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Variants in Fetal Genome Associated with Risk of Preeclampsia in Mother

For the first time, a relationship has been found between fetal genes and the risk of preeclampsia in the mother. Norwegian researchers, including a team from the Norwegian University of Science and Technology (NTNU), figure prominently in the international group that presented the discovery in Nature Genetics, first published online earlier this summer, on June 19, 2017. The article is titled “Variants in the Fetal Genome Near FLT1 Are Associated with Risk Of Preeclampsia.” Preeclampsia affects approximately 3 per cent of births in Norway; worldwide, that number is estimated to be about 5 per cent. In the vast majority of cases, the mother has mild symptoms, typically high blood pressure. Nevertheless, preeclampsia is one of the leading causes of death in both mothers and babies around the time of birth, and sometimes the only way to treat it is to deliver the baby, even prematurely. "For the first time ever, we have discovered a fetal gene that increases the risk of preeclampsia," says Dr. Ann-Charlotte Iversen at the Department of Clinical and Molecular Medicine at NTNU. She says there has not been much research on the role of fetal genes in triggering the illness. Preeclampsia usually begins with a problem in the placenta, which is mainly composed of fetal cells. For that reason, it makes sense that fetal cells might have a hand in causing the illness, Dr. Iversen said, even though it is the mother's symptoms during the last part of the pregnancy that lead to the diagnosis. Dr. Iversen is head of a research group at NTNU's Centre of Molecular Inflammation Research (CEMIR). "Our findings are particularly solid for three reasons: we analyzed a large number of individuals, we found several genetic variables that all point to the same gene associated with the risk, and two independent population studies confirmed that this gene is associated with the risk," Dr. Iversen said. There are also a number of major studies that support the conclusions. CEMIR is one of 12 partners from 6 different countries in an EU project called InterPregGen, which was created in 2011.

"We are all working together to uncover the genetic risk factors for preeclampsia in the mother and fetus. We have linked a number of major European population studies to conduct the world's largest genetic study of preeclampsia," says Dr. Iversen. "Our contribution to the project has been information on a group of women from the HUNT study who have had problematic and healthy pregnancies, as well as information from the Preeclampsia Biobank, which has been collected independently."

The Nature Genetics article includes analyses of material from the Preeclampsia Biobank, including blood samples and tissue samples from placentas that have been collected at St. Olavs and Haukeland University Hospitals.


The genetic variants identified by the researchers are associated with the FLT-1 gene, which encodes a protein that in soluble form is known as a biomarker for preeclampsia.

The protein contributes to damaging the mother's vascular system so that she develops symptoms such as high blood pressure and an increased amount of protein in the urine. This happens as a result of problems with the placenta, essentially because fetal cells in the placenta produce the protein.

"We have shown here that the risk of disease may be because changes in the gene affect how the protein works and how it affects the mother. This is a fetal gene that gives the mother an increased risk of developing preeclampsia. This find clearly brings us closer to a better understanding of preeclampsia," Dr. Iversen said.


CEMIR's contribution to the effort came in the form of three researchers: Gabriela Silva, a PhD candidate; gynecologist and postdoctoral physician Dr. Liv Cecilie Vestrheim Thomsen (who also works at Helse Vest, the Western Norway Regional Health Authority), and Dr. Iversen herself. The research center has solid expertise in molecular analyses of the activation of the placenta.

"The EU project has brought together geneticists, statisticians, and clinicians. NTNU and CEMIR's expertise has been a complementary strength," says Dr. Iversen.

Gabriela Silva analyzed the protein expression of FLT-1 in placental samples from sick and healthy pregnant women, while Dr. Thomsen has been central in collecting the placentas.

"We have compared the result with the occurrence of the genes associated with the risk. This means that we have conducted a functional follow-up of the gene discovery, which has now been published," Dr. Iversen says.

CEMIR is one of the foremost research centers in Norway and has been selected as a Centre of Excellence by the Research Council of Norway.


"CEMIR's Research Group for inflammation in pregnancy has as its goal to figure out which disease mechanisms cause problems with the placenta and lead to the development of preeclampsia," says Dr. Iversen.

The group is working to understand what goes wrong so they can detect problems early in a pregnancy. The goal is to predict which women will develop the disease.

"Our molecular analyses have identified specialized fetal cells in the placenta as the main actors in preeclampsia. These are the same fetal cells that have been identified with this new genetic discovery. This reinforces our conviction that fetal cells play an active role, and represents a big change in thinking, because research has previously focused most on the mother's immune system. If we want to prevent preeclampsia, we have to understand the foundation for the disease," says Dr. Iversen.

[Press release] [Nature Genetics abstract]