Medical researchers have obtained a breakthrough in identifying genes that increase the chance for mothers to have dizygotic twins. Researchers believe the findings represent a significant advance in the identification of key mechanisms controlling ovarian function and provide a greater understanding of female fertility and infertility.
Twinning has fascinated human beings over the centuries. Twins are relatively common and occur more than one time per 100 maternities. Roughly two-thirds of all twin pairs are dizygotic or non-identical and are genetically as alike as other siblings.
It has been firmly established that dizygotic twinning has a maternal genetic component, but no one so far has succeeded in identifying the genes for spontaneous DZ twinning after decades of investigations.
An international collaboration* on the genetics of dizygotic twinning led by Dr Hamdi Mbarek and Prof. Dorret Boomsma from the Vrije Universiteit Amsterdam has obtained a breakthrough in identifying genes that increase the chance for mothers to have dizygotic twins. One of these genes also has significant effects on fertility measures, including the age of a girl’s first menstruation, age at menopause, number of children, and age at first (and last) child, but also on polycystic ovary syndrome, which is a major cause of infertility in women.
The findings appear online today in the international scientific journal The American Journal of Human Genetics. Researchers believe the findings represent a significant advance in the identification of key mechanisms controlling ovarian function and provide a greater understanding of female fertility and infertility.
Mbarek and colleagues report two genetic variants. The first variant is close to the gene coding for the secretion of follicle stimulating hormone (the FSHB gene) by the pituitary, the small brain organ that governs almost all major hormonal events in the body. The second variant relates to the so-called SMAD3 gene and is likely to be involved in the way the ovaries respond to follicle stimulating hormone. Both variants result in the multiple follicle growth that is obviously needed for the development of non-identical twins. Non-identical twins develop from 2 separate eggs from separate follicles fertilized by separate sperm cells. Whereas identical twins develop from one embryo that splits in half, dizygotic twinning thus starts with a multiple ovulation, a maternal characteristic.
The research brought together a large number of mothers who gave birth to spontaneous dizygotic twins. The mothers were carefully chosen not to have received fertility treatments, such as IVF, which may also lead to twin pregnancies. Their genetic profiles were compared to those from a large group of people who were not related, either as mothers or as family members, to dizygotic twins. An important strength of the study was that the findings were replicated by the famous deCODE group in another large population cohort from Iceland.
The relative risk of a mother having dizygotic twins is increased by 29% if she has one copy of the twinning gene (or alleles) at both contributing locations in the genome.