Social policies, separation and second birth spacing in Western Europe

The research leading to these results received funding from the European Union’s Seventh Framework Programme (FP7/2007–2013) under grant agreement no. 320116 for the research project FamiliesAndSocieties. We also acknowledge funds from the Academy of Finland (decision number 275030 and 293103) and the German Science Foundation (KR 2855/3–1 and TR 457/7–1).Objective: This paper studies postseparation fertility behavior. The aim is to investigate whether, and if so how, separation affects second birth spacing in Western European countries. Methods: This analysis makes use of rich survey data from Belgium, France, Germany, Italy, Spain, and the United Kingdom, as well as from Finnish register data. We thus cover the behavior of a large proportion of the population of Western Europe. We also use descriptive measures, such as Kaplan‒Meier survival functions and cumulative incidence curves. In the multivariate analysis, we employ event history modeling to show how education relates to postseparation fertility behavior. Results: There are large differences in postseparation fertility behavior across European countries. For Spain and Italy, we find that only a negligibly small proportion of the population have a second child after separating from the other parent of the firstborn child. The countries with the highest proportion of second children with a new partner are the United Kingdom, Germany, and Finland. In all countries, separation after first birth leads to a sharp increase in the birth interval between first and second births. Contribution: Our study is a contribution to the demographic literature that aims at understanding birth spacing patterns in Western Europe. Furthermore, we draw attention to the role of postseparation policies in explaining country differences in fertility behavior in contemporary societies.Publisher PDFPeer reviewe

Nanoscale Phase Separation in Colossal Magnetoresistance Materials: A Lesson for the Cuprates?

A recent vast experimental and theoretical effort in manganites has shown that the colossal magnetoresistance effect can be understood based on the competition of charge-ordered and ferromagnetic phases. The general aspects of the theoretical description appear to be valid for any compound with intrinsic phase competition. In high temperature superconductors, recent experiments have shown the existence of intrinsic inhomogeneities in many materials, revealing a phenomenology quite similar to that of manganese oxides. Here, the results for manganites are briefly reviewed with emphasis on the general aspects. In addition, theoretical speculations are formulated in the context of Cu-oxides by mere analogy with manganites. This includes a tentative explanation of the spin-glass regime as a mixture of antiferromagnetic and superconducting islands, the rationalization of the pseudogap temperature T* as a Griffiths temperature where clusters start forming upon cooling, the prediction of "colossal" effects in cuprates, and the observation that quenched disorder may be far more relevant in Cu-oxides than previously anticipated.Comment: 25 pages, 14 figures, post-muSR2002 Superconductivity Worksho

A comparative study on fertility among the descendants of immigrants in Europe

This study investigates the childbearing patterns of the descendants of immigrants in selected European countries, with a focus on ethnic minority women whose parents arrived in Europe from high-fertility countries. While the fertility levels of immigrants to Europe have been examined in the recent literature, the childbearing patterns among their descendants have received little attention. Using longitudinal data from eight European countries and applying Poisson regression models, the study shows that many descendants of immigrants exhibit first-birth levels that are similar to the ‘native’ population in their respective countries; however, first-birth levels are elevated among women of Pakistani and Bangladeshi origin in the UK and for those of Turkish descent in France and Belgium. Transition rates to a second child vary less across ethnic groups. Most ethnic minority women in the UK, France and Belgium show significantly higher third-birth levels than ‘natives’ in those countries. The inclusion of women’s level of education in the analysis has little effect on fertility differences across the ethnic groups. Overall, the childbearing behaviour of the descendants of immigrants falls in between the fertility pathways experienced by their parents’ generation and the respective ‘native’ populations. The analysis supports the idea that both the mainstream society and the minority subculture shape the childbearing patterns of the descendants of immigrants in Europe

The systemic lupus erythematosus IRF5 risk haplotype is associated with systemic sclerosis

Systemic sclerosis (SSc) is a fibrotic autoimmune disease in which the genetic component plays an important role. One of the strongest SSc association signals outside the human leukocyte antigen (HLA) region corresponds to interferon (IFN) regulatory factor 5 (IRF5), a major regulator of the type I IFN pathway. In this study we aimed to evaluate whether three different haplotypic blocks within this locus, which have been shown to alter the protein function influencing systemic lupus erythematosus (SLE) susceptibility, are involved in SSc susceptibility and clinical phenotypes. For that purpose, we genotyped one representative single-nucleotide polymorphism (SNP) of each block (rs10488631, rs2004640, and rs4728142) in a total of 3,361 SSc patients and 4,012 unaffected controls of Caucasian origin from Spain, Germany, The Netherlands, Italy and United Kingdom. A meta-analysis of the allele frequencies was performed to analyse the overall effect of these IRF5 genetic variants on SSc. Allelic combination and dependency tests were also carried out. The three SNPs showed strong associations with the global disease (rs4728142: P = 1.34×10<sup>−8</sup>, OR = 1.22, CI 95% = 1.14–1.30; rs2004640: P = 4.60×10<sup>−7</sup>, OR = 0.84, CI 95% = 0.78–0.90; rs10488631: P = 7.53×10<sup>−20</sup>, OR = 1.63, CI 95% = 1.47–1.81). However, the association of rs2004640 with SSc was not independent of rs4728142 (conditioned P = 0.598). The haplotype containing the risk alleles (rs4728142*A-rs2004640*T-rs10488631*C: P = 9.04×10<sup>−22</sup>, OR = 1.75, CI 95% = 1.56–1.97) better explained the observed association (likelihood P-value = 1.48×10<sup>−4</sup>), suggesting an additive effect of the three haplotypic blocks. No statistical significance was observed in the comparisons amongst SSc patients with and without the main clinical characteristics. Our data clearly indicate that the SLE risk haplotype also influences SSc predisposition, and that this association is not sub-phenotype-specific

Temperature calibration along the NW Iberian margin : multi-proxy approach

1 poster presented at the European Geosciences Union General Assembly 2012, Vienna, Austria, 22 – 27 April 2012Marine sediments, mainly the ones from coastal upwelling areas, are valuable archives for past reconstructions, including climate changes, global and regional oceanography, and the cycles of biochemical components in the ocean. However, the regional calibrations of the sediment properties (“proxy” data) to the present-day oceanographic and biological conditions are necessary for interpretation of high-resolution sediment-derived information. Many works have contributed directly or indirectly to improving proxy calibrations related to upwelling and nutrient cycling parameters, but there are few studies with a multi-proxy approach for the same region. Along NW Iberian margin, little work has been done regarding with calibration of proxy data. Thus, we lack understanding on (1) how the seasonally variable hydrography affects the various plankton groups and (2) how much of the water column signal is preserved in the sediments and available for paleo-reconstructions. In order to minimize this lack of information from the upper water column temperature point of view, we investigate trace element and stable isotopes from planktonic foraminifera, and alkenone Uk’37 index from a large set of core-top sediment samples from the NW Iberian margin (41.5-42.5ºN; 9-10ºW). Sediment data are compared with present-day water column data (CTD, stable isotopes, satellite measurements) and to “global” calibration data sets of the proxies with sea surface temperature. We explore reconstructing upper water column structure using three species (G. bulloides, N. pachyderma dextral, and G. inflata) with different depth habitats, different seasonal abundances, and linked to specific hydrographic conditions in this region. Preliminary results show that Mg/Ca and 18O temperatures of all species are consistent with seasonal temperatures observed in present-day water column data. In addition G. bulloides and N. pachyderma dextral appears with temperatures related with subtropical and subpolar Eastern North Atlantic Central Waters, respectively.N

A genome-wide association study follow-up suggests a possible role for PPARG in systemic sclerosis susceptibility

Introduction: A recent genome-wide association study (GWAS) comprising a French cohort of systemic sclerosis (SSc) reported several non-HLA single-nucleotide polymorphisms (SNPs) showing a nominal association in the discovery phase. We aimed to identify previously overlooked susceptibility variants by using a follow-up strategy.<p></p> Methods: Sixty-six non-HLA SNPs showing a P value <10-4 in the discovery phase of the French SSc GWAS were analyzed in the first step of this study, performing a meta-analysis that combined data from the two published SSc GWASs. A total of 2,921 SSc patients and 6,963 healthy controls were included in this first phase. Two SNPs, PPARG rs310746 and CHRNA9 rs6832151, were selected for genotyping in the replication cohort (1,068 SSc patients and 6,762 healthy controls) based on the results of the first step. Genotyping was performed by using TaqMan SNP genotyping assays. Results: We observed nominal associations for both PPARG rs310746 (PMH = 1.90 × 10-6, OR, 1.28) and CHRNA9 rs6832151 (PMH = 4.30 × 10-6, OR, 1.17) genetic variants with SSc in the first step of our study. In the replication phase, we observed a trend of association for PPARG rs310746 (P value = 0.066; OR, 1.17). The combined overall Mantel-Haenszel meta-analysis of all the cohorts included in the present study revealed that PPARG rs310746 remained associated with SSc with a nominal non-genome-wide significant P value (PMH = 5.00 × 10-7; OR, 1.25). No evidence of association was observed for CHRNA9 rs6832151 either in the replication phase or in the overall pooled analysis.<p></p> Conclusion: Our results suggest a role of PPARG gene in the development of SSc

Common Variants of the Liver Fatty Acid Binding Protein Gene Influence the Risk of Type 2 Diabetes and Insulin Resistance in Spanish Population

SummaryThe main objective was to evaluate the association between SNPs and haplotypes of the FABP1-4 genes and type 2 diabetes, as well as its interaction with fat intake, in one general Spanish population. The association was replicated in a second population in which HOMA index was also evaluated.Methods1217 unrelated individuals were selected from a population-based study [Hortega study: 605 women; mean age 54 y; 7.8% with type 2 diabetes]. The replication population included 805 subjects from Segovia, a neighboring region of Spain (446 females; mean age 52 y; 10.3% with type 2 diabetes). DM2 mellitus was defined in a similar way in both studies. Fifteen SNPs previously associated with metabolic traits or with potential influence in the gene expression within the FABP1-4 genes were genotyped with SNPlex and tested. Age, sex and BMI were used as covariates in the logistic regression model.ResultsOne polymorphism (rs2197076) and two haplotypes of the FABP-1 showed a strong association with the risk of DM2 in the original population. This association was further confirmed in the second population as well as in the pooled sample. None of the other analyzed variants in FABP2, FABP3 and FABP4 genes were associated. There was not a formal interaction between rs2197076 and fat intake. A significant association between the rs2197076 and the haplotypes of the FABP1 and HOMA-IR was also present in the replication population.ConclusionsThe study supports the role of common variants of the FABP-1 gene in the development of type 2 diabetes in Caucasians

Adjuvant dabrafenib and trametinib for patients with resected BRAF-mutated melanoma: DESCRIBE-AD real-world retrospective observational study

BRAF and MEK inhibitor, dabrafenib plus trametinib, adjuvant therapy is effective for high-risk resected melanoma patients with BRAF-V600 mutations. However, real-world evidence is limited. We aimed to determine the feasibility of this therapy in routine clinical practice. DESCRIBE-AD, a retrospective observational study, collected real-world data from 25 hospitals in Spain. Histologically confirmed and resected BRAF-mutated melanoma patients aged & GE;18 years who were previously treated with dabrafenib plus trametinib adjuvant therapy, were included. The primary objectives were treatment discontinuation rate and time to discontinuation. The secondary objectives included safety and efficacy. From October 2020 to March 2021, 65 patients were included. Dabrafenib and trametinib discontinuation rate due to treatment-related adverse events (TRAEs) of any grade was 9%. Other reasons for discontinuation included patients' decisions (6%), physician decisions (6%), unrelated adverse events (3%), disease progression (5%), and others (5%). The median time to treatment discontinuation was 9 months [95% confidence interval (CI), 5-11]. G3-4 TRAEs occurred in 21.5% of patients, the most common being pyrexia (3%), asthenia (3%), and diarrhoea (3%). Unscheduled hospitalisations and clinical tests occurred in 6 and 22% of patients, respectively. After 20-month median follow-up (95% CI, 18-22), 9% of patients had exitus due to disease progression, with a 12-month relapse-free survival and overall survival rates of 95.3% and 100%, respectively. Dabrafenib and trametinib adjuvant therapy proved effective for melanoma patients in a real-world setting, with a manageable toxicity profile. Toxicity frequencies were low leading to low incidence of unscheduled medical visits, tests, and treatment discontinuations