Is there increased monozygotic twinning after assisted reproductive technology?
1Reproductive Services, Melbourne IVF, The Royal Women's Hospital, Melbourne, Australia. manuela.toledo@mivf.com.au
The Australian & New Zealand Journal of Obstetrics & Gynaecology
|September 21, 2005
Summary
Assisted reproductive technologies may increase the risk of monozygotic twinning. Further research is needed to understand the causes and implications of this association for twin pregnancies.
Area of Science:
- Reproductive medicine
- Maternal-fetal medicine
- Genetics
Background:
- An observed association exists between assisted reproductive technologies (ART) and an increased incidence of monozygotic twinning over the past two decades.
- The precise mechanisms underlying ART-related monozygotic twinning remain unclear, with several theories proposed.
- Established risks associated with monozygotic twins, including increased perinatal morbidity and mortality, underscore the importance of understanding this association.
Purpose of the Study:
- To review assisted reproductive technologies potentially linked to a higher risk of monozygotic twinning.
- To highlight specific ART procedures, such as intracytoplasmic sperm injection, assisted hatching, and blastocyst transfers, that may contribute to this risk.
- To emphasize the clinical significance of determining the true incidence of monozygotic twinning following ART.
Main Methods:
- Literature review of studies investigating the link between assisted reproductive technologies and monozygotic twinning.
- Analysis of proposed mechanisms and theories for ART-induced monozygotic twinning.
- Examination of specific ART procedures and their potential association with increased monozygotic twinning rates.
Main Results:
- Several assisted reproductive technologies, including intracytoplasmic sperm injection, assisted hatching, and blastocyst transfers, are implicated in the increased risk of monozygotic twinning.
- The exact causal pathways remain incompletely understood.
- The review synthesizes current knowledge on ART-associated monozygotic twinning.
Conclusions:
- Understanding the incidence of monozygotic twinning after ART is crucial due to the known higher risks for twins.
- Further research is warranted to elucidate the causative factors and refine ART protocols to mitigate risks.
- Accurate data on monozygotic twinning rates post-ART are essential for informed clinical practice and patient counseling.
Related Concept Videos
Nondisjunction
During meiosis, chromosomes occasionally separate improperly. This occurs due to failure of homologous chromosome separation during meiosis I or failed sister chromatid separation during meiosis II. In some species, notably plants, nondisjunction can result in an organism with an entire additional set of chromosomes, which is called polyploidy. In humans, nondisjunction can occur during male or female gametogenesis and the resulting gametes possess one too many or one too few chromosomes.
Nondisjunction
Nondisjunction is the failure of homologous chromosomes or sister chromatids to separate correctly and move to the opposite poles of the cells. This produces daughter cells with abnormal chromosome numbers. Nondisjunction is common during anaphase I or anaphase II of meiosis. Mutations in synaptonemal complex proteins that attach homologous chromosomes increase the chances of nondisjunction in anaphase I of meiosis I. In contrast, mutations in topoisomerases and condensins that hold sister...
Meiosis vs. Mitosis
Cell division is necessary for growth and reproduction in organisms. Mitosis aids cell growth and development by dividing somatic cells. In contrast, meiosis causes the division of germ cells and plays an essential role in sexual reproduction. Due to their unique functional requirements, mitosis and meiosis differ from each other in multiple aspects.
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
Before the start of mitosis and meiosis I, the cell synthesizes DNA, resulting in two homologous copies of each chromosome. DNA synthesis is...
In Vitro Fertilization
In vitro fertilization (IVF) is a form of assisted reproductive technology where an egg is fertilized with sperm in a controlled laboratory environment before transferring the resulting embryo into the uterus. This process is designed to help individuals and couples experiencing difficulties conceiving.
The IVF process begins with ovarian stimulation, during which reproductive endocrinologists prescribe hormonal medications to stimulate the ovaries to produce multiple eggs instead of the single...
The IVF process begins with ovarian stimulation, during which reproductive endocrinologists prescribe hormonal medications to stimulate the ovaries to produce multiple eggs instead of the single...
Meiosis I
Meiosis is a carefully orchestrated set of cell divisions, the goal of which—in humans—is to produce haploid sperm or eggs, each containing half the number of chromosomes present in somatic cells elsewhere in the body. Meiosis I is the first such division, and involves several key steps, among them: condensation of replicated chromosomes in diploid cells; the pairing of homologous chromosomes and their exchange of information; and finally, the separation of homologous chromosomes by a...
Meiosis II
Meiosis II is the second and final stage of meiosis. It relies on the haploid cells produced during meiosis I, each of which contain only 23 chromosomes—one from each homologous initial pair. Importantly, each chromosome in these cells is composed of two joined copies, and when these cells enter meiosis II, the goal is to separate such sister chromatids using the same microtubule-based network employed in other division processes. The result of meiosis II is two haploid cells, each containing...


