345 Aging Skin Barrier
also reported that reaction to another strong irritant, octanoic acid was significantly lower
in subjects more than 55 years old while reactions to the weaker irritants acetic acid and
decanol were only directionally reduced with age.83 Bowman et al. performed a 10 day
cumulative irritation test comparing 26 subjects 18–45 with 26 subjects 65–80 using 11
products of widely varying irritancy.84 They found no statistically significant differences in
response between the age groups, but the response was directionally less in the older age
group for all the compounds that produced significant irritation.
While the static barrier function of the epidermis does not seem to diminish with age,
recovery of barrier function after disruption has been found to be significantly slower in
older skin. Ghadially et al. disrupted SC by either tape stripping or acetone treatment to the
point that TEWL was increased to the range of 20–30 g/m2-hr.85 Recovery of the barrier
was quantified by measuring TEWL over the next several days. After acetone treatment
young skin (under age 30) recovered its barrier function by 50% at 24 hours, while older
skin (over 80) had only recovered 15% at 24 hours. Younger subjects took about 4 days
to recover to 90% of their original SC barrier to TEWL while older skin required 7 days
to recover by 90% after either tape stripping or acetone extraction. The slower recovery of
SC barrier function may be related to slower rates of epidermal renewal in older skin as
discussed below.
AGE AND SC TURNOVER
It is well known that corneocytes are continually shed into the environment and are being
continually replaced by cells generated in the SG (see above). The SC “turnover time” is
most frequently measured by staining the SC with the fluorescent dye, dansyl chloride, and
monitoring the rate of dye disappearance with a UV light. When all of the fluorescence
has disappeared the SC has turned over completely.86 Grove and coworkers reported that
SC turnover time is increased in elderly skin.24,56 Data from taken from Grove et al. are
presented in Table II.
Figure 4. Scatter plot of TEWL versus age for 452 Chinese women along with a quadratic regression fi.
Figure courtesy of G.G. Hillebrand, used with permission.
346 JOURNAL OF COSMETIC SCIENCE
The total time for SC on the volar forearm to turn over increased from 19.8 ± 1.4 days in
the under 35 years old group to 28.1 ± 2.7 days in an over 60 age group.56 Similar changes
were seen on the upper inner arm as shown in Table II. Their results agree with the positive
correlation between age and the time to turn over the SC reported by Roberts and Marks.87
Grove found the number of SC cell layers was approximately constant between age groups
(Table II) indicating that the increased SC turnover time results from decreased epidermal
cell proliferation rates with age.24,56 Marks reported a small but statistically significant
decline with age in the number of epidermal cells in the DNA synthesis phase.88 Engelke
et al. investigated differences between young normal skin, young dry skin, aged normal
skin, and aged dry skin89 using an antibody that stains the nuclei of proliferating cells (Ki-
S3).90 Their data also indicate a significant reduction in epidermal proliferation rate in aged
“normal skin” compared to young normal skin. A slower rate of epidermal cell proliferation
is consistent with the significant increase in time to repair a disrupted SC barrier reported
by Ghadially et al.85 Grove also reported that small chemically induced blisters healed
more slowly in subjects between 65–70 years of age than in subjects 18–25 years of age.91
DRY SKIN IN THE ELDERLY
The greater tendency of older subjects to develop dry skin is well known.4,92–94 Elderly dry
skin is especially prone to itching which can sometimes be severe.48–50
It is not entirely clear why older subjects are more prone to developing dry skin. One
possibility is lower levels of NMF with age as NMF levels are reported to be lower in dry
skin.40 Data on the effect of age on NMF levels do not present a consistent picture. One
of the key moisturizing components of NMF is PCA.34,40 Harding et al. reported lower
levels of PCA in older subjects and the difference was more marked deeper in the stratum
corneum.99 Horii et al. reported a general decrease in free amino acids with increasing
levels of dry skin in elderly subjects.100 On the other hand Jacobson et al. found that some
SC amino acids decreased with age while others increased, but no difference was seen in
total NMF free amino acids (FAA) normalized to protein content between young and old
subjects.101 Takahashi and Tezuka102 reported that NMF FAA increased in older subjects.
However, both groups sampled the stratum corneum by scraping skin flakes from the
surface rather than tape stripping to sample from lower levels of the SC as Harding et al.
did. Further, as Tagami103 has pointed out Takahashi and Tezuka reported their results
as FAA/corneocyte. Thus, the higher levels of NMF FAA they report could be due to the
presence of larger corneocytes in older skin25,26,56 as discussed above.
Table II
Measurements of Epidermal Turnover Rate From Grove et. al56
Site Age Transit time
(days)
Number of
cell layers
Turnover rate
(hours/layer)
Volar forearm 35 19.8 ± 1.39 17.0 ± 0.83 28.3 ± 1.2
Volar forearm 60 28.1 ± 2.66 16.8 ± 0.66 40.1** ± 3.8
Upper inner arm 35 17.7 ± 2.02 14.3 ± 0.61 30.0 ± 2.6
Upper inner arm 60 25.5 ± 2.63 13.9 ± 0.81 46.6 ± 6.5
Results are presented as mean ± S.E. Calculated from the data due to a typographical error in
paper.
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Extracted Text (may have errors)

345 Aging Skin Barrier
also reported that reaction to another strong irritant, octanoic acid was significantly lower
in subjects more than 55 years old while reactions to the weaker irritants acetic acid and
decanol were only directionally reduced with age.83 Bowman et al. performed a 10 day
cumulative irritation test comparing 26 subjects 18–45 with 26 subjects 65–80 using 11
products of widely varying irritancy.84 They found no statistically significant differences in
response between the age groups, but the response was directionally less in the older age
group for all the compounds that produced significant irritation.
While the static barrier function of the epidermis does not seem to diminish with age,
recovery of barrier function after disruption has been found to be significantly slower in
older skin. Ghadially et al. disrupted SC by either tape stripping or acetone treatment to the
point that TEWL was increased to the range of 20–30 g/m2-hr.85 Recovery of the barrier
was quantified by measuring TEWL over the next several days. After acetone treatment
young skin (under age 30) recovered its barrier function by 50% at 24 hours, while older
skin (over 80) had only recovered 15% at 24 hours. Younger subjects took about 4 days
to recover to 90% of their original SC barrier to TEWL while older skin required 7 days
to recover by 90% after either tape stripping or acetone extraction. The slower recovery of
SC barrier function may be related to slower rates of epidermal renewal in older skin as
discussed below.
AGE AND SC TURNOVER
It is well known that corneocytes are continually shed into the environment and are being
continually replaced by cells generated in the SG (see above). The SC “turnover time” is
most frequently measured by staining the SC with the fluorescent dye, dansyl chloride, and
monitoring the rate of dye disappearance with a UV light. When all of the fluorescence
has disappeared the SC has turned over completely.86 Grove and coworkers reported that
SC turnover time is increased in elderly skin.24,56 Data from taken from Grove et al. are
presented in Table II.
Figure 4. Scatter plot of TEWL versus age for 452 Chinese women along with a quadratic regression fi.
Figure courtesy of G.G. Hillebrand, used with permission.
346 JOURNAL OF COSMETIC SCIENCE
The total time for SC on the volar forearm to turn over increased from 19.8 ± 1.4 days in
the under 35 years old group to 28.1 ± 2.7 days in an over 60 age group.56 Similar changes
were seen on the upper inner arm as shown in Table II. Their results agree with the positive
correlation between age and the time to turn over the SC reported by Roberts and Marks.87
Grove found the number of SC cell layers was approximately constant between age groups
(Table II) indicating that the increased SC turnover time results from decreased epidermal
cell proliferation rates with age.24,56 Marks reported a small but statistically significant
decline with age in the number of epidermal cells in the DNA synthesis phase.88 Engelke
et al. investigated differences between young normal skin, young dry skin, aged normal
skin, and aged dry skin89 using an antibody that stains the nuclei of proliferating cells (Ki-
S3).90 Their data also indicate a significant reduction in epidermal proliferation rate in aged
“normal skin” compared to young normal skin. A slower rate of epidermal cell proliferation
is consistent with the significant increase in time to repair a disrupted SC barrier reported
by Ghadially et al.85 Grove also reported that small chemically induced blisters healed
more slowly in subjects between 65–70 years of age than in subjects 18–25 years of age.91
DRY SKIN IN THE ELDERLY
The greater tendency of older subjects to develop dry skin is well known.4,92–94 Elderly dry
skin is especially prone to itching which can sometimes be severe.48–50
It is not entirely clear why older subjects are more prone to developing dry skin. One
possibility is lower levels of NMF with age as NMF levels are reported to be lower in dry
skin.40 Data on the effect of age on NMF levels do not present a consistent picture. One
of the key moisturizing components of NMF is PCA.34,40 Harding et al. reported lower
levels of PCA in older subjects and the difference was more marked deeper in the stratum
corneum.99 Horii et al. reported a general decrease in free amino acids with increasing
levels of dry skin in elderly subjects.100 On the other hand Jacobson et al. found that some
SC amino acids decreased with age while others increased, but no difference was seen in
total NMF free amino acids (FAA) normalized to protein content between young and old
subjects.101 Takahashi and Tezuka102 reported that NMF FAA increased in older subjects.
However, both groups sampled the stratum corneum by scraping skin flakes from the
surface rather than tape stripping to sample from lower levels of the SC as Harding et al.
did. Further, as Tagami103 has pointed out Takahashi and Tezuka reported their results
as FAA/corneocyte. Thus, the higher levels of NMF FAA they report could be due to the
presence of larger corneocytes in older skin25,26,56 as discussed above.
Table II
Measurements of Epidermal Turnover Rate From Grove et. al56
Site Age Transit time
(days)
Number of
cell layers
Turnover rate
(hours/layer)
Volar forearm 35 19.8 ± 1.39 17.0 ± 0.83 28.3 ± 1.2
Volar forearm 60 28.1 ± 2.66 16.8 ± 0.66 40.1** ± 3.8
Upper inner arm 35 17.7 ± 2.02 14.3 ± 0.61 30.0 ± 2.6
Upper inner arm 60 25.5 ± 2.63 13.9 ± 0.81 46.6 ± 6.5
Results are presented as mean ± S.E. Calculated from the data due to a typographical error in
paper.

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