Evidence map›Paper›PMID 37147937›Full record

ArticleAsian journal of andrology2023

Altered microRNA expression profiles of human spermatozoa in normal fertile men of different ages.

Ming-Jia Zhao, Yao-Nan Zhang, Yong-Ping Zhao, Xian-Bing Chen, Bao-Sheng Han, Ning Ding, Yi-Qun Gu, Shu-Song Wang, Jing Ma, Mei-Ling Liu

Abstract read
In one paragraph

Article in Asian journal of andrology, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

7 citing papers in PubMed.

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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

10 authors.

Ming-Jia ZhaoGraduate School of Peking Union Medical College, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
Yao-Nan ZhangNational Health Commission Key Laboratory of Male Reproductive Health, National Research Institute for Family Planning, Beijing 100081, China.
Yong-Ping ZhaoDepartment of Family Planning and Reproductive Medicine, Peking University People's Hospital, Beijing 100081, China.
Xian-Bing ChenDepartment of Family Planning and Reproductive Medicine, Peking University People's Hospital, Beijing 100081, China.
Bao-Sheng HanDepartment of Reproduction and Genetics, Maternity and Child Health Care Hospital, Tangshan 063000, China.
Ning DingNational Health Commission Key Laboratory of Male Reproductive Health, National Research Institute for Family Planning, Beijing 100081, China.
Yi-Qun GuGraduate School of Peking Union Medical College, Peking Union Medical College, Chinese Academy of Medical Sciences, Beijing 100730, China.
Shu-Song WangHebei Key Laboratory of Reproductive Medicine, Hebei Institute of Reproductive Health Science and Technology, Shijiazhuang 050071, China.
Jing MaHebei Key Laboratory of Reproductive Medicine, Hebei Institute of Reproductive Health Science and Technology, Shijiazhuang 050071, China.
Mei-Ling LiuNational Health Commission Key Laboratory of Male Reproductive Health, National Research Institute for Family Planning, Beijing 100081, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

MicroRNAs (miRNAs) are mediators of the aging process. The purpose of this work was to analyze the miRNA expression profiles of spermatozoa from men of different ages with normal fertility. Twenty-seven donors were divided into three groups by age (Group A, n = 8, age: 20-30 years; Group B, n = 10, age: 31-40 years; and Group C, n = 9, age: 41-55 years) for high-throughput sequencing analysis. Samples from 65 individuals (22, 22, and 21 in Groups A, B, and C, respectively) were used for validation by quantitative real-time polymerase chain reaction (qRT-PCR). A total of 2160 miRNAs were detected: 1223 were known, 937 were newly discovered and unnamed, of which 191 were expressed in all donors. A total of 7, 5, and 17 differentially expressed microRNAs (DEMs) were found in Group A vs B, Group B vs C, and Group A vs C comparisons, respectively. Twenty-two miRNAs were statistically correlated with age. Twelve miRNAs were identified as age-associated miRNAs, including hsa-miR-127-3p, mmu-miR-5100_L+2R-1, efu-miR-9226_L-2_1ss22GA, cgr-miR-1260_L+1, hsa-miR-652-3p_R+1, pal-miR-9993a-3p_L+2R-1, hsa-miR-7977_1ss6AG, hsa-miR-106b-3p_R-1, hsa-miR-186-5p, PC-3p-59611_111, hsa-miR-93-3p_R+1, and aeca-mir-8986a-p5_1ss1GA. There were 9165 target genes of age-associated miRNAs. Gene Ontology (GO) analysis of the target genes identified revealed enrichment of protein binding, membrane, cell cycle, and so on. The Kyoto Encyclopedia of Genes and Genomes (KEGG) enrichment analysis of age-related miRNAs for target genes revealed 139 enriched pathways, such as signaling pathways regulating stem cell pluripotency, metabolic pathways, and the Hippo signaling pathway. This suggests that miRNAs play a key role in male fertility changes with increasing age and provides new evidence for the study of the mechanism of age-related male fertility decline.

Indexed as

MicroRNAsAdultGene Expression ProfilingHumansMaleMiddle AgedSignal TransductionSpermatozoaYoung AdultMicroRNAsMIRN186 microRNA, humanMIRN7977 microRNA, human

Identifiers

PMID37147937
PMCPMC10715607

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.