Approximative two-flavor framework for neutrino oscillations with nonstandard interactions

In this paper, we develop approximative two-flavor neutrino oscillation formulas including subleading nonstandard interaction effects. Especially, the limit when the small mass-squared difference approaches zero is investigated. The approximate formulas are also tested against numerical simulations in order to determine their accuracy and they will probably be most useful in the GeV energy region, which is the energy region where most upcoming neutrino oscillation experiments will be operating. Naturally, it is important to have analytical formulas in order to interpret the physics behind the degeneracies between standard and nonstandard parameters.Comment: 21 pages, 7 figures, REVTeX4. Final version published in Phys. Rev.

On the evolution of an entangled lepton-neutrino pair

The evolution of the entangled muon-neutrino system emerging from charged pion decay is explored both in vacuum and in matter. The study is based on a Weisskopf-Wigner type wave-packet description. Explicit formulae are derived displaying modulation and attenuation of the oscillations due to additional time scales characterising the production process. The case of neutrinos disentangled due to the detection of the muon is also considered

Probing non-unitary mixing and CP-violation at a Neutrino Factory

A low energy non-unitary leptonic mixing matrix is a generic feature of many extensions of the Standard Model. In such a case, the task of future precision neutrino oscillation experiments is more ambitious than measuring the three mixing angles and the leptonic (Dirac) CP-phase, i.e., the accessible parameters of a unitary leptonic mixing matrix. A non-unitary mixing matrix has 13 parameters that affect neutrino oscillations, out of which four are CP-violating. In the scheme of Minimal Unitarity Violation (MUV) we analyse the potential of a Neutrino Factory for determining or constraining the parameters of the non-unitary leptonic mixing matrix, thereby testing the origin of CP-violation in the lepton sector.Comment: 21 pages, 8 eps figures, REVTeX

Signatures from an extra-dimensional seesaw model

We study the generation of small neutrino masses in an extra-dimensional model, where right-handed neutrinos are allowed to propagate in the extra dimension, while the Standard Model particles are confined to a brane. Motivated by the fact that extra-dimensional models are non-renormalizable, we truncate the Kaluza-Klein towers at a maximal extra-dimensional momentum. The structure of the bulk Majorana mass term, motivated by the Sherk-Schwarz mechanism, implies that the right-handed Kaluza-Klein neutrinos pair to form Dirac neutrinos, except for a number of unpaired Majorana neutrinos at the top of each tower. These heavy Majorana neutrinos are the only sources of lepton number breaking in the model, and similarly to the type-I seesaw mechanism, they naturally generate small masses for the left-handed neutrinos. The lower Kaluza-Klein modes mix with the light neutrinos, and the mixing effects are not suppressed with respect to the light-neutrino masses. Compared to conventional fermionic seesaw models, such mixing can be more significant. We study the signals of this model at the Large Hadron Collider, and find that the current low-energy bounds on the non-unitarity of the leptonic mixing matrix are strong enough to exclude an observation.Comment: 17 pages, 3 figures, REVTeX4. Final version published in Phys. Rev.

Cerebrospinal fluid Aβ42/40 corresponds better than Aβ42 to amyloid PET in Alzheimer’s disease

Background: Decreased concentrations of amyloid-β 1-42 (Aβ(42)) in cerebrospinal fluid (CSF) and increased retention of Aβ tracers in the brain on positron emission tomography (PET) are considered the earliest biomarkers of Alzheimer’s disease (AD). However, a proportion of cases show discrepancies between the results of the two biomarker modalities which may reflect inter-individual differences in Aβ metabolism. The CSF Aβ(42/40) ratio seems to be a more accurate biomarker of clinical AD than CSF Aβ(42) alone. Objective: We tested whether CSF Aβ(42) alone or the Aβ(42/40) ratio corresponds better with amyloid PET status and analyzed the distribution of cases with discordant CSF-PET results. Methods: CSF obtained from a mixed cohort (n = 200) of cognitively normal and abnormal research participants who had undergone amyloid PET within 12 months (n = 150 PET-negative, n = 50 PET-positive according to a previously published cut-off) was assayed for Aβ(42) and Aβ(40) using two recently developed immunoassays. Optimal CSF cut-offs for amyloid positivity were calculated, and concordance was tested by comparison of the areas under receiver operating characteristic (ROC) curves (AUC) and McNemar’s test for paired proportions. Results: CSF Aβ(42/40) corresponded better than Aβ(42) with PET results, with a larger proportion of concordant cases (89.4% versus 74.9%, respectively, p < 0.0001) and a larger AUC (0.936 versus 0.814, respectively, p < 0.0001) associated with the ratio. For both CSF biomarkers, the percentage of CSF-abnormal/PET-normal cases was larger than that of CSF-normal/PET-abnormal cases. Conclusion: The CSF Aβ(42/40) ratio is superior to Aβ(42) alone as a marker of amyloid-positivity by PET. We hypothesize that this increase in performance reflects the ratio compensating for general between-individual variations in CSF total Aβ

Serum Neurofilament Light Protein as a Marker for Diffuse Axonal Injury: Results from a Case Series Study

Diffuse axonal injury (DAI) is an important cause of morbidity in patients with traumatic brain injury (TBI). There is currently no simple and reliable technique for early identification of patients with DAI, or to prognosticate long-term outcome in this patient group. In the present study, we examined acute serum concentrations of neurofilament light (NFL) in nine patients with severe TBI and DAI using a novel ultrasensitive single molecule array (Simoa) assay. The relationships between the NFL concentrations and MRI in the acute stage as well as clinical outcome and magnetic resonance diffusion tensor imaging (MR-DTI) parameters at 12 months were analyzed. We found that the mean NFL concentrations among the patients displayed a 30-fold increase compared with controls, and that NFL completely discriminated between the patients and controls. We also found a relationship between serum NFL and MR-DTI parameters, with higher NFL concentrations in patients with higher trace (R2 = 0.79) and lower fractional anisotropy (FA) (R 2 = 0.83). These results suggest that serum NFL may be a valuable blood biomarker for TBI, reflecting the severity of DAI

Testing matter effects in propagation of atmospheric and long-baseline neutrinos

We quantify our current knowledge of the size and flavor structure of the matter effects in the evolution of atmospheric and long-baseline neutrinos based solely on the analysis of the corresponding neutrino data. To this aim we generalize the matter potential of the Standard Model by rescaling its strength, rotating it away from the e-e sector, and rephasing it with respect to the vacuum term. This phenomenological parametrization can be easily translated in terms of non-standard neutrino interactions in matter. We show that in the most general case, the strength of the potential cannot be determined solely by atmospheric and long-baseline data. However its flavor composition is very much constrained and the present determination of the neutrino masses and mixing is robust under its presence. We also present an update of the constraints arising from this analysis in the particular case in which no potential is present in the e-mu and e-tau sectors. Finally we quantify to what degree in this scenario it is possible to alleviate the tension between the oscillation results for neutrinos and antineutrinos in the MINOS experiment and show the relevance of the high energy part of the spectrum measured at MINOS.Comment: PDFLaTeX file using JHEP3 class, 25 pages, 7 figures included. Accepted for publication in JHE

Amyloid mis-metabolism in idiopathic normal pressure hydrocephalus

BACKGROUND: Patients with idiopathic normal pressure hydrocephalus (iNPH) have reduced cerebrospinal fluid (CSF) concentrations of amyloid-β (Aβ) and α- and β-cleaved soluble forms of amyloid precursor protein (sAPPα and sAPPβ). The aims of this study were to examine if changes could also be seen in the CSF for secreted metabolites of APP-like protein 1 (APLP1) and to explore the prognostic value of amyloid-related CSF biomarkers, as well as markers of neuronal injury and astroglial activation, as regards to clinical outcome after shunt surgery. METHODS: Twenty patients diagnosed with iNPH, 10 improved and 10 unchanged by shunt surgery, and 20 neurologically healthy controls were included. All patients were examined clinically prior to surgery and at 6-month follow-up after surgery using the iNPH scale. Lumbar puncture was performed pre-operatively. CSF samples were analyzed for neurofilament light (NFL), Aβ isoforms Aβ38, Aβ40 and Aβ42, sAPPα, sAPPβ, APLP1 β-derived peptides APL1β25, APL1β 27 and APL1β 28 and YKL40 by immunochemical methods. RESULTS: The concentrations of all soluble forms of APP, all Aβ isoforms and APL1β28 were lower, whilst APL1β25 and APL1β27 were higher in the CSF of iNPH patients compared to controls. There was no difference in biomarker concentrations between patients who improved after surgery and those who remained unchanged. CONCLUSIONS: The reduced CSF concentrations of Aβ38, Aβ40, Aβ42, sAPPα and sAPPβ suggest that APP expression could be downregulated in iNPH. In contrast, APLP1 concentration in the CSF seems relatively unchanged. The increase of APL1β25 and APL1β27 in combination with a slight decreased APL1β28 could be caused by more available γ-secretase due to reduced availability of its primary substrate, APP. The data did not support the use of these markers as indicators of shunt responsiveness