Diabetes Care, Vol 15, Issue 8 953-959, Copyright © 1992 by American Diabetes Association
Is combination sulfonylurea and insulin therapy useful in NIDDM patients? A metaanalysis
JA Pugh, ML Wagner, J Sawyer, G Ramirez, M Tuley and SJ Friedberg
Audie L. Murphy Memorial Veterans Hospital, San Antonio, Texas 78284.
OBJECTIVE--To assess the efficacy of combination therapy with insulin and
sulfonylurea in the treatment of NIDDM. RESEARCH DESIGN AND
METHODS--Studies published between January 1966 and January 1991 were
identified through a computerized Medline search and by hand searching the
bibliographies of identified articles. We identified 17 eligible
randomized, controlled trials of combination therapy in NIDDM. These trials
had a minimum duration of 8 wk and at least one of three outcome measures
(fasting glucose, HbA1, or C-peptide) with SD or SE of the mean reported to
do metaanalysis. With standardized forms, three independent reviews
abstracted measures of study quality and specific descriptive information
about population, intervention, and outcome measurements. RESULTS--We
calculated effect size and weighted mean changes of the three outcome
measures for control and treatment groups. In the treatment group, the
fasting plasma glucose decreased from a mean of 11.4 mM (206 mg/dl) at
baseline to a mean of 9.16 mM (165 mg/dl) posttreatment, whereas the
control group decreased from (11.3 to 10.8 mM) (204 to 194 mg/dl) (effect
size 0.39, P less than 0.0001). For HbA1, the treatment group decreased
from a baseline of 11.0 to 10.2% compared to 11.0 and 11.2% in the control
group (effect size 0.43, P less than 0.0001). For fasting C-peptide, the
treatment group increased from 0.49 to 0.58 nM (1.45 to 1.75 ng/ml)
compared with 0.47 and 0.43 (1.42 and 1.30) for the control group (effect
size 0.26, P less than 0.017). CONCLUSION--Combined insulin-sulfonylurea
therapy leads to modest improvement in glycemic control compared with
insulin therapy alone. With combined therapy, lower insulin doses may be
used to achieve similar control. Obese patients with higher fasting
C-peptides may be more likely to respond than others.