27 research outputs found
The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation : efficacy and safety
Background: Predictive genetic testing has high impact on cancer prevention for BRCA carriers and passing this information in BRCA families is important. Mostly, this is proband-mediated but this path is defective and denies relatives lifesaving information.
Objective: To assess the efficacy/safety of an intervention, in which relatives are actively informed.
Design: Sequential prospective study in new BRCA families. The proband informed relatives about predictive testing (phase I). After 6 months, a letter was sent to adult relatives who had not been reached (phase II). Then a phone call was made to obtain a final notion of their wishes. All subjects received psychometric testing (State-Trait Anxiety Inventory, STAI), an interview and routine counselling.
Results: Twenty families were included. Twenty-four of the relatives could not be reached, 59 were 'decliners', 47 participated by the proband and 42 by the letter. Predictive testing was performed in 98 % of the participants of which 30 were mutation carriers. The intervention is psychologically safe: the 95 % CI for the estimated mean difference in STAI DY1 between phase II/I subjects (mean difference -1.07, 95 % CI -4.4 to 2.35, p = 0.53) shows that the mean STAI DY1 score (measured at first consult) for phase II is no more than 2.35 units higher than for phase I, which is not relevant.
Conclusions: A protocol directly informing relatives nearly doubles the number of relatives tested and is psychologically safe. This should lead to a change in counselling guidelines in families with a strong germline predisposition for cancer
A Genome-Wide Association Study of Pulmonary Function Measures in the Framingham Heart Study
The ratio of forced expiratory volume in one second to forced vital capacity (FEV1/FVC) is a measure used to diagnose airflow obstruction and is highly heritable. We performed a genome-wide association study in 7,691 Framingham Heart Study participants to identify single-nucleotide polymorphisms (SNPs) associated with the FEV1/FVC ratio, analyzed as a percent of the predicted value. Identified SNPs were examined in an independent set of 835 Family Heart Study participants enriched for airflow obstruction. Four SNPs in tight linkage disequilibrium on chromosome 4q31 were associated with the percent predicted FEV1/FVC ratio with p-values of genome-wide significance in the Framingham sample (best p-value = 3.6e-09). One of the four chromosome 4q31 SNPs (rs13147758; p-value 2.3e-08 in Framingham) was genotyped in the Family Heart Study and produced evidence of association with the same phenotype, percent predicted FEV1/FVC (p-value = 2.0e-04). The effect estimates for association in the Framingham and Family Heart studies were in the same direction, with the minor allele (G) associated with higher FEV1/FVC ratio levels. Results from the Family Heart Study demonstrated that the association extended to FEV1 and dichotomous airflow obstruction phenotypes, particularly among smokers. The SNP rs13147758 was associated with the percent predicted FEV1/FVC ratio in independent samples from the Framingham and Family Heart Studies producing a combined p-value of 8.3e-11, and this region of chromosome 4 around 145.68 megabases was associated with COPD in three additional populations reported in the accompanying manuscript. The associated SNPs do not lie within a gene transcript but are near the hedgehog-interacting protein (HHIP) gene and several expressed sequence tags cloned from fetal lung. Though it is unclear what gene or regulatory effect explains the association, the region warrants further investigation
Assessment of a primary and tertiary care integrated management model for chronic obstructive pulmonary disease
<p>Abstract</p> <p>Background</p> <p>The diagnosis and treatment of patients with chronic obstructive pulmonary disease (COPD) in Spain continues to present challenges, and problems are exacerbated when there is a lack of coordinated follow-up between levels of care. This paper sets out the protocol for assessing the impact of an integrated management model for the care of patients with COPD. The new model will be evaluated in terms of 1) improvement in the rational utilization of health-care services and 2) benefits reflected in improved health status and quality of life for patients.</p> <p>Methods/Design</p> <p>A quasi-experimental study of the effectiveness of a COPD management model called COPD PROCESS. The patients in the study cohorts will be residents of neighborhoods served by two referral hospitals in Barcelona, Spain. One area comprises the intervention group (n = 32,248 patients) and the other the control group (n = 32,114 patients). The study will include pre- and post-intervention assessment 18 months after the program goes into effect. Analyses will be on two datasets: clinical and administrative data available for all patients, and clinical assessment information for a cohort of 440 patients sampled randomly from the intervention and control areas. The main endpoints will be the hospitalization rates in the two health-care areas and quality-of-life measures in the two cohorts.</p> <p>Discussion</p> <p>The COPD PROCESS model foresees the integrated multidisciplinary management of interventions at different levels of the health-care system through coordinated routine clinical practice. It will put into practice diagnostic and treatment procedures that are based on current evidence, multidisciplinary consensus, and efficient use of available resources. Care pathways in this model are defined in terms of patient characteristics, level of disease severity and the presence or absence of exacerbation. The protocol covers the full range of care from primary prevention to treatment of complex cases.</p
The impact of an interventional counselling procedure in families with a BRCA1/2 gene mutation: efficacy and safety
Plasmaconcentraties van de voortplantingshormonen (LH, Psub4, Esub2), GH en cortisol gedurende de oestrale cyclus van het schaap (Ovis aries)
KKULeuven Campusbibliotheek Exacte Wetenschappen / UCL - Université Catholique de LouvainSIGLEBEBelgiu
Comparison of the ecology and distribution of the Poaceae flora on inselbergs embedded in savannah (Benin) or in rain forest (Western Central Africa)
The ecology and distribution of Poaceae species found on 12 inselbergs embedded in savannah and woodland (Benin) and on 25 inselbergs enclosed in rain forest (CEG: Cameroon, Equatorial Guinea and Gabon) are described. A total of 77 species were observed, 46 in Benin and 36 in CEG. Five species were strictly saxicolous in Benin and three in CEG, but most species (83%) were also present in the vegetation surrounding the inselbergs (the matrix). In Benin, 46% of the species were present on half of the inselbergs, while only one species did so in CEG. This unequal distribution of the species amongst sites in CEG could originate from dispersal limitation due to the strong ecological contrast between the inselberg biotope and the rain forest. Ecological conditions on the inselbergs are more similar to that of a savannah and woodland matrix, which could explain the homogeneity of inselberg vegetation in Benin. In CEG, four species were mainly distributed outside the lowland rain forest region: two in savannah and woodland, and two in mountainous vegetation. The discontinuous distribution of these species with inselberg satellite populations in the lowland rainforest is probably related to Quaternary vegetation changes. Inselberg in both study area contribute significantly to the regional species diversity by the presence of strictly saxicolous species or of species from other phytochoria. The inselberg habitat should therefore be considered in conservation policies. © 2006 Royal Botanical Society of Belgium.SCOPUS: ar.jinfo:eu-repo/semantics/publishe