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Characterization of the protein expression and localization of hnRNP family members during murine spermatogenesis. 小鼠精子发生过程中hnRNP家族成员蛋白表达和定位的研究。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202273
Xiao-Li Wang, Jin-Mei Li, Shui-Qiao Yuan

Mammalian testis exhibits remarkably high transcriptome complexity, and spermatogenesis undergoes two periods of transcriptional cessation. These make the RNA-binding proteins (RBPs) the utmost importance during male germ cell development. Heterogeneous nuclear ribonucleoproteins (hnRNPs) are a large family of RBPs implicated in many steps of RNA processing; however, their roles in spermatogenesis are largely unknown. Here, we investigated the expression pattern of 12 hnRNP family members in mouse testes and found that most detected members are highly expressed in the testis. Furthermore, we found that most of the detected hnRNP proteins (hnRNPD, hnRNPK, hnRNPQ, hnRNPU, and hnRNPUL1) display the highest signals in the nuclei of pachytene spermatocytes, round spermatids, and Sertoli cells, whereas hnRNPE1 exclusively concentrates in the manchette of elongating spermatids. The expression of these hnRNP proteins showed both similarities and specificity, suggesting their diverse roles in spermatogenesis.

哺乳动物睾丸表现出非常高的转录组复杂性,精子发生经历了两个转录停止期。这使得rna结合蛋白(rbp)在男性生殖细胞发育过程中发挥着至关重要的作用。异质核核糖核蛋白(hnRNPs)是一个涉及RNA加工许多步骤的rbp大家族;然而,它们在精子发生中的作用在很大程度上是未知的。在这里,我们研究了12个hnRNP家族成员在小鼠睾丸中的表达模式,发现大多数检测到的成员在睾丸中高表达。此外,我们发现大多数hnRNP蛋白(hnRNPD、hnRNPK、hnRNPQ、hnRNPU和hnRNPUL1)在粗线精母细胞、圆形精母细胞和Sertoli细胞的细胞核中表现出最高的信号,而hnRNPE1只集中在细长精母细胞的细胞核中。这些hnRNP蛋白的表达具有相似性和特异性,提示它们在精子发生中的不同作用。
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引用次数: 2
Clinical significance of distally located periurethral calcification in patients with lower urinary tract symptoms of benign prostate hyperplasia. 下尿路良性前列腺增生患者尿道周围远端钙化的临床意义。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202245
Seong Hyeon Yu, Do Gyeong Lim, Sun-Ouck Kim

This study evaluated the association of periurethral calcification (PUC) with uroflowmetric parameters and symptom severity in male patients with lower urinary tract symptoms (LUTS) of benign prostatic hyperplasia (BPH). The data were collected from a prospectively maintained database of 1321 men with LUTS of BPH who visited Chonnam National University Hospital (Gwang-ju, Korea) from January 2015 to December 2019. PUC severity and location were evaluated on the midsagittal plane during transrectal ultrasonography. Relationships among age, prostate-related parameters, International Prostate Symptom Score (IPSS), and uroflowmetric parameters were assessed. Among the 1321 patients in this study, 530 (40.1%) had PUC. Patients with PUC had significantly higher IPSS (mean ± standard deviation [s.d.]: 15.1 ± 8.7 vs 13.1 ± 7.9; P < 0.001) and lower peak flow rate (Qmax; mean ± s.d.: 12.4 ± 6.6 ml s-1 vs 14.7 ± 13.3 ml s-1; P < 0.001), compared with patients who did not have PUC. Analyses according to PUC severity revealed that patients with severe PUC had higher prostate-specific antigen (PSA) level (P = 0.009), higher total IPSS (P < 0.001), lower Qmax (P = 0.002), and smaller prostate volume (P < 0.001), compared with patients who had non-severe (mild or moderate) PUC. Multivariate analysis showed that distal PUC was independently associated with high total IPSS (P = 0.02), voiding symptom score (P = 0.04), and storage symptom score (P = 0.023), and low Qmax (P = 0.015). In conclusion, PUC was significantly associated with worse LUTS parameters in terms of IPSS and Qmax. Furthermore, distally located PUC was independently associated with worse LUTS of BPH in men.

本研究评估了男性良性前列腺增生(BPH)下尿路症状(LUTS)患者尿道周围钙化(PUC)与尿流指标和症状严重程度的关系。数据收集自2015年1月至2019年12月在全南国立大学医院(韩国光州)就诊的1321名BPH男性LUTS前瞻性维护数据库。经直肠超声检查PUC的严重程度和位置。评估年龄、前列腺相关参数、国际前列腺症状评分(IPSS)和尿流测量参数之间的关系。在本研究的1321例患者中,530例(40.1%)患有PUC。PUC患者的IPSS显著增高(均数±标准差[s.d。: 15.1±8.7 vs 13.1±7.9;P < 0.001),峰值流量较低(Qmax;平均±s.d: 12.4±6.6 ml s-1 vs 14.7±13.3 ml s-1;P < 0.001),与没有PUC的患者相比。根据PUC严重程度的分析显示,重度PUC患者的前列腺特异性抗原(PSA)水平高于非重度(轻度或中度)PUC患者(P = 0.009),总IPSS较高(P < 0.001), Qmax较低(P = 0.002),前列腺体积较小(P < 0.001)。多因素分析显示,远端PUC与高总IPSS (P = 0.02)、排尿症状评分(P = 0.04)、储尿症状评分(P = 0.023)和低Qmax (P = 0.015)独立相关。综上所述,PUC在IPSS和Qmax方面与较差的LUTS参数显著相关。此外,远端PUC与男性BPH的LUTS恶化独立相关。
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引用次数: 0
Genetically predicted insomnia causally increases the risk of erectile dysfunction. 基因预测的失眠会增加勃起功能障碍的风险。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202261
Yang Xiong, Fu-Xun Zhang, Yang-Chang Zhang, Chang-Jing Wu, Feng Qin, Jiu-Hong Yuan
Sleep has attracted extensive attention due to its significance in health. However, its association with erectile dysfunction (ED) is insufficiently investigated. To investigate the potential causal links between sleep traits (insomnia, sleep duration, and chronotype) and ED, this study was performed. The single-nucleotide polymorphisms (SNPs) associated with insomnia, sleep duration, and chronotype were retrieved from previous genome-wide association studies (GWAS). A conventional two-sample Mendelian randomization (MR) was used to estimate the causal links between sleep traits and ED. The summary statistics of ED were from individuals of European ancestry (6175 cases vs 217 630 controls). As shown by the random effect inverse-variance-weighting (IVW) estimator, genetically predicted insomnia was causally associated with a 1.15-fold risk of ED (95% confidence interval: 1.07–1.23, P < 0.001). Sleep duration and morningness were not causally associated with ED, as indicated by the IVW (all P > 0.05). These findings were consistent with the results of sensitivity analyses. Based on genetic data, this study provides causal evidence that genetically predicted insomnia increases the risk of ED, whereas sleep duration and chronotype do not.
睡眠因其对健康的重要性而受到广泛关注。然而,其与勃起功能障碍(ED)的关系尚不充分研究。为了调查睡眠特征(失眠、睡眠时间和睡眠类型)与ED之间的潜在因果关系,进行了这项研究。与失眠、睡眠时间和睡眠类型相关的单核苷酸多态性(snp)是从之前的全基因组关联研究(GWAS)中检索到的。采用传统的双样本孟德尔随机化(MR)来估计睡眠特征与ED之间的因果关系。ED的汇总统计数据来自欧洲血统的个体(6175例与21730例对照)。随机效应反方差加权(IVW)估计显示,基因预测的失眠与ED的1.15倍风险有因果关系(95%置信区间:1.07-1.23,P < 0.001)。IVW显示,睡眠时间和晨起与ED无因果关系(均P > 0.05)。这些发现与敏感性分析的结果一致。基于基因数据,这项研究提供了因果证据,表明基因预测的失眠会增加ED的风险,而睡眠时间和睡眠类型则不会。
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引用次数: 12
Transrectal ultrasound examination of prostate cancer guided by fusion imaging of multiparametric MRI and TRUS: avoiding unnecessary mpMRI-guided targeted biopsy. 多参数MRI与TRUS融合成像引导下的前列腺癌经直肠超声检查:避免不必要的mpmri引导下的靶向活检。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202276
Guang Xu, Jun-Heng Li, Li-Hua Xiang, Bin Yang, Yun-Chao Chen, Yi-Kang Sun, Bing-Hui Zhao, Jian Wu, Li-Ping Sun, Hui-Xiong Xu

The purpose of this study was to explore transrectal ultrasound (TRUS) findings of prostate cancer (PCa) guided by multiparametric magnetic resonance imaging (mpMRI) and to improve the Prostate Imaging Reporting and Data System (PI-RADS) system for avoiding unnecessary mpMRI-guided targeted biopsy (TB). From January 2018 to October 2019, fusion mpMRI and TRUS-guided biopsies were performed in 162 consecutive patients. The study included 188 suspicious lesions on mpMRI in 156 patients, all of whom underwent mpMRI-TRUS fusion imaging-guided TB and 12-core transperineal systematic biopsy (SB). Univariate analyses were performed to investigate the relationship between TRUS features and PCa. Then, logistic regression analysis with generalized estimating equations was performed to determine the independent predictors of PCa and obtain the fitted probability of PCa. The detection rates of PCa based on TB alone, SB alone, and combined SB and TB were 55.9% (105 of 188), 52.6% (82 of 156), and 62.8% (98 of 156), respectively. The significant predictors of PCa on TRUS were hypoechogenicity (odds ratio [OR]: 9.595, P = 0.002), taller-than-wide shape (OR: 3.539, P = 0.022), asymmetric vascular structures (OR: 3.728, P = 0.031), close proximity to capsule (OR: 3.473, P = 0.040), and irregular margins (OR: 3.843, P = 0.041). We propose subgrouping PI-RADS score 3 into categories 3a, 3b, 3c, and 3d based on different numbers of TRUS predictors, as the creation of PI-RADS 3a (no suspicious ultrasound features) could avoid 16.7% of mpMRI-guided TBs. Risk stratification of PCa with mpMRI-TRUS fusion imaging-directed ultrasound features could avoid unnecessary mpMRI-TBs.

本研究旨在探讨多参数磁共振成像(mpMRI)引导下前列腺癌(PCa)的经直肠超声(TRUS)表现,并改进前列腺成像报告和数据系统(PI-RADS)系统,以避免不必要的mpMRI引导下的靶向活检(TB)。2018年1月至2019年10月,我们连续对162例患者进行了mpMRI融合活检和trus引导活检。该研究包括156例患者的188个mpMRI可疑病变,所有患者都接受了mpMRI- trus融合成像引导下的TB和12核经会阴系统活检(SB)。采用单变量分析来研究TRUS特征与PCa之间的关系。然后利用广义估计方程进行logistic回归分析,确定主成分的独立预测因子,得到主成分的拟合概率。单独检测TB、单独检测SB、合并检测SB和TB的PCa检出率分别为55.9%(105 / 188)、52.6%(82 / 156)和62.8%(98 / 156)。前列腺癌在TRUS上的显著预测因子为低回声性(比值比[OR]: 9.595, P = 0.002)、高过宽的形状(OR: 3.539, P = 0.022)、不对称的血管结构(OR: 3.728, P = 0.031)、靠近包膜(OR: 3.473, P = 0.040)和不规则的边缘(OR: 3.843, P = 0.041)。基于不同数量的TRUS预测因子,我们建议将PI-RADS评分3分为3a、3b、3c和3d类,因为PI-RADS 3a(无可疑超声特征)的创建可以避免16.7%的mpmri引导下的tb。采用mpMRI-TRUS融合成像定向超声特征对PCa进行风险分层,可避免不必要的mpMRI-TBs。
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引用次数: 0
Retraction Note: PlncRNA-1 induces apoptosis through the Her-2 pathway in prostate cancer cells. 注:PlncRNA-1通过Her-2通路诱导前列腺癌细胞凋亡。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202318
Qing Yang, Zi-Lian Cui, Qin Wang, Xun-Bo Jin, Yong Zhao, Mu-Wen Wang, Wei Song, Hua-Wei Qu, Wei-Ting Kang
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引用次数: 0
Biallelic mutations in WDR12 are associated with male infertility with tapered-head sperm. WDR12双等位基因突变与锥形头精子男性不育有关。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202269
Juan Hua, Lan Guo, Yao Yao, Wen Hu, Yang-Yang Wan, Bo Xu

Teratozoospermia is a rare disease associated with male infertility. Several recurrent genetic mutations have been reported to be associated with abnormal sperm morphology, but the genetic basis of tapered-head sperm is not well understood. In this study, whole-exome sequencing (WES) identified a homozygous WD repeat domain 12 (WDR12; p.Ser162Ala/c.484T>G) variant in an infertile patient with tapered-head spermatozoa from a consanguineous Chinese family. Bioinformatic analysis predicted this mutation to be a pathogenic variant. To verify the effect of this variant, we analyzed WDR12 protein expression in spermatozoa of the patient and a control individual, as well as in the 293T cell line, by Western blot analysis, and found that WDR12 expression was significantly downregulated. To understand the role of normal WDR12, we evaluated its mRNA and protein expression in mice at different ages. We observed that WDR12 expression was increased in pachytene spermatocytes, with intense staining visible in round spermatid nuclei. Based on these results, the data suggest that the rare biallelic pathogenic missense variant (p.Ser162Ala/c.484T>G) in the WDR12 gene is associated with tapered-head spermatozoa. In addition, after intracytoplasmic sperm injection (ICSI), a successful pregnancy was achieved. This finding indicates that infertility associated with this WDR12 homozygous mutation can be overcome by ICSI. The present results may provide novel insights into understanding the molecular mechanisms of male infertility.

畸形精子症是一种罕见的与男性不育相关的疾病。据报道,一些复发性基因突变与精子形态异常有关,但锥形头精子的遗传基础尚不清楚。在这项研究中,全外显子组测序(WES)鉴定了一个纯合子WD重复结构域12 (WDR12;p.Ser162Ala/c.484T>G)在一个来自中国近亲家庭的锥形头精子不育患者中的变异。生物信息学分析预测该突变是一种致病变异。为了验证该变异的作用,我们通过Western blot分析了患者和对照个体精子以及293T细胞系中WDR12蛋白的表达,发现WDR12表达明显下调。为了了解正常WDR12的作用,我们在不同年龄的小鼠中评估了其mRNA和蛋白的表达。我们观察到粗线精母细胞中WDR12表达增加,圆形精母细胞核中可见强烈染色。基于这些结果,数据提示WDR12基因中罕见的双等位致病错义变异(p.Ser162Ala/c.484T>G)与锥形头精子有关。此外,经卵胞浆内单精子注射(ICSI)后,成功怀孕。这一发现表明,与WDR12纯合突变相关的不孕症可以通过ICSI来克服。本研究结果可能为理解男性不育的分子机制提供新的见解。
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引用次数: 1
Association between semen collection time and semen parameters: an observational study. 精液采集时间与精液参数之间的关系:一项观察性研究。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202268
Shun Bai, Xian-Chao Dou, Hao-Lin Qi, Yan-Song Zhu, Yin-Tao Zhang, Yi-Xun Liu, Xue-Chun Hu, Cheng Cao, Xian-Hong Tong, Bo Xu, Li-Min Wu, Xiao-Hua Jiang

The process of semen collection plays a key role in the quality of semen specimens. However, the association between semen collection time and semen quality is still unclear. In this study, ejaculates by masturbation from 746 subfertile men or healthy men who underwent semen analysis were examined. The median (interquartile range) semen collection time for all participants was 7.0 (5.0-11.0) min, and the median time taken for semen collection was lower in healthy men than that in subfertile men (6.0 min vs 7.0 min). An increase in the time required to produce semen samples was associated with poorer semen quality. Among those undergoing assisted reproductive technology (ART), the miscarriage rate was positively correlated with the semen collection time. After adjusting for confounders, the highest quartile (Q4) of collection time was negatively associated with semen volume and sperm concentration. A longer time to produce semen samples (Q3 and Q4) was negatively correlated with progressive and total sperm motility. In addition, there was a significant negative linear association between the semen collection time and the sperm morphology. Higher risks of asthenozoospermia (adjusted odds ratio [OR] = 2.06, 95% confidence interval [CI]: 1.31-3.25, P = 0.002) and teratozoospermia (adjusted OR = 1.98, 95% CI: 1.10-3.55, P = 0.02) were observed in Q3 than those in Q1. Our results indicate that a higher risk of abnormal semen parameter values was associated with an increase in time for semen collection, which may be related to male fertility through its association with semen quality.

精液采集过程对精液标本的质量起着关键作用。然而,精液采集时间与精液质量之间的关系尚不清楚。在这项研究中,对746名不育男性或健康男性的手淫射精进行了精液分析。所有参与者的精液收集时间中位数(四分位数范围)为7.0(5.0-11.0)分钟,健康男性的精液收集时间中位数低于低生育能力男性(6.0分钟vs 7.0分钟)。制作精液样本所需时间的增加与精液质量下降有关。在接受辅助生殖技术(ART)的患者中,流产率与精液采集时间呈正相关。在调整混杂因素后,收集时间的最高四分位数(Q4)与精液量和精子浓度呈负相关。产生精液样本(Q3和Q4)的时间越长,精子的进步性和总活力越低。此外,精液采集时间与精子形态呈显著的负线性相关。第三季度出现弱精子症(校正比值比[OR] = 2.06, 95%可信区间[CI]: 1.31-3.25, P = 0.002)和畸形精子症(校正比值比[OR] = 1.98, 95% CI: 1.10-3.55, P = 0.02)的风险高于第一季度。我们的研究结果表明,精液参数值异常的高风险与精液采集时间的增加有关,这可能与男性生育能力有关,因为它与精液质量有关。
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引用次数: 0
Glutathione S-transferase genetic polymorphisms and fluoride-induced reproductive toxicity in men with idiopathic infertility. 特发性不育症男性谷胱甘肽s -转移酶遗传多态性和氟化物诱导的生殖毒性。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202271
Jun He, Yi Mu, Miao Liu, Bang-Wei Che, Wen-Jun Zhang, Ke-Hang Chen, Kai-Fa Tang

Male infertility caused by idiopathic oligoasthenospermia (OAT) is known as idiopathic male infertility. Glutathione S-transferase (GST) and fluoride may play important roles in idiopathic male infertility, but their effects are still unknown. Our study examined the relationship between GST polymorphisms and fluoride-induced toxicity in idiopathic male infertility and determined the underlying mechanism. Sperm, blood, and urine samples were collected from 560 males. Fluoride levels were measured by a highly selective electrode method, and GST genotypes were identified using polymerase chain reaction (PCR) and PCR-restriction fragment length polymorphism (PCR-RFLP). Semen parameters, DNA fragmentation index (DFI), mitochondrial membrane potential (MMP), and oxidative stress (OS) biomarkers were statistically assessed at the P < 0.05 level. Compared with healthy fertile group, semen parameters, fluoride levels, OS biomarkers, sex hormone levels, and MMP and DFI levels were lower in the idiopathic male infertility group. For glutathione S-transferase M1 (GSTM1[-]) and glutathione S-transferase T1 (GSTT1[-]) or glutathione S-transferase P1 (GSTP1) mutant genotypes, levels of semen fluoride, OS, MMP, and DFI were considerably higher, and the mean levels of sperm parameters and testosterone were statistically significant in GSTM1(+), GSTT1(+), and GSTP1 wild-type genotypes. Both semen and blood fluoride levels were associated with oxidative stress in idiopathic male infertility patients. Elevated fluoride in semen with the genotypes listed above was linked to reproductive quality in idiopathic male infertility patients. In conclusion, GST polymorphisms and fluorine may have an indicative relationship between reproductive quality and sex hormone levels, and OS participates in the development of idiopathic male infertility.

由特发性少弱精子症(OAT)引起的男性不育被称为特发性男性不育。谷胱甘肽s -转移酶(GST)和氟化物可能在特发性男性不育症中起重要作用,但其作用尚不清楚。我们研究了特发性男性不育症中GST多态性与氟化物毒性之间的关系,并确定了其潜在机制。收集了560名男性的精子、血液和尿液样本。采用高选择性电极法测定氟化物水平,采用聚合酶链反应(PCR)和限制性片段长度多态性(PCR- rflp)鉴定GST基因型。精液参数、DNA片段化指数(DFI)、线粒体膜电位(MMP)和氧化应激(OS)生物标志物在P < 0.05水平上进行统计学评估。与健康不育组相比,特发性男性不育组的精液参数、氟化物水平、OS生物标志物、性激素水平、MMP和DFI水平均较低。对于谷胱甘肽s -转移酶M1(GSTM1[-])和谷胱甘肽s -转移酶T1(GSTT1[-])或谷胱甘肽s -转移酶P1 (GSTP1)突变基因型,精液氟化物、OS、MMP和DFI水平均显著升高,GSTM1(+)、GSTT1(+)和GSTP1野生型的精子参数和睾酮平均水平均有统计学意义。特发性男性不育症患者的精液和血液氟化物水平与氧化应激有关。具有上述基因型的精液中氟化物含量升高与特发性男性不育症患者的生殖质量有关。综上所述,GST多态性与氟可能与生殖质量和性激素水平存在指示性关系,OS参与了特发性男性不育的发生发展。
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引用次数: 0
A novel homozygous frameshift variant in DNAH8 causes multiple morphological abnormalities of the sperm flagella in a consanguineous Pakistani family. 在巴基斯坦的一个近亲家庭中,一种新的DNAH8纯合子移码变异导致精子鞭毛的多种形态异常。
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202274
Sobia Dil, Asad Khan, Ahsanullah Unar, Meng-Lei Yang, Imtiaz Ali, Aurang Zeb, Huan Zhang, Jian-Teng Zhou, Muhammad Zubair, Khalid Khan, Shun Bai, Qing-Hua Shi

Multiple morphological abnormalities of the sperm flagella (MMAF) is a severe form of asthenozoospermia categorized by immotile spermatozoa with abnormal flagella in ejaculate. Whole-exome sequencing (WES) is used to detect pathogenic variants in patients with MMAF. In this study, a novel homozygous frameshift variant (c.6158_6159insT) in dynein axonemal heavy chain 8 (DNAH8) from two infertile brothers with MMAF in a consanguineous Pakistani family was identified by WES. Reverse transcription-polymerase chain reaction (RT-PCR) confirmed DNAH8 mRNA decay in these patients with the DNAH8 mutation. Hematoxylin-eosin staining and transmission electron microscopy revealed highly divergent morphology and ultrastructure of sperm flagella in these patients. Furthermore, an immunofluorescence assay showed the absence of DNAH8 and a reduction in its associated protein DNAH17 in the patients' spermatozoa. Collectively, our study expands the phenotypic spectrum of patients with DNAH8-related MMAF worldwide.

精子鞭毛多重形态异常(MMAF)是一种严重的弱精子症,表现为精子不动,射精时鞭毛异常。全外显子组测序(WES)用于检测MMAF患者的致病变异。在本研究中,我们从巴基斯坦一个近亲家庭中患有MMAF的不育兄弟中发现了一种新的纯合子移码变异(c.6158_6159insT)。逆转录聚合酶链反应(RT-PCR)证实了这些DNAH8突变患者的DNAH8 mRNA衰变。苏木精-伊红染色和透射电镜显示,这些患者的精子鞭毛形态和超微结构高度不同。此外,免疫荧光分析显示,患者精子中DNAH8缺失,其相关蛋白DNAH17减少。总的来说,我们的研究扩大了全球范围内与dnah8相关的MMAF患者的表型谱。
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引用次数: 1
Outcomes of radical prostatectomy in a 20-year localized prostate cancer single institution series in China. 中国20年局部前列腺癌根治性前列腺切除术的结果
IF 2.9 2区 医学 Q2 ANDROLOGY Pub Date : 2023-05-01 DOI: 10.4103/aja202264
Xiao-Hao Ruan, Tsun Tsun Stacia Chun, Da Huang, Hoi-Lung Wong, Brian Sze-Ho Ho, Chiu-Fung Tsang, Terence Chun-Ting Lai, Ada Tsui-Lin Ng, Rong Na, James Hok-Leung Tsu

The long-term survival outcomes of radical prostatectomy (RP) in Chinese prostate cancer (PCa) patients are poorly understood. We conducted a single-center, retrospective analysis of patients undergoing RP to study the prognostic value of pathological and surgical information. From April 1998 to February 2022, 782 patients undergoing RP at Queen Mary Hospital of The University of Hong Kong (Hong Kong, China) were included in our study. Multivariable Cox regression analysis and Kaplan-Meier analysis with stratification were performed. The 5-year, 10-year, and 15-year overall survival (OS) rates were 96.6%, 86.8%, and 70.6%, respectively, while the 5-year, 10-year, and 15-year PCa-specific survival (PSS) rates were 99.7%, 98.6%, and 97.8%, respectively. Surgical International Society of Urological Pathology PCa grades (ISUP Grade Group) ≥4 was significantly associated with poorer PSS (hazard ratio [HR] = 8.52, 95% confidence interval [CI]: 1.42-51.25, P = 0.02). Pathological T3 stage was not significantly associated with PSS or OS in our cohort. Lymph node invasion and extracapsular extension might be associated with worse PSS (HR = 20.30, 95% CI: 1.22-336.38, P = 0.04; and HR = 7.29, 95% CI: 1.22-43.64, P = 0.03, respectively). Different surgical approaches (open, laparoscopic, or robotic-assisted) had similar outcomes in terms of PSS and OS. In conclusion, we report the longest timespan follow-up of Chinese PCa patients after RP with different approaches.

中国前列腺癌(PCa)患者根治性前列腺切除术(RP)的长期生存预后尚不清楚。我们对接受RP的患者进行了单中心回顾性分析,以研究病理和手术信息对预后的价值。从1998年4月到2022年2月,782名在香港大学玛丽医院(中国香港)接受RP的患者被纳入我们的研究。采用多变量Cox回归分析和分层Kaplan-Meier分析。5年、10年和15年总生存率(OS)分别为96.6%、86.8%和70.6%,而5年、10年和15年前列腺癌特异性生存率(PSS)分别为99.7%、98.6%和97.8%。国际泌尿外科病理学会PCa分级(ISUP分级组)≥4级与PSS较差显著相关(风险比[HR] = 8.52, 95%可信区间[CI]: 1.42-51.25, P = 0.02)。在我们的队列中,病理性T3分期与PSS或OS无显著相关性。淋巴结浸润和囊外延伸可能与PSS恶化相关(HR = 20.30, 95% CI: 1.22-336.38, P = 0.04;HR = 7.29, 95% CI: 1.22 ~ 43.64, P = 0.03)。不同的手术入路(开放、腹腔镜或机器人辅助)在PSS和OS方面有相似的结果。总之,我们报告了不同入路的中国PCa患者RP术后最长随访时间。
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Asian Journal of Andrology
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