| |
American journal of kidney diseases : the official journal of the National Kidney Foundation, Vol. 54, No. 5. (November 2009), pp. 810-819.
Abstract
BACKGROUND: We examined whether atorvastatin affects diabetic kidney disease and whether the effect of atorvastatin on cardiovascular disease (CVD) varies by kidney status in patients with diabetes. STUDY DESIGN: The Collaborative Atorvastatin Diabetes Study (CARDS) randomized placebo-controlled trial. SETTING & PARTICIPANTS: Patients with type 2 diabetes and no prior CVD (n = 2,838). INTERVENTION: Random allocation to atorvastatin, 10 mg/d, or placebo, with a median follow-up of 3.9 years. OUTCOMES: Estimated glomerular filtration rate (eGFR), albuminuria, CVD. MEASUREMENTS: Baseline and follow-up ...
|
| |
Journal of internal medicine, Vol. 266, No. 6. (December 2009), pp. 527-536.
by G. Gruden, G. Bruno, N. Chaturvedi, et al.D. Burt, S. Pinach, C. Schalkwijk, C. D. Stehouwer, D. R. Witte, J. H. Fuller, P. Cavallo-Perin, EURODIAB Prospective Complications Study Group
Abstract
OBJECTIVES: The heat shock proteins 60 and 70 (HSP60, HSP70) play an important role in cytoprotection. Under stress conditions they are released into the circulation and elicit an immune response. Anti-HSP60 and anti-HSP70 antibody levels have been associated with cardiovascular disease. Type 1 diabetes is associated with a greatly increased risk of micro- and macrovascular complications. Therefore, we investigated whether anti-HSP60 and anti-HSP70 antibody levels were associated with micro- and macrovascular complications in type 1 diabetic patients. DESIGN: A cross-sectional nested ...
|
| |
Annals of internal medicine, Vol. 151, No. 1. (7 July 2009)
Abstract
BACKGROUND: Microalbuminuria in diabetes is strongly predictive of nephropathy, end-stage renal disease, and premature cardiovascular morbidity and mortality. Effective preventive therapies are therefore a clinical priority. OBJECTIVE: To determine whether the angiotensin-receptor blocker candesartan compared with placebo affects microalbuminuria incidence or rate of change in albuminuria in type 1 and type 2 diabetes. DESIGN: 3 randomized trials of the DIRECT (Diabetic Retinopathy Candesartan Trials) Program. SETTING: 309 secondary care centers. PATIENTS: 3326 and 1905 patients with type 1 and type 2 ...
|
| |
Diabetologia
Abstract
Abstract Aims/hypothesis Plasma soluble receptor for AGE (sRAGE) may reflect the activity of the AGE–RAGE axis, which has been proposed as a potential mechanism linking hyperglycaemia to vascular complications in diabetes. We have therefore investigated: (1) whether sRAGE is associated with greater prevalence of cardiovascular disease (CVD) and microvascular complications in type 1 diabetic individuals; and (2) the extent to which any such associations are explained by markers of endothelial and renal dysfunction and inflammation. Methods The study included 477 individuals (234 women; ...
|
| |
Diabetologia, Vol. 47, No. 6. (June 2004), pp. 1020-1028.
Abstract
AIMS/HYPOTHESIS: Type 1 diabetic patients who develop microalbuminuria are clearly disadvantaged in terms of their risk of morbidity and mortality from renal and cardiovascular diseases. It is therefore important to identify potential factors that can predict progression to macroalbuminuria. METHODS: This is a 7-year follow-up study of 352 microalbuminuric Type 1 diabetic patients from 31 European centres. Risk factors at baseline were compared in patients who progressed to macroalbuminuria and in patients who remained microalbuminuric or reverted to normoalbuminuria. Risk factors ...
|
| |
Cochrane database of systematic reviews (Online), No. 4. (2007)
Abstract
BACKGROUND: Hypertension and diabetes mellitus are closely associated diseases which are both strongly related to the risk of cardiovascular disease. OBJECTIVES: To assess the effect of intervention, both pharmacological and non-pharmacological, to reduce blood pressure in people with diabetes mellitus on all cause mortality, specific causes of death, including cardiovascular disease, stroke, ischaemic heart disease and renal disease, morbidity associated with macro- and microvascular complications of diabetes mellitus and also side effects of the interventions and their influence on quality of ...
|
| |
Nature Biotechnology, Vol. 26, No. 5. (27 April 2008), pp. 561-569.
by Akin Akinc, Andreas Zumbuehl, Michael Goldberg, et al.Elizaveta S. Leshchiner, Valentina Busini, Naushad Hossain, Sergio A. Bacallado, David N. Nguyen, Jason Fuller, Rene Alvarez, Anna Borodovsky, Todd Borland, Rainer Constien, Antonin de Fougerolles, J. Robert Dorkin, K. Narayanannair Jayaprakash, Muthusamy Jayaraman, Matthias John, Victor Koteliansky, Muthiah Manoharan, Lubomir Nechev, June Qin, Timothy Racie, Denitza Raitcheva, Kallanthottathil G. Rajeev, Dinah W. Y. Sah, Jurgen Soutschek, Ivanka Toudjarska, Hans-Peter Vornlocher, Tracy S. Zimmermann, Robert Langer, Daniel G. Anderson
Abstract
The safe and effective delivery of RNA interference (RNAi) therapeutics remains an important challenge for clinical development. The diversity of current delivery materials remains limited, in part because of their slow, multi-step syntheses. Here we describe a new class of lipid-like delivery molecules, termed lipidoids, as delivery agents for RNAi therapeutics. Chemical methods were developed to allow the rapid synthesis of a large library of over 1,200 structurally diverse lipidoids. From this library, we identified lipidoids that facilitate high levels of ...
|
| |
Ann Rheum Dis, Vol. 65, No. 10. (1 October 2006), pp. 1368-1372.
by L. R. Harrold, R. A. Yood, T. R. Mikuls, et al.S. E. Andrade, J. Davis, J. Fuller, K. A. Chan, D. Roblin, M. A. Raebel, A. Von Worley, R. Platt, K. G. Saag
Abstract
Background: Little is known about the characteristics, evaluation and treatment of women with gout. Objective: To examine the epidemiological differences and differences in treatment between men and women in a large patient population. Methods: The data from approximately 1.4 million people who were members of seven managed care plans in the USA for at least 1 year between 1 January 1999 and 31 December 2003 were examined. Adult members who had pharmacy benefits and at least two ambulatory claims ...
|