quito; Ministerio de Salud Pública; 2011. 42 p.
Monography in Spanish | PIE | ID: biblio-1006617

ABSTRACT

La!muerte!de!una!mujer!durante!el!embarazo,!o!dentro!de!los!42!días!siguientes!a! la! terminación! de! éste,! es! una! tragedia! familiar! y! comunitaria,! con! profundas! consecuencias! sociales! y! económicas.! La! mayoría! de! estas! muertes! pueden! ser!! prevenibles! con! acciones! dirigidas! a! ! evitar! el! embarazo! no! planificado,! con! controles! prenatales! adecuados! para! detección! y! tratamiento! oportuno! de! las! complicaciones!y!una!!adecuada!atención!del!parto!y!puerperio.!


Subject(s)
Humans , Female , Pregnancy , Maternal Health , Health Services Accessibility , Maternal Health Services , Ecuador
3.
Public Health Genomics ; 13(3): 171-80, 2010.
Article in English | MEDLINE | ID: mdl-19844075

ABSTRACT

Ecuador has a heterogeneous population of almost 14 million people and a complex health care system provided through provincial and national health programs by government and private hospitals. There are public health facilities at regional and territorial level. Ecuador has a small cadre of genetic professionals that provide clinical genetic services in a few private medical centers in the main cities. Prenatal screening is offered exclusively in a few individual hospitals, with variable uptake as part of prenatal care. Surveillance of the effect of prenatal screening and diagnosis on the birth prevalence of congenital anomalies is limited by gaps and variations in surveillance systems. Newborn screening programs are almost inexistent. There is broad variation in optional participation in laboratory quality assurance schemes, and there are no regulatory frameworks that are directly pertinent to genetic testing services or population genetics. Health technology assessment in Ecuador is conducted by a diverse collection of organizations, several of which have produced reports related to genetics.


Subject(s)
Congenital Abnormalities/diagnosis , Genomics/methods , Neonatal Screening/methods , Prenatal Diagnosis/methods , Public Health/methods , Community Health Services , Ecuador , Ethics, Medical , Genetic Testing/methods , Geography , Health Policy , Health Priorities , Health Services Accessibility , Humans , Infant, Newborn
4.
Int J Legal Med ; 123(6): 527-33, 2009 Nov.
Article in English | MEDLINE | ID: mdl-19693525

ABSTRACT

Single nucleotide polymorphisms (SNPs) in the flanking regions of microsatellite loci (SNPSTRs) help to increase the power of discrimination of short tandem repeat (STR) loci. SNPs are positions in the genome that have been well-conserved over the course of evolution, so analysing them can help distinguish between STR alleles in which the number of repetitions matches due to descent from those which match by chance. This provides support for the determination of biological paternity and other kinship analyses in which mutation needs to be ruled out as grounds for exclusion. Locus D7S820 shows a variable position, SNP rs59186128, in the 5' flanking region. This study is set out (1) to determine the frequencies of SNP rs59186128 in populations with various geographical origins and (2) to estimate the possible contribution of rs59186128 to the allele discrimination of locus D7S820. To that end, individuals from European Caucasoid, Hispanic, and Afro-American populations are studied using denaturing high-performance liquid chromatography, which enables locus rs59186128 to be quickly and highly cost-effectively screened. Moreover, a method is established for determining the haplotypes of SNPSTR rs59186128_D7820. The results show that SNP rs59186128 has a T allele frequency of more than 0.15 in one of the Afro-American populations studied, and the haplotype analysis shows that there is no preferential association between the alleles of SNPSTR rs59186128_D7S820, which supports the idea that they could be useful in forensic applications.


Subject(s)
Genetics, Population , Polymorphism, Single Nucleotide , Racial Groups/genetics , Tandem Repeat Sequences , Chromatography, High Pressure Liquid , DNA Fingerprinting , Gene Frequency , Genotype , Haplotypes , Humans
5.
Leg Med (Tokyo) ; 11 Suppl 1: S366-7, 2009 Apr.
Article in English | MEDLINE | ID: mdl-19282222

ABSTRACT

Aggression against healthcare workers is a problem of important consequences which is becoming a focus of research. However, its possible effects on psychological health have not been studied sufficiently in spite of the fact that they may be of importance even in the absence of physical aggression [Winstnaley S, Whittington R. Aggression towards health care staff in a UK general hospital: variation among professions. J Clin Nurs 2004;13:3-10,[1]].


Subject(s)
Aggression/psychology , Health Personnel/psychology , Anxiety/epidemiology , Burnout, Professional/psychology , Cross-Sectional Studies , Depression/epidemiology , Humans , Job Satisfaction , Medicine , Spain/epidemiology , Specialties, Surgical
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