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Serum ACE Predicts Severe Hypoglycemia in Children and Adolescents With Type 1 Diabetes
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OBJECTIVE—To investigate whether risk of severe hypoglycemia is related to serum (S) ACE level during intensive treatment in type 1 diabetic children.
RESEARCH DESIGN AND METHODS—A cohort of 86 intensively treated type 1 diabetic patients was studied during 1999–2000. In 1999, the age range was 7–19 years (median 12.8), diabetes duration was 1.2–14.7 years (5.3), insulin dose was 0.4–1.7 units · kg−1 · 24 h−1 (1.0), and the HbA1c year mean was 4.7–10.2% (6.8). HbA1c, insulin doses, and events of severe hypoglycemia (needing assistance from another person) were prospectively registered at regular visits, scheduled quarterly. S-ACE was determined once.
RESULTS—Severe hypoglycemia was correlated to S-ACE (r = 0.22, 95% CI 0.01–0.41, P = 0.0093). The square root of severe hypoglycemia was correlated to S-ACE (r = 0.27, 95% CI 0.06–0.45, P = 0.0093). Patients with S-ACE at the median level or above (n = 44) reported a mean of 3.0 yearly events of severe hypoglycemia compared with 0.5 events in patients with S-ACE lower than the median (n = 42) (P = 0.0079). Of the patients with an S-ACE at the median level or above, 27 (61%) reported severe hypoglycemia, compared with 17 (40%) patients with an S-ACE lower than the median (P = 0.0527). Insulin dose, HbA1c, age, onset age, duration, C-peptide, and sex did not differ between these two groups. S-ACE was negatively correlated with age (r = −0.27, 95% CI −0.46 to 0.07, P = 0.0265) but not with HbA1c, duration, or blood pressure.
CONCLUSIONS—The elevated rate of severe hypoglycemia among patients with higher S-ACE suggests, among other factors, that a genetic determinant for severe hypoglycemia exists. Further evaluation is needed before the clinical usefulness of this test can be elucidated.
Title: Serum ACE Predicts Severe Hypoglycemia in Children and Adolescents With Type 1 Diabetes
Description:
OBJECTIVE—To investigate whether risk of severe hypoglycemia is related to serum (S) ACE level during intensive treatment in type 1 diabetic children.
RESEARCH DESIGN AND METHODS—A cohort of 86 intensively treated type 1 diabetic patients was studied during 1999–2000.
In 1999, the age range was 7–19 years (median 12.
8), diabetes duration was 1.
2–14.
7 years (5.
3), insulin dose was 0.
4–1.
7 units · kg−1 · 24 h−1 (1.
0), and the HbA1c year mean was 4.
7–10.
2% (6.
8).
HbA1c, insulin doses, and events of severe hypoglycemia (needing assistance from another person) were prospectively registered at regular visits, scheduled quarterly.
S-ACE was determined once.
RESULTS—Severe hypoglycemia was correlated to S-ACE (r = 0.
22, 95% CI 0.
01–0.
41, P = 0.
0093).
The square root of severe hypoglycemia was correlated to S-ACE (r = 0.
27, 95% CI 0.
06–0.
45, P = 0.
0093).
Patients with S-ACE at the median level or above (n = 44) reported a mean of 3.
0 yearly events of severe hypoglycemia compared with 0.
5 events in patients with S-ACE lower than the median (n = 42) (P = 0.
0079).
Of the patients with an S-ACE at the median level or above, 27 (61%) reported severe hypoglycemia, compared with 17 (40%) patients with an S-ACE lower than the median (P = 0.
0527).
Insulin dose, HbA1c, age, onset age, duration, C-peptide, and sex did not differ between these two groups.
S-ACE was negatively correlated with age (r = −0.
27, 95% CI −0.
46 to 0.
07, P = 0.
0265) but not with HbA1c, duration, or blood pressure.
CONCLUSIONS—The elevated rate of severe hypoglycemia among patients with higher S-ACE suggests, among other factors, that a genetic determinant for severe hypoglycemia exists.
Further evaluation is needed before the clinical usefulness of this test can be elucidated.
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