Rs. Mazze, DETECTION OF GLUCOSE-INTOLERANCE IN PREGNANCY, International journal of clinical pharmacology, therapy and toxicology, 31(9), 1993, pp. 440-448
Current methods for the screening and diagnosis of glucose intolerance
first discovered in pregnancy are reviewed and innovative approaches
to the detection of metabolic disturbances in pregnancy are presented.
Glucose intolerance first detected in pregnancy, termed gestational d
iabetes mellitus (GDM), is amongst the most significant risks of adver
se fetal and maternal outcome. Normal pregnancy is characterized by bo
th insulin resistance and pancreatic B cell compensation. In those pre
gnancies complicated by glucose intolerance reflected in hyperglycemia
, insulin resistance appears to be heightened, both blood flow and tra
nscapillary transport of insulin are compromised and insulin receptor
and post receptor defects are exacerbated. The resulting hyperinsuline
ma and hyperglycemia have, in turn, been associated with accumulated m
aternal fat deposition and fetal macrosomia. This cascade of events co
nstitutes GDM or impaired glucose tolerance. The discovery of GDM is m
ade through a process of screening and diagnosis, employing standardiz
ed oral glucose challenge tests. These tests were designed to identify
those women at risk for subsequent development of non-insulin depende
nt diabetes mellitus. The current efficacy of glucose challenge tests
has been questioned in light of increasing concern over their usefulne
ss in detecting those women at risk for maternal and fetal complicatio
ns of pregnancy. Alternative methods, including both the modification
of the standardized tests, as well as the introduction of newer method
ologies, such as capillary blood glucose monitoring, have been propose
d. The implementation of newer approaches may result in improved detec
tion of those women whose infants are at high risk for both metabolic
and morphologic complications of persistent hyperglycemia in pregnancy
.