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PMID: 32653083 Published · ppublish English Journal Article

Relationships between the age of 25,445 men attending infertility clinics and sperm chromatin structure assay (SCSA®) defined sperm DNA and chromatin integrity.

Fertility and sterility ·Vol. 114 ·No. 2 ·2020-00-00 ·Pages 311-320

Evenson DP, Djira G, Kasperson K, Christianson J

Abstract

To determine relationships between age of men with potential male factor infertility and sperm chromatin structure assay (SCSA) measures of sperm DNA fragmentation (SDF) and high DNA stainable sperm (HDS), and to compare these data with those obtained from healthy donor men without reproductive issues. Retrospective study. Infertility clinics and diagnostic laboratory. A total of 25,445 men attending infertility clinics. Donors were 87 men working at Lawrence Livermore National Laboratory. None. SCSA measures (% DNA fragmentation index (DFI), X DFI, SD DFI, and %HDS) of men aged 21-80 years. In the study population, advancing paternal age was associated with increased sperm DNA fragmentation (SDF) scored as increased percentage of sperm in semen ejaculates with measurable DNA strand breaks (%DFI). The slope of increase in %DFI prior to age 41.6 years was 0.39, which increased after age 41.6 to more than double at a slope of 0.86. These changes in DNA/chromatin in more than 25,000 aging men attending infertility clinics are similar to those seen over the same age span (20-80 years) in 87 nonpatient, healthy men without reproductive issues. For the age group 20-50 years, there was no major significant difference in %DFI between patients and donor men. According to a logistic regression model, the estimated probability is that, for example, a 40-year-old and a 50-year-old man have a 20% and 40% chance, respectively, to have a pathological DFI ≥25% by age factor alone. The condensation of sperm chromatin in patients increased with age in a linear fashion, from a mean of 12.2 %HDS at age 20-25 to a mean of 7.9 %HDS at age 60-65. Patients had a greater %HDS than donors across all ages. The great heterogeneity of both DFI and HDS values at a specific age prevents the automatic translation of age into an index of DNA fragmentation. However, it reinforces the idea that both DFI and HDS evaluation can play a role in detecting potential male infertility in cases that are not resolved by routine testing and in cases of multiple miscarriages. DFI and HDS data can help clinicians to predict a man's fertility potential, to consider corrective therapeutic approaches, as well as to assess the risk to the offspring's health.

Keywords
Male infertility SCSA test age healthy donors
MeSH Terms
Adult Aged Aged, 80 and over Chromatin/pathology DNA Fragmentation Fertility Fertility Clinics Flow Cytometry Humans Infertility, Male/pathology,physiopathology,therapy Male Middle Aged Paternal Age Predictive Value of Tests Retrospective Studies Risk Assessment Risk Factors Semen Analysis Spermatozoa/pathology Young Adult
Chemicals
Chromatin
Authors & Affiliations
4 authors, click to expand affiliations / ORCID
Evenson Donald P
SCSA Diagnostics Inc., Brookings; Sanford Medical School, University of South Dakota, Sioux Falls. Electronic address: [email protected].
Djira Gemechis
Department of Mathematics and Statistics, South Dakota State University, Brookings, South Dakota.
Kasperson Kay
SCSA Diagnostics Inc., Brookings.
Christianson Jennifer
SCSA Diagnostics Inc., Brookings.
Article Info
Journal
Fertility and sterility
Abbr.
Fertil Steril
ISSN
1556-5653
Published
2020-00-00
Epub
2020-00-09
Pages
311-320
Language
English
Region
United States
NLM ID
0372772
Subset
IM
Corrections
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