精子
DNA
人口
染色质
精子质量
男科
精子细胞
吞吐量
化学
生物
分子生物学
计算生物学
遗传学
计算机科学
医学
环境卫生
电信
无线
作者
Mohammad Simchi,Jason Riordon,Yihe Wang,Christopher McCallum,Jae Bem You,Keith Jarvi,Reza Nosrati,David Sinton
出处
期刊:Analyst
[Royal Society of Chemistry]
日期:2023-01-01
卷期号:148 (16): 3748-3757
被引量:3
摘要
Clinical semen quality assessment is critical to the treatment of infertility. Sperm DNA integrity testing provides critical information that can steer treatment and influence outcomes and offspring health. Flow cytometry is the gold standard approach to assess DNA integrity, but it is not commonly applied at the clinical level. The sperm chromatin dispersion (SCD) assay provides a simpler and cheaper alternative. However, SCD is low-throughput and non-quantitative - sperm assessment is serial, manual and suffers inter- and intra-observer variations. Here, an automated SCD analysis method is presented that enables quantitative sperm DNA quality assessment at the single-cell and population levels. Levering automated optical microscopy and a chromatin diffusion-based analysis, a sample of thousands of sperm that would otherwise require 5 hours is assessed in under 10 minutes - a clinically viable workflow. The sperm DNA diffusion coefficient (DDNA) measurement correlates (R2 = 0.96) with DNA fragmentation index (DFI) from the cytometry-based sperm chromatin structure assay (SCSA). The automated measurement of population-level sperm DNA fragmentation (% sDF) prevents inter-observer variations and shows a good agreement with the SCSA % DFI (R2 = 0.98). This automated approach standardizes and accelerates SCD-based sperm DNA analysis, enabling the clinical application of sperm DNA integrity assessment.
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