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1.
Article in English | MEDLINE | ID: mdl-24329312

ABSTRACT

It is well known that sexually transmitted diseases (STD) spread across a network of human sexual contacts. This network is most often bipartite, as most STD are transmitted between men and women. Even though network models in epidemiology have quite a long history now, there are few general results about bipartite networks. One of them is the simple dependence, predicted using the mean field approximation, between the epidemic threshold and the average and variance of the degree distribution of the network. Here we show that going beyond this approximation can lead to qualitatively different results that are supported by numerical simulations. One of the new features, that can be relevant for applications, is the existence of a critical value for the infectivity of each population, below which no epidemics can arise, regardless of the value of the infectivity of the other population.


Subject(s)
Models, Biological , Sexually Transmitted Diseases/epidemiology , Sexually Transmitted Diseases/transmission , Female , Humans , Male
2.
Transl Psychiatry ; 2: e119, 2012 May 22.
Article in English | MEDLINE | ID: mdl-22832964

ABSTRACT

The identification and exploration of genetic loci that influence smoking behaviors have been conducted primarily in populations of the European ancestry. Here we report results of the first genome-wide association study meta-analysis of smoking behavior in African Americans in the Study of Tobacco in Minority Populations Genetics Consortium (n = 32,389). We identified one non-coding single-nucleotide polymorphism (SNP; rs2036527[A]) on chromosome 15q25.1 associated with smoking quantity (cigarettes per day), which exceeded genome-wide significance (ß = 0.040, s.e. = 0.007, P = 1.84 × 10(-8)). This variant is present in the 5'-distal enhancer region of the CHRNA5 gene and defines the primary index signal reported in studies of the European ancestry. No other SNP reached genome-wide significance for smoking initiation (SI, ever vs never smoking), age of SI, or smoking cessation (SC, former vs current smoking). Informative associations that approached genome-wide significance included three modestly correlated variants, at 15q25.1 within PSMA4, CHRNA5 and CHRNA3 for smoking quantity, which are associated with a second signal previously reported in studies in European ancestry populations, and a signal represented by three SNPs in the SPOCK2 gene on chr10q22.1. The association at 15q25.1 confirms this region as an important susceptibility locus for smoking quantity in men and women of African ancestry. Larger studies will be needed to validate the suggestive loci that did not reach genome-wide significance and further elucidate the contribution of genetic variation to disparities in cigarette consumption, SC and smoking-attributable disease between African Americans and European Americans.


Subject(s)
Black or African American/genetics , Smoking/genetics , Adult , Aged , Chromosomes, Human, Pair 10/genetics , Chromosomes, Human, Pair 15/genetics , Female , Genetic Loci/genetics , Genetic Predisposition to Disease/genetics , Genetic Variation/genetics , Genome-Wide Association Study , Genotype , Humans , Male , Middle Aged , Nerve Tissue Proteins/genetics , Phenotype , Polymorphism, Single Nucleotide/genetics , Proteoglycans/genetics , Receptors, Nicotinic/genetics , Statistics as Topic
3.
Theriogenology ; 78(3): 612-9, 2012 Aug.
Article in English | MEDLINE | ID: mdl-22538010

ABSTRACT

Seminal coagulum formation in spider monkeys (Ateles geoffroyi) interferes with the efficient recovery and evaluation of spermatozoa. The main objective was to assess the effect of increasing concentrations of trypsin on dissolution of seminal coagulum and spermatic parameters. Seminal coagulum was incubated at 37 °C without trypsin or in the presence of increasing trypsin concentrations (0.1%, 1.0%, and 5.0%). For each sample, coagulum dissolution time was measured, and sperm concentration, viability, motility, and morphology were evaluated using light microscopy and/or transmission electronic microscopy (TEM). Trypsin concentrations of 1.0% and 5.0% more rapidly liquefied seminal coagulum, averaging 32 and 21 min, respectively, compared with nontrypsinized controls, with maintenance of greater sperm viability (70.8% and 72.5%, respectively). Coagulum treated with 1.0% trypsin and the liquid ejaculate fraction averaged higher sperm motility (40.1% and 55.6%, respectively) than control samples, and both 1.0% and 5.0% trypsin treatment allowed recovery of increased numbers of motile spermatozoa. There was greater sperm fragmentation at the head and midpiece level after treatment with 1.0% and 5.0% trypsin (55.8% and 55.9%); however, the percentage of normal morphology in structurally intact spermatozoa did not differ relative to controls. With transmission electronic microscopy imaging, there were similar percentages of spermatozoa with plasma membrane swelling in the midpiece and acrosomal regions in trypsin-treated samples and controls. In conclusion, trypsin treatment of spider monkey seminal coagulum exerted a concentration-dependent effect on dissolution time and various spermatic parameters. Higher trypsin concentrations caused more rapid liquefaction of coagulum and recovery of greater numbers of motile spermatozoa, but may adversely affect fragmentation of spermatozoa and could compromise sperm function and cryopreservation potential.


Subject(s)
Atelinae , Semen/drug effects , Spermatozoa/drug effects , Trypsin/administration & dosage , Acrosome/ultrastructure , Animals , Cell Membrane/ultrastructure , Cell Survival , Male , Microscopy, Electron, Transmission , Semen/chemistry , Sperm Count , Sperm Midpiece/ultrastructure , Sperm Motility , Spermatozoa/physiology
4.
Neurology ; 63(3): 554-6, 2004 Aug 10.
Article in English | MEDLINE | ID: mdl-15304594

ABSTRACT

The authors recently have shown that triplication of the alpha-synuclein gene (SNCA) can cause Parkinson disease (PD) and diffuse Lewy body disease within the same kindred. The authors assessed 101 familial PD probands, 325 sporadic PD cases, 65 patients with dementia with Lewy bodies, and 366 neurologically normal control subjects for SNCA multiplication. The authors did not identify any subjects with multiplication of SNCA and conclude this mutation is a rare cause of disease.


Subject(s)
Gene Duplication , Lewy Body Disease/genetics , Nerve Tissue Proteins/genetics , Parkinson Disease/genetics , Adult , Aged , Aged, 80 and over , Cohort Studies , DNA Mutational Analysis , England/epidemiology , Family Health , Female , Finland/epidemiology , Gene Dosage , Gene Expression Regulation , Genetic Predisposition to Disease , Hispanic or Latino/genetics , Humans , Lewy Body Disease/epidemiology , Male , Middle Aged , Nerve Tissue Proteins/physiology , Parkinson Disease/epidemiology , Synucleins , United States/epidemiology , White People/genetics , alpha-Synuclein
5.
Ann Neurol ; 50(5): 658-61, 2001 Nov.
Article in English | MEDLINE | ID: mdl-11706972

ABSTRACT

We investigated the association of Parkinson's disease with tau gene haplotypes. In a sample of 319 unrelated Parkinson's disease patients and 196 control subjects, we observed an increased risk of Parkinson's disease for persons with the H1/H1 genotype (odds ratio = 1.5; 95% confidence interval: 0.98-2.23); however, the finding was not statistically significant. The results remained similar after adjusting for the possible misclassification of progressive supranuclear palsy patients as Parkinson's disease, but became statistically significant after restricting the analysis to nondemented subjects.


Subject(s)
Parkinson Disease/genetics , tau Proteins/genetics , Adult , Aged , Aged, 80 and over , Case-Control Studies , Europe/ethnology , Female , Gene Frequency , Genetic Linkage , Genetic Predisposition to Disease , Genetic Testing , Genotype , Haplotypes/genetics , Humans , Male , Middle Aged , Odds Ratio , Parkinson Disease/epidemiology , Parkinson Disease/ethnology , Risk Assessment , United States/epidemiology , White People/genetics
6.
Trans R Soc Trop Med Hyg ; 89(2): 189-90, 1995.
Article in English | MEDLINE | ID: mdl-7778146

ABSTRACT

We report the use of cultures of mosquito cells (TRA-284) to detect dengue virus in serum from cases of dengue fever in the state of Puebla, México. Using the conventional procedure 56 of 171 samples (32.7%) were positive. The negative sera (67.3%) were passaged 'blind' in mosquito cell cultures but no virus was detected. However, when these sera were incubated in the presence of actinomycin D (an inhibitor of deoxyribonucleic acid transcription) 20 of the 115 samples (17.4%) became positive. This procedure increased the virus detection rate from 32.7% to 44.4%. Serotypes 1 and 4 were identified for the first time in the state of Puebla, where the transmission of dengue virus is increasing. The addition of actinomycin D to mosquito cell cultures may improve the detection of dengue virus and could be a useful tool for virological surveillance in endemic countries.


Subject(s)
Dactinomycin/pharmacology , Dengue Virus/isolation & purification , Animals , Cells, Cultured , Culicidae , Dengue/blood , Humans , Transcription, Genetic/drug effects , Virology/methods
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