Study of Pregnancy Regulation of Insulin and Glucose
Status: | Recruiting |
---|---|
Conditions: | Diabetes |
Therapuetic Areas: | Endocrinology |
Healthy: | No |
Age Range: | 18 - 44 |
Updated: | 4/17/2018 |
Start Date: | February 2016 |
End Date: | August 2021 |
Contact: | Camille E Powe, MD |
Email: | SPRING@partners.org |
Phone: | 617-643-9459 |
It is unknown whether beta cell dysfunction and insulin resistance in Gestational Diabetes
Mellitus (GDM) is representative of a chronic maternal defect, unmasked by pregnancy, or
whether it is the result of an imbalance of a placental hormones. Undiscovered placental
factors which vary between pregnancies likely contribute to the pathogenesis of GDM. To
elucidate the pathophysiology underlying GDM, the investigators will attempt to discover
these factors and characterize pregnancy-associated changes in insulin secretion and
sensitivity in women with and without GDM.
Mellitus (GDM) is representative of a chronic maternal defect, unmasked by pregnancy, or
whether it is the result of an imbalance of a placental hormones. Undiscovered placental
factors which vary between pregnancies likely contribute to the pathogenesis of GDM. To
elucidate the pathophysiology underlying GDM, the investigators will attempt to discover
these factors and characterize pregnancy-associated changes in insulin secretion and
sensitivity in women with and without GDM.
Gestational diabetes mellitus (GDM) complicates 3-7% of pregnancies in the United States and
is associated with perinatal morbidity and a high risk of future maternal type 2 diabetes.
Current prevention and treatment of GDM relies on techniques developed in the type 2 diabetes
population, without regard to unique physiology in pregnancy. GDM occurs in the setting of
profound pregnancy changes in glucose metabolism: late pregnancy is normally characterized by
marked insulin resistance. In order to maintain normal glucose levels and avoid GDM,
pancreatic beta cells must augment insulin secretion to compensate. Women with GDM have
inadequate beta-cell compensation for pregnancy-induced insulin resistance, resulting in
hyperglycemia. It is unknown whether beta cell dysfunction and insulin resistance in GDM is
representative of a chronic maternal defect, unmasked by pregnancy, or whether it is the
result of an imbalance of a placental hormones. Undiscovered placental factors which vary
between pregnancies likely contribute to the pathogenesis of GDM. Discovery of these factors
and elucidation of the pathophysiology underlying GDM will allow for the development better
GDM-specific prevention and treatment strategies.
is associated with perinatal morbidity and a high risk of future maternal type 2 diabetes.
Current prevention and treatment of GDM relies on techniques developed in the type 2 diabetes
population, without regard to unique physiology in pregnancy. GDM occurs in the setting of
profound pregnancy changes in glucose metabolism: late pregnancy is normally characterized by
marked insulin resistance. In order to maintain normal glucose levels and avoid GDM,
pancreatic beta cells must augment insulin secretion to compensate. Women with GDM have
inadequate beta-cell compensation for pregnancy-induced insulin resistance, resulting in
hyperglycemia. It is unknown whether beta cell dysfunction and insulin resistance in GDM is
representative of a chronic maternal defect, unmasked by pregnancy, or whether it is the
result of an imbalance of a placental hormones. Undiscovered placental factors which vary
between pregnancies likely contribute to the pathogenesis of GDM. Discovery of these factors
and elucidation of the pathophysiology underlying GDM will allow for the development better
GDM-specific prevention and treatment strategies.
Inclusion Criteria:
- Women, age 18-44, non-pregnant OR in the 1st trimester of pregnancy (4-14 weeks
gestation),
- Who had GDM in a previous pregnancy
- At risk for diabetes mellitus, as specified by the American Diabetes Association
(ADA):
- BMI ≥ 25 kg/m2 (or BMI ≥ 23 kg/m2 if Asian-American) PLUS one or more of the
following:
- history of giving birth to a neonate weighing > 9 lbs
- first-degree family member with diabetes mellitus
- high-risk ethnic or racial group (African-American, Hispanic, Native American,
Asian-American, or Pacific Islander)
- polycystic ovary syndrome
- hypertension, dyslipidemia if known (HDL<45 and/or triglyceride level >250), or
cardiovascular disease
- physical inactivity
Exclusion Criteria:
- Known pre-existing diabetes mellitus, based on patient report or medical record review
- A1C ≥ 6.5%, detected at study visit 1
- Use of medications known to affect glucose tolerance including corticosteroids,
metformin, sulfonylureas, and others as determined by the investigators.
We found this trial at
1
site
185 Cambridge Street
Boston, Massachusetts 02114
Boston, Massachusetts 02114
617-724-5200
Phone: 617-643-9459
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