Abstract
Context
Functional hypothalamic amenorrhea (HA) is a common, acquired form of hypogonadotropic hypogonadism that occurs in the setting of energy deficits and/or stress. Variability in individual susceptibility to these stressors, HA heritability, and previous identification of several rare sequence variants (RSVs) in genes associated with the rare disorder, isolated hypogonadotropic hypogonadism (IHH), in individuals with HA suggest a possible genetic contribution to HA susceptibility.
Objective
We sought to determine whether the burden of RSVs in IHH-related genes is greater in women with HA than controls.
Design
We compared patients with HA to control women.
Setting
The study was conducted at secondary referral centers.
Patients and Other Participants
Women with HA (n = 106) and control women (ClinSeq study; n = 468).
Interventions
We performed exome sequencing in all patients and controls.
Main Outcome Measure(s)
The frequency of RSVs in 53 IHH-associated genes was determined using rare variant burden and association tests.
Results
RSVs were overrepresented in women with HA compared with controls (P = .007). Seventy-eight heterozygous RSVs in 33 genes were identified in 58 women with HA (36.8% of alleles) compared to 255 RSVs in 41 genes among 200 control women (27.2%).
Conclusions
Women with HA are enriched for RSVs in genes that cause IHH, suggesting that variation in genes associated with gonadotropin-releasing hormone neuronal ontogeny and function may be a major determinant of individual susceptibility to developing HA in the face of diet, exercise, and/or stress.
OR11-6 Rare Sequence Variants in GnRH-Associated Genes May Contribute to Variable Susceptibility to Environmental Stressors in Functional Hypothalamic Amenorrhea
