43 research outputs found
Evolution of high-frequency gravitational waves in some cosmological models
We investigate Isaacson's high-frequency gravitational waves which propagate
in some relevant cosmological models, in particular the FRW spacetimes. Their
time evolution in Fourier space is explicitly obtained for various metric forms
of (anti--)de Sitter universe. Behaviour of high-frequency waves in the
anisotropic Kasner spacetime is also described.Comment: 14 pages, 8 figures, to appear in Czech. J. Phy
Time-Like Shock Hadronization of a Supercooled Quark-Gluon Plasma
We study the energy-momentum and baryonic number conservation laws for
quark-gluon plasma discontinuity transitions into hadron matter states. We find
that the time-like shock hadronization of a supercooled quark-gluon plasma
(when the normal vector to the discontinuity hypersurface is time-like) should
take place. We consider some properties of this process, which is different
from the standard space-like shock hadronization.Comment: 10 pages in Latex + 4 ps figures , preprint UP-TP 94/
Domain Wall Spacetimes: Instability of Cosmological Event and Cauchy Horizons
The stability of cosmological event and Cauchy horizons of spacetimes
associated with plane symmetric domain walls are studied. It is found that both
horizons are not stable against perturbations of null fluids and massless
scalar fields; they are turned into curvature singularities. These
singularities are light-like and strong in the sense that both the tidal forces
and distortions acting on test particles become unbounded when theses
singularities are approached.Comment: Latex, 3 figures not included in the text but available upon reques
Mendelian randomization supports bidirectional causality between telomere length and clonal hematopoiesis of indeterminate potential
Human genetic studies support an inverse causal relationship between leukocyte telomere length (LTL) and coronary artery disease (CAD), but directionally mixed effects for LTL and diverse malignancies. Clonal hematopoiesis of indeterminate potential (CHIP), characterized by expansion of hematopoietic cells bearing leukemogenic mutations, predisposes both hematologic malignancy and CAD. TERT (which encodes telomerase reverse transcriptase) is the most significantly associated germline locus for CHIP in genome-wide association studies. Here, we investigated the relationship between CHIP, LTL, and CAD in the Trans-Omics for Precision Medicine (TOPMed) program (n = 63,302) and UK Biobank (n = 47,080). Bidirectional Mendelian randomization studies were consistent with longer genetically imputed LTL increasing propensity to develop CHIP, but CHIP then, in turn, hastens to shorten measured LTL (mLTL). We also demonstrated evidence of modest mediation between CHIP and CAD by mLTL. Our data promote an understanding of potential causal relationships across CHIP and LTL toward prevention of CAD
Genetic determinants of telomere length from 109,122 ancestrally diverse whole-genome sequences in TOPMed
Genetic studies on telomere length are important for understanding age-related diseases. Prior GWASs for leukocyte TL have been limited to European and Asian populations. Here, we report the first sequencing-based association study for TL across ancestrally diverse individuals (European, African, Asian, and Hispanic/Latino) from the NHLBI Trans-Omics for Precision Medicine (TOPMed) program. We used whole-genome sequencing (WGS) of whole blood for variant genotype calling and the bioinformatic estimation of telomere length in n = 109,122 individuals. We identified 59 sentinel variants (p < 5 × 10−9) in 36 loci associated with telomere length, including 20 newly associated loci (13 were replicated in external datasets). There was little evidence of effect size heterogeneity across populations. Fine-mapping at OBFC1 indicated that the independent signals colocalized with cell-type-specific eQTLs for OBFC1 (STN1). Using a multi-variant gene-based approach, we identified two genes newly implicated in telomere length, DCLRE1B (SNM1B) and PARN. In PheWAS, we demonstrated that our TL polygenic trait scores (PTSs) were associated with an increased risk of cancer-related phenotypes