Endo
Primary Ovarian Insufficiency
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Primary Ovarian Insufficiency
, Premature Ovarian Failure, Hypergonadotrophic Ovarian Failure
See Also
Amenorrhea
Secondary Amenorrhea
Menopause
Epidemiology
Incidence
: 1% of women
Pathophysiology
Follicle depletion or dysfunction resulting in impaired ovarian function
Causes
Idiopathic (>90%)
Chromosomal Abnormality
X-
Chromosome
abnormality (e.g.
Turner Syndrome
)
Y-
Chromosome
presence abnormality
Infection (e.g.
Mumps
)
Autoimmune Disease
directed at
Ovary
Empty Sella Syndrome
Chemotherapy
or
Radiation Exposure
related
Associated Conditions
FMR1
Gene
premutation
Associated with risk of
Fragile X Syndrome
in children
Thyroid
autoimmune disorders
Consider testing for
Thyroid
autoantibodies
Adrenal autoimmune disorders
Consider testing for adrenal autoantibodies
Turner Syndrome
May present only as
Short Stature
and
Amenorrhea
Obtain karyotype from women with
Short Stature
and Primary Ovarian Insufficiency
Multi-system implications of
Turner Syndrome
require surveillance and highlight the importance of testing
Diagnosis
Woman younger than age 40 years old with
Amenorrhea
or
Oligomenorrhea
>=4 months AND
Follicle Stimulating Hormone
in menopausal range (>25 mIU/ml)
Single FSH >25 mIU/ml is sufficient
Previously required 2 consecutive tests, one month apart (an may still consider)
Symptoms
See
Vasomotor Symptoms of Menopause
Hot Flushes
Vaginal Dryness
Amenorrhea
Labs
First Line
See
Secondary Amenorrhea
See
Markers of Ovarian Reserve
Anti-Mullerian Hormone
Thyroid Stimulating Hormone
Follicle Stimulating Hormone
Used as part of diagnosis above
Labs
Second-Line Testing for Non-Iatrogenic Causes
Primary Ovarian Insufficiency labs
FMR1
Gene
Premutation (fragile-X gene)
21-Hydroxylase autoantibodies (
Autoimmune Adrenalitis
and
Addison's Disease
)
Premature Ovarian Insufficiency secondary to Autoimmune Polyendocrine Syndrome
Karyotype
Turner Syndrome
Monosomy X (45,X)
Mosaicism (e.g. 45,X / 46,XX)
Y Chromatin (Y
Chromosome
)
Swyer syndrome (46,XY gonadal dysgenesis)
Mosaic
Turner Syndrome
Labs
Other (as Indicated for secondary cause)
Fastin
g
Serum Glucose
Calcium
Phosphorus
Total
Protein
Albumin to globulin ratio
Complete Blood Count
(CBC)
Erythrocyte Sedimentation Rate
(ESR)
Rheumatoid Factor
(RF)
Antinuclear Antibody
(ANA)
Thyroid Stimulating Hormone
(TSH)
Morning
Serum Cortisol
Level
Management
Adults
Estrogen Replacement Therapy
Continue until at least average typical
Menopause
age (e.g. age 50 years old)
Medications
Transdermal Estradiol
100 mcg (or oral forms of
Estradiol
>=2 mg/day) AND
Progesterone
(if intact
Uterus
)
See
Sequential Estrogen Replacement
See
Continuous Estrogen Replacement
Efficacy
Reduces
Osteoporosis
and
Fracture
risk
Reduces
Vasomotor Symptoms of Menopause
Reduces uterine atrophy
Pregnancy
Risk of variable fertility (10% have spontaneous resolution and risk of pregnancy)
Consider combined
Hormonal Contraception
instead of
Estrogen Replacement
to prevent pregnancy
Otherwise pregnancy is possible with donor implantation
Osteoporosis Prevention
Calcium Supplementation
1200 mg daily
Vitamin D Supplement
ation 800 IU daily (or more)
DEXA Scan
at baseline and then every 1-3 years
Cardiovascular Disease Prevention
Annual
Blood Pressure Measurement
Hyperlipidemia
screening every 5 years
Management
Adolescents
Estrogen
therapy
Consult pediatric endocrinology
Start at age 11-12 years with phased hormonal dosing
Monitoring
Serum Estradiol
Obtain every 4-6 months
Pelvic
Ultrasound
Evaluate for
Uterine Size
and endometrial thickness
Periodically during induction phase
Repeat at
Puberty
completion
Wrist XRay
Obtain yearly (until induction completion)
DEXA Scan
Obtain at initiation of hormonal therapy
Repeat every 1-3 years
References
Klein (2026) Am Fam Physician 114(1): 72-85 [PubMed]
Klein (2013) Am fam Physician 87(11): 781-8 [PubMed]
Nelson (2009) N Engl J Med 360(6): 606-14 [PubMed]
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