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Circulating angiotensin II type I receptor - autoantibodies in diabetic pregnancies
被引:2
|作者:
Linge, Lydia Lande
[1
,2
]
Sugulle, Meryam
[1
,2
,5
,6
,7
]
Wallukat, Gerd
[3
]
Dechend, Ralf
[3
,4
]
Staff, Anne Cathrine
[1
,2
]
机构:
[1] Univ Oslo, Inst Clin Med, Fac Med, Oslo, Norway
[2] Oslo Univ Hosp, Div Gynaecol & Obstet, Oslo, Norway
[3] Expt & Clin Res Ctr, Joint Cooperat Max Delbruck Ctr Mol Med Helmholtz, Berlin, Germany
[4] HELIOS Klin, Dept Cardiol & Nephrol, Berlin, Germany
[5] Oslo Univ Hosp, Div Gynaecol & Obstet, Oslo, Norway
[6] Univ Oslo, Oslo, Norway
[7] POB 4956,Nydalen, N-0424 Oslo, Norway
关键词:
Angiotensin II Type I Receptor autoantibodies;
Biomarkers;
Cardiovascular disease;
Diabetes mellitus;
Placental growth factor;
Pregnancy;
Renin-angiotensin-aldosterone system;
Soluble fms-like tyrosine kinase-1;
PLACENTAL GROWTH-FACTOR;
AGONISTIC ANTIBODIES;
CARDIOVASCULAR-DISEASE;
SYSTEM;
AT(1);
RISK;
PREVENTION;
D O I:
10.1016/j.jri.2022.103777
中图分类号:
R392 [医学免疫学];
Q939.91 [免疫学];
学科分类号:
100102 ;
摘要:
Pregnant women with either pre-existing or gestational diabetes mellitus are at increased risk of preeclampsia as well as future cardiovascular disease. The renin-angiotensin system is dysregulated in both diabetes mellitus and preeclampsia. In preeclampsia, maternal levels of circulating agonistic autoantibodies against the angiotensin II Type I receptor (AT1-AAs) are increased. Circulating AT1-AAs are thought to contribute to both the patho-physiology of preeclampsia and the increased risk of future cardiovascular disease. Studies exploring AT1-AA in diabetes outside pregnancy suggest their potential for both metabolic and cardiovascular pathogenicity. No studies have investigated AT1-AAs in diabetic pregnancies. We hypothesized elevated maternal circulating AT1- AA levels in pregnancies complicated by any type of diabetes mellitus. Third-trimester maternal serum from 39 women (controls: n symbolscript 10; type 1 diabetes: n symbolscript 9; type 2 diabetes: n symbolscript 10; gestational symbolscript were analyzed for AT1-AA using an established bioassay method. Circulating AT1-AAs were present in 70% (7/10) of the controls and 83% (24/29) of the diabetes group (P symbolscript 0.399). Presence of AT1-AA was correlated to hsCRP levels (P symbolscript 0.036), but neither with maternal circulating angiogenic factors (soluble fms-like tyrosine kinase-1 and placental growth factor), nor with maternal or fetal characteristics indicative of metabolic disease or placental dysfunction. Our study is the first to demonstrate presence of circulating AT1-AAs in pregnant women with any type of diabetes. Our findings suggest AT1-AAs presence in pregnancy independently of placental dysfunction, nuancing the current view on their pathogenicity. Whether AT1-AAs per se contribute to increased risk of adverse pregnancy outcomes and future cardiovascular disease remains currently unanswered.
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