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1.
Reprod Biomed Online ; 41(2): 203-216, 2020 Aug.
Article in English | MEDLINE | ID: mdl-32546334

ABSTRACT

Fertility care providers have an obligation to provide safe and effective care to patients. When a user of assisted reproductive technology (ART) is living with a blood-borne viral infection (BBVI: HIV, hepatitis C or hepatitis B), physicians and ART laboratory personnel need to know the requirements for providing quality care. Recent developments in the treatment of BBVI and understanding of transmission have changed these requirements. This guideline from the Canadian Fertility and Andrology Society (CFAS) provides comprehensive, evidence-based guidelines for reducing horizontal transmission and cross-contamination in the ART setting.


Subject(s)
Antiviral Agents/therapeutic use , Blood-Borne Infections/prevention & control , HIV Infections/prevention & control , Hepatitis B/prevention & control , Hepatitis C/prevention & control , Infection Control/methods , Reproductive Techniques, Assisted/adverse effects , Blood-Borne Infections/drug therapy , Canada , Female , HIV Infections/drug therapy , Hepatitis B/drug therapy , Hepatitis C/drug therapy , Humans
2.
PLoS One ; 14(2): e0212043, 2019.
Article in English | MEDLINE | ID: mdl-30779748

ABSTRACT

Psoriasis and its associated inflammatory arthritis, psoriatic arthritis (PsA), have a clear heritable component, but a large proportion of the heritable risk remains unexplained by gene sequence variation. This study aimed to determine if epigenetic factors contribute to the missing heritability in psoriatic disease. DNA methylation profiling was performed on sperm cells from 23 probands with psoriasis without PsA (PsC), 13 PsA probands, and 18 unaffected controls. Differentially methylated CpGs and regions (DMRs) were identified and validated by pyrosequencing. Underlying AluY and copy number variation (CNV) in the HCG26 and IL22 genes, respectively, were assessed by genotyping. Array, subject's age, age of psoriasis onset, psoriasis severity, and medication usage were found to influence methylation at many genes and were included as covariates in the analysis. Between PsC probands vs. controls, 169 DMRs were found; 754 DMRs were found between PsA probands vs. controls, and 86 between PsA and PsC probands (adjusted p<0.05). Differences in methylation across DMRs were generally subtle (<10%) but correlated well with pyrosequencing. Biological inference prioritized notable DMRs associated with skin disease (SIGLEC14, JAM3, PCOLCE, RXRB), skin and/or joint disease (MBP, OSBPL5, SNORD115, HCG26), and joint disease (IL22, ELF5, PPP2R2D, PTPRN2, HCG26). Hypermethylation of the DMR within the first exon of arthritis-associated IL22 showed significant correlation (rho = 0.34, 95% CI 0.06-0.57, p = 0.01) between paired sperm and blood samples, independent of a CNV within the same region. Further studies are needed to rule out underlying genetic causes and determine if these represent heritable, constitutional epimutations, or are the result of exposure of germ cells to endogenous or exogenous environmental factors.


Subject(s)
Arthritis, Psoriatic/genetics , Epigenomics/methods , Interleukins/genetics , Spermatozoa/chemistry , Adult , Age of Onset , Aged , Case-Control Studies , CpG Islands , DNA Methylation , Genetic Predisposition to Disease , High-Throughput Nucleotide Sequencing , Humans , Male , Middle Aged , Sequence Analysis, DNA , Interleukin-22
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