Ερευνα του 2009 λεει οτι φιναστεριδη σε μορφη gel 1% εχει τα ιδια αποτελεσματα με φιναστεριδη σε happy
Comparing the therapeutic effects of finasteride gel and tablet in treatment of the androgenetic alopecia
Zohreh Hajheydari1, Jafar Akbari2, Majid Saeedi2, Leila Shokoohi1
1 Department of Dermatology, Boo Ali Sina (Avicenna) Hospital, Mazandaran University of Medical Sciences, Sari, Iran
2 Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran
Abstract
Background: Finasteride, a type P-selective 5a-reductase inhibitor, as a causative agent of decreasing dihydroxy testestrone (DHT) level, is effective in the treatment of male androgenic alopecia. Aim: We compared the local and oral finasteride in the treatment of androgenic alopecia. Method: This is a double blind, randomized clinical trial study of 45 male patients, who were referred with alopecia to the private clinics and departments in Boo-Ali Sina Hospital, in Sari. Patients with male androgenic alopecia were selected according to the history and physical examinations. The patients were randomly divided into two: topical finasteride (A) and oral finasteride (B) groups. Topical finasteride group (A) received a topical gel of 1% finasteride and placebo tablets, while the oral finasteride group (B) received finasteride tablets (1 mg) and gel base (without drug) as placebo for 6 months. The patients were followed by clinical observation and recording of side effects prior to the treatment and at the end of first week, and then by a monthly follow-up. The size of bald area, total hair count, and terminal hair were studied. Data were analyzed by descriptive and Chi-square statistical test. Results: The mean duration of hair loss was 18.8±23.10 months. Each month the terminal hair, size of bald area and hair count between the two groups were compared. There were no significant differences between the two groups as a viewpoint of hair thickness, hair counts and the size of bald area. Serial measurements indicated a significant increase in hair counts and terminal hair counts between the two groups. Conclusions: The results of this study showed that the therapeutic effects of both finasteride gel and finasteride tablet were relatively similar to each other.
Introduction
Loss of hair and alopecia are the most common problems of modern societies, which create many economical and psychological effects. Recently, a great effort has been made to treat hair loss and alopecia, in which some of them were successful. One of the most common types of alopecia is baldness or androgenetic alopecia. This kind of alopecia is recognized by progressive narrowing of hair in the vertex and fronto- temporal area of scalp, in persons with genetic potency. The alopecia is hereditary in nature and is formed due to the high testosterone receptors in scalps of involved persons. Dihydroxy testosterone is an active form of testosterone that is produced by enzyme type II, 5-a reductase from testosterone. [1] Testosterone affects hair follicle, resulting in hair shaft thinning, shortening of anagen phase and prolongation of telogen phase.[2] The most recommended treatment for androgenic alopecia is composed of local minoxidil, hormonal therapy such as local and oral anti- androgen or local progesterone containing products. [3],[4],[5],[6],[7],[8] Finasteride is an effective drug for treatment of male alopecia that can be used orally or locally. The drug decreases loss of hair by inhibiting 5-α reductase enzyme activity, which converts testosterone to its active form, namely di-hydrotestosterone which is the main cause of male pattern hair loss. [9],[10],[11],[12] Topical finasteride 0.005% is used to treat male alopecia. [10] Since, long-term drug therapy by finasteride is needed for treatment of male alopecia; its oral route is associated by complications such as decreased libido, erectile dysfunction, and decrease volume of ejaculation, depression and gynecomastia . [8],[13] In this research, during a controlled study, we attempted to compare the effect of local finasteride gel on scalp, its target and to measure fewer complications with the oral type of finasteride, in treatment of androgenic alopecia in men. If topical form is effective, it will prevent the undesirable side effects of systemic form of drug. In addition, it will be a suitable treatment for this social problem, especially in adolescence and young age groups in which hair protection, as a cosmetic, is important for
Methods
This is a double blind clinical trial study. The number of samples (according to previous studies) was 45 young adult men . [3],[9] They were selected among patients referred to private clinics and Dermatology department in the City of Sari, during July 2003 to February of 2005. All of the subjects were having androgenetic alopecia, according to their history and clinical examination. They were placed in the study after they wrote the letter of agreement and satisfaction.
Inclusion criteria were as follows: males under 30 years of age, hair loss duration less than 5 years; maximum hair density 20 hairs/cm²; maximum diameter of the bald area less than 10 cm; and having complete physical and psychological health. Exclusion criteria were patients with male alopecia that were under treated, and patients with baseline disease that causes hair loss.
Method of finasteride gel preparation
Since the water solubility of Finesteride gel is very low, thus, at the beginning of work, solubility had to be increased. For this reason, solvent-aid was used. The solvents-aid is water mixable organic solvents, in which by decreasing solubility, and with surface tension of water, will cause increase water solubility of non-polar materials. An adequate amount of ethanol to increase solubility was determined by several examinations and by setting the drug solubility in different percentages of water-ethanol. After setting and preparing the suitable solvent to solve finasteride, several examinations to select the best polymer were done by different materials. For this reason, first the selected polymer was poured on a glass surface, containing an adequate drug solving system, and was maintained in lab temperature for 24 hours. Then, the receiving system was mixed by an electric mixer by velocity of 600 cycles per minute, until it was completely pure. The results showed that 40% water and 60% ethanol are the best solvent system, and hydroxyl propyl methyl cellulose (HPMC) is the best polymer. Preparation of this drug did not need a preservative. Physical stability of the drug as a viewpoint of deposition or opacity in 4°C in refrigerator was evaluated. Since the time frame between drug production and consumption was about one week, there was no need for chemical assessment. In addition, the placebo gel without drug was prepared by the same system. Because, finasteride 1% has the most dermal absorption, therefore, in this study finasteride gel 1% was prepared and used.
Method
A two-part questionnaire was prepared. The first part was related to the demographic characteristics, and the second part was related to record the information about hair loss (size of bald area, number of terminal hair, and vellus hair).
The patients entered the study based on inclusion criteria, and divided in two groups randomly; Group A (Finasteride gel and placebo tablet), and group B (Finasteride tablet and placebo gel). Finasteride tablet and gel, as well as placebo tablet and gel in the same size, shape and color were made by pharmaceutics faculty of Mazandaran Medical Center, and were given to the researchers by a code, which was kept secretive until the end of this study.
Therapeutic method
Patients in two groups received one tablet daily (Finasteride or placebo), associated with local gel (placebo or finasteride). The patients were advised to use the gel twice daily by gently massaging their scalps. Duration of treatment was six months. To evaluate the drug effectiveness, prognosis and side effect, patients visited before the study and the end of first week of treatment, and then followed-up monthly. To assess therapeutic response, the shoblons already made by size of 10 cm² was used . Then the shoblons were placed on the defect and at least 3 squares, selected randomly, and the size of bald area, the number of total hair counts and the number of terminal hair were counted by naked eye. The mean was calculated, and finally, the result number was recorded in the form.
Using variables for therapeutic response were categorized as size of bald area; the total hair count; and the terminal hair count. To evaluate the total response to treatment, the following descriptions was defined: the size of bald area per cm (8.1-9.5 cm : point 1, 6.6-8 cm : point 2, 5.1-6.5 cm : point 3, 3.5-5 cm : point 4); the total hair count(100-124 : point 1, 125-149: point 2, 150-174 : point 3, 175-200 : point 4), and the number of terminal hair (65-89 : point 1, 90-114 : point 2 , 115-139 : point 3, 140-165 : point 4). The resulting scores were summarized: the score 3-6 was considered as bad response, the score 7-9 moderate response, and the score 10-12 good response to the treatment. [14] Finally, the analysis was done by descriptive and Chi-square statistical approach.
Results
Of the 45 androgenetic alopecia patients who were enrolled, 7 were excluded from the study due to incomplete or discontinuation of the entire study period. The patient's age range was 22.8±3.3 years. The average time of hair loss in patients, were 23.10 ±18.8 months. Seven (18.4%) were married and 31(81.6%) were single. Among referred patients, 31(81.6%) had a positive family history of male alopecia and in 7(18.4%), it was negative. Nineteen patients entered in group A, while 19 in group B randomly.
The average total hair count, terminal hair count and the size of bald area in both groups in the beginning and end of treatment respectively are shown in [table 1].
There were no significant statistical differences in the terminal hairs, size of alopecia area and hair count between two groups.
In A group (Finasteride gel and placebo tablet), increased terminal hair count were observed at the third month of treatment ( P =0.001), but increased in terminal hair count was shown in the second months in the B group (Finasteride tablet and placebo gel) ( P =0.015). During therapeutic period, the size of alopecia area was not significantly altered in group A, but in group B, the change in size of alopecia area was significant in the fourth month of treatment ( P =0.027). Increased hair count in two groups were significant in 4 months of treatment ( P =0.001, in group A and P =0.000 in group B). Therapeutic response during therapeutic period in both A and B groups was evaluated by scoring system which shown in [table 2].
Only one of the patients complained the erythema in affected site as a complication of using local finasteride gel that was subsided immediately after discontinuation of the gel. One of the finasteride tablet user described the decreasing libido.
Discussion
The results of this study revealed the moderate therapeutic response, but not a good response, in both groups. Comparing finasteride gel 1%, with finasteride tablet (54.5% versus 56%) showed the relatively similar therapeutic response, that was not statistically significant ( P =0.643). 5a-reductase enzyme causes testosterone convertion to di-hydrotestosterone. The therapeutic effect of the enzyme inhibitors on androgenetic alopecia such as finasteride by dose of 1mg orally, has been proven in different studies. [1],[2],[15],[16],[17] In addition, in this study, serial measurements of hair count and terminal hair increase showed that increasing in total hair count and terminal hair in both therapeutic groups between the beginning and end of study was significant. Like other studies, the total hair in both groups, finasteride gel and tablet, demonstrated significant differences between first referral and 6 months after therapy ( P =0.000), this indicates the therapeutic efficacy of both drugs. [1],[10] The terminal hairs in finasteride gel group were always more than the finasteride tablet group, until third month of therapy. However, they were similar in both groups during the fourth month of treatment. At 5 th and 6 th months, the terminal hair counts were more in the group who were receiving tablets, thus explaining the efficacy of the tablet during therapeutic period. [1] The size of bald area in tablet and gel groups had significant decrease at fourth month, noting there was no change in gel group, which indicates the greater therapeutic effect of tablet than gel. Although, the total hair growth in both groups was significant during the fourth month, in the gel group, we did not find any decrease in the size of alopecia area and consequently the better appearance of person.
Over all, in this recent study, by comparing finasteride tablet and gel groups with each other, it was found that in second, third and fourth months of patients being referred, the therapeutic response to the tablet group was better than gel group, but in fifth and sixth months of treatment, the therapeutic response in both groups was the same.
In previous studies, the finasteride tablet efficacy began after third to sixth months of therapy and if the patient had no response after 12 to 24 months, continuation of usage probably did not appear to be effective. [2] In our study, there was no significant positive therapeutic response in both groups; one reason could be the duration of treatment that was only for 6 months, thus, if the duration of treatment was longer, the results could have indicated a better therapeutic effect.
Like other studies, these results show local finasteride gel, [5],[11],[12] has a considerable efficacy and if used for male alopecia patients, who experienced hair loss in recent years, it will be a good replacement of oral therapy, especially in those who worry about oral drug complications.
Finally, we suggest replication study of more samples, with longer period and assessment of patients' satisfaction after treatment.
Acknowledgement
This work was supported by a grant from the research council of the Mazandaran University of Medical Sciences. Also, the authors offer Dr. Khademloo and Ms. F.shokoohi their profound thanks because of their liberal cooperation.
References
1. Price VH, Menefee E, Sanchez M, Ruane P, Kaufman KD. Changes in hair weight and hair count in men with androgenetic alopecia after treatment with finasteride, 1 mg, and daily. J Am Acad Dermatol 2002;46:517-23. Back to cited text no. 1 [PUBMED] [FULLTEXT]
2. Dunlop F. Androgenetic alopecia in men and women: An overview of cause and treatment. 2005. Available from: http://www.folicle.com\ section 2\2.html. Back to cited text no. 2
3. Olsen EA, Dunlap FE, Funicella T, Koperski JA, Swinehart JM, Tschen EH, et al . A randomized clinical trial of 5% topical minoxidil versus 2% topical minoxidil and placebo in the treatment of androgenetic alopecia in men. J Am Acad Dermatol 2002;47:377-85. Back to cited text no. 3 [PUBMED] [FULLTEXT]
4. Hugo Perez BS. Ketokonazole as an adjunct of finasteride in the treatment of androgenetic alopecia in men. Med Hypotheses 2004;62:112-5. Back to cited text no. 4 [PUBMED] [FULLTEXT]
5. Sintova A, Serafimovich S, Gilhar A. New topical ant androgenic formulation can stimulate hair growth in human bald scalp grafted onto mice. Int J Pharm 2000;194:125-34. Back to cited text no. 5
6. Vexiau P, Chaspoux C, Boudou P, Fiet J, Jouanique C, Hardy N, et al . Effects of minoxidil 2% versus cyproterone acetate treatment on female androgenetic alopecia: A controlled, 12- month randomized trial. Br J Dermatol 2002;146:992-9. Back to cited text no. 6 [PUBMED] [FULLTEXT]
7. Shapiro J, Kaufman KD. Use of finasteride in the treatment of men with androgenetic alopecia (Male pattern hair loss). J Investig Dermatol Symp Proc 2003;8:20-3. Back to cited text no. 7 [PUBMED]
8. Shokree J, Javadzadeh Y, Aayatollahi M, Asnaashari S, Mateen A. Local finasteride formulation and assessment of its dermal absorption. Drug Sci 2004;1:97-106. Back to cited text no. 8
9. Lucas KJ. Finasteride cream in hirsutism. Endocr Pract 2001;7:5-10. Back to cited text no. 9 [PUBMED] [FULLTEXT]
10. Mazzarella F, Loconsole F, Cammisa A, Mastrolonardo M, Vena GA. Topical finasteride in the treatment of androgenetic alopecia: Preliminary evaluation after a 16-month therapy course. J Dermatol Treatment 1997;8:189-92. Back to cited text no. 10
11. Hajheydari Z, Jamshidi M, Akbari J, Mohammadpour R. Combination of topical garlic gel and betamethasone valerate cream in the treatment of localized alopecia areata: A double-blind randomized controlled study. Indian J Dermatol Venereol Leprol 2007;73:29-32. Back to cited text no. 11 [PUBMED] Medknow Journal
12. Dallob AL, Sadick NS, Unger W, Lipert S, Geissler LA, Gregoire SL. The effect of Finasteride, a 5a-reductase inhibitor, on scalp skin testosterone and dihydro-testosterone concentration in patients with male pattern baldness. J Clin Endocrinol Metab 1994;79:703-6. Back to cited text no. 12
13. Kaufman KD, Olsen EA, Whiting D, Savin R, DeVillez R, Bergfeld W, et al . Finasteride in the treatment of men with androgenetic alopecia: Finasteride Male Pattern Hair Loss Study Group. J Am Acad Dermatol 1998;39:578-89. Back to cited text no. 13 [PUBMED] [FULLTEXT]
14. Roberts JL, Fiedler V, Imperato-McGinley J, Whiting D, Olsen E, Shupack J, et al . Clinical dose ranging studies with finasteride, a type 2 5alpha-reductase inhibitor, in men with male pattern hair loss. J Am Acad Dermatol 1999;41:555-63. Back to cited text no. 14 [PUBMED]
15. Hamilton JB. Drug category. Available from: http://www.emedicine.com/derm/topic21.htm. [cited on 2003]. Back to cited text no. 15
16. Burkhart CG, Burkhart CN. 5 alpha reductase and finasteride in pattern alopecia and acne. J Drug Dermatol 2004;3:363-4. Back to cited text no. 16
17. Altomare G. Capella G. Depression circumstantially related to the administration for androgenetic alopecia. J Dermatol 2002;29:665-9. Back to cited text no. 17
πηγη http://www.ijdvl.com/article.asp?issn=0378-6323;year=2009;volume=75;issue=1;spage=47;epage=51;aulast=Hajheydari
Πολυ ενδιαφερον αποτελεσματα!!!
Comparing the therapeutic effects of finasteride gel and tablet in treatment of the androgenetic alopecia
Zohreh Hajheydari1, Jafar Akbari2, Majid Saeedi2, Leila Shokoohi1
1 Department of Dermatology, Boo Ali Sina (Avicenna) Hospital, Mazandaran University of Medical Sciences, Sari, Iran
2 Department of Pharmaceutics, Faculty of Pharmacy, Mazandaran University of Medical Sciences, Sari, Iran
Abstract
Background: Finasteride, a type P-selective 5a-reductase inhibitor, as a causative agent of decreasing dihydroxy testestrone (DHT) level, is effective in the treatment of male androgenic alopecia. Aim: We compared the local and oral finasteride in the treatment of androgenic alopecia. Method: This is a double blind, randomized clinical trial study of 45 male patients, who were referred with alopecia to the private clinics and departments in Boo-Ali Sina Hospital, in Sari. Patients with male androgenic alopecia were selected according to the history and physical examinations. The patients were randomly divided into two: topical finasteride (A) and oral finasteride (B) groups. Topical finasteride group (A) received a topical gel of 1% finasteride and placebo tablets, while the oral finasteride group (B) received finasteride tablets (1 mg) and gel base (without drug) as placebo for 6 months. The patients were followed by clinical observation and recording of side effects prior to the treatment and at the end of first week, and then by a monthly follow-up. The size of bald area, total hair count, and terminal hair were studied. Data were analyzed by descriptive and Chi-square statistical test. Results: The mean duration of hair loss was 18.8±23.10 months. Each month the terminal hair, size of bald area and hair count between the two groups were compared. There were no significant differences between the two groups as a viewpoint of hair thickness, hair counts and the size of bald area. Serial measurements indicated a significant increase in hair counts and terminal hair counts between the two groups. Conclusions: The results of this study showed that the therapeutic effects of both finasteride gel and finasteride tablet were relatively similar to each other.
Introduction
Loss of hair and alopecia are the most common problems of modern societies, which create many economical and psychological effects. Recently, a great effort has been made to treat hair loss and alopecia, in which some of them were successful. One of the most common types of alopecia is baldness or androgenetic alopecia. This kind of alopecia is recognized by progressive narrowing of hair in the vertex and fronto- temporal area of scalp, in persons with genetic potency. The alopecia is hereditary in nature and is formed due to the high testosterone receptors in scalps of involved persons. Dihydroxy testosterone is an active form of testosterone that is produced by enzyme type II, 5-a reductase from testosterone. [1] Testosterone affects hair follicle, resulting in hair shaft thinning, shortening of anagen phase and prolongation of telogen phase.[2] The most recommended treatment for androgenic alopecia is composed of local minoxidil, hormonal therapy such as local and oral anti- androgen or local progesterone containing products. [3],[4],[5],[6],[7],[8] Finasteride is an effective drug for treatment of male alopecia that can be used orally or locally. The drug decreases loss of hair by inhibiting 5-α reductase enzyme activity, which converts testosterone to its active form, namely di-hydrotestosterone which is the main cause of male pattern hair loss. [9],[10],[11],[12] Topical finasteride 0.005% is used to treat male alopecia. [10] Since, long-term drug therapy by finasteride is needed for treatment of male alopecia; its oral route is associated by complications such as decreased libido, erectile dysfunction, and decrease volume of ejaculation, depression and gynecomastia . [8],[13] In this research, during a controlled study, we attempted to compare the effect of local finasteride gel on scalp, its target and to measure fewer complications with the oral type of finasteride, in treatment of androgenic alopecia in men. If topical form is effective, it will prevent the undesirable side effects of systemic form of drug. In addition, it will be a suitable treatment for this social problem, especially in adolescence and young age groups in which hair protection, as a cosmetic, is important for
Methods
This is a double blind clinical trial study. The number of samples (according to previous studies) was 45 young adult men . [3],[9] They were selected among patients referred to private clinics and Dermatology department in the City of Sari, during July 2003 to February of 2005. All of the subjects were having androgenetic alopecia, according to their history and clinical examination. They were placed in the study after they wrote the letter of agreement and satisfaction.
Inclusion criteria were as follows: males under 30 years of age, hair loss duration less than 5 years; maximum hair density 20 hairs/cm²; maximum diameter of the bald area less than 10 cm; and having complete physical and psychological health. Exclusion criteria were patients with male alopecia that were under treated, and patients with baseline disease that causes hair loss.
Method of finasteride gel preparation
Since the water solubility of Finesteride gel is very low, thus, at the beginning of work, solubility had to be increased. For this reason, solvent-aid was used. The solvents-aid is water mixable organic solvents, in which by decreasing solubility, and with surface tension of water, will cause increase water solubility of non-polar materials. An adequate amount of ethanol to increase solubility was determined by several examinations and by setting the drug solubility in different percentages of water-ethanol. After setting and preparing the suitable solvent to solve finasteride, several examinations to select the best polymer were done by different materials. For this reason, first the selected polymer was poured on a glass surface, containing an adequate drug solving system, and was maintained in lab temperature for 24 hours. Then, the receiving system was mixed by an electric mixer by velocity of 600 cycles per minute, until it was completely pure. The results showed that 40% water and 60% ethanol are the best solvent system, and hydroxyl propyl methyl cellulose (HPMC) is the best polymer. Preparation of this drug did not need a preservative. Physical stability of the drug as a viewpoint of deposition or opacity in 4°C in refrigerator was evaluated. Since the time frame between drug production and consumption was about one week, there was no need for chemical assessment. In addition, the placebo gel without drug was prepared by the same system. Because, finasteride 1% has the most dermal absorption, therefore, in this study finasteride gel 1% was prepared and used.
Method
A two-part questionnaire was prepared. The first part was related to the demographic characteristics, and the second part was related to record the information about hair loss (size of bald area, number of terminal hair, and vellus hair).
The patients entered the study based on inclusion criteria, and divided in two groups randomly; Group A (Finasteride gel and placebo tablet), and group B (Finasteride tablet and placebo gel). Finasteride tablet and gel, as well as placebo tablet and gel in the same size, shape and color were made by pharmaceutics faculty of Mazandaran Medical Center, and were given to the researchers by a code, which was kept secretive until the end of this study.
Therapeutic method
Patients in two groups received one tablet daily (Finasteride or placebo), associated with local gel (placebo or finasteride). The patients were advised to use the gel twice daily by gently massaging their scalps. Duration of treatment was six months. To evaluate the drug effectiveness, prognosis and side effect, patients visited before the study and the end of first week of treatment, and then followed-up monthly. To assess therapeutic response, the shoblons already made by size of 10 cm² was used . Then the shoblons were placed on the defect and at least 3 squares, selected randomly, and the size of bald area, the number of total hair counts and the number of terminal hair were counted by naked eye. The mean was calculated, and finally, the result number was recorded in the form.
Using variables for therapeutic response were categorized as size of bald area; the total hair count; and the terminal hair count. To evaluate the total response to treatment, the following descriptions was defined: the size of bald area per cm (8.1-9.5 cm : point 1, 6.6-8 cm : point 2, 5.1-6.5 cm : point 3, 3.5-5 cm : point 4); the total hair count(100-124 : point 1, 125-149: point 2, 150-174 : point 3, 175-200 : point 4), and the number of terminal hair (65-89 : point 1, 90-114 : point 2 , 115-139 : point 3, 140-165 : point 4). The resulting scores were summarized: the score 3-6 was considered as bad response, the score 7-9 moderate response, and the score 10-12 good response to the treatment. [14] Finally, the analysis was done by descriptive and Chi-square statistical approach.
Results
Of the 45 androgenetic alopecia patients who were enrolled, 7 were excluded from the study due to incomplete or discontinuation of the entire study period. The patient's age range was 22.8±3.3 years. The average time of hair loss in patients, were 23.10 ±18.8 months. Seven (18.4%) were married and 31(81.6%) were single. Among referred patients, 31(81.6%) had a positive family history of male alopecia and in 7(18.4%), it was negative. Nineteen patients entered in group A, while 19 in group B randomly.
The average total hair count, terminal hair count and the size of bald area in both groups in the beginning and end of treatment respectively are shown in [table 1].
There were no significant statistical differences in the terminal hairs, size of alopecia area and hair count between two groups.
In A group (Finasteride gel and placebo tablet), increased terminal hair count were observed at the third month of treatment ( P =0.001), but increased in terminal hair count was shown in the second months in the B group (Finasteride tablet and placebo gel) ( P =0.015). During therapeutic period, the size of alopecia area was not significantly altered in group A, but in group B, the change in size of alopecia area was significant in the fourth month of treatment ( P =0.027). Increased hair count in two groups were significant in 4 months of treatment ( P =0.001, in group A and P =0.000 in group B). Therapeutic response during therapeutic period in both A and B groups was evaluated by scoring system which shown in [table 2].
Only one of the patients complained the erythema in affected site as a complication of using local finasteride gel that was subsided immediately after discontinuation of the gel. One of the finasteride tablet user described the decreasing libido.
Discussion
The results of this study revealed the moderate therapeutic response, but not a good response, in both groups. Comparing finasteride gel 1%, with finasteride tablet (54.5% versus 56%) showed the relatively similar therapeutic response, that was not statistically significant ( P =0.643). 5a-reductase enzyme causes testosterone convertion to di-hydrotestosterone. The therapeutic effect of the enzyme inhibitors on androgenetic alopecia such as finasteride by dose of 1mg orally, has been proven in different studies. [1],[2],[15],[16],[17] In addition, in this study, serial measurements of hair count and terminal hair increase showed that increasing in total hair count and terminal hair in both therapeutic groups between the beginning and end of study was significant. Like other studies, the total hair in both groups, finasteride gel and tablet, demonstrated significant differences between first referral and 6 months after therapy ( P =0.000), this indicates the therapeutic efficacy of both drugs. [1],[10] The terminal hairs in finasteride gel group were always more than the finasteride tablet group, until third month of therapy. However, they were similar in both groups during the fourth month of treatment. At 5 th and 6 th months, the terminal hair counts were more in the group who were receiving tablets, thus explaining the efficacy of the tablet during therapeutic period. [1] The size of bald area in tablet and gel groups had significant decrease at fourth month, noting there was no change in gel group, which indicates the greater therapeutic effect of tablet than gel. Although, the total hair growth in both groups was significant during the fourth month, in the gel group, we did not find any decrease in the size of alopecia area and consequently the better appearance of person.
Over all, in this recent study, by comparing finasteride tablet and gel groups with each other, it was found that in second, third and fourth months of patients being referred, the therapeutic response to the tablet group was better than gel group, but in fifth and sixth months of treatment, the therapeutic response in both groups was the same.
In previous studies, the finasteride tablet efficacy began after third to sixth months of therapy and if the patient had no response after 12 to 24 months, continuation of usage probably did not appear to be effective. [2] In our study, there was no significant positive therapeutic response in both groups; one reason could be the duration of treatment that was only for 6 months, thus, if the duration of treatment was longer, the results could have indicated a better therapeutic effect.
Like other studies, these results show local finasteride gel, [5],[11],[12] has a considerable efficacy and if used for male alopecia patients, who experienced hair loss in recent years, it will be a good replacement of oral therapy, especially in those who worry about oral drug complications.
Finally, we suggest replication study of more samples, with longer period and assessment of patients' satisfaction after treatment.
Acknowledgement
This work was supported by a grant from the research council of the Mazandaran University of Medical Sciences. Also, the authors offer Dr. Khademloo and Ms. F.shokoohi their profound thanks because of their liberal cooperation.
References
1. Price VH, Menefee E, Sanchez M, Ruane P, Kaufman KD. Changes in hair weight and hair count in men with androgenetic alopecia after treatment with finasteride, 1 mg, and daily. J Am Acad Dermatol 2002;46:517-23. Back to cited text no. 1 [PUBMED] [FULLTEXT]
2. Dunlop F. Androgenetic alopecia in men and women: An overview of cause and treatment. 2005. Available from: http://www.folicle.com\ section 2\2.html. Back to cited text no. 2
3. Olsen EA, Dunlap FE, Funicella T, Koperski JA, Swinehart JM, Tschen EH, et al . A randomized clinical trial of 5% topical minoxidil versus 2% topical minoxidil and placebo in the treatment of androgenetic alopecia in men. J Am Acad Dermatol 2002;47:377-85. Back to cited text no. 3 [PUBMED] [FULLTEXT]
4. Hugo Perez BS. Ketokonazole as an adjunct of finasteride in the treatment of androgenetic alopecia in men. Med Hypotheses 2004;62:112-5. Back to cited text no. 4 [PUBMED] [FULLTEXT]
5. Sintova A, Serafimovich S, Gilhar A. New topical ant androgenic formulation can stimulate hair growth in human bald scalp grafted onto mice. Int J Pharm 2000;194:125-34. Back to cited text no. 5
6. Vexiau P, Chaspoux C, Boudou P, Fiet J, Jouanique C, Hardy N, et al . Effects of minoxidil 2% versus cyproterone acetate treatment on female androgenetic alopecia: A controlled, 12- month randomized trial. Br J Dermatol 2002;146:992-9. Back to cited text no. 6 [PUBMED] [FULLTEXT]
7. Shapiro J, Kaufman KD. Use of finasteride in the treatment of men with androgenetic alopecia (Male pattern hair loss). J Investig Dermatol Symp Proc 2003;8:20-3. Back to cited text no. 7 [PUBMED]
8. Shokree J, Javadzadeh Y, Aayatollahi M, Asnaashari S, Mateen A. Local finasteride formulation and assessment of its dermal absorption. Drug Sci 2004;1:97-106. Back to cited text no. 8
9. Lucas KJ. Finasteride cream in hirsutism. Endocr Pract 2001;7:5-10. Back to cited text no. 9 [PUBMED] [FULLTEXT]
10. Mazzarella F, Loconsole F, Cammisa A, Mastrolonardo M, Vena GA. Topical finasteride in the treatment of androgenetic alopecia: Preliminary evaluation after a 16-month therapy course. J Dermatol Treatment 1997;8:189-92. Back to cited text no. 10
11. Hajheydari Z, Jamshidi M, Akbari J, Mohammadpour R. Combination of topical garlic gel and betamethasone valerate cream in the treatment of localized alopecia areata: A double-blind randomized controlled study. Indian J Dermatol Venereol Leprol 2007;73:29-32. Back to cited text no. 11 [PUBMED] Medknow Journal
12. Dallob AL, Sadick NS, Unger W, Lipert S, Geissler LA, Gregoire SL. The effect of Finasteride, a 5a-reductase inhibitor, on scalp skin testosterone and dihydro-testosterone concentration in patients with male pattern baldness. J Clin Endocrinol Metab 1994;79:703-6. Back to cited text no. 12
13. Kaufman KD, Olsen EA, Whiting D, Savin R, DeVillez R, Bergfeld W, et al . Finasteride in the treatment of men with androgenetic alopecia: Finasteride Male Pattern Hair Loss Study Group. J Am Acad Dermatol 1998;39:578-89. Back to cited text no. 13 [PUBMED] [FULLTEXT]
14. Roberts JL, Fiedler V, Imperato-McGinley J, Whiting D, Olsen E, Shupack J, et al . Clinical dose ranging studies with finasteride, a type 2 5alpha-reductase inhibitor, in men with male pattern hair loss. J Am Acad Dermatol 1999;41:555-63. Back to cited text no. 14 [PUBMED]
15. Hamilton JB. Drug category. Available from: http://www.emedicine.com/derm/topic21.htm. [cited on 2003]. Back to cited text no. 15
16. Burkhart CG, Burkhart CN. 5 alpha reductase and finasteride in pattern alopecia and acne. J Drug Dermatol 2004;3:363-4. Back to cited text no. 16
17. Altomare G. Capella G. Depression circumstantially related to the administration for androgenetic alopecia. J Dermatol 2002;29:665-9. Back to cited text no. 17
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