Trends in cardiovascular risk factor management in type 1 diabetes by sex

https://doi.org/10.1016/j.jdiacomp.2018.01.003Get rights and content

Abstract

Aims

DCCT showed that intensive type 1 diabetes management reduces complication incidence but did not focus on other cardiovascular disease risk factors, whose control in type 1 diabetes has not been well-studied. We assessed trends in cardiovascular risk factors in type 1 diabetes and attainment of concurrent American Diabetes Association (ADA) guidelines/recommendations (for HbA1c, blood pressure, LDL cholesterol, triglycerides) for complication prevention.

Methods

Individuals with childhood-onset type 1 diabetes (n = 658; 49.4% women; baseline (1986–1988) median age 27 and duration 19 years) were followed biennially for up to 25 years, with surveys and/or examinations.

Results

At the latest recorded follow-up, achievement of concurrent ADA recommendations increased for HbA1c (from 9.7 to 25.6%, p < .0001); was unchanged for blood pressure (from 89.7% to 87.4%, p = .36); and decreased for LDL cholesterol (from 62.3 to 39.7%, p < .0001). Adoption of intensive insulin therapy (from 5.9 to 64.4%, p < .0001) and hypercholesterolemia (from 67.3 to 78.9%, p = .0006) also increased. Overall, the proportion meeting all four recommendations was essentially unaltered (from 6.8% to 7.6%) (p = .69). Results were similar by gender.

Conclusions

Although the adoption of intensive insulin therapy and obtaining ADA HbA1c recommendations are increasing, overall cardiovascular risk factor compliance remains low and merits further intervention.

Introduction

The incidence of type 1 diabetes continues to increase annually1 and with that comes a growing concern for the burden posed by diabetes-associated microvascular and macrovascular complications.2 Increased risk of cardiovascular disease (CVD) has been repeatedly recognized as a complication of type 1 diabetes, and recent data still suggest a 10-fold greater risk.3 There are multiple modifiable risk factors, such as HbA1c, blood pressure, lipids, smoking, and obesity, which can be intervened upon to reduce CVD risk in type 1 diabetes.4 Indeed, results from the Diabetes Control and Complications Trial (DCCT) demonstrated that intensive management of hyperglycemia greatly reduces the development and progression of micro5- and macro-vascular6 disease in type 1 diabetes, transforming care for these individuals. Unfortunately, years after the advent of intensive insulin therapy, the rates of CVD are still higher in type 1 diabetes compared to the general population, suggesting that tighter control of non-glycemic factors might be beneficial. However, to what extent improvements in cardiovascular risk factor control have occurred in the general type 1 diabetes population and whether they may differ between men and women, is not clear. An earlier study suggested poor adherence.7 In the present study, we aimed to assess trends in CVD risk factors among men and women over the 25-year follow-up of a cohort study of individuals with childhood-onset type 1 diabetes.

For >20 years, the American Diabetes Association (ADA) has disseminated key recommendations for diabetes care standards and guidelines in an attempt to improve management.8 Understanding how well these guidelines are attained may give insight into what areas of care are needed to potentially reduce the continuing high CVD rates. We therefore aimed to determine the proportion of individuals within this type 1 diabetes cohort falling within the guidelines set by the ADA for the prevention and management of diabetes complications. We additionally assessed trends over time in the proportions adopting intensive insulin therapy as well as in the proportions of overweight/obesity, hypercholesterolemia and hypertension, given their close interrelation with ADA goal attainment.

Section snippets

The Pittsburgh epidemiology of diabetes complications (EDC) study

The EDC study is a historical prospective cohort study of risk factors for complications resulting from childhood-onset (<17 years old) type 1 diabetes. Participants were either diagnosed, or seen within 1 year of diagnosis, at Children's Hospital of Pittsburgh between 1950 and 1980. The cohort, which has been shown to be representative of the Allegheny County, Pennsylvania, type 1 diabetes population,9 has been described in detail elsewhere.10,11 Briefly, participants have been followed by

Results

The baseline characteristics for the total cohort of childhood-onset type 1 diabetes (n = 658, 49.4% female), as well as the characteristics stratified by gender, are presented in Table 1. Overall, the median (interquartile range) age and duration of diabetes were 27 (21.9, 33.3) years and 18.5 (13.2, 25.5) years, respectively. HbA1c was high for both men and women, with an overall median of 8.6% (7.7%, 9.7%) or 70 mmol/mol (61 mmol/mol, 83 mmol/mol). The cohort had a median body mass index

Discussion

In this cohort of individuals with childhood-onset type 1 diabetes, we observed that the proportion falling within the ADA recommendations for HbA1c increased, whereas the proportion meeting the ADA recommendations for LDL-C gradually decreased over the 25-year follow up period, reflecting the lowering of LDL-C goals. On the contrary, attainment of blood pressure and triglyceride goals remained high throughout follow-up. When analyses were restricted to individuals age 35–45 years at each time

Conflict of interest statement

The authors declare no conflicts of interest.

Acknowledgments

We thank all study participants for their invaluable contributions as well as the Epidemiology of Diabetes Complications (EDC) study staff.

Funding sources

This research was supported by NIH grant DK34818 and the Rossi Memorial Fund.

Author contributions

KS conducted the analysis and wrote the manuscript; TC researched, analyzed data, and wrote/edited the manuscript; TJO designed the EDC study and reviewed/edited the manuscript. This study was part of author KS’ Master's essay.

Prior presentation

Preliminary results were presented in abstract form at the 76th Scientific Sessions of the American Diabetes Association, New Orleans, LA, 10–14 June 2016.

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