57 research outputs found
Recognition and Stigma of Prescription Drug Abuse Disorder: Personal and Community Determinants
Background
Prescription drug abuse (PDA) disorders continue to contribute to the current American opioid crisis. Within this context, our study seeks to improve understanding about stigma associated with, and symptom recognition of, prescription drug abuse. Aims
Model the stigma and symptom recognition of PDA in the general population. Methods
A randomized, nation-wide, online, vignette-focused survey of the general public (N = 631) was implemented with an oversample for rural counties. Logit estimation was used for analysis, with regional and county-level sociodemographic variables as controls. Results
Individual respondents that self-identify as having or having had “a prescription drug abuse issue” were less likely to correctly identify the condition and were 4 times more likely to exhibit stigma. Male respondents were approximately half as likely to correctly identify PDA as female respondents while older respondents (55+) were more likely to correctly identify PDA, relative to those aged 35–54. Being both male and younger was associated with slightly more stigma, in that they were less likely to disagree with the stigma statement. Conclusions
In light of the continued risks that individuals with PDA behaviors face in potentially transitioning to illicit opioid use, the findings of this survey suggested a continued need for public education and outreach. Of particular note is the perspective of those who have self-identified with the condition, as this population faces the largest risks of adverse health outcomes from illicit drug use within the survey respondents
Detecting autozygosity through runs of homozygosity: A comparison of three autozygosity detection algorithms
<p>Abstract</p> <p>Background</p> <p>A central aim for studying runs of homozygosity (ROHs) in genome-wide SNP data is to detect the effects of autozygosity (stretches of the two homologous chromosomes within the same individual that are identical by descent) on phenotypes. However, it is unknown which current ROH detection program, and which set of parameters within a given program, is optimal for differentiating ROHs that are truly autozygous from ROHs that are homozygous at the marker level but vary at unmeasured variants between the markers.</p> <p>Method</p> <p>We simulated 120 Mb of sequence data in order to know the true state of autozygosity. We then extracted common variants from this sequence to mimic the properties of SNP platforms and performed ROH analyses using three popular ROH detection programs, PLINK, GERMLINE, and BEAGLE. We varied detection thresholds for each program (e.g., prior probabilities, lengths of ROHs) to understand their effects on detecting known autozygosity.</p> <p>Results</p> <p>Within the optimal thresholds for each program, PLINK outperformed GERMLINE and BEAGLE in detecting autozygosity from distant common ancestors. PLINK's sliding window algorithm worked best when using SNP data pruned for linkage disequilibrium (LD).</p> <p>Conclusion</p> <p>Our results provide both general and specific recommendations for maximizing autozygosity detection in genome-wide SNP data, and should apply equally well to research on whole-genome autozygosity burden or to research on whether specific autozygous regions are predictive using association mapping methods.</p
Evidence for Positive Selection on the Osteogenin (BMP3) Gene in Human Populations
BACKGROUND: Human skeletal system has evolved rapidly since the dispersal of modern humans from Africa, potentially driven by selection and adaptation. Osteogenin (BMP3) plays an important role in skeletal development and bone osteogenesis as an antagonist of the osteogenic bone morphogenetic proteins, and negatively regulates bone mineral density. METHODOLOGY/PRINCIPAL FINDINGS: Here, we resequenced the BMP3 gene from individuals in four geographically separated modern human populations. Features supportive of positive selection in the BMP3 gene were found including the presence of an excess of nonsynonymous mutations in modern humans, and a significantly lower genetic diversity that deviates from neutrality. The prevalent haplotypes of the first exon region in Europeans demonstrated features of long-range haplotype homogeneity. In contrast with findings in European, the derived allele SNP Arg192Gln shows higher extended haplotype homozygosity in East Asian. The worldwide allele frequency distribution of SNP shows not only a high-derived allele frequency in Asians, but also in Americans, which is suggestive of functional adaptation. CONCLUSIONS/SIGNIFICANCE: In conclusion, we provide evidence for recent positive selection operating upon a crucial gene in skeletal development, which may provide new insight into the evolution of the skeletal system and bone development
The effect of nutrients on pyrrolizidine alkaloids in Senecio plants and their interactions with herbivores and pathogens
The aim of this review is to combine the knowledge of studies on effects of nutrients on pyrrolizidine alkaloids (PAs) in Senecio with those studies of effects of PAs on herbivores and pathogens in order to predict the effects that nutrients may have on herbivores and pathogens via changes in PAs. We discuss whether these predictions match with the outcome of studies where the effect of nutrients on herbivores and insects were measured. PA concentrations in S. jacobaea, S. vulgaris and S. aquaticus were mostly reduced by NPK fertilization, with genotype-specific effects occurring. Plant organs varied in their response to increased fertilization; PA concentrations in flowers remained constant, while shoot and roots were mostly negatively affected. Biomass change is probably largely responsible for the change in concentrations. Nutrients affect both the variety and the levels of PAs in the plant. The reduced PA concentrations after NPK fertilization was expected to benefit herbivores, but no or negative responses from insect herbivores were observed. Apparently other changes in the plant after fertilization are overriding the effect of PAs. Pathogens do seem to benefit from the lower PA concentrations after fertilization; they were more detrimental to fertilized plants than to unfertilized control plants. Future studies should include the effect of each element of nutrients separately and in combinations in order to gain more insight in the effect of specific nutrients on PA content in Senecio plants
Inferring the joint demographic history of multiple populations from multidimensional SNP frequency data
Demographic models built from genetic data play important roles in
illuminating prehistorical events and serving as null models in genome scans
for selection. We introduce an inference method based on the joint frequency
spectrum of genetic variants within and between populations. For candidate
models we numerically compute the expected spectrum using a diffusion
approximation to the one-locus two-allele Wright-Fisher process, involving up
to three simultaneous populations. Our approach is a composite likelihood
scheme, since linkage between neutral loci alters the variance but not the
expectation of the frequency spectrum. We thus use bootstraps incorporating
linkage to estimate uncertainties for parameters and significance values for
hypothesis tests. Our method can also incorporate selection on single sites,
predicting the joint distribution of selected alleles among populations
experiencing a bevy of evolutionary forces, including expansions, contractions,
migrations, and admixture. As applications, we model human expansion out of
Africa and the settlement of the New World, using 5 Mb of noncoding DNA
resequenced in 68 individuals from 4 populations (YRI, CHB, CEU, and MXL) by
the Environmental Genome Project. We also combine our demographic model with a
previously estimated distribution of selective effects among newly arising
amino acid mutations to accurately predict the frequency spectrum of
nonsynonymous variants across three continental populations (YRI, CHB, CEU).Comment: 17 pages, 4 figures, supporting information included with sourc
Human and Non-Human Primate Genomes Share Hotspots of Positive Selection
Among primates, genome-wide analysis of recent positive selection is currently
limited to the human species because it requires extensive sampling of genotypic
data from many individuals. The extent to which genes positively selected in
human also present adaptive changes in other primates therefore remains unknown.
This question is important because a gene that has been positively selected
independently in the human and in other primate lineages may be less likely to
be involved in human specific phenotypic changes such as dietary habits or
cognitive abilities. To answer this question, we analysed heterozygous Single
Nucleotide Polymorphisms (SNPs) in the genomes of single human, chimpanzee,
orangutan, and macaque individuals using a new method aiming to identify
selective sweeps genome-wide. We found an unexpectedly high number of
orthologous genes exhibiting signatures of a selective sweep simultaneously in
several primate species, suggesting the presence of hotspots of positive
selection. A similar significant excess is evident when comparing genes
positively selected during recent human evolution with genes subjected to
positive selection in their coding sequence in other primate lineages and
identified using a different test. These findings are further supported by
comparing several published human genome scans for positive selection with our
findings in non-human primate genomes. We thus provide extensive evidence that
the co-occurrence of positive selection in humans and in other primates at the
same genetic loci can be measured with only four species, an indication that it
may be a widespread phenomenon. The identification of positive selection in
humans alongside other primates is a powerful tool to outline those genes that
were selected uniquely during recent human evolution
Ancient and Recent Adaptive Evolution of Primate Non-Homologous End Joining Genes
In human cells, DNA double-strand breaks are repaired primarily by the non-homologous end joining (NHEJ) pathway. Given their critical nature, we expected NHEJ proteins to be evolutionarily conserved, with relatively little sequence change over time. Here, we report that while critical domains of these proteins are conserved as expected, the sequence of NHEJ proteins has also been shaped by recurrent positive selection, leading to rapid sequence evolution in other protein domains. In order to characterize the molecular evolution of the human NHEJ pathway, we generated large simian primate sequence datasets for NHEJ genes. Codon-based models of gene evolution yielded statistical support for the recurrent positive selection of five NHEJ genes during primate evolution: XRCC4, NBS1, Artemis, POLλ, and CtIP. Analysis of human polymorphism data using the composite of multiple signals (CMS) test revealed that XRCC4 has also been subjected to positive selection in modern humans. Crystal structures are available for XRCC4, Nbs1, and Polλ; and residues under positive selection fall exclusively on the surfaces of these proteins. Despite the positive selection of such residues, biochemical experiments with variants of one positively selected site in Nbs1 confirm that functions necessary for DNA repair and checkpoint signaling have been conserved. However, many viruses interact with the proteins of the NHEJ pathway as part of their infectious lifecycle. We propose that an ongoing evolutionary arms race between viruses and NHEJ genes may be driving the surprisingly rapid evolution of these critical genes
Explaining Perceptions of Climate Change in the US
A significant proportion of the US population does not believe that climate change is a serious problem and immediate action is necessary. We ask whether individuals' experiences with long-run changes in their local climate can override the power of partisanship that appears to dominate this opinion process. We merge individual-level data on climate change perceptions and the main determinants previously identified by the literature with county-level data on an exogenous measure of local climate change. While we find that local climate change significantly affects perceptions and in the expected direction, partisanship and political ideology maintain the strongest effect. We then field a randomized online experiment to test whether partisanship also drives support for pro-climate policies and the willingness to make environmentally friendly individual choices
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RESIDENTIAL MOBILITY, FAMILY STRUCTURE, AND THE CELL-ONLY POPULATION
The cell-phone-only (CPO) population has grown rapidly over the past several years, causing concern for researchers who rely mostly on random digit dialing (RDD) of landlines to conduct their research. While early research on CPOs has focused largely on age differences, CPOs may differ from those with landlines in many other ways even after controlling for age. In this article, we use the Cooperative Congressional Election Study—an Internet survey based on matched random sampling—and the American National Election Study—an in-person survey based on stratified residential sampling— to examine the potential effects of the cell-only population for survey research. These surveys are ideal for studying the causes and consequences of cell-only lifestyles for survey research because they reach cell-only and landline respondents through a single sampling frame. We reach two main conclusions: (1) CPO households are not simply a function of age, but of other factors as well, especially residential mobility and family structure; and (2) there are notable differentials in vote preferences and turnout between CPOs and others.Governmen
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