| 0 |
Normal stratum corneum |
| 1 |
Hyperkeratosis of the primary and secondary lines and/or the
appendageal orifices |
| 2 |
Hyperkeratosis covering less than 30% of the plateaus |
| 3 |
Hyperkeratosis covering more than 30% of the plateaus |
| 4 |
Diffuse confluent scales |
| 5 |
Thick, uneven scales covering the entire surface,
obliterating the skin surface furrows |
The mean and SD of the a* and ITA° values were calculated.
Intra-individual comparisons were made for each colorimetric value
between the forehead skin and lesional skin using the two-tailed
paired Student t test. Correlations between the values of these
parameters were searched for using regression model analysis with
calculation of the coefficient of correlation r. Similar
statistical assessments were performed to evaluate the
relationships between, on the one hand, ITA° values and, on the
other hand, xerosis severity as assessed by dry dermoscopy, and the
ULEV and CSSS methods. A p value lower than 0.05 was
considered statistically significant.
Results
Erythema as assessed by the a* parameter was similar
(p = 0.46) on the forehead (8.3 ± 1.3) and on
the legs (8.5 ± 1.5). By contrast, the ITA° value of the
forehead (– 33 ± 3) was significantly lower
(p < 0.01) than on leg ashiness
(– 29.7 ± 6.6). A weak correlation was found between
the a* and ITA° values on the forehead (r = 0.42), but
was absent on leg ashiness (r = – 0.02).
Xerosis of leg ashiness (Fig. 1) was recognized by
dry dermoscopy grading (2.7 ± 0.8), ULEV assessment
(3.3 ± 0.9) and CSSS xerosis grading
(3.7 ± 0.9). Correlations were found between each of the
3 rating methods of xerosis and ITA° values (Table III, Figs. 2- 4).
Table III. Coefficients of
correlation r between the individual typology angle (ITA°) and
xerosis ratings by dry dermoscopy, ultraviolet light enhanced
visualization (ULEV) and by cyanoacrylate skin surface stripping
(CSSS) examination
|
ULEV |
CSSS |
ITA° |
| Dry
dermoscopy |
0.65 |
0.68 |
0.73 |
| ULEV |
|
0.83 |
0.76 |
| CSSS |
|
|
0.83 |
Discussion
Xerosis responsible for ashiness reduces the natural skin shine
and presents as whitish areas in darker skinned individuals.
Cross-polarized imaging combining image analysis and clinical
pattern recognition has been suggested to quantify this skin
condition [5]. Skin weathering, particularly during winter, results
in some physiological and structural changes [11, 15-25]. Exposure
to a cold environment alters the activity of desquamatory enzymes
[11, 26]. This effect is amplified when the relative humidity of
air is reduced with ensuing water depletion in the outer stratum
corneum [19, 23]. The combination of cold and dry threat can be
expressed by dew point variations [15, 20]. The resulting effect of
such a process is the development of a peculiar type of xerosis
[11, 21, 27] due to a defect in corneodesmolysis and desquamation
[28-30]. The altered specific enzymes are proteases, particularly
serine and cathepsin-like enzymes.
The present study was performed combining colorimetric assessments
and xerosis ratings by visual inspection, and by the ULEV and CSSS
methods. It shows that skin ashiness is similarly objectivated by
assessing the stratum corneum texture than by measuring skin
colour. The whitish, dull and opaque appearance results from the
overall increase in diffuse light scattering and a reduction in
Fresnel reflection (optical phenomenon responsible for skin glare)
at the skin surface. This optical phenomenon is responsible for the
variations in skin glare.
Erythema was not evidenced by measurements of parameter a* at the
site of skin ashiness. This suggests the absence of
clinically-relevant inflammation at the origin of this skin
condition.
In conclusion, ashiness as a consequence of skin weathering does
not appear to be related to inflammation. Xerosis with a reduction
of Fresnel reflexion seems to be the major cause of this common
skin condition in individuals with a dark skin complexion. n
Acknowledgements. This work was supported by the
“Fonds d'Investissement de la Recherche Scientifique” of the
University Hospital of Liège.
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