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引用本文的文献

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Obstetrical and Perinatal Outcomes Are Not Associated with Advanced Paternal Age in IVF or ICSI Pregnancies with Autologous Oocytes.在使用自体卵母细胞进行体外受精(IVF)或卵胞浆内单精子注射(ICSI)的妊娠中,产科和围产期结局与父亲高龄无关。
Biology (Basel). 2023 Sep 20;12(9):1256. doi: 10.3390/biology12091256.

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2
The trend in delayed childbearing and its potential consequences on pregnancy outcomes: a single center 9-years retrospective cohort study in Hubei, China.晚育趋势及其对妊娠结局的潜在影响:中国湖北一项单中心 9 年回顾性队列研究。
BMC Pregnancy Childbirth. 2022 Jun 24;22(1):514. doi: 10.1186/s12884-022-04807-8.
3
Parental Age and Childhood Lymphoma and Solid Tumor Risk: A Literature Review and Meta-Analysis.父母年龄与儿童淋巴瘤和实体瘤风险:文献回顾与荟萃分析。
JNCI Cancer Spectr. 2022 May 2;6(3). doi: 10.1093/jncics/pkac040.
4
Sperm deoxyribonucleic acid fragmentation (by terminal deoxynucleotidyl transferase biotin dUTP nick end labeling assay) does not impair reproductive success measured as cumulative live birth rates per donor metaphase II oocyte used.精子脱氧核糖核酸碎片化(通过末端脱氧核苷酸转移酶生物素 dUTP 缺口末端标记检测法)不会损害以每个供体使用的中期 II 卵母细胞的累积活产率来衡量的生殖成功。
Fertil Steril. 2022 Jul;118(1):79-89. doi: 10.1016/j.fertnstert.2022.04.002. Epub 2022 May 23.
5
Cumulative live birth rates in donor oocyte ICSI cycles are not improved by magnetic-activated cell sorting sperm selection.在供体卵母细胞胞浆内单精子注射周期中,磁激活细胞分选精子选择法并不能提高累积活产率。
Reprod Biomed Online. 2022 Apr;44(4):677-684. doi: 10.1016/j.rbmo.2021.09.024. Epub 2021 Oct 8.
6
Maternal and perinatal complications according to maternal age: A systematic review and meta-analysis.按产妇年龄划分的孕产妇及围产儿并发症:系统评价和荟萃分析。
Int J Gynaecol Obstet. 2022 Oct;159(1):43-55. doi: 10.1002/ijgo.14100. Epub 2022 Feb 7.
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Advanced paternal age and risk of schizophrenia in offspring - Review of epidemiological findings and potential mechanisms.高龄父亲与子女精神分裂症风险的关联:流行病学研究结果与潜在机制的综述。
Schizophr Res. 2021 Jul;233:72-79. doi: 10.1016/j.schres.2021.06.016. Epub 2021 Jul 6.
8
Effect of paternal age on offspring birth defects: a systematic review and meta-analysis.父亲年龄对后代出生缺陷的影响:系统评价和荟萃分析。
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9
Relationship between male age, semen parameters and assisted reproductive technology outcomes.男性年龄、精液参数与辅助生殖技术结局的关系。
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Association between advanced paternal age and congenital heart defects: a systematic review and meta-analysis.父亲年龄较大与先天性心脏病之间的关联:系统评价和荟萃分析。
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在使用捐赠卵子的人类体外受精或卵胞浆内单精子注射后,父亲年龄较大并不影响与医学相关的产科和围产期结局。

Advanced Paternal Age Does Not Affect Medically-Relevant Obstetrical and Perinatal Outcomes following IVF or ICSI in Humans with Donated Oocytes.

作者信息

Navarro-Gomezlechon Ana, Gil Juliá María, Hervás Irene, Mossetti Laura, Rivera-Egea Rocío, Garrido Nicolás

机构信息

IVI Foundation-Instituto de Investigación Sanitaria La Fe (IIS La Fe), Av. Fernando Abril Martorell, 106, Torre A, 46026 Valencia, Spain.

IVF Laboratory, IVIRMA Roma, Via Federico Calabresi, 11, 00169 Rome, Italy.

出版信息

J Clin Med. 2023 Jan 28;12(3):1014. doi: 10.3390/jcm12031014.

DOI:10.3390/jcm12031014
PMID:36769665
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9918020/
Abstract

BACKGROUND

Concomitant with delays in childbearing, concerns have been raised of whether advanced paternal age is associated with adverse reproductive outcomes, but the evidence is controversial in part due to the uncertain threshold in which to consider advanced paternal age and confounding maternal factors. This retrospective study aimed to evaluate the effect of paternal age on reproductive outcomes related to the pregnancy and perinatal health of the offspring.

METHODS

We retrospectively evaluated 16,268 cases of patients who underwent IVF or ICSI (using autologous sperm and donated oocytes, between January 2008 and March 2020, at Spanish IVIRMA clinics. Patients were divided based on paternal age at conception [≤30 ( = 204), 31-40 ( = 5752), and >40 years ( = 10,312)], and the differences in obstetrical and perinatal outcomes were analyzed by descriptive analysis, followed by univariate and multivariate analysis.

RESULTS

Fathers 31-40 and >40 years old were associated with lower odds of caesarean delivery [AOR 0.63 (95% CI, 0.44-0.90; = 0.012) and AOR 0.61 (95% CI, 0.41-0.91; = 0.017), respectively] and longer pregnancies [ARC 5.09 (95% CI, 2.39-7.79; < 0.001) and ARC 4.54 (95% CI, 1.51-7.58; = 0.003), respectively] with respect to fathers ≤30 years old. Furthermore, fathers aged 31-40 years old had lower odds of having a female infant (AOR, 0.70; 95% CI, 0.49-0.99; = 0.045) than those ≤30. The rest of obstetrical and perinatal outcomes, which we deemed more medically-relevant as they were considered serious for health, were comparable between groups with our adjusted model.

CONCLUSIONS

Despite this hopeful message to fathers of advanced paternal age, future studies should consider the short- and long-term outcomes of the offspring and try to better elucidate the associations of advanced paternal age with reproductive outcomes and the molecular mechanisms underlying the observed associations.

摘要

背景

随着生育延迟,人们开始关注父亲年龄偏大是否与不良生殖结局有关,但部分证据存在争议,这在一定程度上是由于难以确定父亲年龄偏大的阈值以及母亲因素的混杂作用。这项回顾性研究旨在评估父亲年龄对与后代妊娠和围产期健康相关的生殖结局的影响。

方法

我们回顾性评估了2008年1月至2020年3月期间在西班牙IVIRMA诊所接受体外受精(IVF)或卵胞浆内单精子注射(ICSI)(使用自体精子和捐赠卵子)的16268例患者。根据受孕时父亲的年龄将患者分为三组[≤30岁(n = 204)、31 - 40岁(n = 5752)和>40岁(n = 10312)],通过描述性分析分析产科和围产期结局的差异,随后进行单因素和多因素分析。

结果

与≤30岁的父亲相比,31 - 40岁和>40岁的父亲剖宫产几率较低[调整后比值比(AOR)分别为0.63(95%置信区间,0.44 - 0.90;P = 0.012)和AOR 0.61(95%置信区间,0.41 - 0.91;P = 0.017)],妊娠时间较长[平均差(ARC)分别为5.09(95%置信区间,2.39 - 7.79;P < 0.001)和ARC 4.54(95%置信区间,1.51 - 7.58;P = 0.003)]。此外,31 - 40岁的父亲生育女婴的几率低于≤30岁的父亲(AOR,0.70;95%置信区间,0.49 - 0.99;P = 0.045)。在我们的调整模型中,其余我们认为在医学上更相关(因其被视为对健康有严重影响)的产科和围产期结局在各组之间具有可比性。

结论

尽管这一信息对父亲年龄偏大的情况来说是个好消息,但未来的研究应考虑后代的短期和长期结局,并努力更好地阐明父亲年龄偏大与生殖结局之间的关联以及所观察到的关联背后的分子机制。