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      Geometric classification of scalp hair for valid drug testing, 6 more reliable than 8 hair curl groups

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          Abstract

          Introduction

          Curly hair is reported to contain higher lipid content than straight hair, which may influence incorporation of lipid soluble drugs. The use of race to describe hair curl variation (Asian, Caucasian and African) is unscientific yet common in medical literature (including reports of drug levels in hair). This study investigated the reliability of a geometric classification of hair (based on 3 measurements: the curve diameter, curl index and number of waves).

          Materials and methods

          After ethical approval and informed consent, proximal virgin (6cm) hair sampled from the vertex of scalp in 48 healthy volunteers were evaluated. Three raters each scored hairs from 48 volunteers at two occasions each for the 8 and 6-group classifications. One rater applied the 6-group classification to 80 additional volunteers in order to further confirm the reliability of this system. The Kappa statistic was used to assess intra and inter rater agreement.

          Results

          Each rater classified 480 hairs on each occasion. No rater classified any volunteer’s 10 hairs into the same group; the most frequently occurring group was used for analysis. The inter-rater agreement was poor for the 8-groups (k = 0.418) but improved for the 6-groups (k = 0.671). The intra-rater agreement also improved (k = 0.444 to 0.648 versus 0.599 to 0.836) for 6-groups; that for the one evaluator for all volunteers was good (k = 0.754).

          Conclusions

          Although small, this is the first study to test the reliability of a geometric classification. The 6-group method is more reliable. However, a digital classification system is likely to reduce operator error. A reliable objective classification of human hair curl is long overdue, particularly with the increasing use of hair as a testing substrate for treatment compliance in Medicine.

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          Most cited references27

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          Hair cortisol as a biological marker of chronic stress: current status, future directions and unanswered questions.

          The detrimental effects of stress on human health are being increasingly recognized. There is a critical need for the establishment of a biomarker that accurately measures its intensity and course over time. Such a biomarker would allow monitoring of stress, increase understanding of its pathophysiology and may help identify appropriate and successful management strategies. Whereas saliva and urine cortisol capture real-time levels, hair cortisol analysis presents a complementary means of monitoring stress, capturing systemic cortisol exposure over longer periods of time. This novel approach for cortisol quantification is being increasingly used to identify the effects of stress in a variety of pathological situations, from chronic pain to acute myocardial infarctions. Because of its ability to provide a long-term, month-by-month measure of systemic cortisol exposure, hair cortisol analysis is becoming a useful tool, capable of answering clinical questions that could previously not be answered by other tests. In this paper we review the development, current status, limitations and outstanding questions regarding the use of hair cortisol as a biomarker of chronic stress. Copyright © 2011 Elsevier Ltd. All rights reserved.
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            Dermal papilla cell number specifies hair size, shape and cycling and its reduction causes follicular decline.

            Although the hair shaft is derived from the progeny of keratinocyte stem cells in the follicular epithelium, the growth and differentiation of follicular keratinocytes is guided by a specialized mesenchymal population, the dermal papilla (DP), that is embedded in the hair bulb. Here we show that the number of DP cells in the follicle correlates with the size and shape of the hair produced in the mouse pelage. The same stem cell pool gives rise to hairs of different sizes or types in successive hair cycles, and this shift is accompanied by a corresponding change in DP cell number. Using a mouse model that allows selective ablation of DP cells in vivo, we show that DP cell number dictates the size and shape of the hair. Furthermore, we confirm the hypothesis that the DP plays a crucial role in activating stem cells to initiate the formation of a new hair shaft. When DP cell number falls below a critical threshold, hair follicles with a normal keratinocyte compartment fail to generate new hairs. However, neighbouring follicles with a few more DP cells can re-enter the growth phase, and those that do exploit an intrinsic mechanism to restore both DP cell number and normal hair growth. These results demonstrate that the mesenchymal niche directs stem and progenitor cell behaviour to initiate regeneration and specify hair morphology. Degeneration of the DP population in mice leads to the types of hair thinning and loss observed during human aging, and the results reported here suggest novel approaches to reversing hair loss.
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              Measurement of cortisol in human hair as a biomarker of systemic exposure.

              Current methods for measuring long-term endogenous production of cortisol can be challenging due to the need to take multiple urine, saliva or serum samples. Hair grows approximately 1 centimeter per month, and hair analysis accurately reflects exposure to drug abuse and environmental toxins. Here we describe a new assay for measurement of cortisol in hair, and determined a reference range for non-obese subjects. For measurement of cortisol in hair we modified an immunoassay originally developed for measuring cortisol in saliva. We compared hair samples obtained from various parts of the head, and assessed the effect of hair dying. We analyzed hair samples from non-obese subjects, in whom we also obtained urine, saliva and blood samples for cortisol measurements. The mean extraction recovery for hair cortisol standards of 100 ng/ml, 50 ng/ml and 2 ng/ml (n=6) was 87.9%, 88.9% and 87.4%, respectively. Hair cortisol levels were not affected by hair color or by dying hair samples after they were obtained. Cortisol levels were decreased in hair that was artificially colored before taking the sample. The coefficient of variation was high for cortisol levels in hair from different sections of the head (30.5 %), but was smaller when comparing between hair samples obtained from the vertex posterior (15.6%). The reference range for cortisol in hair was 17.7-153.2 pg/mg of hair (median 46.1 pg/mg). Hair cortisol levels correlated significantly with cortisol in 24-hour urine (r=0.33; P=0.041). The correlation of hair cortisol with 24-hour urine cortisol supports its relevance as biomarker for long-term exposure.

                Author and article information

                Contributors
                Role: Editor
                Journal
                PLoS One
                PLoS ONE
                plos
                plosone
                PLoS ONE
                Public Library of Science (San Francisco, CA USA )
                1932-6203
                1 June 2017
                2017
                : 12
                : 6
                : e0172834
                Affiliations
                [1 ]Hair and Skin Research Lab, Division of Dermatology, Groote Schuur Hospital, Cape Town, South Africa
                [2 ]Department of Human Biology, Faculty of Health Sciences, University of Cape Town, Cape Town, South Africa
                [3 ]Statistical Sciences, Faculty of Science, University of Cape Town, Cape Town, South Africa
                [4 ]Engineering, University of Cape Town, Cape Town, South Africa
                Northwestern University Feinberg School of Medicine, UNITED STATES
                Author notes

                Competing Interests: The authors have declared that no competing interests exist.

                • Conceptualization: NPK.

                • Data curation: KM.

                • Formal analysis: FG KM.

                • Funding acquisition: NPK.

                • Investigation: KM JCVW NS.

                • Methodology: KM LMD NPK.

                • Project administration: KM.

                • Resources: NPK LMD.

                • Software: FG KM.

                • Supervision: NPK LMD.

                • Validation: JCVW NS.

                • Visualization: FG KM.

                • Writing – original draft: KM.

                • Writing – review & editing: NPK LMD JCVW NS MN FG KM.

                ‡ These authors also contributed equally to this work.

                Article
                PONE-D-16-23253
                10.1371/journal.pone.0172834
                5453415
                28570555
                46b42f52-91d4-48c7-ab54-066f5e6c5850
                © 2017 Mkentane et al

                This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.

                History
                : 9 June 2016
                : 9 February 2017
                Page count
                Figures: 2, Tables: 4, Pages: 10
                Funding
                Funded by: funder-id http://dx.doi.org/10.13039/501100001321, National Research Foundation;
                Award ID: South African Research Chair in Dermatology and Toxicology
                Award Recipient : Nonhlanhla P Khumalo
                Funded by: funder-id http://dx.doi.org/10.13039/501100001322, South African Medical Research Council;
                Award ID: Self Initiated Research Grant
                Award Recipient : Nonhlanhla P Khumalo
                This work received Seed Funding from The University of Cape Town.
                Categories
                Research Article
                Biology and Life Sciences
                Anatomy
                Integumentary System
                Hair
                Medicine and Health Sciences
                Anatomy
                Integumentary System
                Hair
                Biology and Life Sciences
                Anatomy
                Head
                Scalp
                Medicine and Health Sciences
                Anatomy
                Head
                Scalp
                Research and Analysis Methods
                Research Assessment
                Research Validity
                Biology and Life Sciences
                Biochemistry
                Lipids
                People and Places
                Demography
                Physical Sciences
                Mathematics
                Geometry
                Curvature
                Medicine and Health Sciences
                Pharmacology
                Drug Screening
                Research and Analysis Methods
                Mathematical and Statistical Techniques
                Statistical Methods
                Multivariate Analysis
                Principal Component Analysis
                Physical Sciences
                Mathematics
                Statistics (Mathematics)
                Statistical Methods
                Multivariate Analysis
                Principal Component Analysis
                Custom metadata
                All relevant data are within the paper and its Supporting Information files.

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