91 research outputs found
Consensus document on Lipoprotein(a) from the Italian Society for the Study of Atherosclerosis (SISA)
Aims: In view of the consolidating evidence on the causal role of Lp(a) in cardiovascular disease, the Italian Society for the Study of Atherosclerosis (SISA) has assembled a consensus on Lp(a) genetics and epidemiology, together with recommendations for its measurement and current and emerging therapeutic approaches to reduce its plasma levels. Data on the Italian population are also provided.
Data synthesis: Lp(a) is constituted by one apo(a) molecule and a lipoprotein closely resembling to a low-density lipoprotein (LDL). Its similarity with an LDL, together with its ability to carry oxidized phospholipids are considered the two main features making Lp(a) harmful for cardiovascular health. Plasma Lp(a) concentrations vary over about 1000 folds in humans and are genetically determined, thus they are quite stable in any individual. Mendelian Randomization studies have suggested a causal role of Lp(a) in atherosclerotic cardiovascular disease (ASCVD) and aortic valve stenosis and observational studies indicate a linear direct correlation between cardiovascular disease and Lp(a) plasma levels. Lp(a) measurement is strongly recommended once in a patient's lifetime, particularly in FH subjects, but also as part of the initial lipid screening to assess cardiovascular risk. The apo(a) size polymorphism represents a challenge for Lp(a) measurement in plasma, but new strategies are overcoming these difficulties. A reduction of Lp(a) levels can be currently attained only by plasma apheresis and, moderately, with PCSK9 inhibitor treatment.
Conclusions: Awaiting the approval of selective Lp(a)-lowering drugs, an intensive management of the other risk factors for individuals with elevated Lp(a) levels is strongly recommended
The SMART personalised self-management system for congestive heart failure: results of a realist evaluation
Background: Technology has the potential to provide support for self-management to people with congestive heart failure (CHF). This paper describes the results of a realist evaluation of the SMART Personalised Self-Management System (PSMS) for CHF. Methods: The PSMS was used, at home, by seven people with CHF. Data describing system usage and usability as well as questionnaire and interview data were evaluated in terms of the context, mechanism and outcome hypotheses (CMOs) integral to realist evaluation. Results: The CHF PSMS improved heart failure related knowledge in those with low levels of knowledge at baseline, through providing information and quizzes. Furthermore, participants perceived the self-regulatory aspects of the CHF PSMS as being useful in encouraging daily walking. The CMOs were revised to describe the context of use, and how this influences both the mechanisms and the outcomes. Conclusions: Participants with CHF engaged with the PSMS despite some technological problems. Some positive effects on knowledge were observed as well as the potential to assist with changing physical activity behaviour. Knowledge of CHF and physical activity behaviour change are important self-management targets for CHF, and this study provides evidence to direct the further development of a technology to support these targets. Keywords: Technology, Realist evaluation, User-centred design, Heart failure, Self-managemen
Nonlinearity and Topology
The interplay of nonlinearity and topology results in many novel and emergent
properties across a number of physical systems such as chiral magnets, nematic
liquid crystals, Bose-Einstein condensates, photonics, high energy physics,
etc. It also results in a wide variety of topological defects such as solitons,
vortices, skyrmions, merons, hopfions, monopoles to name just a few.
Interaction among and collision of these nontrivial defects itself is a topic
of great interest. Curvature and underlying geometry also affect the shape,
interaction and behavior of these defects. Such properties can be studied using
techniques such as, e.g. the Bogomolnyi decomposition. Some applications of
this interplay, e.g. in nonreciprocal photonics as well as topological
materials such as Dirac and Weyl semimetals, are also elucidated
Addition of either pioglitazone or a sulfonylurea in type 2 diabetic patients inadequately controlled with metformin alone: impact on cardiovascular events. A randomized controlled trial
Background and aims: Metformin is the first-line therapy in type 2 diabetes. In
patients inadequately controlled with metformin, the addition of a sulfonylurea or pioglitazone
are equally plausible options to improve glycemic control. However, these drugs have
profound differences in their mechanism of action, side effects, and impact on cardiovascular
risk factors. A formal comparison of these two therapies in terms of cardiovascular morbidity
and mortality is lacking. The TOSCA.IT study was designed to explore the effects of adding pioglitazone
or a sulfonylurea on cardiovascular events in type 2 diabetic patients inadequately
controlled with metformin. Methods: Multicentre, randomized, open label, parallel group trial of 48 month duration. Type
2 diabetic subjects, 50e75 years, BMI 20e45 Kg/m2, on secondary failure to metformin monotherapy
will be randomized to add-on a sulfonylurea or pioglitazone. The primary efficacy
outcome is a composite endpoint of all-cause mortality, nonfatal myocardial infarction,
nonfatal stroke, and unplanned coronary revascularization. Principal secondary outcome is
a composite ischemic endpoint of sudden death, fatal and non-fatal myocardial infarction
and stroke, endovascular or surgical intervention on the coronary, leg or carotid arteries,
major amputations. Side effects, quality of life and economic costs will also be evaluated. Efficacy,
safety, tolerability, and study conduct will be monitored by an independent Data Safety
Monitoring Board. End points will be adjudicated by an independent external committee.
Conclusions: TOSCA.IT is the first on-going study investigating the head-to-head comparison of
adding a sulfonylurea or pioglitazone to existing metformin treatment in terms of hard cardiovascular
outcomes
Prediction of 6 months left ventricular dilatation after myocardial infarction in relation to cardiac morbidity and mortality - Application of a new dilatation model to GISSI-3 data
Aims To predict the long-term left ventricular volume index early after myocardial infarction and to investigate the relationship between long-term left ventricular dilatation risk and clinical outcome. Methods and Results By applying a previously developed dilatation model, we predicted the 6-month left ventricular volume index early after myocardial infarction (median 9 days) in 13 679 GISSI-3 patients, to identify patients at high risk of long-term left ventricular dilatation. The left ventricular systolic and diastolic volume indexes at 6 months were predicted with r=0.72 and r=0.68. respectively. in the subgroup of patients in whom a pre-discharge echo was available (n=7842). Patients predicted to be at risk for long-term left ventricular dilatation had an increased risk of mortality (R.R. 1.87. 95% CI: 1.48 to 2.36) and heart failure at 6 months (RR 2.59, 95% CI:2.04 to 3.28), but no increased risk of reinfarction at 6 months (RR 1.12, 95% CI: 0.87 to 1.45) or of angina pectoris (RR 1.07, 95% CI: 0.95 to 1.20). Conclusion Our prediction of long-term left ventricular dilatation, obtained by applying our new dilatation model in over 13 000 GISSI-3 patients, correlated well with mortality and heart failure after myocardial infarction, Therefore, our new dilatation model may contribute to more efficient risk stratification early after myocardial infarction. (C) 2001 The European Society of Cardiology
Addition of either pioglitazone or a sulfonylurea in type 2 diabetic patients inadequately controlled with metformin alone: Impact on cardiovascular events. A randomized controlled trial.
BACKGROUND AND AIMS:
Metformin is the first-line therapy in type 2 diabetes. In patients inadequately controlled with metformin, the addition of a sulfonylurea or pioglitazone are equally plausible options to improve glycemic control. However, these drugs have profound differences in their mechanism of action, side effects, and impact on cardiovascular risk factors. A formal comparison of these two therapies in terms of cardiovascular morbidity and mortality is lacking. The TOSCA.IT study was designed to explore the effects of adding pioglitazone or a sulfonylurea on cardiovascular events in type 2 diabetic patients inadequately controlled with metformin.
METHODS:
Multicentre, randomized, open label, parallel group trial of 48 month duration. Type 2 diabetic subjects, 50-75 years, BMI 20-45 Kg/m(2), on secondary failure to metformin monotherapy will be randomized to add-on a sulfonylurea or pioglitazone. The primary efficacy outcome is a composite endpoint of all-cause mortality, nonfatal myocardial infarction, nonfatal stroke, and unplanned coronary revascularization. Principal secondary outcome is a composite ischemic endpoint of sudden death, fatal and non-fatal myocardial infarction and stroke, endovascular or surgical intervention on the coronary, leg or carotid arteries, major amputations. Side effects, quality of life and economic costs will also be evaluated. Efficacy, safety, tolerability, and study conduct will be monitored by an independent Data Safety Monitoring Board. End points will be adjudicated by an independent external committee.
CONCLUSIONS:
TOSCA.IT is the first on-going study investigating the head-to-head comparison of adding a sulfonylurea or pioglitazone to existing metformin treatment in term of hard cardiovascular outcomes. Registration: Clinicaltrials.gov ID NCT00700856
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