Placental Aromatase Deficiency

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Rupashi; José Eduardo Riceto Loyola Junior, M.D.[2]

Aromatase deficiency is an autosomal recessive disorder in which there is a decrease or absence in the level of aromatase in the body, which leads to impairment in the conversion of androgens to estrogen. This is due to a genetic mutation in the CYP19A1, a subtype of cytochrome P450. Patients affected by this disease typically present with maternal virilization, amenorrhea during puberty in females. Males are rarely affected.

• The evidence of the disease goes back to the year of 1991, when the first case of aromatase deficiency occurred in a 24-year old primigravida and the female fetus showed pseudohermaphroditism.^[1]
• The majority of affected individuals were women during the third trimester of pregnancy manifesting with maternal virilization resulting in hirsutism and acne.

• There is no established system for the classification of placental aromatase deficiency.

• Placental aromatase deficiency is a rare autosomal recessive disorder.
• The CYP19A1 gene is responsible for the production of the enzyme aromatase, which converts androgens to different forms of estrogen.
• Mutation is inherited in an autosomal recessive mode.
• Estrogen is involved in sexual development in females prior to birth and the levels peak during pregnancy. Mutation in the CYP19A1 gene leads to deficiency or absence of activity of aromatase.
• As a result, there is a decrease in the production of estrogen due to lack of conversion of androgens to estrogen and an increase in testosterone and androstenedione levels.
• In pregnant women, excess androgens cross the placenta and enter into the maternal circulation leading to virilization. Female fetuses who are affected have ambiguous genitalia while males develop osteoporosis.^[2]

• CYP19A1 gene mutation primarily causes placental aromatase deficiency and the placenta is not capable of converting androgenic precursors of estrogen to estradiol. Mutations on exons 3,5, and 9 have been reported.^[3]
• Studies suggest that it is more prevalent in consanguineous marriages and both are heterozygous carriers of the mutation.

• Congenital adrenal hyperplasia can be considered as a differential in female patients.^[4]
• While, in male patients, it should be differentiated from:
  • 5 alpha-reductase deficiency, which the levels of both testosterone is low to normal and dihydrotestosterone level is decreased.^[5]
  • Estrogen resistance syndrome
  • 46,XY disorder of sex development due to isolated 17, 20 lyase deficiency.
  • Congenital adrenal hyperplasia due to cytochrome P450 oxidoreductase deficiency.
  • Congenital hypogonadotropic hypogonadism.

• The prevalence of placental aromatase deficiency is unknown.^[6]
• There are only a few cases that have been described in literature.
• The first case in males was reported in 1995.^[7]

• The risk factors evident with placental aromatase deficiency include placental ischemia and preeclampsia.^[8]

• There is insufficient evidence to recommend routine screening for Placental aromatase deficiency.

• Placental aromatase deficiency is a rare entity.
• Defective synthesis of estrogen in aromatase deficiency may result in :
• Delayed Puberty
• Insulin resistance
• Polycystic ovary syndrome^[2]
• Bone disorders such as osteoporosis

• There are no established criteria for the diagnosis of placental aromatase deficiency. The diagnosis may be made clinically.
• Genetic analysis and location of a mutation in the CYP19A1 gene may be done for the confirmation of the placental aromatase deficiency.^[9]

• The hallmark of placental aromatase deficiency is maternal virilization. A positive history of hirsutism, deepening of the voice, and cystic acne is suggestive of placental aromatase deficiency.^[6][10]

• Physical examination of patients with Placental Aromatase Deficiency is usually remarkable for virilization and masculinization in mother during pregnancy, clitoromegaly, and primary amenorrhea in girls during childhood and puberty.^[11]
• Males are usually normal. They may be tall and have reduced bone age.

• An elevated concentration of serum testosterone and reduced levels of estrogen is diagnostic of placental aromatase deficiency.^[12]
• In aromatase deficient girls, basal and GnRH-stimulated FSH levels are elevated.^[6]
• Urinary levels of androgens are usually normal or elevated.

• There are no ECG findings associated with placental aromatase deficiency.

• An x-ray may be helpful in the diagnosis of osteoporosis which manifests mainly in males.^[13] Findings on an x-ray suggestive of osteoporosis include loss of bone mass, cortical thinning, and minor fractures.

• Ultrasound may be helpful in the diagnosis of polycystic ovary syndrome which occurs as a sequela in female patients.^[2]

• There are no CT scan findings associated with placental aromatase deficiency.

• There are no MRI findings associated with placental aromatase deficiency.

• There are no other imaging findings associated with placental aromatase deficiency.

• There are no other diagnostic studies associated with placental aromatase deficiency.

• In patients with aromatase deficiency, lifetime hormone replacement therapy is mandatory.
• Hormone replacement therapy, like oral conjugated estrogen, may be useful to stimulate pubertal growth spurt, breast development, and induce menstruation in females. This may also lead to the resolution of cystic ovaries and promote bone growth.
• After 14 years of age, the combination oral contraceptive may be used.^[6]
• Treatment options for males include transdermal estradiol that helps in increasing bone mineral density.^[10]

• Surgical intervention may be an option for ambiguous genitalia.^[14]

• There are no established measures for the primary prevention of placental aromatase deficiency.

• There are no established measures for the secondary prevention of placental aromatase deficiency.