Adrenal antibodies detect asymptomatic auto-immune adrenal insufficiency in young women with spontaneous premature ovarian failure.

@article{Bakalov2002AdrenalAD,
  title={Adrenal antibodies detect asymptomatic auto-immune adrenal insufficiency in young women with spontaneous premature ovarian failure.},
  author={Vladimir K. Bakalov and Vien H. Vanderhoof and Carolyn A. Bondy and Lawrence M. Nelson},
  journal={Human reproduction},
  year={2002},
  volume={17 8},
  pages={
          2096-100
        }
}
BACKGROUND Auto-immune adrenal insufficiency is a potentially fatal disorder. Young women with spontaneous premature ovarian failure (POF) are at increased risk of developing this condition. METHODS We further characterized auto-immune adrenal insufficiency in this population by conducting an in-depth cross-sectional evaluation of adrenal function in a series of 123 women. RESULTS We uncovered a new diagnosis of adrenal insufficiency in four women [3.2%, 95% confidence interval (CI) 0.2-6.4… 

Tables from this paper

Adrenal cortex autoantibodies in subjects with normal adrenal function.

Premature ovarian insufficiency (POI) and autoimmunity-an update appraisal

Further large clinical studies are needed to investigate the true impact of autoimmunity on POI and to identify the selected groups of patients who are most likely to benefit from immunossuprresive treatment.

Possible role of autoimmunity in patients with premature ovarian insufficiency.

It is presumed that the presence of anti-ovarian antibodies together with abnormalities of cellular immunity may in some cases potentially represent the involvement of an autoimmune mechanism in idiopathic POI.

Premature ovarian insufficiency: evaluation and management

Management of ovarian function before the age of 40 years should address psychological well being, ovarian hormone replacement, and restoration of fertility, and management of associated endocrinopathies, co-morbidity and genetic counseling are also of great relevance.

The hypothalamic-pituitary-adrenal axis in pregnancy: challenges in disease detection and treatment.

Challenges in diagnosis and management of disorders of the hypothalamic-pituitary-adrenal axis in pregnancy are discussed and Appropriate treatment andManagement of labor are reviewed.

Premature ovarian failure.

  • R. Rebar
  • Medicine, Biology
    Obstetrics and gynecology
  • 2009
Hormone therapy should be provided to eliminate symptoms of estrogen deficiency and help prevent osteopenia, but will not necessarily (and inexplicably) prevent pregnancy in the 5-10% of women who conceive spontaneously after the diagnosis is made.

Phenotyping and genetic studies of 357 consecutive patients presenting with premature ovarian failure.

A genetic cause of POF was identified in 25 patients, i.e. 7% of the whole cohort, and novel strategies of P OF phenotyping are in such content mandatory to improve the rate of PTO patients for whom etiology is identified.
...

References

SHOWING 1-10 OF 22 REFERENCES

The natural history of adrenal function in autoimmune patients with adrenal autoantibodies.

Adrenal autoantibodies were found in 23 of 2571 patients with organ-specific autoimmune diseases, in one of 632 first-degree relatives of insulin-dependent diabetic patients, and in none of 375 normal controls; patients who developed Addison's disease showed significant association with HLA-B8 phenotype.

Extra-adrenal endocrine deficiencies in Addison's disease.

Organ-specific autoimmunity in patients with premature ovarian failure

The detection of antiovarian antibodies in only one patient confirms that they are probably detectable in a short period of the disease, and is consistent with previous immunohistochemical data which indicate that autoimmune disorders are common in patients with POF.

II. Adrenal cortex and steroid 21-hydroxylase autoantibodies in children with organ-specific autoimmune diseases: markers of high progression to clinical Addison's disease.

In children with autoimmune endocrine diseases, ACA/21-hydroxylase autoantibodies are important predictive markers for the development of Addison's disease.

Adrenal and ovarian autoimmunity.

Addison’s disease, described first by Thomas Addison (1), is quite rare and has been described in 40–110 cases per 1 000 000 inhabitants (2–4). Currently, in the developed countries the most common

Adrenal-cortex autoantibodies and steroid-producing cells autoantibodies in patients with Addison's disease: comparison of immunofluorescence and immunoprecipitation assays.

A high association between these two markers in patients with different forms of autoimmune Addison's disease and in those with short- or long-standing disease was found; the only case negative for all these three markers suffered from Turner's syndrome.

Lesson of the Week: Addison's disease

Two fatal cases of autoimmune Addison's disease that were diagnosed only at necropsy are reported, which are associated with other immune disorders, including thyroid disease, diabetes mellitus, pernicious anaemia, hypoparathyroidism, and ovarian failure.

Sudden death due to auto-immune Addison’s disease in a 12-year-old girl

Abstract A 12-year-old female suffering from adreno-cortical insufficiency showed symptoms similar to a gastro-enteritis, and severe electrolytic and acid/base disturbances which progressed into

The prevalence of Addison's disease in Coventry, UK.

A prevalence study using a postal survey of general practitioners in Coventry concludes that Addison's disease is 2.4 times more common than previously reported.

Clinical gynecologic endocrinology and infertility

Clinical gynecologic endocrinology and infertility , Clinical gynecologic endocrinology and infertility , کتابخانه دیجیتال جندی شاپور اهواز