hair loss news, information, faqs, articles

Archive for the ‘General’ Category

Male androgenetic alopecia and cardiovascular risk factors: A case-control study

Thursday, April 29th, 2010

BACKGROUND AND OBJECTIVES: The relationship between androgenetic alopecia and cardiovascular disease has been studied by some authors in the past, although the results of epidemiological studies have been variable. The objective of this study was to determine the prevalence of metabolic syndrome and carotid arteriosclerosis in patients with early-onset androgenetic alopecia. PATIENTS AND METHODS: Seventy men were studied, 35 with diagnosis of early-onset (before 35 years of age) androgenetic alopecia and 35 control subjects who consulted for other skin conditions. In both groups, the criteria for metabolic syndrome according to the Adult Treatment Panel-III were studied (obesity, triglycerides, high-density lipoprotein cholesterol, systolic and diastolic blood pressure, and blood glucose), presence of atheromatous plaques, and carotid intima-media thickness using Doppler ultrasonography. Other cardiovascular risk factors, hormones, and acute-phase reactants were also analyzed. RESULTS: Criteria for metabolic syndrome were met by 57.1% of the patients with androgenetic alopecia compared to 14.3% of the controls (P<0001). Thirty-four percent of the patients with androgenetic alopecia had atheromatous plaques compared to 8.6% of the controls (P=.018). In an independent correlation analysis, abdominal obesity, systolic blood pressure, triglycerides, and blood glucose levels were significantly greater among patients with androgenetic alopecia. Testosterone and sex hormone binding globulin levels were similar in the 2 groups whereas insulin and aldosterone levels were higher in patients with androgenetic alopecia (P<05). CONCLUSIONS: The high frequency of metabolic syndrome and carotid atheromatous plaques in patients with androgenetic alopecia suggests cardiovascular screening should be done to enable early detection of individuals at risk and initiation of preventive treatment before cardiovascular disease becomes established.
Arias-Santiago S, Gutiérrez-Salmerón MT, Castellote-Caballero L, Buendía-Eisman A, Naranjo-Sintes R.

Servicio de Dermatología, Hospital Clínico San Cecilio, Granada, España. salvadorarias@hotmail.es
Actas Dermosifiliogr. 2010 Apr;101(3):248-56.

creatine monohydrate supplementation affects dihydrotestosterone to testosterone ratio

Sunday, April 18th, 2010

Three weeks of creatine monohydrate supplementation affects dihydrotestosterone to testosterone ratio in college-aged rugby players.
OBJECTIVE: This study investigated resting concentrations of selected androgens after 3 weeks of creatine supplementation in male rugby players. It was hypothesized that the ratio of dihydrotestosterone (DHT, a biologically more active androgen) to testosterone (T) would change with creatine supplementation. DESIGN: Double-blind placebo-controlled crossover study with a 6-week washout period. SETTING: Rugby Institute in South Africa. PARTICIPANTS: College-aged rugby players (n = 20) volunteered for the study, which took place during the competitive season. INTERVENTIONS: Subjects loaded with creatine (25 g/day creatine with 25 g/day glucose) or placebo (50 g/day glucose) for 7 days followed by 14 days of maintenance (5 g/day creatine with 25 g/day glucose or 30 g/day glucose placebo). MAIN OUTCOME MEASURES: Serum T and DHT were measured and ratio calculated at baseline and after 7 days and 21 days of creatine supplementation (or placebo). Body composition measurements were taken at each time point. RESULTS: After 7 days of creatine loading, or a further 14 days of creatine maintenance dose, serum T levels did not change. However, levels of DHT increased by 56% after 7 days of creatine loading and remained 40% above baseline after 14 days maintenance (P < 0.001). The ratio of DHT:T also increased by 36% after 7 days creatine supplementation and remained elevated by 22% after the maintenance dose (P < 0.01). CONCLUSIONS: Creatine supplementation may, in part, act through an increased rate of conversion of T to DHT. Further investigation is warranted as a result of the high frequency of individuals using creatine supplementation and the long-term safety of alterations in circulating androgen composition. STATEMENT OF CLINICAL RELEVANCE: Although creatine is a widely used ergogenic aid, the mechanisms of action are incompletely understood, particularly in relation to dihydrotestosterone, and therefore the long-term clinical safety cannot be guaranteed.

van der Merwe J, Brooks NE, Myburgh KH.

Department of Clin J Sport Med. 2009 Sep;19(5):399-404.

Changes of metabolic profile in men treated for androgenetic alopecia with 1 mg finasteride.

Saturday, March 27th, 2010



Changes of metabolic profile in men treated for androgenetic alopecia with 1 mg finasteride.

Duskova M, Hill M, Starka L.

Objective. Androgenetic alopecia is recognized as a risk factor for cardiovascular diseases, glucose metabolism disorders, and benign prostate hyperplasia and/or carcinoma. Finasteride, used for treatment of androgenetic alopecia at a dose of 1mg/day, is an effective inhibitor of type II 5alpha-reductase, the enzyme responsible for the reduction of testosterone to dihydrotestosterone. Recent studies reported that dihydrotestosterone, among other activities, might play some role in visceral fat metabolism. It thus seemed reasonable to examine whether finasteride treatment of androgenetic alopecia ameliorates some features of metabolic syndrome frequently seen associated with this condition.
Methods. We examined 12 men with premature balding (defined as frontoparietal and vertex hair loss before age 30 with alopecia defined as grade 3 vertex or more on the Norwood-modified Hamilton alopecia classification). Hormonal levels and metabolic parameters were determined and insulin tolerance tests performed for all individuals. Finasteride (1 mg/day) was administrated for 12 months. The hormonal profile and lipid spectrum were monitored after 4, 8 and 12 months of treatment and insulin tolerance tests were repeated after 12 months of the treatment.
Results. After treatment with finasteride the expected changes in the steroid spectrum were seen, namely a decrease in dihydrotestosterone and increase in testosterone, androstenedione and free testosterone index.
We observed an initial increase in total cholesterol and HDL- and LDL-cholesterol, which stabilized with prolonged treatment. We founded a significant decrease in glycated hemoglobin HbA1c and insulin resistance measured using rate constant for plasma glucose disappearance (kITT) showed only a borderline decrease.
Conclusions. Finasteride is an efficient 5alpha-reductase inhibitor even at low doses of 1mg/day. In men treated with this dose for 12 months, we observed mild differences in metabolic profile with slight amelioration of glucose metabolism regulation. Keywords: Finasteride – Androgenetic alopecia – Androgens – Lipids – Insulin sensitivity – Metabolic disorders.

hair loss

hair loss

Treatment of Androgenetic Alopecia with the combo : Propecia , Rogaine and Retin-A

Tuesday, November 17th, 2009

Finasteride is an effective oral medication in the treatment of androgenetic alopecia (AGA). Minoxidil has a direct effect on hair growth by stimulating dermal papillae or follicular hair matrix cells.
Article by Gwang Seong Choi, Sung Joo Lee

Author: Gwang Seong Choi, Sung Joo Lee.
Department of Dermatology, Inha University, Inchon, Korea

Study Results:

Finasteride is an effective oral medication in the treatment of androgenetic alopecia (AGA). Minoxidil has a direct effect on hair growth by stimulating dermal papillae or follicular hair matrix cells. Simultaneous administration of topical minoxidil with tretinoin may enhance the response of AGA to minoxidil.

We treated 41 AGA patients from 23 to 43 years of age (grade III and VI, according to the Norwood-Hamilton classification scale) with combination therapy. The results were evaluated by patient self assessment and investigator assessment by comparision of clinical photography. Every 3 months, clinical evaluation and adverse events were assessed.
At month 12, of the 41 patient enrolled, Effective results, including excellent results and good results, were observed in 27 (65.9%) patients. Progressed hair loss compared to baseline were 2 (4.9%) patients. Adverse effects including sexual dysfunctions and skin irritation were observed in 2 (4.9%) and 6 (14.6%) patients, respectively. The results between self assessment and investigator assessment showed similarity.

The combination therapy of oral finasteride 1mg/day, topical 3% minoxidil, and 0.025% tretinoin improved AGA more efficiently comparing to monotherapy. We recommended combination therapy in those patients with AGA who desire medical therapy.

http://www.hairway.org/upload/08111715283937.jpg http://www.all-rx.com/images/products/propecia.gif http://www.irxmedicine.com/images/products/RetinA.jpg