Department of Clinical Sciences and Community Health, University of Milan, 20100, Milan, Italy.
Department of Endocrine and Metabolic Diseases and Laboratory of Endocrine and Metabolic Research, IRCCS Istituto Auxologico Italiano, Piazzale Brescia 20, 20149, Milan, Italy.
Hum Genet. 2021 Jan;140(1):77-111. doi: 10.1007/s00439-020-02147-1. Epub 2020 Mar 21.
A genetic basis of congenital isolated hypogonadotropic hypogonadism (CHH) can be defined in almost 50% of cases, albeit not necessarily the complete genetic basis. Next-generation sequencing (NGS) techniques have led to the discovery of a great number of loci, each of which has illuminated our understanding of human gonadotropin-releasing hormone (GnRH) neurons, either in respect of their embryonic development or their neuroendocrine regulation as the "pilot light" of human reproduction. However, because each new gene linked to CHH only seems to underpin another small percentage of total patient cases, we are still far from achieving a comprehensive understanding of the genetic basis of CHH. Patients have generally not benefited from advances in genetics in respect of novel therapies. In most cases, even genetic counselling is limited by issues of apparent variability in expressivity and penetrance that are likely underpinned by oligogenicity in respect of known and unknown genes. Robust genotype-phenotype relationships can generally only be established for individuals who are homozygous, hemizygous or compound heterozygotes for the same gene of variant alleles that are predicted to be deleterious. While certain genes are purely associated with normosmic CHH (nCHH) some purely with the anosmic form (Kallmann syndrome-KS), other genes can be associated with both nCHH and KS-sometimes even within the same kindred. Even though the anticipated genetic overlap between CHH and constitutional delay in growth and puberty (CDGP) has not materialised, previously unanticipated genetic relationships have emerged, comprising conditions of combined (or multiple) pituitary hormone deficiency (CPHD), hypothalamic amenorrhea (HA) and CHARGE syndrome. In this review, we report the current evidence in relation to phenotype and genetic peculiarities regarding 60 genes whose loss-of-function variants can disrupt the central regulation of reproduction at many levels: impairing GnRH neurons migration, differentiation or activation; disrupting neuroendocrine control of GnRH secretion; preventing GnRH neuron migration or function and/or gonadotropin secretion and action.
先天性孤立性促性腺激素低下症(CHH)的遗传基础在近 50%的病例中可以确定,但不一定是完整的遗传基础。下一代测序(NGS)技术已经发现了大量的基因座,每个基因座都阐明了我们对人类促性腺激素释放激素(GnRH)神经元的理解,无论是在其胚胎发育方面,还是在作为人类生殖“指示灯”的神经内分泌调节方面。然而,由于与 CHH 相关的每个新基因似乎只支持总患者病例的另一个小百分比,因此我们仍然远未全面了解 CHH 的遗传基础。患者一般无法从遗传学的新疗法中受益。在大多数情况下,即使是遗传咨询也受到明显表达和外显率可变性的限制,这些可变性可能是由已知和未知基因的寡基因性所支撑的。只有当个体是同一基因的纯合子、半合子或复合杂合子时,通常才能建立稳健的基因型-表型关系,这些个体的变异等位基因预测是有害的。虽然某些基因纯粹与正常嗅觉 CHH(nCHH)相关,某些基因纯粹与嗅觉缺失型(Kallmann 综合征-KS)相关,而其他基因可能与 nCHH 和 KS 相关-有时甚至在同一个家族中。尽管 CHH 与生长和青春期发育迟缓(CDGP)的遗传重叠并未实现,但已经出现了以前未预料到的遗传关系,包括联合(或多种)垂体激素缺乏症(CPHD)、下丘脑性闭经(HA)和 CHARGE 综合征。在这篇综述中,我们报告了与 60 个基因相关的表型和遗传特征的当前证据,这些基因的功能丧失变异可以在许多层面上破坏生殖的中枢调节:损害 GnRH 神经元的迁移、分化或激活;破坏 GnRH 分泌的神经内分泌控制;阻止 GnRH 神经元迁移或功能以及/或促性腺激素的分泌和作用。