Multiple risk factor interventions and inflammatory biomarkers in high risk individuals with type 2 diabetes

2012 ◽  
Vol 95 (3) ◽  
pp. 386-388 ◽  
Author(s):  
Andre Pascal Kengne ◽  
Eugene Sobngwi ◽  
John Chalmers
2019 ◽  
Vol 21 (5) ◽  
Author(s):  
Caroline Holm Nørgaard ◽  
Mitra Mosslemi ◽  
Christina J.-Y. Lee ◽  
Christian Torp-Pedersen ◽  
Nathan D. Wong

2005 ◽  
Vol 142 (5) ◽  
pp. 313 ◽  
Author(s):  
George Davey Smith ◽  
Yiscah Bracha ◽  
Kenneth H. Svendsen ◽  
James D. Neaton ◽  
Steven M. Haffner ◽  
...  

2001 ◽  
Vol 3 (1) ◽  
pp. 1-8 ◽  
Author(s):  
John R. Cockcroft ◽  
Ian B. Wilkinson ◽  
Hannele Yki-Järvinen

2014 ◽  
Vol 13 (1) ◽  
pp. 95 ◽  
Author(s):  
Norbert J Tripolt ◽  
Sophie H Narath ◽  
Michaela Eder ◽  
Thomas R Pieber ◽  
Thomas C Wascher ◽  
...  

2020 ◽  
Author(s):  
Digsu N. Koye ◽  
Joanna Ling ◽  
John Dibato ◽  
Kamlesh Khunti ◽  
Olga Montvida ◽  
...  

<b>Objectives: </b>To evaluate temporal prevalence trend, cardiometabolic risk factors, and the risk of atherosclerotic cardiovascular disease (ASCVD) and all-cause mortality (ACM) in incident young- and usual-onset type 2 diabetes. <p><b>Research Design and Methods: </b>From the UK primary care database, 370,854 people with new diagnosis of type 2 diabetes from 2000 to 2017 were identified. Analyses were conducted by age groups (18-39, 40-49, 50-59, 60-69, 70-79 years) and high/low risk status without history of ASCVD at diagnosis - ≥ two of current smoking, high SBP, high LDL-C or chronic kidney disease were classified as high-risk. </p> <p><b>Results:</b> Proportion of people aged <50 years at diagnosis increased during 2000-2010 and then stabilised. The incidence rates of ASCVD and ACM declined in people aged ≥50 years, but did not decrease in people <50 years. Compared to people aged ≥50 years, those aged 18-39 years at diagnosis had higher obesity (71% obese), higher HbA1c (8.6%), 71% had high LDL-C, while only 18% were on cardio-protective therapy. Although 2% in this age group had ASCVD at diagnosis, 23% were identified as high-risk. In the 18-39 years group, the adjusted average years to ASCVD /ACM in high-risk individuals (years (95% CI): 9.1 (8.2–10.0) /9.3 (8.1–10.4)) were similar to those with low-risk (years (95% CI): 10.0 (9.5 – 10.5) /10.5 (9.7–11.2)). However, individuals ≥50 years with high-risk were likely to experience an ASCVD event 1.5 - 2 years earlier and death 1.1 – 1.5 years earlier compared to low-risk groups (p<0.01). </p> <p><b>Conclusions: </b>Unlike usual-onset,<b> </b>young-onset type 2 diabetes have similar cardiovascular and mortality risk irrespective of their cardiometabolic risk factor status at diagnosis. The guidelines on the management of young-onset type 2 diabetes for intensive risk-factor management and cardioprotective therapies need to be urgently re-evaluated through prospective studies.<b> </b></p>


2019 ◽  
Vol 65 (6) ◽  
pp. 781-790 ◽  
Author(s):  
Thomas A Zelniker ◽  
David A Morrow ◽  
Ofri Mosenzon ◽  
Yared Gurmu ◽  
Kyungah Im ◽  
...  

Abstract BACKGROUND Cardiac and renal diseases commonly occur with bidirectional interactions. We hypothesized that cardiac and inflammatory biomarkers may assist in identification of patients with type 2 diabetes mellitus (T2DM) at high risk of worsening renal function. METHODS In this exploratory analysis from SAVOR-TIMI 53, concentrations of high-sensitivity cardiac troponin T (hs-TnT), N-terminal pro–B-type natriuretic peptide (NT-proBNP), and high-sensitivity C-reactive protein (hs-CRP) were measured in baseline serum samples of 12310 patients. The primary end point for this analysis was a ≥40% decrease in estimated glomerular filtration rate (eGFR) at end of treatment (EOT) at a median of 2.1 years. The relationships between biomarkers and the end point were modeled using adjusted logistic and Cox regression. RESULTS After multivariable adjustment including baseline renal function, each biomarker was independently associated with an increased risk of ≥40% decrease in eGFR at EOT [Quartile (Q) Q4 vs Q1: hs-TnT adjusted odds ratio (OR), 5.63 (3.49–9.10); NT-proBNP adjusted OR, 3.53 (2.29–5.45); hs-CRP adjusted OR, 1.84 (95% CI, 1.27–2.68); all P values ≤0.001]. Furthermore, each biomarker was independently associated with higher risk of worsening of urinary albumin-to-creatinine ratio (UACR) category (all P values ≤0.002). Sensitivity analyses in patients without heart failure and eGFR &gt;60 mL/min provided similar results. In an adjusted multimarker model, hs-TnT and NT-proBNP remained significantly associated with both renal outcomes (all P values &lt;0.01). CONCLUSIONS hs-TnT, NT-proBNP, and hs-CRP were each associated with worsening of renal function [reduction in eGFR (≥40%) and deterioration in UACR class] in high-risk patients with T2DM. Patients with high cardiac or inflammatory biomarkers should be treated not only for their risk of cardiovascular outcomes but also followed for renal deterioration.


2012 ◽  
Vol 95 (3) ◽  
pp. 389-398 ◽  
Author(s):  
Xanthia F. Samaropoulos ◽  
Laney Light ◽  
Walter T. Ambrosius ◽  
Santica M. Marcovina ◽  
Jeffrey Probstfield ◽  
...  

Sign in / Sign up

Export Citation Format

Share Document