This project seeks to improve the clinical care available to patients with disorders of ovarian follicle function and ovulation through research using animal models as well as clinical protocols. In pursuing this goal, we expect to expand understanding of the ovarian follicle in health and disease. We have focused on premature ovarian failure, a condition that prematurely terminates ovarian function and fertility in 1% of women. We have particular interest in autoimmunity as a cause of ovarian failure. In a mouse model, we found that autoantibodies from mice with experimental autoimmune oophoritis bind to MATER, a novel 120 kd protein that is specific to the oocyte cytoplasm. Mater is a novel oocyte-specific maternal effect gene whose product is essential for embryonic development beyond the two-cell stage. MATER provides a new determinant with which to investigate the mechanisms of autoimmune premature ovarian failure as well as mechanisms of early embryonic developmental failure. In the clinic, we have found that premature ovarian failure is more complex than merely a premature menopause. One half of these young women have ovarian follicles remaining that function intermittently. We are investigating the mechanisms of this ovarian follicle dysfunction. In some cases the dysfunction is caused by autoimmune oophoritis; in other cases it is due to low follicle number. We are also investigating other adverse health consequences of premature ovarian failure. We found that these young women have deficient circulating free testosterone levels, and, surprisingly, two thirds of our patients have a reduced bone density that may place them at increased risk of hip fracture. We have clinical studies underway to develop hormone replacement methods appropriate specifically to these young women, and we are working to develop a clinically useful test that will detect ovarian insufficiency earlier in its course. Approximately 3% of women with premature ovarian failure will also develop autoimmune adrenal insufficiency, and we are also working to develop an efficient screening test to detect this earlier in its course. Premature ovarian failure is clearly a more complex condition than has been previously recognized.

Project Start
Project End
Budget Start
Budget End
Support Year
10
Fiscal Year
2000
Total Cost
Indirect Cost
Name
U.S. National Inst/Child Hlth/Human Dev
Department
Type
DUNS #
City
State
Country
United States
Zip Code
Popat, Vaishali B; Calis, Karim A; Vanderhoof, Vien H et al. (2009) Bone mineral density in estrogen-deficient young women. J Clin Endocrinol Metab 94:2277-83
Hubayter, Ziad R; Popat, Vaishali; Vanderhoof, Vien H et al. (2009) A prospective evaluation of antral follicle function in women with 46,XX spontaneous primary ovarian insufficiency. Fertil Steril :
Kalantaridou, Sophia N; Vanderhoof, Vien H; Calis, Karim A et al. (2008) Sexual function in young women with spontaneous 46,XX primary ovarian insufficiency. Fertil Steril 90:1805-11
McConkie-Rosell, Allyn; Abrams, Liane; Finucane, Brenda et al. (2007) Recommendations from multi-disciplinary focus groups on cascade testing and genetic counseling for fragile X-associated disorders. J Genet Couns 16:593-606
Ventura, June L; Fitzgerald, O Ray; Koziol, Deloris E et al. (2007) Functional well-being is positively correlated with spiritual well-being in women who have spontaneous premature ovarian failure. Fertil Steril 87:584-90
Wittenberger, Michael D; Hagerman, Randi J; Sherman, Stephanie L et al. (2007) The FMR1 premutation and reproduction. Fertil Steril 87:456-65
Armstrong, Alicia Y; Calis, Karim A; Nelson, Lawrence M (2007) Do survivors of childhood cancer have an increased incidence of primary ovarian insufficiency? Nat Clin Pract Endocrinol Metab 3:326-7
Di Pasquale, Elisa; Rossetti, Raffaella; Marozzi, Anna et al. (2006) Identification of new variants of human BMP15 gene in a large cohort of women with premature ovarian failure. J Clin Endocrinol Metab 91:1976-9
Tung, Joyce Y; Rosen, Mitchell P; Nelson, Lawrence M et al. (2006) Novel missense mutations of the Deleted-in-AZoospermia-Like (DAZL) gene in infertile women and men. Reprod Biol Endocrinol 4:40
Corrigan, Emily C; Nelson, Lawrence M; Bakalov, Vladimir K et al. (2006) Effects of ovarian failure and X-chromosome deletion on body composition and insulin sensitivity in young women. Menopause 13:911-6

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