Elizabeth Hughes
University of Birmingham
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Featured researches published by Elizabeth Hughes.
International Journal of Clinical Practice | 2007
A. Gunarathne; Jeetesh V. Patel; R. Potluri; B. Gammon; S. Jessani; Elizabeth Hughes; G. Y. H. Lip
Background: Stroke is a major cause of premature mortality in Britain, but its burden is markedly greater amongst South Asians. Because of the paucity of data in this area, we investigated the magnitude and impact of risk from cardiovascular comorbidities on survival amongst South Asian stroke patients.
Journal of Hypertension | 2006
Jeetesh V. Patel; Hoong Sern Lim; Sunil Nadar; Muzahir Tayebjee; Elizabeth Hughes; Gregory Y.H. Lip
Background Abnormal inflammation, platelets and angiogenesis are involved in the pathophysiology of cardiovascular disease (CVD). Objective To test the hypothesis that concentrations of high sensitive C-reactive protein (CRP, an index of inflammation) and soluble CD40 ligand (sCD40L, an index of platelet activation) would be abnormal in hypertension, and in turn, be related to plasma indices of angiogenesis, the angiopoietins-1 and -2, and vascular endothelial growth factor (VEGF), in addition to the presence or absence of CVD. Methods Using a cross-sectional approach, we measured plasma concentrations of CRP, sCD40L, VEGF, and angiopoietins-1 and -2 in 147 patients with hypertension (85 with a history of CVD event/s, 62 CVD event-free) and 68 age- and sex-matched healthy controls. Results Concentrations of sCD40L (P = 0.039), CRP (P < 0.001), angiopoietin-1 (P < 0.001), angiopoietin-2 (P = 0.003) and VEGF (P < 0.001) were all greater amongst hypertensive patients than in controls. There were no significant differences in sCD40L and VEGF concentrations between hypertensive individuals with and without CVD events, but CRP and angiopoietin-1 concentrations were significantly greater amongst those with CVD events. On multiple regression analysis, sCD40L was associated with angiopoietin-2 (P = 0.01) and VEGF (P = 0.007) in hypertensive individuals, but no such associations were found within the healthy control group. Conclusion In patients with hypertension, sCD40L was associated with increased circulating markers of abnormal angiogenesis (angiopoietin-2, VEGF). The interaction between sCD40L and angiogenesis may contribute to the pathophysiology of CVD in hypertension.
International Journal of Clinical Practice | 2007
K. M. Sharobeem; Jeetesh V. Patel; Alistair Ritch; G. Y. H. Lip; Paramjit Gill; Elizabeth Hughes
Background: Stroke is a continuing cause of excess cardiovascular disease (CVD) mortality amongst migrants from the Indian subcontinent (South Asians) living in Britain. However, little is known about the dyslipidaemia associated with stroke in South Asians. In particular, the highly atherogenic lipoprotein (a) [Lp(a)] and high apolipoprotein (Apo) B to AI ratio are emerging risk factors for CVD.
Journal of Thrombosis and Haemostasis | 2010
Jeetesh V. Patel; Inessa Tracey; Elizabeth Hughes; Gregory Y.H. Lip
Summary. The consumption of long chain omega‐3 polyunsaturated acids (PUFA) is considered to protect against cardiovascular disease and promote longevity following a heart attack. Historically, research in this area was fuelled by compelling reports of the cardiovascular benefits of omega‐3 PUFA in select populations and cultures. More recent studies, in wider populations, suggest discordant findings: differences that are difficult to reconcile as the mechanism of action of omega‐3 PUFA are poorly understood. As such, the use of this ‘natural treatment’ for cardiovascular disease is increasingly controversial, and potentially one of unfulfilled promise. To what extent does ethnicity influence the impact that omega‐3 PUFA have on cardiovascular disease and its associated complications? We were interested to review the benefits of omega‐3 PUFA in the management of cardiovascular risk amongst diverse ethnic groups. Using a systematic review of literature relating to omega‐3 PUFA and cardiovascular disease, we found ethnicity to be a factor that accounts for inconsistency between studies. Some of the effects of omega‐3 PUFA are limited to cultures with a very high omega‐3 intake, and in turn, ethnicity moderates the efficiency with which PUFA are derived from the diet. Moreover, omega‐3 PUFA are an important health care intervention in the current climate of globalization, where supplementation is likely to give protection to cultural groups undergoing dietary transition. Future epidemiological research into the efficacy of omega‐3 PUFA in cardiovascular disease should consider the influence of ethnicity.
European Journal of Heart Failure | 2010
Jeetesh V. Patel; Abraheem Abraheem; John Creamer; Mark Gunning; Elizabeth Hughes; Gregory Y.H. Lip
To compare the performance of apolipoproteins (Apo) and oxidized LDL against routine clinical lipid profiles in the discrimination of atherosclerotic burden and cardiac function in stable coronary artery disease (CAD) patients.
Data in Brief | 2018
Philippe Moulin; Robert Dufour; Maurizio Averna; Marcello Arca; Angelo B. Cefalù; Davide Noto; Laura D’Erasmo; Alessia Di Costanzo; Christophe Marçais; Luis Álvarez-Sala Walther; Maciej Banach; Jan Borén; Robert Cramb; Ioanna Gouni-Berthold; Elizabeth Hughes; Colin Johnson; Xavier Pintó; Željko Reiner; Jeanine E. Roeters van Lennep; Handrean Soran; Claudia Stefanutti; Erik S.G. Stroes; Eric Bruckert
Data presented in this article are supplementary material to our article entitled “Identification and diagnosis of patients with familial chylomicronaemia syndrome (FCS): expert panel recommendations and proposal of an “FCS Score” (Moulin et al., 2018, in press). The data describe the genotypes of patients with familial chylomicronaemia syndrome (FCS) and multifactorial chylomicronaemia syndrome (MCS), from the validation and replication cohorts.
Atherosclerosis | 2018
Philippe Moulin; Robert Dufour; Maurizio Averna; Marcello Arca; Angelo B. Cefalù; Davide Noto; L. D'Erasmo; Alessia Di Costanzo; Christophe Marçais; Luis Álvarez-Sala Walther; Maciej Banach; Jan Borén; Robert Cramb; Ioanna Gouni-Berthold; Elizabeth Hughes; Colin Johnson; Xavier Pintó; Željko Reiner; Jeanine E. Roeters van Lennep; Handrean Soran; Claudia Stefanutti; Erik S.G. Stroes; Eric Bruckert
Familial chylomicronaemia syndrome (FCS) is a rare, inherited disorder characterised by impaired clearance of triglyceride (TG)-rich lipoproteins from plasma, leading to severe hypertriglyceridaemia (HTG) and a markedly increased risk of acute pancreatitis. It is due to the lack of lipoprotein lipase (LPL) function, resulting from recessive loss of function mutations in the genes coding LPL or its modulators. A large overlap in the phenotype between FCS and multifactorial chylomicronaemia syndrome (MCS) contributes to the inconsistency in how patients are diagnosed and managed worldwide, whereas the incidence of acute hypertriglyceridaemic pancreatitis is more frequent in FCS. A panel of European experts provided guidance on the diagnostic strategy surrounding FCS and proposed an algorithm-based diagnosis tool for identification of these patients, which can be readily translated into practice. Features included in this FCS score comprise: severe elevation of plasma TGs (fasting TG levels >10 mmol/L [885 mg/dL] on multiple occasions), refractory to standard TG-lowering therapies, a young age at onset, the lack of secondary factors (except for pregnancy and oral oestrogens) and a history of episodes of acute pancreatitis. Considering 53 FCS patients from three cohorts and 52 MCS patients from three cohorts, the overall sensitivity of the FCS score (≥10) was 88% (95% confidence interval [CI]: 0.76, 0.97) with an overall specificity of 85% (95% CI: 0.75, 0.94). Receiver operating characteristic curve area was 0.91. Pragmatic clinical scoring, by standardising diagnosis, may help differentiate FCS from MCS, may alleviate the need for systematic genotyping in patients with severe HTG and may help identify high-priority candidates for genotyping.
International Journal of Clinical Practice | 2012
Jeetesh V. Patel; G. Y. H. Lip; D. Prabharkaran; Kolli Srinath Reddy; Paramjit Gill; Elizabeth Hughes
rently (dual use). We acknowledge that the participants’ memory for these dates were likely imprecise, but it appears that many of those surveyed quit tobacco soon after starting e-cigs and they remained quit. The figure also suggests that a very small proportion (around 3%) stopped using tobacco more than a couple of weeks prior to starting to use e-cigs. Initiation of e-cig use by non-tobacco users is bound to occur on occasion and this should be discouraged, particularly among young people. It remains to be seen whether this will occur primarily in ‘at risk’ youth who may otherwise initiate far more harmful cigarette smoking (i.e. acting to prevent uptake of smoking), or whether e-cigs may act as a ‘gateway’ to smoking for some youth who otherwise would not. One recent study in Korea found that 0.5% (22 ⁄ 4341) of school students had tried e-cigs and five (0.1%) of these students described themselves as never smokers (2). However, this pales in comparison with the proportion (19%) who had tried cigarettes. E-cigs should clearly not be available to adolescents either over the counter or via the internet. One small (n = 40) clinical trial of e-cigs (without a comparison group) in smokers not planning to quit has now been published (3). Encouragingly, that study found that 23% had quit smoking 6 months later. We agree that e-cigs have potential as aids to smoking cessation (4) and that larger randomized trials are required.
Atherosclerosis | 2013
Jeetesh V. Patel; Julia Chackathayil; Brian Gammon; Inessa Tracey; Adam Lovick; Paramjit Gill; Amitava Banerjee; Charlotte A. Scarff; James H. Scrivens; Gregory Y.H. Lip; Elizabeth Hughes
Archive | 2018
Jeetesh V. Patel; Prabir Bandyopadhyay; Elizabeth Hughes