Skip to main content

FINASTERIDE IN THE TREATMENT OF FEMALE ANDROGENIC ALOPECIA

academics

 

Clinical research courses

{ DOWNLOAD AS PDF }

ABOUT AUTHORS
Priyanka T*, Giri raja sekhar D, Lekhanth A, Revanth.A
Department of Pharmacy Practice,
Annamacharya College of Pharmacy
Rajampet, Andhra Pradesh, India
*priyankat283@gmail.com

ABSTRACT
Hair loss in women is twice more distressing in women when compared to men. The most common cause of hair loss in women is Female Androgenic Alopecia (FAGA) which shows Ludwig, Christmas tree, Hamilton pattern. Androgenic alopecia is due to the increased activity of 5α-reductase in the hair follicles which results in the gradual transformation of large, terminal follicles to small, miniaturized follicles. Finasteride is a 5α-reductase II enzyme which inhibits the conversion of testosterone to dihydro testosterone and is effectively used in the management of the male pattern androgenic alopecia with a dose of 1mg/day but this article mainly reviews the use of Finasteride in the female androgenic alopecia. Studies so far reported increased scalp hair counts, hair density, hair regrowth both by the patient assessment and photographs by the blinded expert panel. Relevant literatures were chosen to determine the efficacy of Finasteride in the treatment of female Androgenic Alopecia.

REFERENCE ID: PHARMATUTOR-ART-2282

PharmaTutor (ISSN: 2347 - 7881)

Volume 2, Issue 11

Received On: 27/09/2014; Accepted On: 01/10/2014; Published On: 01/11/2014

How to cite this article: T Priyanka, GR sekhar, A Lekhanth; Finasteride in the Treatment of Female Androgenic Alopecia; PharmaTutor; 2014; 2(11); 10-15

BACKGROUND
Hair loss can be distressing for the female patient, with women being twice as likely as men to be very-to-extremely upset and up to 70% of women reporting high levels of distress over their hair loss.[1] Female androgenic alopecia (FAGA), or female pattern alopecia, is the most common form of hair loss in women. The incidence increases with age with 50% to 75% of women older than 65 years with FAGA compared to 6% to 12% of women aged 20 to 30 years.[2]

Pathophysiology
Androgenic alopecia (AGA) is induced by androgens in genetically susceptible women and men. Hair follicles of women and men with AGA have increased 5α-reductase activity and increased levels of dihydro testosterone (DHT). DHT, which is formed by the peripheral conversion of testosterone by 5α-reductase, is thought to be responsible for the characteristic miniaturization of scalp hair follicles in AGA. In genetically susceptible hair follicles, DHT binds to the androgen receptor, and the hormone-receptor complex then activates the genes responsible for the gradual transformation of large, terminal follicles to small, miniaturized follicles. Over successive hair cycles in AGA, the duration of anagen shortens and matrix size decreases, resulting in smaller follicles that produce shorter, finer, miniaturized hairs that cover the scalp less and less well. These miniaturized hairs of various lengths and diameters are the hallmark of AGA. The number of follicles per unit area, however, remains the same. [3]

Clinical features:
Three different patterns of hair loss can be observed:
1. Diffuse thinning of the crown region with preservation of the frontal hairline (Ludwig’s type). The severity of this pattern can be evaluated using the 3-point Ludwig scale or the 5-point Sinclair scale.

2. Frontal midline recession/breach with thinning and widening of the central part of the scalp without diffuse hair loss, best known as “Christmas tree pattern” as described by Olsen. This pattern also involves the superior part of the scalp but the thinning is wider in the frontal scalp giving the alopecic area a triangular shaped figure resembling a christmas tree.

3. Thinning associated with bitemporal recession (Hamilton type). This presentation has the same classical distribution of male pattern baldness: thinning evident in the lateral-frontal part of the superior scalp and vertex. [4]

Source: Medscape. Available at medscape.com/viewarticle/735007_7

Finasteride with antiandrogenic effect:
Finasteride works by inhibiting 5α-reductase II enzyme, which is responsible for catalyzing the conversion of testosterone to the much more active chemical 5 Dihydrotestosterone. Thus, finasteride suppresses overall androgen activity by restricting total circulating androgen activity. [5] Finasteride reduces hair loss and stimulates hair regrowth by increasing hair counts in men taking 1 mg daily. [6]

Finasteride in the female hair loss
The effectiveness of the Finasteride in the male androgenic alopecia is well documented but to study the effectiveness of the Finasteride in the female androgenic alopecia is evaluated in this earlier study.This study was a double-blind, placebo-controlled, randomized, multicenter trial which included 137 members between the age 41-60 years. Selected patients were randomized into Finasteride and placebo group where they receive Finasteride 1 mg/day or placebo for 1 year. The therapeutic endpoint of the study was to evaluate scalp hair counts, patient and investigator assessments, assessment of global photographs by a blinded expert panel, and histological analysis of scalp biopsy specimens.

The results of the study after 12 months were that Finasteride group did not show any difference from the placebo group despite of the reduced serum dihydrotestosterone .[7]

Later many evidences reported in the improvement of hair growth after long term use and high doses of Finasteride. In a case series 41 postmenopausal women with increased androgen levels and SAHA (seborrhea, acne, hirsut­ism, and alopecia) were given 2.5 mg/d for 2 years and noted hair regrowth in all 41 women. [8]

Finasteride 1.25mg/d was given in 4 postmenopausal women with hyperandrogenism having hair loss with characteristics of both male and female patterns. And was reported improvement in hair loss and hair growth after 6 month-2.5 years. [9] 

Finasteride 5mg/week was given in 67 year old women with normoandrogenic levels for 12 months and patient reported increased hair density. [10]

Finasteride 2.5-5 mg/day is given to 5 postmenopausal women with normal androgen levels for 1 year and the outcome measures evaluated were patient and investigator assessments, and review of photographs taken at baseline and at months 6, 12 and 18. The results of the study were that patients reported decreased hair loss, increased hair growth and improved appearance of hair which was confirmed by investigator assessments and photographs.[11]

Valsecchi et al., reported a case of 51 year old patient who was normoandrogenic and not responsive to minoxidil therapy and was started on Finasteride 1mg/d showed a hair regrowth after 12-13 months of therapy.[12]

Iorizzo et al conducted a study to determine the efficacy of Finasteride in the premenopausal women using oral contraceptives by giving a oral dose of Finasteride 2.5mg/d for 12 months and the efficacy of the treatment is measured by self administered questionnaire to patients, global photography and the hair density score from videodermoscopy and the results showed improvement in 23 patients, no improvement in 13 patients and 1 showed worsening of the condition. [13]

Finasteride 2.5mg/d in postmenopausal women of age 47 years showed hair loss stabilization at 6 months and hair regrowth at 10 months who had hair loss due to treatment with estrogen and testosterone after the hysterectomy and bilateral salpingo-oophorectomy. [14]

Finasteride 5mg/d was given in 12 normoandrogenic patients in which 9 showed improvement from the treatment and the other 3did not show improvement due to the other reasons of alopecia.[15]  A 44 year old premenopausal women with normal androgen levels was given 2.5 mg/d of Finasteride for 3.5 months and showed decreased hair loss and hair regrowth. [2]

Finasteride 5mg/d was administered in 40 normoandrogenic postmenopausal women with androgenic alopecia for 18 months and the outcome measures were patient's satisfaction and global photograph assessment. The results of the study were that on patient satisfaction 22 showed improvement, 12 showed moderate improvement and 6 showed no improvement. On global photo assessment, 8 patients showed no improvement, 16 showed moderate improvement and 16 showed significant improvements at the 6th month and a slight improvement was observed in 12 and 18th month. Four patients reported  reduced libido and one patient showed elevated liver enzymes. [16]

In contrast, 48 hyperandrogenic women with alopecia were randomized into three groups in which cyproterone acetate (50 mg), flutamide (250 mg) and finasteride (5 mg) daily were given and the efficacy of the treatment was checked after 1 year and was found that flutamide showed reduction in 21% of Ludwig scores whereas treatment with finasteride did not show hair growth. [17]

NOW YOU CAN ALSO PUBLISH YOUR ARTICLE ONLINE.

SUBMIT YOUR ARTICLE/PROJECT AT editor-in-chief@pharmatutor.org

Subscribe to Pharmatutor Alerts by Email

FIND OUT MORE ARTICLES AT OUR DATABASE

Treatment of female androgenic alopecia with oral Finasteride :

Reference, year

Study type

Number of women

Androgen  levels

Menopausal state

Treatment dose

Length of treatment

Primary findings

Price et al

(2000)[7]

Double blind, randomized, placebo-controlled trial

137(67 in the treatment group; 70 in the placebo group

Normal

Postmeno
pausal


1 mg/day

1 yr

No difference between Finasteride group and placebo group

Camacho(2001) [8]

Case series

41

Increased (due to SAHA)


Postmeno
pausal


2.5 mg/d

2 yr

Improvement in all 41 women with SAHA

Shum et al(2002) [9]

Case series

4

increased

Postmeno
pausal


1.25 mg/d

Upto 2.5yr

Improvement in all women


Thai et al.,

2002 [10]

Case report

1

Normal

Postmeno
pausal


5 mg/week

12 months

Hair regrowth

Carmina et al., 2003 [17]

Randomized study

48

increased

premeno
pausal

5mg/ daily

1 yr

No improvement

Trüeb; Swiss

Trichology Study Group

(2004)[11]

Case series

5

Normal

Postmeno
pausal


Four women were treated with 2.5 mg/d and 1 women treated with 5mg/day

1 yr

Improved in all women after 6 months of initiation of treatment


Valsecchi et al.,

(2004) [12]

Case report

1

normal

postmeno
pausal

1 mg/d

13 months

Hair regrowth

Iorizzo et al (2006) [13]

Case series

37

increased

Premeno
pausal


2.5 mg/d and oral contraceptives

12 months

23 were improved.No improvement in 13 patients. 1 patient worsening of the condition.

Hong et al

(2007) [14]

Case report

1

increased

Postmeno
pausal


2.5 mg/d

10 months

Hair regrowth


Kohler et al.,2007 [15]

Retrospective study

12

Normal

Premeno
pausal

5 mg/d


9 improved, 3 no improvement

 Olga Boychenko et al.,

2012 [2]

Case report

1

Normal

Premeno
pausal

1.25 mg/d

3.5 months

Hair regrowth

Oliveira et al., 2013 [16]


40

Normal

Postmeno
pausal

5mg/d

18 months

22 patients significant improvement, 12 patients moderate improvement, 6 patients no improvement.

CONCLUSION
Finasteride is potential in treating the androgenic alopecia of postmenopausal and premenopausal women but however not effective in all patients. As Finasteride belongs to the pregnancy category X its use in premenopausal patients should not be overlooked. Further evaluations can be done to know the safety and efficacy of Finasteride in different doses and populations.

REFERENCES
1. British Columbia poison and drug information centre. Available at dpic.org/article/professional/finasteride-hair-loss-womenaccessed on (25/08/2014).
2. Olga Boychenko, Robert M. Bernstein, Eric S. Schweiger. Finasteride in the Treatment of Female Pattern (Androgenic) Alopecia: A Case Report and Review of the Literature.cutaneous medicine for the practitioner.2012;90:73-76.
3. Vera H Price. Androgenetic Alopecia in Women. Journal of Investigative Dermatology Symposium Proceedings. 2003;8: 24–27.
4. Ingrid Herskovitz, Antonella Tosti. Female Pattern Hair Loss. International Journal of Endocrinology and Metabolism. 2013 Oct; 11(4): e9860.1-8
5. Quan Q Dinh, Rodney Sinclair. Female pattern hair loss: Current treatment concepts. Clinical Interventions in Aging. 2007; 2(2): 189–199.
6. Blumeyer A, Tosti A, Messenger A, Reygagne P, Del Marmol V, Spuls PI, et al. Evidence-based (S3) guideline for the treatment of androgenetic alopecia in women and in men. Journal of the German Society of Dermatology. 2011;9 Suppl 6:S1-57
7. Price VH, Roberts JL, Hordinsky M, et al. Lack of effi¬cacy of finasteride in postmenopausal women with andro¬genetic alopecia. Journal of the American Academy of Dermatology. 2000;43(5, pt 1):768-776.
8. Camacho F. Hirsutismo. enfoque clinico terapéutico. Actualizaciones Terapeuticas Dermatologicas 2001;24:190-206.
9. Shum KW, Cullen DR, Messenger AG. Hair loss in women with hyperandrogenism: four cases responding to finaster-ide. Journal of the American Academy of Dermatology. 2002;47:733-739.
10. Thai KE, Sinclair RD. Finasteride for female androgenetic alopecia. British Journal of Dermatology. 2002; 147: 812-813.
11. Trüeb RM; Swiss Trichology Study Group. Finaster-ide treatment of patterned hair loss in normoandro¬genic postmenopausal women. Dermatology. 2004;209:202-207.
12. Valsecchi R, Leghissa P, Riva M. Female pattern alopecia treated by finasteride: a case forward. Acta Dermato Venerologica. 2004; 84: 488-489.
13. Iorizzo M, Vincenzi C, Voudouris S, et al. Finasteride treatment of female pattern hair loss. Archives of Dermatology. 2006;142:298-302.
14. Hong JB, Chiu HC, Chan JY, et al. A woman with iat¬rogenic alopecia responding to finasteride [published online ahead of print January 30, 2007]. British Journal of Dermatology. 2007;156:754-755.
15. Kohler C, Tschumi K, Bodmer C, Schneiter M, Birkhauser M. Effect of finasteride 5 mg (Proscar®) on acne and alopecia in female patients with normal serum levels of free testosterone. Gynecology Endocrinology. 2007; 23: 142-145.
16. R Oliveira-Soares, J Maia e Silva, M Peres Correia, Marisa C André. Finasteride 5 mg/day Treatment of Patterned Hair Loss in Normo-androgenetic Postmenopausal Women. International Journal of Trichology. 2013; 5(1): 22–25.
17. Carmina E, Lobo RA. Treatament of hyperandrogenic aloipecia in women. Fertility and  Sterility. 2003; 79: 91-95.

NOW YOU CAN ALSO PUBLISH YOUR ARTICLE ONLINE.

SUBMIT YOUR ARTICLE/PROJECT AT editor-in-chief@pharmatutor.org

Subscribe to Pharmatutor Alerts by Email

FIND OUT MORE ARTICLES AT OUR DATABASE