Publications by authors named "Yoshitomo Kobori"

Objective: To develop a core outcome set for male infertility trials.

Design: A two-round Delphi survey and consensus development workshop were undertaken with healthcare professionals, researchers and clinicians globally.

Subjects: 334 participants from 39 countries participated in the Delphi Survey, while 44 participants from 21 countries participated in the consensus development workshop.

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Study Question: Can a core outcome set be developed through a global consensus to standardize outcome selection, collection, comparison, and reporting in future male infertility trials?

Summary Answer: A minimum dataset, known as a 'core outcome set', has been developed for randomized controlled trials (RCTs) and systematic reviews evaluating potential interventions for male infertility.

What Is Known Already: Numerous factors, including a failure to consider the perspectives of men with lived experiences of infertility or their partners when developing and conducting RCTs can limit their clinical utility. Selection of outcomes, variations in outcome definitions, and the selective reporting of outcomes based on statistical analysis make the results of infertility research challenging to interpret, compare, and implement.

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Background: This randomized controlled trial provided LC16m8 pre-exposure prophylaxis to high-risk individuals to assess its efficacy for mpox prevention, safety, and immunogenicity.

Methods: This multicenter, randomized, open-label trial enrolled men and women aged ≥18 years at high risk of mpox. Participants were randomly assigned 1:1 to early- or late-vaccination groups.

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Case: A 40-year-old Japanese man with nonobstructive azoospermia (NOA) was found to carry rare variants in a newly identified causative gene for spermatogenic failure. This patient was identified through mutation screening of in 97 men with etiology-unknown isolated NOA.

Outcome: The patient had two heterozygous variants in that affect consensus sequences of splice-donor sites [c.

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Article Synopsis
  • Isodicentric Y chromosomes are common structural variants in humans, particularly with unclear mechanisms behind those involving short arm breakpoints (idic(Yq)).
  • A Japanese man with azoospermia (lack of sperm) and short stature was diagnosed with a unique karyotype featuring a mix of chromosomal abnormalities, including an ∼1.8 Mb deletion in his Y chromosome.
  • The findings suggest the idic(Yq) condition arose from multiple DNA breaks in a specific region (PAR1) of the Y chromosome, and the patient's symptoms might be linked to genetic factors affecting his growth and fertility.
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  • * Findings reveal that harmful CNVs and damaging genetic mutations likely account for at least 8% each of the genetic causes of NOA, while mutations in other genes have a minor influence.
  • * Analysis of 115 unrelated patients identified various AZF-linked CNVs in over half the cases, suggesting a higher prevalence than seen in previous studies from Japan and China.
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  • * In the U.S., a specific strain, called the US N. meningitidis urethritis clade (US_NmUC), is responsible for these urethral infections, and researchers have identified similar strains in Japan known as the Japan N. meningitidis urethritis clade (J_NmUC).
  • * The study highlights the need for global monitoring of these urethritis-linked meningococci to better understand their spread and characteristics, as they may have a common ancestor that is found worldwide.
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Article Synopsis
  • The study aims to create a core outcome set specifically for male infertility research to standardize data collection and enhance research quality.
  • Existing challenges in male infertility research include inconsistencies in outcome measures and lack of participant perspectives, which the new core set will address.
  • An international steering group will use systematic reviews and consensus methods, like the modified Delphi method, to gather input from various stakeholders and determine prioritized outcomes.
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Semen analysis has long been used to evaluate male fertility. Recently, several sperm function tests have been developed. Of those, the sperm DNA fragmentation index (DFI), which describes the status of the sperm DNA, is thought to be a suitable parameter for evaluating male fertility.

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Objectives: To evaluate whether the long-term usage of mirabegron, which was reported to have potential side effects on male reproductive organs in animal studies, was harmful to spermatogenesis in human testis.

Methods: Thirty consecutive patients with spinal cord injury (20-48 years old) who performed clean intermittent catheterization were involved in this study. Ten patients were treated with mirabegron (50 mg/d) for more than 2 years and refrained from using an antimuscarinic agent due to the side effects of constipation and dry mouth.

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The risk of a gonadal tumor is high in testicular disorder of sexual development (DSD) with the Y chromosome, but cases of DSD without the Y chromosome are extremely rare. We reported a gonadal tumor in a phenotypically male individual with 46, XX testicular DSD. A testicular tumor was incidentally found in a 32-year-old phenotypic male who was presented to the hospital with male infertility.

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Purpose: Cryptorchidism is one of the most common causes of non-obstructive azoospermia (NOA) in adulthood. Even if early orchidopexy is performed to preserve fertility potential, some patients still suffer from azoospermia. Fertility potential is significantly lower in bilateral than unilateral cryptorchidism.

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As testicular torsion is a medical emergency, it requires quick diagnosis and treatment. Color Doppler ultrasound (CDUS) is useful for the diagnosis of testicular torsion. An accurate diagnosis can be difficult when CDUS indicates the preservation of blood flow in the testis.

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Purpose: Mosaic loss of chromosome Y (mLOY) is a common feature in elderly men. If mLOY can also occur in young men, it may lead to spermatogenic failure due to loss of spermatogenic genes. Indeed, previous studies detected the 45,X/46,XY karyotype in a few young men with spermatogenic failure.

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The majority of facilities in Japan that offer artificial insemination as part of assisted reproduction programs currently perform semen collection in the early morning. The total motile sperm count of the semen used in intrauterine insemination is an important factor in achieving successful fertilization and subsequent childbirth. The present study was initiated to determine whether semen parameters varied with the time of day at which the semen sample was collected.

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Background: X chromosome inactivation (XCI) is an indispensable process in the development of human female embryos. Reportedly, XCI occurs when a blastocyst contains 10-12 embryonic progenitor cells. To date, it remains unclear whether XCI ratios are normally preserved in Klinefelter syndrome (KS) patients with 47,XXY karyotype.

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Article Synopsis
  • * The study compares semen samples from infertile men with varicocele to fertile men without, revealing that those with varicocele had lower sperm qualities but higher serum FSH and increased levels of seminal oxidation-reduction potential (ORP) and DFI.
  • * A significant positive correlation exists between ORP and DFI in men with varicocele, while both measures negatively correlate with sperm concentration, motility, and total sperm count in these infertile men.
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The azoospermia factor (AZF) region is important for spermatogenesis, and deletions within these regions are a common cause of oligozoospermia and azoospermia. Although several studies have reported this cause, the present research, to the best of our knowledge, is the first large-scale study assessing this factor in Japan. In this study, 1030 male patients with infertility who were examined for Y chromosome microdeletion using the polymerase chain reaction-reverse sequence-specific oligonucleotide (PCR-rSSO) method, a newly developed method for Y chromosome microdeletion screening, were included.

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  • The PROPHET study aims to assess the effectiveness of p2PSA-related indexes in diagnosing prostate cancer in men with PSA levels under 10 ng/ml.
  • Between April 2015 and March 2017, 421 men were evaluated, with substantial findings related to Gleason Grade Group prostate cancer diagnoses.
  • The results indicate that p2PSA-related indexes are more effective than traditional PSA tests at detecting clinically significant prostate cancer and could prevent unnecessary biopsies in 35% to 42% of men without aggressive forms of the disease.
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Pyoderma gangrenosum (PG) is a skin disease characterized by an unknown neutrophilic infiltration in dermis and a nonbacterial destructive ulcer. Post-operative PG is an extremely rare type that occurs around surgical sites during the immediate post-operative period. It is usually diagnosed as surgical site infection at the time of presentation.

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Male factor infertility contributes to about 50% of the incidence of infertility in couples. Semen analysis is key to the diagnosis of the reproductive potential of a male subject. In current practice, men must attend a clinic or other hospital facility to have their semen analyzed.

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  • A 25-year-old male patient with gender identity disorder (GID) in Japan opted for sperm cryopreservation before undergoing male-to-female (MTF) sex reassignment surgery to potentially have children in the future.
  • The institution's ethics committee reviewed and approved the cryopreservation, marking a significant decision for the patient.
  • Unlike in some other countries, Japan currently lacks established guidelines for sperm cryopreservation in individuals with GID.
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Objective: To examine the association between human papillomavirus (HPV) infection and penile cancer among Japanese patients.

Methods: Thirty-four patients with penile cancer were enrolled in this study. DNA was extracted from paraffin-embedded tumor tissue samples, and HPV-DNA tests and genotyping were performed.

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Synopsis of recent research by authors named "Yoshitomo Kobori"

  • - Yoshitomo Kobori's research primarily focuses on male infertility, exploring genetic causes, structural variants, and diagnostic methods related to conditions such as nonobstructive azoospermia and Y chromosome abnormalities.
  • - Recent findings indicate significant genetic factors contributing to isolated nonobstructive azoospermia, including rare gene variants and copy-number variations, along with an urgent need for improved diagnostic techniques in male reproductive health.
  • - Kobori's studies also highlight the prevalence of infectious agents like Neisseria meningitidis in urethritis cases and propose standardized outcome measures for male infertility research to enhance consistency and clarity in clinical applications.