Elsevier

Fertility and Sterility

Volume 95, Issue 2, February 2011, Pages 658-662.e3
Fertility and Sterility

Menopause
Skin wrinkles and rigidity in early postmenopausal women vary by race/ethnicity: baseline characteristics of the skin ancillary study of the KEEPS trial

https://doi.org/10.1016/j.fertnstert.2010.09.025Get rights and content

Objective

To characterize skin wrinkles and rigidity in recently menopausal women.

Design

Baseline assessment of participants before randomization to study drug.

Setting

Multicenter trial, university medical centers.

Patient(s)

Recently menopausal participants enrolled in the Kronos Early Estrogen Prevention Study (KEEPS).

Intervention(s)

Skin wrinkles were assessed at 11 locations on the face and neck using the Lemperle wrinkle scale. Skin rigidity was assessed at the forehead and cheek using a durometer.

Main Outcome Measure(s)

Skin wrinkles and rigidity were compared among race/ethnic groups. Skin wrinkles and rigidity were correlated with age, time since menopause, weight, and body mass index (BMI).

Result(s)

In early menopausal women, wrinkles, but not skin rigidity, vary significantly among races, where black women have the lowest wrinkle scores. In white women, chronological age was significantly correlated with worsening skin wrinkles, but not with rigidity. Skin rigidity correlated with increasing length of time since menopause, however, only in the white subgroup. In the combined study group, increasing weight was associated with less skin wrinkling.

Conclusion(s)

Skin characteristics of recently menopausal women are not well studied. Ethnic differences in skin characteristics are widely accepted, but poorly described. In recently menopausal women not using hormone therapy (HT), significant racial differences in skin wrinkling and rigidity exist. Continued study of the KEEPS population will provide evidence of the effects of HT on the skin aging process in early menopausal women.

Section snippets

Materials and methods

The KEEPS trial is a multicenter, double-blind, randomized placebo-controlled trial designed to compare the effects of early initiation of oval versus transdermal E, each with cyclic P, on cardiovascular end points. Subjects enrolled in the parent KEEPS trial were offered participation in this ancillary skin study to evaluate the effects of HT on skin aging at two of the nine participating sites (Yale University, New Haven, CT and Albert Einstein College of Medicine, Bronx, NY) under approved

Demographics

Baseline skin assessment was completed in 106 participants from KEEPS. Mean age of these participants was 53.3 years (±2.7 years) and had an average duration of 1.8 years (±1.0 year) since menopause. Baseline demographics were also analyzed by racial group, which were broken into black (n = 21), white (n = 65), and other (n = 16). Race was not recorded for three participants (Table 1). Past or current tobacco smoking, age and years since onset of menopause were comparable among racial groups,

Discussion

Although the effects of E on the skin are widely studied, characterization of the skin near the menopausal transition is lacking. Furthermore, data on racial differences in skin aging are sparse and conflicting (33). In the present study we describe skin characteristics in recently menopausal women, and also delineate skin differences that exist among racial groups. Our finding that black women have significantly fewer wrinkles overall is the first to quantify such a racial difference in

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      The lack of dermal elasticity increases the likelihood of skin sagging. However, research utilising a durometer showed no correlation between body mass index (BMI) and skin wrinkles at eleven locations on the face in early postmenopausal women [26]. Some facial creases are utilised for identification of the living [27], but the use of facial creases for identification of the dead has not been previously studied.

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    E.W. has nothing to disclose. L.P. has nothing to disclose. T.A. has nothing to disclose. R.M. has nothing to disclose. R.F. has nothing to disclose. H.A. has nothing to disclose. M.H. has nothing to disclose. N.S. has nothing to disclose. H.S.T. has nothing to disclose.

    Supported by the Kronos Longevity Research Institute; the Reproductive Scientist Development Program NIH K12HD00849 and The Berlex Foundation to Erin Wolff; and the National Institutes of Health grant U54 HD052668 to Hugh S. Taylor.

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