Paternal Age and Fetal Aneuploidy

Ovo Clinic

Status: Completed

Conditions: Trisomy 21

Treatments: Diagnostic Test: Optimo prenatal screening test

Study type: Observational

Funder types: Industry

Identifiers

NCT05981521

3321

Details and patient eligibility

About

Trisomy 21, commonly known as down syndrome, is the most common chromosomal abnormality in humans. Advanced maternal age (AMA) is a well-recognized risk factor for trisomy 21, with the risk increasing significantly beyond the age of 35. Research on the effects of paternal age on the prenatal risk of trisomy 21 is lacking, with inconsistent findings in the literature.

The Harmony® prenatal test is an Non-Invasive Prenatal Testing (NIPT) that screens maternal blood for chromosomal abnormalities in the Cell-Free Fetal DNA (cfDNA). The harmony® prenatal test can detect conditions such as trisomy 13, 18, and 21, as well as sex chromosome abnormalities.

The Optimo test is a prenatal screening test that screens for trisomies 13, 18 and 21 in the developing fetus using extended biochemical screening in maternal. The Optimo test has shown high sensitivity and specificity in detecting trisomy 21.

Enrollment: 7,141 patients

Sex: Female

Ages: 18+ years old

Volunteers: No Healthy Volunteers

Inclusion criteria

• Pregnant women aged 18 years or older (at the time of trisomy 18 and 21 screening) and who were able to complete the questionnaire in either French or English
• Pregnant women who completed the entire trisomy 21 screening process at clinique ovo were included

Exclusion criteria

• Patients who did not indicate the male partner/donor's age were excluded
• Patients who did not complete or sign the clinical information form