Category | Fasting plasma glucose before test | Plasma glucose 2 hours after ingestion of 1.75 g/kg glucose | Clinical outcomes |
Normal glucose tolerance (NGT)* | <126 mg/dL (7 mmol/L) | <140 mg/dL (7.8 mmol/L) | In general, clinically stable |
Prediabetes categories | |||
Indeterminate glycemia (INDET) | <126 mg/dL (7 mmol/L) | <140 mg/dL (7.8 mmol/L), with a mid-point peak >200 mg/dL (11.1 mmol/L) | Clinical impact unclear but evidence suggests increased risk of morbidity |
Impaired glucose tolerance (IGT) | <126 mg/dL (7 mmol/L) | 140 to 200 mg/dL (7.8 to 11.1 mmol/L) | |
CFRD | |||
CFRD without fasting hyperglycemia¶ | <126 mg/dL (7 mmol/L) | ≥200 mg/dL (11.1 mmol/L) | Increased morbidity and mortality |
CFRD with fasting hyperglycemia¶ | ≥126 mg/dL (7 mmol/L) | OGTT not necessary |
CFRD: cystic fibrosis-related diabetes; OGTT: oral glucose tolerance test.
* In the past, fasting plasma glucose 100 to <126 mg/dL (5.6 to 7 mmol/L) has been termed impaired fasting glucose. However, because the clinical significance of impaired fasting glucose in people with cystic fibrosis is unclear, it is not generally used as a diagnostic category in the CFRD spectrum.
¶ Historically, CFRD was subcategorized by the absence or presence of fasting hyperglycemia (fasting plasma glucose ≥126 mg/dL [7.0 mmol/L]). Fasting hyperglycemia usually represents a more advanced stage of disease and is associated with microvascular complications[1]. However, because treatment may be beneficial for patients with and without fasting hyperglycemia, this distinction is no longer made[2].
Adapted from: Moran A, Hardin D, Rodman D, Allen HF, Beall RJ, Borowitz D, et al. Diagnosis, screening and management of cystic fibrosis related diabetes mellitus: a consensus conference report. Diabetes Research Clin Practice 1999; 45:61.
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