184 research outputs found
Spin-Dependent Cyclotron Decay Rates in Strong Magnetic Fields
Cyclotron decay and absorption rates have been well studied in the
literature, focusing primarily on spectral, angular and polarization
dependence. Astrophysical applications usually do not require retention of
information on the electron spin state, and these are normally averaged in
obtaining the requisite rates. In magnetic fields, higher order quantum
processes such as Compton scattering become resonant at the cyclotron frequency
and its harmonics, with the resonances being formally divergent. Such
divergences are usually eliminated by accounting for the finite lifetimes of
excited Landau states. This practice requires the use of spin-dependent
cyclotron rates in order to obtain accurate determinations of process rates
very near cyclotronic resonances, the phase space domain most relevant for
certain applications to pulsar models. This paper develops previous results in
the literature to obtain compact analytic expressions for cyclotron decay
rates/widths in terms of a series of Legendre functions of the second kind;
these expressions can be expediently used in astrophysical models. The rates
are derived using two popular eigenstate formalisms, namely that due to Sokolov
and Ternov, and that due to Johnson and Lippmann. These constitute two sets of
eigenfunctions of the Dirac equation that diagonalize different operators, and
accordingly yield different spin-dependent cyclotron rates. This paper
illustrates the attractive Lorentz transformation characteristics of the
Sokolov and Ternov formulation, which is another reason why it is preferable
when electron spin information must be explicitly retained.Comment: 11 pages, 2 embedded figures, apjgalley format, To appear in The
Astrophysical Journal, Vol 630, September 1, 2005 issu
Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects
An overview of anti-diabetic plants used in Gabon: Pharmacology and Toxicology
© 2017 Elsevier B.V. All rights reserved.Ethnopharmacological relevance: The management of diabetes mellitus management in African communities, especially in Gabon, is not well established as more than 60% of population rely on traditional treatments as primary healthcare. The aim of this review was to collect and present the scientific evidence for the use of medicinal plants that are in currect by Gabonese traditional healers to manage diabetes or hyperglycaemia based here on the pharmacological and toxicological profiles of plants with anti-diabetic activity. There are presented in order to promote their therapeutic value, ensure a safer use by population and provide some bases for further study on high potential plants reviewed. Materials and methods: Ethnobotanical studies were sourced using databases such as Online Wiley library, Pubmed, Google Scholar, PROTA, books and unpublished data including Ph.D. and Master thesis, African and Asian journals. Keywords including ‘Diabetes’ ‘Gabon’ ‘Toxicity’ ‘Constituents’ ‘hyperglycaemia’ were used. Results: A total of 69 plants currently used in Gabon with potential anti-diabetic activity have been identified in the literature, all of which have been used in in vivo or in vitro studies. Most of the plants have been studied in human or animal models for their ability to reduce blood glucose, stimulate insulin secretion or inhibit carbohydrates enzymes. Active substances have been identified in 12 out of 69 plants outlined in this review, these include Allium cepa and Tabernanthe iboga. Only eight plants have their active substances tested for anti-diabetic activity and are suitables for further investigation. Toxicological data is scarce and is dose-related to the functional parameters of major organs such as kidney and liver. Conclusion: An in-depth understanding on the pharmacology and toxicology of Gabonese anti-diabetic plants is lacking yet there is a great scope for new treatments. With further research, the use of Gabonese anti-diabetic plants is important to ensure the safety of the diabetic patients in Gabon.Peer reviewedFinal Accepted Versio
A Genetic Signature of Spina Bifida Risk from Pathway-Informed Comprehensive Gene-Variant Analysis
Despite compelling epidemiological evidence that folic acid supplements reduce the frequency of neural tube defects (NTDs) in newborns, common variant association studies with folate metabolism genes have failed to explain the majority of NTD risk. The contribution of rare alleles as well as genetic interactions within the folate pathway have not been extensively studied in the context of NTDs. Thus, we sequenced the exons in 31 folate-related genes in a 480-member NTD case-control population to identify the full spectrum of allelic variation and determine whether rare alleles or obvious genetic interactions within this pathway affect NTD risk. We constructed a pathway model, predetermined independent of the data, which grouped genes into coherent sets reflecting the distinct metabolic compartments in the folate/one-carbon pathway (purine synthesis, pyrimidine synthesis, and homocysteine recycling to methionine). By integrating multiple variants based on these groupings, we uncovered two provocative, complex genetic risk signatures. Interestingly, these signatures differed by race/ethnicity: a Hispanic risk profile pointed to alterations in purine biosynthesis, whereas that in non-Hispanic whites implicated homocysteine metabolism. In contrast, parallel analyses that focused on individual alleles, or individual genes, as the units by which to assign risk revealed no compelling associations. These results suggest that the ability to layer pathway relationships onto clinical variant data can be uniquely informative for identifying genetic risk as well as for generating mechanistic hypotheses. Furthermore, the identification of ethnic-specific risk signatures for spina bifida resonated with epidemiological data suggesting that the underlying pathogenesis may differ between Hispanic and non-Hispanic groups
Management of subclinical hyperthyroidism
The ideal approach for adequate management of subclinical hyperthyroidism (low levels
of thyroid-stimulating hormone [TSH] and normal thyroid hormone level) is a matter of
intense debate among endocrinologists. The prevalence of low serum TSH levels ranges
between 0.5% in children and 15% in the elderly population. Mild subclinical hyperthyroid
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ism is more common than severe subclinical hyperthyroidism. Transient suppression of
TSH secretion may occur because of several reasons; thus, corroboration of results from
different assessments is essential in such cases. During differential diagnosis of hyperthy
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roidism, pituitary or hypothalamic disease, euthyroid sick syndrome, and drug-mediated
suppression of TSH must be ruled out. A low plasma TSH value is also typically seen in
the first trimester of gestation. Factitial or iatrogenic TSH inhibition caused by excessive
intake of levothyroxine should be excluded by checking the patient’s medication history.
If these nonthyroidal causes are ruled out during differential diagnosis, either transient
or long-term endogenous thyroid hormone excess, usually caused by Graves’ disease or
nodular goiter, should be considered as the cause of low circulating TSH levels.
We recommend the following 6-step process for the assessment and treatment of this
common hormonal disorder: 1) confirmation, 2) evaluation of severity, 3) investiga
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tion of the cause, 4) assessment of potential complications, 5) evaluation of the neces
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sity of treatment, and 6) if necessary, selection of the most appropriate treatment.
In conclusion, management of subclinical hyperthyroidism merits careful monitoring
through regular assessment of thyroid function. Treatment is mandatory in older patients
(> 65 years) or in presence of comorbidities (such as osteoporosis and atrial fibrillation
Herbal supplements in the print media: communicating benefits and risks
Background The rise in use of food supplements based on botanical ingredients (herbal supplements) is depicted as part of a trend empowering consumers to manage their day-to-day health needs, which presupposes access to clear and accurate information to make effective choices. Evidence regarding herbal supplement efficacy is extremely variable so recent regulations eliminating unsubstantiated claims about potential effects leave producers able to provide very little information about their products. Medical practitioners are rarely educated about herbal supplements and most users learn about them via word-of-mouth, allowing dangerous misconceptions to thrive, chief among them the assumption that natural products are inherently safe. Print media is prolific among the information channels still able to freely discuss herbal supplements. Method This study thematically analyses how 76 newspaper/magazine articles from the UK, Romania and Italy portray the potential risks and benefits of herbal supplements. Results Most articles referenced both risks and benefits and were factually accurate but often lacked context and impartiality. More telling was how the risks and benefits were framed in service of a chosen narrative, the paucity of authoritative information allowing journalists leeway to recontextualise herbal supplements in ways that serviced the goals and values of their specific publications and readerships. Conclusion Providing sufficient information to empower consumers should not be the responsibility of print media, instead an accessible source of objective information is required.</p
Clinical, behavioural and pharmacogenomic factors influencing the response to levothyroxine therapy in patients with primary hypothyroidism—protocol for a systematic review
19-base pair deletion polymorphism of the dihydrofolate reductase (DHFR) gene: maternal risk of Down syndrome and folate metabolism
Study protocol; Thyroid hormone Replacement for Untreated older adults with Subclinical hypothyroidism - a randomised placebo controlled Trial (TRUST)
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