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Published on: August 29, 2019
Insight on multiple morphological abnormalities of sperm flagella in male infertility: what is new?
Wei-Li Wang1, Chao-Feng Tu1, Yue-Qiu Tan1,2,3
1Institute of Reproductive and Stem Cell Engineering, School of Basic Medical Science, Central South University, Changsha 410078, China.
Abstract:
The syndrome of multiple morphological abnormalities of the sperm flagella (MMAF) is a specific kind of asthenoteratozoospermia with a mosaic of flagellar morphological abnormalities (absent, short, bent, coiled, and irregular flagella). MMAF was proposed in 2014 and has attracted increasing attention; however, it has not been clearly understood. In this review, we elucidate the definition of MMAF from a systematical view, the difference between MMAF and other conditions with asthenoteratozoospermia or asthenozoospermia (such as primary mitochondrial sheath defects and primary ciliary dyskinesia), the knowledge regarding its etiological mechanism and related genetic findings, and the clinical significance of MMAF for intracytoplasmic sperm injection and genetic counseling. This review provides the basic knowledge for MMAF and puts forward some suggestions for further investigations.
Insights
Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) is a complex sperm disorder. This review clarifies MMAF definition, causes, genetics, and clinical implications for fertility treatments.
Area of Science:
- Reproductive Biology
- Human Genetics
- Medical Science
Background:
- Multiple Morphological Abnormalities of the Sperm Flagella (MMAF) is a specific asthenoteratozoospermia characterized by diverse flagellar defects.
- While recognized since 2014, MMAF remains incompletely understood.
- Distinguishing MMAF from similar sperm motility disorders is crucial for accurate diagnosis.
Purpose of the Study:
- To systematically define MMAF and differentiate it from other conditions like primary mitochondrial sheath defects and primary ciliary dyskinesia.
- To review current knowledge on the etiological mechanisms and genetic factors associated with MMAF.
- To discuss the clinical significance of MMAF in the context of assisted reproductive technologies and genetic counseling.
Main Methods:
- Systematic review of existing literature on MMAF.
- Comparative analysis of MMAF with other asthenoteratozoospermia and asthenozoospermia conditions.
- Synthesis of etiological, genetic, and clinical data.
Main Results:
- MMAF presents with a spectrum of flagellar abnormalities including absent, short, bent, coiled, and irregular flagella.
- Genetic underpinnings and etiological pathways of MMAF are being elucidated.
- Understanding MMAF is vital for guiding intracytoplasmic sperm injection (ICSI) and genetic counseling.
Conclusions:
- This review provides a foundational understanding of MMAF.
- Further research is recommended to fully elucidate MMAF's mechanisms and clinical management.
- Accurate diagnosis and genetic insights into MMAF improve reproductive outcomes.
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