Ferti$can
Development and validation of an innovative method for the diagnosis and prognosis of male infertility
About
FERTI$CAN aims to develop and validate an innovative diagnostic device for the diagnosis, prognosis, and therapeutic guidance of male infertility.
Male infertility accounts for nearly half of infertility cases worldwide. However, its clinical evaluation still relies predominantly on conventional semen analysis, a method with limited diagnostic and prognostic value. FERTI$CAN proposes a disruptive solution: a molecular-based diagnostic array capable of characterizing sperm quality at the protein and RNA level, complementing traditional semen assessment.
By integrating validated biomarkers into a customizable diagnostic platform, FERTI$CAN seeks to improve patient stratification, predict assisted reproductive technology (ART) outcomes, and support personalized treatment strategies.
The Challenge & Motivation
Infertility is a growing global health concern, affecting approximately 1 in 6 individuals worldwide. Despite major technological advances in reproductive medicine, the diagnosis of male infertility remains insufficient.
The Problem: Around 30–40% of male infertility cases are classified as idiopathic, meaning that no clear cause is identified after routine clinical evaluation. Conventional semen analysis cannot detect molecular defects that compromise fertilization potential.
The Gap: There is currently no clinically validated molecular diagnostic platform capable of predicting reproductive success or guiding treatment selection in male infertility.
The Opportunity: Advances in proteomics and transcriptomics have revealed distinct molecular signatures in sperm associated with infertility-related conditions. Translating this knowledge into a diagnostic tool represents a major step toward precision reproductive medicine.
Scientific Innovation
FERTI$CAN is built upon years of research in sperm molecular profiling conducted at the University of Aveiro, particularly within the Institute of Biomedicine (iBiMED).
Our approach integrates:
1. Biomarker Identification
Systematic review and meta-analysis of existing literature combined with previous in-house discoveries to identify robust candidate biomarkers (proteins and RNAs) associated with sperm quality and infertility phenotypes.
2. Molecular Validation
Validation of selected biomarkers in well-characterized human cohorts, including fertile donors and patients with infertility-related conditions.
3. Diagnostic Array Development
Design of a prototype molecular array capable of simultaneously evaluating multiple validated biomarkers in human sperm samples.
4. Clinical Stratification
Establishment of threshold values for each biomarker to enable:
• Diagnosis of idiopathic infertility
• Prediction of ART success
• Selection of the most appropriate reproductive technique
• Monitoring of treatment efficacy
Unlike conventional semen analysis, FERTI$CAN evaluates sperm at the molecular level, providing objective and reproducible data to support clinical decision-making.
Impact & Sustainability
FERTI$CAN has the potential to transform male infertility management across multiple dimensions:
Clinical Impact
• Improve diagnosis of idiopathic infertility
• Predict ART outcomes
• Reduce unnecessary invasive treatments
• Support personalized reproductive medicine
Economic Impact
Male reproductive disorders represent a significant burden on healthcare systems. By improving diagnostic precision and treatment selection, FERTI$CAN may reduce unnecessary ART cycles and associated costs.
Scientific Impact
• Advance knowledge in reproductive biology
• Stimulate biomarker-driven diagnostics
• Open avenues for future therapeutic interventions
Societal Impact
Male infertility remains underdiagnosed and underprioritized. FERTI$CAN promotes greater awareness and contributes to improved reproductive health outcomes.
The Consortium
This project brings together multidisciplinary expertise in biomedicine, reproductive biology, embryology, and clinical urology.
INSTITUTIONS
Leading Institution:
• University of Aveiro (UA) - Institute of Biomedicine (iBiMED).
Partner Institutions:
• Centro Hospitalar do Baixo Vouga (CHBV);
• Centro Hospitalar de Vila Nova de Gaia/Espinho (CHVNGE).
TEAM
Principal Investigator:
Dr. Joana Santiago, Researcher at the Institute of Biomedicine – iBiMED, University of Aveiro.
Team Members:
• Prof. Margarida Fardilha, Associate Professor with Habilitation at the Department of Medical Sciences and Coordinator of Fardilha's Lab at iBiMED;
• Prof. Maria Teresa Herdeiro, Associate Professor with Habilitation and Principal Researcher at iBiMED
• Dr. Madalena Cabral, Senior Embryologist at CHVNGE;
• Pedro O. Corda, PhD Student at iBiMED;
• Vanessa Bowen, MSc Student at iBiMED.
Clinical consultants:
• Dra. Sandra Lemos, Gynecologist at CHBV;
• Dra. Sara Rocha, Gynecologist at CHBV;
• Dr. António Patrício, Urologist at CHBV;
• Dra. Ilda Pires, Senior Embryologist at CHVNGE.

Duration: 36 Months
Funding: Portugal 2030 / FCT (Foundation for Science and Technology)
E-mail: dcm-fertiscan@ua.pt.
Team
Dr. Joana Santiago
Principal Investigator UA
Prof. Margarida Fardilha
Expert in male fertility biomarkers.

Prof. Maria Teresa Herdeiro
Expert in Public Health
Pedro O. Corda
PhD Student
Madalena Cabral
PhD Student
Vanessa Bowen
MSc Student
This work is financed by FEDER funds through COMPETE2030 and by National Funds through FCT – Foundation for Science and Technology, under the project FERTISCAN (Project 16652; COMPETE2030-FEDER-00783300; 2023.17577.ICDT; https://doi.org/10.54499/2023.17577.ICDT).





