The phase transition and the Quasi-Normal Modes of black Holes

We reexamined the argument that the quasinormal modes could be a probe of the phase transition of a topological black hole to a hairy configuration by investigating general scalar perturbations. We found further evidence in the quasinormal modes for this phase transition. For the general black hole configurations, we observed that although the quasinormal modes can present us different phases of different configurations, there is no dramatic change in the slope of quasinormal frequencies at the critical point of the phase transition. More detailed studies of quasinormal modes are needed to reveal the subtle behavior of the phase transition.Comment: Revised version, accepted for publication in JHE

Intermediate Asymptotics of the Kerr Quasinormal Spectrum

We study analytically the quasinormal mode spectrum of near-extremal (rotating) Kerr black holes. We find an analytic expression for these black-hole resonances in terms of the black-hole physical parameters: its Bekenstein-Hawking temperature T_{BH} and its horizon's angular velocity \Omega, which is valid in the intermediate asymptotic regime 1<<\omega<<1/T_{BH}.Comment: 4 page

Holographic dark energy in the DGP model

The braneworld model proposed by Dvali, Gabadadze and Porrati leads to an accelerated universe without cosmological constant or other form of dark energy. Nevertheless, we have investigated the consequences of this model when an holo- graphic dark energy is included, taken the Hubble scale as IR cutoff. We have found that the holographic dark energy leads to an accelerated universe flat (de Sitter like expansion) for the two branch: {\ko} = \pm1 of the DGP model. Nevertheless, in universes with no null curvature the dark energy presents an EoS corresponding to a phantom fluid during the present era and evolving to a de Sitter like phase for future cosmic time. In the special case in which the holographic parameter c is equal to one we have found a sudden singularity in closed universes. In this case the expansion is decelerating. ManuscriptComment: Latex, 12 pages, 4 figures; Submitted to Phys. Lett.

Notes on interacting holographic dark energy model in a closed universe

We consider interacting holographic dark energy model in Friedmann Robertson Walker space time with positive spatial curvature and investigate the behavior of curvature parameter and dark energy density in accelerated expanding epoch. We also derive some conditions needed to cross the phantom divide line in this model.Comment: 10 pages, typos corrected, some explanations and references added and updated, accepted for publication in JCA

Hypophosphatasia

Hypophosphatasia is a rare inherited disorder characterized by defective bone and teeth mineralization, and deficiency of serum and bone alkaline phosphatase activity. The prevalence of severe forms of the disease has been estimated at 1/100 000

SARS-CoV-2 viral load in nasopharyngeal swabs is not an independent predictor of unfavorable outcome

The aim was to assess the ability of nasopharyngeal SARS-CoV-2 viral load at first patient’s hospital evaluation to predict unfavorable outcomes. We conducted a prospective cohort study including 321 adult patients with confirmed COVID-19 through RT-PCR in nasopharyngeal swabs. Quantitative Synthetic SARS-CoV-2 RNA cycle threshold values were used to calculate the viral load in log10 copies/mL. Disease severity at the end of follow up was categorized into mild, moderate, and severe. Primary endpoint was a composite of intensive care unit (ICU) admission and/or death (n = 85, 26.4%). Univariable and multivariable logistic regression analyses were performed. Nasopharyngeal SARS-CoV-2 viral load over the second quartile (≥ 7.35 log10 copies/mL, p = 0.003) and second tertile (≥ 8.27 log10 copies/mL, p = 0.01) were associated to unfavorable outcome in the unadjusted logistic regression analysis. However, in the final multivariable analysis, viral load was not independently associated with an unfavorable outcome. Five predictors were independently associated with increased odds of ICU admission and/or death: age ≥ 70 years, SpO2, neutrophils > 7.5 × 103/µL, lactate dehydrogenase ≥ 300 U/L, and C-reactive protein ≥ 100 mg/L. In summary, nasopharyngeal SARS-CoV-2 viral load on admission is generally high in patients with COVID-19, regardless of illness severity, but it cannot be used as an independent predictor of unfavorable clinical outcome

Meta-analysis of 49 549 individuals imputed with the 1000 Genomes Project reveals an exonic damaging variant in ANGPTL4 determining fasting TG levels

Background So far, more than 170 loci have been associated with circulating lipid levels through genomewide association studies (GWAS). These associations are largely driven by common variants, their function is often not known, and many are likely to be markers for the causal variants. In this study we aimed to identify more new rare and low-frequency functional variants associated with circulating lipid levels. Methods We used the 1000 Genomes Project as a reference panel for the imputations of GWAS data from ~60 000 individuals in the discovery stage and ~90 000 samples in the replication stage. Results Our study resu

Rare and low-frequency coding variants alter human adult height

Height is a highly heritable, classic polygenic trait with ~700 common associated variants identified so far through genome - wide association studies . Here , we report 83 height - associated coding variants with lower minor allele frequenc ies ( range of 0.1 - 4.8% ) and effects of up to 2 16 cm /allele ( e.g. in IHH , STC2 , AR and CRISPLD2 ) , >10 times the average effect of common variants . In functional follow - up studies, rare height - increasing alleles of STC2 (+1 - 2 cm/allele) compromise d proteolytic inhibition of PAPP - A and increased cleavage of IGFBP - 4 in vitro , resulting in higher bioavailability of insulin - like growth factors . The se 83 height - associated variants overlap genes mutated in monogenic growth disorders and highlight new biological candidates ( e.g. ADAMTS3, IL11RA, NOX4 ) and pathways ( e.g . proteoglycan/ glycosaminoglycan synthesis ) involved in growth . Our results demonstrate that sufficiently large sample sizes can uncover rare and low - frequency variants of moderate to large effect associated with polygenic human phenotypes , and that these variants implicate relevant genes and pathways

KLB is associated with alcohol drinking, and its gene product β-Klotho is necessary for FGF21 regulation of alcohol preference.

Excessive alcohol consumption is a major public health problem worldwide. Although drinking habits are known to be inherited, few genes have been identified that are robustly linked to alcohol drinking. We conducted a genome-wide association metaanalysis and replication study among >105,000 individuals of European ancestry and identified β-Klotho (KLB) as a locus associated with alcohol consumption (rs11940694; P = 9.2 × 10(-12)). β-Klotho is an obligate coreceptor for the hormone FGF21, which is secreted from the liver and implicated in macronutrient preference in humans. We show that brain-specific β-Klotho KO mice have an increased alcohol preference and that FGF21 inhibits alcohol drinking by acting on the brain. These data suggest that a liver-brain endocrine axis may play an important role in the regulation of alcohol drinking behavior and provide a unique pharmacologic target for reducing alcohol consumption