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Published on: December 21, 2016
Serum T50 predicts cardiovascular mortality in individuals with type 2 diabetes: A prospective cohort study
Amarens van der Vaart1,2, Coby Eelderink1, Harry van Goor3
1Departments of Internal Medicine, Divisions of Nephrology, University Medical Center Groningen, University of Groningen, Groningen, the Netherlands.
Insights
The serum T50 test can predict cardiovascular mortality in type 2 diabetes patients. Lower T50 levels indicate a higher risk of death, aiding in risk stratification for better patient outcomes.
Area of Science:
- Cardiology
- Diabetology
- Biochemistry
Background:
- Individuals with type 2 diabetes (T2D) face elevated cardiovascular disease (CVD) risk.
- The serum T50 test measures calciprotein particle transformation time.
- Traditional risk factors do not fully capture CVD risk in T2D.
Purpose of the Study:
- To determine if serum T50 predicts cardiovascular mortality in T2D patients.
- To assess T50's predictive value independent of established risk factors.
Main Methods:
- Prospective cohort study of 621 T2D patients.
- Cox regression models analyzed the association between serum T50 and mortality.
- Risk prediction improvement was assessed using Harrell's C statistic.
Main Results:
- A 60-minute decrease in serum T50 was linked to a 32% increased risk of cardiovascular mortality (HR 1.32).
- Lower T50 levels also correlated with a 15% higher risk of all-cause mortality (HR 1.15).
- These findings remained consistent in sensitivity analyses.
Conclusions:
- Serum T50 enhances cardiovascular and all-cause mortality risk prediction in T2D.
- The T50 test can aid in risk stratification for T2D patients.
- T50 may guide therapeutic strategies to mitigate cardiovascular mortality.
Background And Aims:
Individuals with type 2 diabetes (T2D) have a higher risk of cardiovascular disease, compared with those without T2D. The serum T50 test captures the transformation time of calciprotein particles in serum. We aimed to assess whether serum T50 predicts cardiovascular mortality in T2D patients, independent of traditional risk factors.
Methods:
We analyzed 621 individuals with T2D in this prospective cohort study. Cox regression models were performed to test the association between serum T50 and cardiovascular and all-cause mortality. Causes of death were categorized according to ICD-10 codes. Risk prediction improvement was assessed by comparing Harrell's C for models without and with T50. RESULTS: The mean age was 64.2 ± 9.8 years, and 61% were male. The average serum T50 time was 323 ± 63 min. Higher age, alcohol use, high-sensitive C-reactive protein, and plasma phosphate were associated with lower serum T50 levels. Higher plasma triglycerides, venous bicarbonate, sodium, magnesium, and alanine aminotransferase were associated with higher serum T50 levels. After a follow-up of 7.5[5.4-10.7] years, each 60 min decrease in serum T50 was associated with an increased risk of cardiovascular (fully adjusted HR 1.32, 95% CI 1.08-1.50, and p = 0.01) and all-cause mortality (HR 1.15, 95%CI 1.00-1.38, and p = 0.04). Results were consistent in sensitivity analyses after exclusion of individuals with estimated glomerular filtration rate <45 or <60 mL/min/1.73 m2 and higher plasma phosphate levels.
Conclusions:
Serum T50 improves prediction of cardiovascular and all-cause mortality risk in individuals with T2D. Serum T50 may be useful for risk stratification and to guide therapeutic strategies aiming to reduce cardiovascular mortality in T2D.
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