AI Article Synopsis

  • The study examines the ratio of PRM1 to PRM2 mRNA in testicular biopsies from azoospermia patients to see how it relates to sperm quality and fertilization ability.
  • In the study involving 106 azoospermia patients, the testicular samples were categorized into obstructive azoospermia (OA) and two types of nonobstructive azoospermia (NOA), revealing distinct expressions of certain genes related to sperm production.
  • Results indicated that the PRM1/PRM2 mRNA ratio is significantly increased in the Sertoli cell-only syndrome (SCOS) group, suggesting that this ratio could serve as a more reliable marker for assessing sperm quality in NOA cases.

Article Abstract

Altered protamine 1 (PRM1)/ protamine 2 (PRM2) mRNA ratio in testicular biopsy samples correlates with sperm quality and its fertilising ability. This study is planned to assess PRM1/ PRM2 mRNA ratio in subgroups of azoospermia to suggest a more reliable and accurate marker for assessing sperm quality in nonobstructive azoospermia (NOA). A cross-sectional study was done on testicular biopsy samples, taken from 106 azoospermic patients. Samples were histologically classified into subgroups: 36 obstructive azoospermia (OA), and two groups of NOA: 41 round spermatid maturation arrest (SMA) and 29 Sertoli cell-only syndrome (SCOS). OA samples showed histologically normal spermatogenesis and serve as a positive control. mRNA expression of jumonji domain-containing 1A (JMJD1A), PRM1, PRM2 and transition nuclear proteins (TNP1, TNP2) genes was determined, by RT-qPCR. Significantly lower expression of JMJD1A (p < .001), PRM1 (p = .0265) and PRM2 (p = .0032) has been seen in the SCOS group of NOA. We found significant (p < .001) increase in PRM1/PRM2 mRNA ratio in testicular biopsy samples of SCOS group of NOA patients and significant negative correlation of PRM1/PRM2 mRNA ratio with JMJD1A. Hence, PRM1/PRM2 mRNA ratio may represent a more reliable and accurate marker to assess sperm quality in NOA in addition to standard semen parameters.

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Source
http://dx.doi.org/10.1111/and.13936DOI Listing

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