z-logo
open-access-imgOpen Access
Spiral Artery Lesions in Relation to Metabolic Control in Diabetes Mellitus
Author(s) -
Björk O.,
Persson B.,
Stangenberg M.,
Václavínková V.
Publication year - 1984
Publication title -
acta obstetricia et gynecologica scandinavica
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.401
H-Index - 102
eISSN - 1600-0412
pISSN - 0001-6349
DOI - 10.3109/00016348409154646
Subject(s) - medicine , pregnancy , diabetes mellitus , fetus , pathological , spiral artery , endocrinology , amniotic fluid , obstetrics , placenta , genetics , biology
. Decidual and intramyometrial spiral arteries from 18 insulin‐dependent diabetic and 18 non‐diabetic women were compared histologically. All women were normoten‐sive and none had signs of pre‐eclampsia. None of the infants in either group had intra‐uterine growth retardation. Metabolic control in the diabetic women was assessed by pregnancy glucose level from the last trimester of pregnancy and by C‐peptide in amniotic fluid and cord blood as a measure of the fetal beta‐cell function. The intramyometrial and decidual parts of the spiral artery were normal in the non‐diabetic group. None of the diabetic patients showed pathological changes in the intramyometrial part of the spiral artery. Two of the 18 diabetic patients had pathological changes (intramural fibrosis) in the decidual portion of the spiral artery. These two women had signs of diabetic angiopathy (White's class D and F) and in one of them, the background diabetic retinopathy progressed markedly during pregnancy. The pregnancy glucose level was above normal (>6.2 mM/1) in 3 of 18 diabetics. The C‐peptide values in amniotic fluid and cord blood were above normal in 11 of 17 and in 5 of 17, respectively. Both patients with spiral artery lesions had pregnancy glucose levels in the upper range, 5.86 and 5.98 mM/1, respectively and the highest value of C‐peptide in the amniotic fluid and cord blood, suggesting exaggerated fetal beta‐cell function.

The content you want is available to Zendy users.

Already have an account? Click here to sign in.
Having issues? You can contact us here