Genetics of Male Infertility: A Marker of Overall Health

男性不育的遗传学：整体健康的标志

• 批准号: 10613339
• 负责人: Kyle Edwin Orwig
• 金额: $ 162.38万
• 依托单位: MAGEE-WOMEN'S RES INST AND FOUNDATION
• 依托单位国家: 美国
• 财政年份: 2019
• 资助国家: 美国
• 起止时间: 2019-09-01 至 2025-03-31
• 项目状态: 未结题
• 来源: https://reporter.nih.gov/project-details/10613339
• 关键词: Acceleration; Adoption; Adult; Age; Benefits and Risks; Biological; CRISPR/Cas technology; Cardiovascular Diseases; Cell Maintenance; Center for Translational Science Activities; Child; Cities; Clinic; Collaborations; Communication; Complement; Counseling; Couples; Data; Data Coordinating Center; Development; Diagnosis; Disease; Education; Education and Outreach; Epigenetic Process; Faculty Workshop; Family; Family member; Female; Fertility; Genes; Genetic; Germ Cells; Health; High School Student; Human; Individual; Infertility; Institution; K-12 student; Knowledge; Lead; Learning Module; Life Expectancy; Link; Male Infertility; Malignant Neoplasms; Medical; Medical center; Metabolic syndrome; Middle School Student; Mission; Mutant Strains Mice; Mutation; New York; Oregon; Patient Recruitments; Patients; Phenotype; Pilot Projects; Policies; Pregnancy; Program Description; Questionnaires; Recording of previous events; Reproduction; Reproductive Health; Reproductive Medicine; Research; Research Personnel; Science; Sertoli cell only syndrome; Somatic Cell; Specialized Center; Students; Sum; Technology; Testing; Testis; Time; Translating; Translations; United States; Universities; Variant; Washington; Well in self; Work; assisted reproduction; career; clinical development; clinical diagnostics; comorbidity; comorbidity Index; cost; data exchange; diagnostic screening; effectiveness evaluation; epidemiologic data; epigenome; fertility preservation; gene therapy; genetic variant; genome editing; genome sequencing; human model; idiopathic infertility; improved; individualized medicine; junior high school; laboratory experiment; male; man; medical schools; men; mouse model; novel; personalized medicine; programs; prospective; reproductive; safety and feasibility; sertoli cell; stem cell function; stem cells; targeted treatment; teacher; underserved community; whole genome

Abstract: Overall Azoospermia impacts 1% of men globally, which translates to 645,000 men between the ages of 20 and 50 in the United States. It is estimated that genetic causes explain 50% of infertility. Epidemiological data suggest that fertility status may be a marker of overall health, but the genetic underpinnings are just beginning to be understood. Improved knowledge about the genetic basis of infertility and associated overall health comorbidities will aid in the counseling of infertile couples; justify the development of diagnostic screens; and may lead to patient-specific treatment options. In the current personalized medicine era with reduced cost whole genome sequencing and facile genome editing technologies, it is feasible to discover genetic underpinnings of infertility and overall health comorbidities and develop targeted therapies. Project I will discover genetic variants in men with azoospermia to identify targets for development of clinical diagnostics or therapy. Project I will use Charlson Comorbidity Index questionnaires to determine whether infertile patients or their family members have histories of other overall health comorbidities. Project II will validate infertility- associated genetic variants identified in Project I and characterize the fertility and overall health phenotypes. Project II will also work collaborate with Project III to determine the impact of epigenetic perturbations on spermatogonial stem cell function. Project III will develop Sertoli cell and germ cell gene therapies in mouse models of azoospermia and will produce critical safety and feasibility data to inform the public dialogue on the risks and benefits of gene therapy in and around the germline. The Pilot project will discover the epigenetic landscape of germ cells and somatic cells from the testes of fertile versus infertile men. Core A will provide the administrative oversight and facilitate communications and data exchange among projects and cores to ensure that this P50 program achieves an impact that is greater than the sum of its parts. The Education and Outreach Core will maximize the public impact of this P50 by developing hands-on teaching modules to educate middle school and high school students as well as adults in underserved communities about reproductive medicine and the genetics of infertility. Modules will be tested and validated in the Pitt Mobile Science lab before deploying to teacher workshops in St. Louis, Pittsburgh, Ithaca and New York allowing teachers to implement the modules in their classrooms. Male focused teaching modules will also be shared with P50 centers in Oregon and at Northwestern to complement their existing female-focused hands-on modules.

摘要：总体 无精症影响全球 1% 的男性，即 20 岁至 50 岁之间的男性有 645,000 名 美国。据估计，50% 的不孕症是由遗传原因造成的。流行病学数据表明 生育状况可能是整体健康的一个标志，但遗传基础才刚刚开始 明白了。提高对不孕症遗传基础和相关整体健康状况的了解 合并症将有助于不孕夫妇的咨询；证明诊断技术发展的合理性 屏幕；并可能导致针对患者的具体治疗选择。在当前个性化医疗时代 降低成本的全基因组测序和简便的基因组编辑技术，发现是可行的 不孕症和整体健康合并症的遗传基础，并开发有针对性的治疗方法。项目一 将发现无精子症男性的遗传变异，以确定临床诊断开发的目标 或治疗。项目一将使用查尔森合并症指数问卷来确定不孕患者是否 或其家庭成员有其他整体健康合并症的病史。项目 II 将验证不孕症—— 项目 I 中确定的相关遗传变异，并表征了生育力和整体健康表型。 项目 II 还将与项目 III 合作，以确定表观遗传扰动对 精原干细胞功能。项目 III 将开发小鼠支持细胞和生殖细胞基因疗法 无精子症模型，并将产生关键的安全性和可行性数据，为公众对话提供信息 种系内及其周围基因治疗的风险和益处。该试点项目将发现表观遗传 生育男性和不育男性睾丸的生殖细胞和体细胞的景观。核心A将提供 行政监督并促进项目和核心之间的沟通和数据交换，以确保 该 P50 计划所产生的影响大于其各部分之和。教育和外展 Core 将通过开发实践教学模块来教育中层学生，从而最大限度地提高 P50 的公众影响力 向中小学生以及服务欠缺社区的成年人介绍生殖医学 以及不孕不育的遗传学。模块将在皮特移动科学实验室之前进行测试和验证 部署到圣路易斯、匹兹堡、伊萨卡和纽约的教师讲习班，让教师能够实施 他们教室里的模块。以男性为中心的教学模块也将与 P50 中心共享 俄勒冈州和西北大学，以补充其现有的以女性为中心的实践模块。

项目成果

Germ cell nests in adult ovaries and an unusually large ovarian reserve in the naked mole-rat.

生殖细胞在成年卵巢中筑巢，裸鼹鼠的卵巢储备异常大。

• 发表时间: 2021
• 作者: Place, Ned J;Prado, Alexandra M;Faykoo;Brieño;Albertini, David F;Holmes, Melissa M
• 通讯作者: Holmes, Melissa M

Genomic study of TEX15 variants: prevalence and allelic heterogeneity in men with spermatogenic failure.

TEX15 变体的基因组研究：生精障碍男性的患病率和等位基因异质性。

• 发表时间: 2023
• 作者: Qureshi, Sidra;Hardy, Jimmaline J;Pombar, Christopher;Berman, Andrea J;Malcher, Agnieszka;Gingrich, Tara;Hvasta, Rachel;Kuong, Jannah;Munyoki, Sarah;Hwang, Kathleen;Orwig, Kyle E;Ahmed, Jawad;Olszewska, Marta;Kurpisz, Maciej;Conrad, Donald F
• 通讯作者: Conrad, Donald F

Utilizing artificial intelligence in academic writing: an in-depth evaluation of a scientific review on fertility preservation written by ChatGPT-4.

在学术写作中利用人工智能：对 ChatGPT-4 撰写的关于生育力保存的科学评论的深入评估。

• 发表时间: 2024-04-15
• 影响因子: 3.1
• 作者: Safrai, Myriam;Orwig, Kyle E
• 通讯作者: Orwig, Kyle E

The Sertoli cell expressed gene secernin-1 (Scrn1) is dispensable for male fertility in the mouse.

支持细胞表达的基因 secernin-1 (Scrn1) 对于小鼠的雄性生育能力是必不可少的。

• 发表时间: 2021
• 作者: Houston, Brendan J;Nagirnaja, Liina;Merriner, D Jo;O'Connor, Anne E;Okuda, Hidenobu;Omurtag, Kenan;Smith, Craig;Aston, Kenneth I;Conrad, Donald F;O'Bryan, Moira K
• 通讯作者: O'Bryan, Moira K

Human Spermatogenesis: Insights From the Clinical Care of Men With Infertility.

人类精子发生：不育男性临床护理的见解。

• 发表时间: 2022
• 作者: Schlegel; Peter N
• 通讯作者: Peter N