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Published on: January 7, 2018
Low fasting plasma glucose level predicts morbidity and mortality in symptomatic adults with congenital heart disease
Hideo Ohuchi1, Kenji Yasuda1, Shin Ono1
1Department of Pediatric Cardiology and Adult Congenital Heart Disease, National Cerebral and Cardiovascular Center, Osaka, Japan.
Insights
Low fasting blood glucose (FPG) is common in adults with complex congenital heart disease (ACHD) and predicts hospitalization and mortality in symptomatic patients. This finding is crucial for understanding ACHD prognosis.
Area of Science:
- Cardiology
- Endocrinology
- Metabolic Disorders
Background:
- Adults with complex congenital heart disease (ACHD) exhibit a high prevalence of abnormal glucose regulation (AGR).
- The prognostic implications of AGR in ACHD patients remain incompletely understood.
Purpose of the Study:
- To investigate the prognostic value of abnormal glucose regulation (AGR) in adults with complex congenital heart disease (ACHD).
Main Methods:
- A 75g oral glucose tolerance test was administered to 438 ACHD patients and 27 healthy controls.
- Associations between AGR parameters and clinical events (hospitalization, all-cause mortality) were analyzed.
Main Results:
- Lower fasting blood glucose (FPG) levels were observed in unrepaired and Fontan patients compared to controls.
- Low FPG (≤ 80 mg/dl) was more prevalent in all ACHD groups than in healthy controls.
- New York Heart Association class and low FPG independently predicted hospitalization and mortality, while postprandial glucose was not an independent predictor.
Conclusions:
- Low FPG is a frequent finding in ACHD patients.
- Low FPG serves as a significant predictor of morbidity and all-cause mortality, particularly in symptomatic ACHD individuals.
Background:
Adults with complex congenital heart disease (ACHD) have a high prevalence of abnormal glucose regulation (AGR: impaired glucose tolerance and diabetes mellitus). However, the impact of AGR on the prognosis remains unclear.
Purpose:
Our purpose was to clarify the prognostic value of AGR in ACHD.
Methods And Results:
We performed a 75 g oral glucose tolerance test in 438 consecutive patients with ACHD (age 26 ± 8 years), including 38 unrepaired, 148 Fontan, 252 biventricular, and 27 healthy subjects and investigated associations between AGR and clinical events that required hospitalization or caused deaths from all-causes. When compared with the healthy group, fasting blood glucose level (FPG, mg/dl) was lower in the unrepaired and Fontan subjects (p<0.05-0.01) and the prevalence of low FPG (≤ 80 mg/dl) was also higher in the unrepaired (58%), Fontan (47%), and biventricular group (33%) than in the healthy control (11%) (p<0.0001). Postprandial hyperglycemia (area under the curve of glucose: PG-AUC) was higher in all ACHD groups (p<0.0001 for all). New York Heart Association class and lower FPG independently predicted the hospitalization (FPG ≤ 84 mg/dl) and mortality (FPG ≤ 80 mg/dl) (p<0.05-0.0001), while the PG-AUC was not an independent predictor. When compared with the asymptomatic ACHD, symptomatic ACHD with lower FPG had high hazard ratios of 2.2 (95% confidence interval [CI]: 1.3-3.8, p<0.002) and 3.3 (95% CI: 1.2-11.9, p<0.03) for the hospitalizations and all-cause mortality, respectively.
Conclusions:
Low FPG is not uncommon in ACHD and the low FPG predicts the morbidity and all-cause mortality in symptomatic ACHD.
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