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Texte intégral de l'article
 
  Version imprimable

TrichoScan: combining epiluminescence microscopy with digital image analysis for the measurement of hair growth in vivo


European Journal of Dermatology. Volume 11, Numéro 4, 362-8, July - August 2001, Revues


Summary  

Auteur(s) : R. Hoffmann, Department of Dermatology, Philipp University, Deutschhausstraße 9, 35033 Marburg, Germany..

Illustrations


   
   Figure 1. This is a stepwise illustration of the complete TrichoScan procedure. A: a representative area of the scalp is chosen and the plastic template is applied; B: all hairs are carefully combed through the plastic template; C: the hairs are shaved on the scalp surface; D: the shaved area is 1.8 cm2 in size; E: 1 cm of dye is applied onto a wooden stick; F: 3 drops of developer are mixed (G) with the dye; H: the dye is carefully applied onto the shaved area; I: after 12 min the dye is carefully removed with an alcoholic solution; J: digital images are taken at 20- and 40-fold magnification while the area is still wet.



   
   Figure 2. Example of the TrichoScan analysis of hair number, hair density, cumulative hair thickness and anagen/telogen ratio. The figure illustrates a digital image taken at 20-fold magnification (left side of the image) and shows the area of 0.65 cm2 (blue circle) which is analyzed with the TrichoScan software. The TrichoScan results are illustrated on the right side, where the detected hairs are illustrated with different colors. Red hairs are non-growing hairs (telogen), green hairs are growing hairs (anagen) and yellow hairs touch the borders of the circle. The right lower part of the figure shows a histogram of the different hair lengths detected by the TrichoScan software.



   
  

Figures 3-6. The intra-class correlation of three different measurements in 10 volunteers (subjects) from the same investigator is shown for hair counts (Fig. 3) and for cumulative hair thickness (Fig. 4). The intra-class correlation of one measurement in 5 volunteers (subjects) from two different investigators is shown for hair counts (Fig. 5) and for cumulative hair thickness (Fig. 6).






   
   Figures 7 and 8. Hair counts and cumulative hair thickness were analysed for 6 months in 11 volunteers without AGA, in 5 untreated men with AGA, and in 12 men treated with finasteride (1 mg/day). In controls and untreated men we noticed no significant difference in the number of hairs within the observation time of 6 months (between the values at baseline and after 6 months). In contrast those men treated with finasteride showed a continuous increase (mean with 95% confidence interval) at 3 months (p = 0.055) and at 6 months (p = 0.021) in the number of hairs within the analysed area compared to the values at baseline. Untreated men showed a continuous and significant decrease in the overall thickness of hairs 3 and 6 months after the initial visit (baseline). In contrast those men treated with finasteride showed, in comparison with the baseline visit, a continuous and significant increase in the number of hairs within the analysed area after 3 (p = 0.034) and 6 months (p = 0.006).






   
   Figures 9 and 10. While defining anagen hairs as growing and telogen hairs as non-growing hairs three days after shaving, the TrichoScan is able to calculate a digital trichogram. This figure illustrates the results (mean with 95% confidence interval) from two investigators, who analysed of 18 volunteers with AGA the proportion of anagen hairs (Fig. 9) and the hair growth rate (Fig. 10) at the vertex and at the occiput (only 14 images). Compared to the occiput, the AGA-affected scalp reveals a decreased number of and slower growing anagen hairs. Both investigators produced similar results.



   
    



   
    


 

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