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Continuous subcutaneous insulin infusion in adults: glycemic advantage is predicted by venous plasma C-peptide concentrations.
Diabetes Care. 1985 Sep-Oct; 8(5):447-55.DC

Abstract

Continuous subcutaneous insulin infusion (CSII) has been compared with conventional insulin injection treatment (CIT) supplemented by self-monitoring of capillary blood glucose (SMBG) in 18 nonobese adults with insulin-dependent diabetes mellitus (IDDM). Mean daily insulin dosage and rates of hypoglycemia were similar during CSII (duration of treatment 36 +/- 2 wk mean +/- SE) and CIT (31 +/- 1.6 wk). On the basis of fasting C-peptide concentrations and postintravenous glucagon increments of less than 0.1 pmol/ml, subjects were classified C-peptide negative (CP NEG) (N = 11), or C-peptide positive (CP POS) (N = 7). Relative to CIT, CP NEG subjects on CSII had significant decreases in premeal/bedtime and postmeal plasma glucose concentrations and glycosylated hemoglobin (percent of total). CP POS patients during each of CSII and CIT showed glycemic responses equivalent to those of CP NEG patients on CSII. In neither group could results be explained on the basis of improved beta cell function. Thus, therapeutic advantage of CSII was not apparent in IDDM adults retaining significant C-peptide activity.

Authors

No affiliation info availableNo affiliation info availableNo affiliation info availableNo affiliation info available

Pub Type(s)

Comparative Study
Journal Article
Research Support, Non-U.S. Gov't

Language

eng

PubMed ID

3902423

Citation

Rodger, N W., et al. "Continuous Subcutaneous Insulin Infusion in Adults: Glycemic Advantage Is Predicted By Venous Plasma C-peptide Concentrations." Diabetes Care, vol. 8, no. 5, 1985, pp. 447-55.
Rodger NW, Dupre J, Canny CL, et al. Continuous subcutaneous insulin infusion in adults: glycemic advantage is predicted by venous plasma C-peptide concentrations. Diabetes Care. 1985;8(5):447-55.
Rodger, N. W., Dupre, J., Canny, C. L., & Brown, W. F. (1985). Continuous subcutaneous insulin infusion in adults: glycemic advantage is predicted by venous plasma C-peptide concentrations. Diabetes Care, 8(5), 447-55.
Rodger NW, et al. Continuous Subcutaneous Insulin Infusion in Adults: Glycemic Advantage Is Predicted By Venous Plasma C-peptide Concentrations. Diabetes Care. 1985 Sep-Oct;8(5):447-55. PubMed PMID: 3902423.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Continuous subcutaneous insulin infusion in adults: glycemic advantage is predicted by venous plasma C-peptide concentrations. AU - Rodger,N W, AU - Dupre,J, AU - Canny,C L, AU - Brown,W F, PY - 1985/9/1/pubmed PY - 1985/9/1/medline PY - 1985/9/1/entrez SP - 447 EP - 55 JF - Diabetes care JO - Diabetes Care VL - 8 IS - 5 N2 - Continuous subcutaneous insulin infusion (CSII) has been compared with conventional insulin injection treatment (CIT) supplemented by self-monitoring of capillary blood glucose (SMBG) in 18 nonobese adults with insulin-dependent diabetes mellitus (IDDM). Mean daily insulin dosage and rates of hypoglycemia were similar during CSII (duration of treatment 36 +/- 2 wk mean +/- SE) and CIT (31 +/- 1.6 wk). On the basis of fasting C-peptide concentrations and postintravenous glucagon increments of less than 0.1 pmol/ml, subjects were classified C-peptide negative (CP NEG) (N = 11), or C-peptide positive (CP POS) (N = 7). Relative to CIT, CP NEG subjects on CSII had significant decreases in premeal/bedtime and postmeal plasma glucose concentrations and glycosylated hemoglobin (percent of total). CP POS patients during each of CSII and CIT showed glycemic responses equivalent to those of CP NEG patients on CSII. In neither group could results be explained on the basis of improved beta cell function. Thus, therapeutic advantage of CSII was not apparent in IDDM adults retaining significant C-peptide activity. SN - 0149-5992 UR - https://www.unboundmedicine.com/medline/citation/3902423/Continuous_subcutaneous_insulin_infusion_in_adults:_glycemic_advantage_is_predicted_by_venous_plasma_C_peptide_concentrations_ DB - PRIME DP - Unbound Medicine ER -