TY - JOUR
T1 - Placental peptides regulating islet adaptation to pregnancy: clinical potential in gestational diabetes mellitus
T2 - • Endocrine & Metabolic Diseases • Gastrointestinal
AU - Simpson, Sian
AU - Smith, Lorna
AU - Bowe, James
PY - 2018/12
Y1 - 2018/12
N2 - Pregnancy involves a progressive increase in insulin resistance and the β-cells must adapt to compensate and prevent gestational diabetes (GDM). In this review we discuss the evidence for placental peptides, including placental lactogen, hepatocyte growth factor, adiponectin and leptin, playing a role in the islet adaptation to pregnancy. The difficulties of translating data from rodent models into human pregnancy are covered and we summarise studies investigating associations between serum placental peptides and GDM risk. In conclusion, current data support important roles for placental peptides interacting to support β-cells during pregnancy, however mechanisms involved in humans are unclear. Further work in humans is required, but placental peptides have clinical potential from both a diagnostic and therapeutic perspective.
AB - Pregnancy involves a progressive increase in insulin resistance and the β-cells must adapt to compensate and prevent gestational diabetes (GDM). In this review we discuss the evidence for placental peptides, including placental lactogen, hepatocyte growth factor, adiponectin and leptin, playing a role in the islet adaptation to pregnancy. The difficulties of translating data from rodent models into human pregnancy are covered and we summarise studies investigating associations between serum placental peptides and GDM risk. In conclusion, current data support important roles for placental peptides interacting to support β-cells during pregnancy, however mechanisms involved in humans are unclear. Further work in humans is required, but placental peptides have clinical potential from both a diagnostic and therapeutic perspective.
UR - http://www.scopus.com/inward/record.url?scp=85052927715&partnerID=8YFLogxK
U2 - 10.1016/j.coph.2018.08.004
DO - 10.1016/j.coph.2018.08.004
M3 - Article
SN - 1471-4892
VL - 43
SP - 59
EP - 65
JO - Current Opinion in Pharmacology
JF - Current Opinion in Pharmacology
ER -