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1.
J Therm Biol ; 110: 103349, 2022 Dec.
Article in English | MEDLINE | ID: mdl-36462858

ABSTRACT

The prediction of survival time for those immersed in water remains a key element in the function of search and rescue organisations around the globe. The data on which such predictions are made come from laboratory studies and actual incidents. The UK National Immersion Incident Survey (UKNIIS) represents one of the largest surveys undertaken in this area. The UKNIIS data are obtained by questionnaire from immersion incidents around the British Isles. The survey has been in operation since 1991 and at the time of writing contained almost 1600 cases. The aim of the present work was to analyse these cases with the aim of establishing a model for the prediction of survival time in water. This analysis is described in this paper: two model approaches are presented and their strengths and weaknesses are discussed. Recommendations for the use and development of such models are made.


Subject(s)
Water
2.
Environ Health ; 20(1): 102, 2021 09 13.
Article in English | MEDLINE | ID: mdl-34517898

ABSTRACT

BACKGROUND: Much of the current evidence of associations between long-term PM2.5 and health outcomes relies on national or regional analyses using exposures derived directly from regulatory monitoring data. These findings could be affected by limited spatial coverage of monitoring data, particularly for time periods before spatially extensive monitoring began in the late 1990s. For instance, Pope et al. (2009) showed that between 1980 and 2000 a 10 µg/m3 reduction in PM2.5 was associated with an average 0.61 year (standard error (SE) = 0.20) longer life expectancy. That analysis used 1979-1983 averages of PM2.5 across 51 U.S. Metropolitan Statistical Areas (MSAs) computed from about 130 monitoring sites. Our reanalysis re-examines this association using modeled PM2.5 in order to assess population- or spatially-representative exposure. We hypothesized that modeled PM2.5 with finer spatial resolution provides more accurate health effect estimates compared to limited monitoring data. METHODS: We used the same data for life expectancy and confounders, as well as the same analysis models, and investigated the same 211 continental U.S. counties, as Pope et al. (2009). For modeled PM2.5, we relied on a previously-developed point prediction model based on regulatory monitoring data for 1999-2015 and back-extrapolation to 1979. Using this model, we predicted annual average concentrations at centroids of all 72,271 census tracts and 12,501 25-km national grid cells covering the contiguous U.S., to represent population and space, respectively. We averaged these predictions to the county for the two time periods (1979-1983 and 1999-2000), whereas the original analysis used MSA averages given limited monitoring data. Finally, we estimated regression coefficients for PM2.5 reduction on life expectancy improvement over the two periods, adjusting for area-level confounders. RESULTS: A 10 µg/m3 decrease in modeled PM2.5 based on census tract and national grid predictions was associated with 0.69 (standard error (SE) = 0.31) and 0.81 (0.29) -year increases in life expectancy. These estimates are higher than the estimate of Pope et al. (2009); they also have larger SEs likely because of smaller variability in exposure predictions, a standard property of regression. Two sets of effect estimates, however, had overlapping confidence intervals. CONCLUSIONS: Our approach for estimating population- and spatially-representative PM2.5 concentrations based on census tract and national grid predictions, respectively, provided generally consistent findings to the original findings using limited monitoring data. This finding lends additional support to the evidence that reduced fine particulate matter contributes to extended life expectancy.


Subject(s)
Air Pollutants/analysis , Life Expectancy , Models, Theoretical , Particulate Matter/analysis , Environmental Monitoring , Humans , United States
3.
Osteoarthritis Cartilage ; 28(2): 189-200, 2020 02.
Article in English | MEDLINE | ID: mdl-31843571

ABSTRACT

OBJECTIVE: This paper aims to (i) identify differences in measures of hip morphology between four racial groups using anteroposterior (AP) hip x-rays, and (ii) examine whether these differences vary by sex. METHODS: 912 hip x-rays (456 individuals) from four racial groups (European Caucasians, American Caucasians, African Americans and Chinese) were obtained. Males and females (45-75 years) with no radiographic hip OA (Kellgren and Lawrence < Grade 2 or Croft < Grade 1) were included. Eleven features of hip joint morphology were analysed. Linear regression with generalised estimating equations (GEE) was used to determine race and sex differences in hip morphology. Post-hoc Bonferroni procedure was used to adjust for multiple comparisons. RESULTS: The final analysis included 875 hips. Chinese hips showed significant differences for the majority of measures to other racial groups. Chinese were characterised by more shallow and narrow acetabular sockets, reduced femoral head coverage, smaller femoral head diameter, and a lesser angle of alignment between the femoral neck and shaft. Variation was found between other racial groups, but with few statistically significant differences. The average of lateral centre edge angle, minimum neck width and neck length differed between race and sex (p-value for interaction < 0.05). CONCLUSIONS: Significant differences were found in measures of morphology between Chinese hips compared to African Americans or Caucasian groups; these may explain variation in hip OA prevalence rates between these groups and the lower rate of hip OA in Chinese. Sex differences were also identified, which may further explain male-female prevalence differences for OA.


Subject(s)
Acetabulum/diagnostic imaging , Femur Head/diagnostic imaging , Femur Neck/diagnostic imaging , Hip Joint/diagnostic imaging , Osteoarthritis, Hip/ethnology , Acetabulum/anatomy & histology , Black or African American , Aged , Asian People , Female , Femur Head/anatomy & histology , Femur Neck/anatomy & histology , Hip Joint/anatomy & histology , Humans , Male , Middle Aged , Osteoarthritis, Hip/epidemiology , Radiography , Sex Factors , White People
5.
Eur J Neurol ; 21(11): 1387-93, 2014 Nov.
Article in English | MEDLINE | ID: mdl-25040216

ABSTRACT

BACKGROUND AND PURPOSE: Cognitive deficits are common following stroke. Cognitive function in the acute stroke setting is a predictive factor for mid-term outcome. The Montreal Cognitive Assessment (MoCA) is a screening tool for cognitive impairment. The feasibility of MoCA in the acute phase of stroke was evaluated and factors predictive of cognitive impairment were determined. METHODS: In this prospective, single-centre, explorative and observational study consecutive patients with ischaemic (IS) or haemorrhagic (ICH) stroke were enrolled between March 2011 and September 2012. The routine work-up for each patient encompassed assessment of cardiovascular risk factors, the National Institutes of Health Stroke Scale (NIHSS) and the pre-morbid modified Rankin Scale (mRS) score. Cognitive performance was measured using the German version of the MoCA within the first days of admission. A MoCA score of <26 was considered to indicate cognitive impairment. RESULTS: Between March 2011 and September 2012 a total of 842 patients with IS (89.0%) and ICH (11.0%) were enrolled in our study. MoCA was feasible in 678/842 patients (80.5%). Factors independently associated with non-feasibility were stroke severity (NIHSS), pre-morbid functional status (mRS), age and lower educational level. Mean MoCA was 21.4 (SD 5.7). A total of 498/678 (73.5%) patients appeared cognitively impaired (<26/30). Independent predictive factors for a lower MoCA score were age, educational level, stroke severity (NIHSS) and pre-morbid functional status (mRS). CONCLUSIONS: In the acute phase of stroke, MoCA is feasible in about 80% of eligible patients. At this stage, MoCA identifies a cognitive impairment in 75% of patients.


Subject(s)
Cognition Disorders/diagnosis , Neuropsychological Tests/standards , Psychometrics/instrumentation , Stroke/diagnosis , Aged , Aged, 80 and over , Cardiovascular Diseases/complications , Cognition Disorders/etiology , Feasibility Studies , Female , Humans , Male , Middle Aged , Prospective Studies , Stroke/complications
6.
Aesthet Surg J ; 29(2): 150-7, 2009.
Article in English | MEDLINE | ID: mdl-19371848

ABSTRACT

Most medications, herbal preparations, and nutraceutical supplements have notable effects on biochemical pathways and may influence wound healing, coagulation, and cardiovascular function. They can also interact with other drugs. A large portion of the data available regarding the effects of naturopathic medicines is anecdotal. Marketing of certain products may be misleading and potentially harmful, and quality control standards are highly variable. In order to ensure quality control and standardization of products, it is prudent to work with preparations manufactured by companies that adhere to pharmaceutical (good manufacturing practice [GMP]) standards. However, many of these higher-quality products are not readily available to the public over the counter. A large percentage of patients undergoing plastic surgery use one or more herbal medications, but the disclosure of such medications to allopathic providers is often incomplete. In addition, patients may not understand the importance of discontinuing such medications before surgery. The authors review research on the possible benefits and risks of commonly used herbal medications such as arnica montana, St. John's wort, bromelain, echinacea, ginkgo biloba, ephedra, valerian, and others, focusing on their potentially positive or negative impact during the perioperative period of aesthetic surgery. Good communication with surgical patients, including the administration of a presurgical questionnaire to help identify any use of herbal medications, is emphasized.


Subject(s)
Dietary Supplements/adverse effects , Perioperative Care , Plant Preparations/adverse effects , Plastic Surgery Procedures , Arnica/adverse effects , Arnica/metabolism , Bromelains/adverse effects , Bromelains/metabolism , Drug Interactions , Echinacea/adverse effects , Echinacea/metabolism , Ephedra/adverse effects , Ephedra/metabolism , Ginkgo biloba/adverse effects , Ginkgo biloba/metabolism , Herb-Drug Interactions , Humans , Hypericum/adverse effects , Hypericum/metabolism , Plant Preparations/metabolism , Quality Control , Surgery, Plastic , Valerian/adverse effects , Valerian/metabolism
7.
Diabetologia ; 49(1): 174-82, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16341839

ABSTRACT

AIMS/HYPOTHESIS: An insulin signalling pathway leading from activation of protein kinase B (PKB, also known as Akt) to phosphorylation (inactivation) of glycogen synthase kinase-3 (GSK-3) and activation of glycogen synthase is well characterised. However, in hepatocytes, inactivation of GSK-3 is not the main mechanism by which insulin stimulates glycogen synthesis. We therefore tested whether activation of PKB causes inactivation of glycogen phosphorylase. MATERIALS AND METHODS: We used a conditionally active form of PKB, produced using recombinant adenovirus, to test the role of acute PKB activation in the control of glycogen phosphorylase and glycogen synthesis in hepatocytes. RESULTS: Conditional activation of PKB mimicked the inactivation of phosphorylase, the activation of glycogen synthase, and the stimulation of glycogen synthesis caused by insulin. In contrast, inhibition of GSK-3 caused activation of glycogen synthase but did not mimic the stimulation of glycogen synthesis by insulin. PKB activation and GSK-3 inhibition had additive effects on the activation of glycogen synthase, indicating convergent mechanisms downstream of PKB involving inactivation of either phosphorylase or GSK-3. Glycogen synthesis correlated inversely with the activity of phosphorylase-a, irrespective of whether this was modulated by insulin, by PKB activation or by a selective phosphorylase ligand, supporting an essential role for phosphorylase inactivation in the glycogenic action of insulin in hepatocytes. CONCLUSIONS/INTERPRETATION: In hepatocytes, the acute activation of PKB, but not the inhibition of GSK-3, mimics the stimulation of glycogen synthesis by insulin. This is explained by a pathway downstream of PKB leading to inactivation of phosphorylase, activation of glycogen synthase, and stimulation of glycogen synthesis, independent of the GSK-3 pathway.


Subject(s)
Hepatocytes/physiology , Insulin/pharmacology , Proto-Oncogene Proteins c-akt/physiology , Animals , Cells, Cultured , Enzyme Activation , Glycogen Synthase Kinase 3/metabolism , Hepatocytes/cytology , Hepatocytes/drug effects , Male , Phosphatidylinositol 3-Kinases/metabolism , Phosphorylation , Rats , Rats, Wistar
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