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 Table of Contents  
REVIEW ARTICLE
Year : 2018  |  Volume : 10  |  Issue : 6  |  Page : 262-270  

Scalp condition impacts hair growth and retention via oxidative stress


1 Center for Dermatology and Hair Diseases, University of Zurich, Wallisellen, Switzerland
2 The Procter and Gamble Company, Cincinnati, OH, USA
3 Sharon Woods Innovation Center, Cincinnati, OH, USA

Date of Web Publication1-Feb-2019

Correspondence Address:
Prof. Ralph M Trueb
Center for Dermatology and Hair Diseases, Bahnhofplatz 1A, CH-8304 Wallisellen
Switzerland
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Source of Support: None, Conflict of Interest: None


DOI: 10.4103/ijt.ijt_57_18

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   Abstract 


Conventionally, the medical focus has been either on hair loss or the condition of the scalp in terms of specific dermatological diseases. Indeed, the proximate structural arrangement of the scalp and hair leads to an interdependent relationship between the two. While protective benefits of the hair to the scalp are obvious, the role of the scalp as an incubatory environment for the preemergent hair fiber has largely been ignored. In fact, there is a wealth of observational data on specific dermatological conditions of the scalp providing evidence for the role of the scalp condition in supporting the production of healthy hair. Oxidative stress, the inability of the body to sufficiently counteract the sources of oxidation, is prevalent in many skin conditions, including normal skin aging. On the scalp, the hair appears to be impacted prior to emergence, and oxidative stress appears to play a role in premature hair loss. The scalp commensal organism, Malassezia, has been recognized to be a source of oxidative damage. Therefore, hair care products, specifically shampoos, with active Malassezia inhibitory agents, such as zinc pyrithione, tend to reduce premature hair loss, besides the known benefits in treating specific dermatologic scalp pathologies, and therefore should represent an integral part of every treatment regimen for hair loss, even in individuals not showing symptoms of scalp pathologies.

Keywords: Malassezia spp., oxidative stress, premature hair loss, scalp pathologies, zinc pyrithione-based shampoo


How to cite this article:
Trueb RM, Henry JP, Davis MG, Schwartz JR. Scalp condition impacts hair growth and retention via oxidative stress. Int J Trichol 2018;10:262-70

How to cite this URL:
Trueb RM, Henry JP, Davis MG, Schwartz JR. Scalp condition impacts hair growth and retention via oxidative stress. Int J Trichol [serial online] 2018 [cited 2023 May 30];10:262-70. Available from: https://www.ijtrichology.com/text.asp?2018/10/6/262/251423




   Introduction Top


“Ah, such are the lures of the toilet that none will for long hold aloof from them.

Cosmetics are not going to be a mere prosaic remedy for age and plainness.

From: Max Beerbohm, A Defence of Cosmetics (1894).

The condition of the hair plays an important role in our physical appearance and self-perception. The quantity, quality, and styling of our hair define our gender, age, health, and social status.[1] There are no significant differences in the number of hair follicles between men and women, or between the different races. Differences in the appearance of hair are due to the type of hair produced by the follicle and the type of hair care practiced by the individual.[2]

Conventionally, the medical focus has been either on hair loss or the condition of the scalp in terms of specific dermatological conditions. In fact, the proximate structural arrangement of the scalp and hair leads to an interdependent relationship between the two. The protective benefits of the hair to the scalp, such as ultraviolet radiation (UVR) screening, moisture retention, and mechanical shielding, are obvious, while the role of the scalp as an incubatory environment for the preemergent hair fiber is often overlooked.[3]

It is the aim of this article to provide evidence that the condition of the scalp affects the natural growth and retention of hair, and consequently that appropriate scalp care may deliver fundamental benefits for hair growth and its quality. Preemergent hair can be negatively impacted by the oxidative stress that occurs with an unhealthy scalp, possibly due to the incubatory environment, specifically the metabolic activity of resident microbes. Therefore, hair care products with active agents that reduce the population of respective microbes and restore a healthy scalp while reducing the associated oxidative stress may have an impact on hair health.


   The Scalp in Health and Disease Top


The scalp is the anatomical area bordered by the face at the front and by the neck at the sides and back. It is characterized by a usually high density of terminal hair growth with numerous sebaceous glands that contribute to a specific microenvironment with significant differences from the rest of the skin. The scalp is a rich environment for microbes. Ecologically, sebaceous areas have greater species richness than dry ones, with implications both for skin physiology and pathologic conditions.[4] Specifically, dandruff and seborrheic dermatitis, psoriasis, atopic dermatitis, and ultimately alopecia represent pathologic conditions, in which oxidative stress is very commonly detected.[5] Quantitation of lipid peroxidation is a particularly prevalent method in dermatology to detect the underlying oxidative stress.[6],[7],[8]

Dandruff and seborrheic dermatitis

The specific anatomic features of the scalp skin, such as the large number of terminal hair follicles and the enlarged epidermal surface due to numerous hair canals, contribute to a specific microenvironment of the scalp and higher rate of exfoliation. Even a normal scalp will develop some degree of flaking within 1 or 2 weeks if the hair is not washed, while pathological dandruff results from accelerated proliferation of epidermal cells. This leads to a breakdown of the normal columnar structure of the stratum corneum with increased exfoliation of variously large collections of abnormally keratinizing epidermal cells and formation of cell aggregates, which determine the size of the flakes. The process results from focal inflammation of the scalp with parakeratosis which causes abnormal exfoliation and an altered light refractive index of the keratinized cell aggregates.[9] The clinical appearance of dandruff is determined by the size, adherence, and light refractive characteristics of the flakes. Among the factors that lead to inflamed patches on the scalp are microbial colonization with Malassezia fungi, sebaceous lipids, and individual sensitivity.[10]

Seborrheic dermatitis represents a chronic recurrent condition characterized by scaling and poorly defined erythematous patches, with a predilection for areas rich in sebaceous glands. In contrast to dandruff, in seborrheic dermatitis, the redness and scaling frequently extend beyond the scalp to include the folds of the nose and eyebrow areas. The cause of seborrheic dermatitis is again understood to involve fungi of the genus Malassezia.[10] Therefore, there seems to exist a pathogenic link with dandruff that is understood to represent the mildest form of the clinical presentation of seborrheic dermatitis.

The scalp microbiome consists primarily of Propionibacteria, Staphylococcus bacteria, and Malassezia yeast.[11] Malassezia are responsible for essentially the entire scalp mycobiome. The inflammatory process is believed to be mediated by fungal metabolites, specifically free fatty acids released from sebaceous triglycerides. Both dandruff and seborrheic dermatitis have clear signs of oxidative stress as indicated by perturbed surface and systemic antioxidant enzyme levels.[12],[13],[14],[15] There have also been observations from surface samples of elevated lipid peroxidation accompanying dandruff and seborrheic dermatitis.[16],[17]

Psoriasis

Psoriasis is a chronic inflammatory condition of the scalp, and the most thoroughly studied skin condition linking oxidative stress, the role of Malassezia spp., and risk of hair loss. In contrast to seborrheic dermatitis, the condition is characterized by sharply demarcated erythematosquamous lesions with silver-white scaling. The most dramatic expression of the immune-mediated condition is tumor necrosis factor-alpha inhibition – treatment-induced psoriasiform dermatitis of the scalp with the risk of permanent alopecia from scarring.[18],[19],[20] Overgrowth of the scalp with Malassezia spp. is again a well-known feature of scalp psoriasis.[21] Indicators of oxidative stress in psoriasis include altered antioxidant enzymes,[22] oxidized proteins,[23],[24] as well as oxidized lipids.[25]

Atopic dermatitis

Atopic dermatitis is yet another common, chronic, relapsing, inflammatory skin disorder that may affect the scalp in a significant manner. Its pathogenesis is complex and involves genetics, environmental factors, disrupted permeability of the skin, and immunologic mechanisms. A subset of patients with head-and-neck dermatitis may have a reaction to resident Malassezia flora exacerbating their condition.[26],[27],[28],[29],[30],[31] This reaction is likely related to both humoral- and cell-mediated immunity. Even in the absence of differences in Malassezia spp. colonization, patients with head-and-neck atopic dermatitis are more likely to have positive skin prick test results and Malassezia-specific IgE compared to healthy controls and to patients with atopy without head-and-neck dermatitis.[32]

Again, atopic dermatitis is a condition that is strongly associated with oxidative stress: quantitation of urinary indicators of stress is elevated,[33],[34],[35] as are oxidized surface protein levels, which in addition may be exacerbated by environmental impacts.[36]

Scalp aging

Aging of the scalp underlies the same principles as aging of the skin, except for a natural protection from UVR depending on the amount of scalp hair. Aging represents the accumulation of changes over time, involving both programmed factors and damage-related factors (nonprogrammed factors). Programmed factors follow a biological timetable, perhaps a continuation of the one that regulates childhood growth and development. This regulation would depend on changes in gene expression that affect the systems responsible for maintenance, repair, and defense responses. Damage-related factors include internal and environmental assaults that induce cumulative damage at various levels.

Aging of the hair itself affects hair color (graying), hair production (alopecia), and structural properties of the hair fiber (hair diameter, hair fiber curvature, stretching, bending, and torsional rigidity of the hair fiber, and lipid composition), with its consequence for the manageability and overall appearance of hair.[37]

In contrast, the aging effects on nonbalding scalp are relatively unnoticed. Underneath the hair, the scalp may appear pale and dry, with a certain degree of laxity. In contrast, balding scalp exhibits the features of photo-aged skin, including irregular pigmentation, wrinkling, atrophy, telangiectasia, and findings of cutaneous premalignant and malignant diseases, such as actinic keratosis, basal cell carcinoma, and squamous cell carcinoma. Onset of solar elastosis of the scalp precedes the onset of hair loss in androgenetic alopecia,[38] providing the evidence that scalp hair does not completely protect from the effects of UVR and the need for added scalp UVR protection. Other aging features seen in the sun-damaged scalp include variability in thickness and cellularity in epidermis, unevenly distributed melanocytes, and increased inflammatory cells in the dermis. Due to the decrease in volume and elasticity, the skin becomes thinner and more easily damaged. Moreover, aging skin receives less blood flow and exhibits lower glandular activity. The net result of these effects is the decreasing ability of skin to heal itself, with an increase of skin pathologies.

Remarkably, aging does not appear to follow a perfectly regular course over time. Periods of stability, or even partial remission, alternated with periods of more marked evolution, reflecting perhaps the influence of individual factors such as the individual's general health and nutritional status, life style and hygiene, and risk factors for accelerated aging.


   Role of Oxidative Stress in Scalp Health and Aging Top


Experimental evidence supports the hypothesis that oxidative stress plays a major role in the aging process. In 1956, Harman[39] originally proposed the free radical theory of aging. Free radicals are highly reactive molecules with unpaired electrons that can directly damage various cellular structural membranes, lipids, proteins, and DNA. The damaging effects of these reactive oxygen species are induced internally during normal metabolism and externally through exposure to various oxidative stresses from the environment. While the body possesses endogenous defense mechanisms, such as anti-oxidative enzymes (superoxide dismutase, catalase, and glutathione peroxidase) and nonenzymatic anti-oxidative molecules (Vitamin E, Vitamin C, glutathione, and ubiquinone), to protect it from free radicals by reducing and neutralizing them, with age, the production of free radicals increases, while the endogenous defense mechanisms decrease. This imbalance leads to the progressive damage of cellular structures, presumably resulting in the aging phenotype.

Nishimura (oral communication, 7th World Congress for Hair Research, May 4–6, 2013, Edinburgh, Scotland) found hair follicles to age through defective renewal of hair follicle stem cells much in the manner as maintenance of melanocyte stem cells becomes incomplete with aging.[40] Hair production and pigmentation is fueled by stem cells, which transition between cyclical bouts of rest and activity. Aged hair follicle stem cells exhibit enhanced resting and abbreviated growth phases and are delayed in response to tissue-regenerating cues. Ultimately, aged hair follicle stem cells are poor at initiating proliferation and show diminished self-renewing capacity upon extensive use. Aging-related loss of hair follicle stem cell marker expression starts well before hair follicles have shortened. Using genomic instability syndromes and exposure to ionizing radiation as models, Nishimura proposed an accumulation of DNA damage to be involved in the aging process.

Concept of the pre- and post-emergent hair fiber

Conventionally, the study of hair aging has focused on two main streams of attention: on the one hand, the esthetic problem of aging hair and its management, in other words everything that happens outside the skin, and on the other hand, the biological problem of hair aging, in terms of microscopic, biochemical, and molecular changes within the follicle in the depth of the scalp.

The condition of the hair fiber must be viewed as the result of a combination of preemergent and of postemergent factors.[41] Sources of oxidative stress with impact on the preemergent fiber include oxidative metabolism; smoking;[42],[43] UVR;[44] inflammation from microbial, pollutant, or irritant origins; and oxidized scalp lipids. Sources of oxidative stress with impact on the postemergent fiber include again UVR, and chemical insults from oxidizing hair colorants and pollutants [Figure 1].[41]
Figure 1: Sources of oxidative stress with impact on the condition of the hair fiber

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While age-dependent thinning of hair is understood to be genetically determined and linked to peculiarities of hormone metabolism, it is primarily treated with the respective hair growth-promoting agent minoxidil and the 5-alpha-reductase inhibitors finasteride or dutasteride. Nevertheless, their limited success rate means that further pathogenic pathways must be taken into account.[45] Specifically, Bahta et al.[46] originally demonstrated that cultured dermal papilla cells (DPCs) from balding scalp grow slower in vitro than nonbalding DPCs. Loss of proliferative capacity of balding DPCs was associated with changes in cell morphology, expression of senescence-associated markers, decreased expression of proliferating cell markers, and upregulation of markers of oxidative stress and DNA damage. The finding of premature senescence of balding DPCs in association with the expression of markers of oxidative stress and DNA damage suggests that balding DPCs are particularly sensitive to environmental stress. As one of the major triggers of senescence in vitro stems from oxidative stress, Upton et al.[47] further investigated the effects of oxidative stress on balding and occipital scalp DPCs. Patient-matched DPCs from balding and occipital scalp were cultured at atmospheric (21%) or physiologically normal (2%) O2. At 21% O2, DPCs showed flattened morphology and a significant reduction in mobility, population doubling, increased levels of reactive oxygen species and senescence-associated β-Gal activity, and increased expression of p16 (INK4a) and pRB. Balding DPCs secreted higher levels of the negative hair growth regulators such as transforming growth factor beta 1 and 2 in response to H2O2 but not cell culture-associated oxidative stress. These in vitro findings suggest a role for oxidative stress in the pathogenesis of androgenetic alopecia both in relation to cell senescence and migration, and also to secretion of known hair follicle inhibitory factors. Finally, stress-induced premature senescence of DPCs compromise hair follicle epithelial–mesenchymal interaction underlying hair cycling.[48]

Studies have demonstrated oxidative stress associated with alopecia.[49],[50],[51],[52],[53],[54] The measures are similar to those in other skin conditions: antioxidant enzymes, protein oxidation, and lipid oxidation. The most common manifestation of the oxidative stress is lipid oxidation, and therefore quantitation of lipid peroxidation is a particularly prevalent method in dermatologic research.[7] The oxidized lipids are now understood to negatively influence the normal growth of hair: Naito et al.[55] analyzed the effect of the lipid peroxides on hair follicles and observed that the topical application of linolein hydroperoxides, one of the lipid peroxides, leads to the early onset of the catagen phase in hair cycles. Furthermore, they found that lipid peroxides induced apoptosis of hair follicle cells. They also induced apoptosis in human epidermal keratinocytes by upregulating apoptosis-related genes. These results indicate that lipid peroxides, which can cause free radicals, induce the apoptosis of hair follicle cells, and this is followed by early onset of the catagen phase.

Ultimately, in the context of scalp condition and its impact on the preemergent hair and aging, Malassezia is a proven source of oxidative stress,[56],[57] with a correlation between Malassezia presence and the degree of oxidative stress.[58],[59]

An unhealthy scalp leads to unhealthy hair

There is ample evidence from data involving collections and characterization of hair samples from various unhealthy scalp conditions to help establish a link between scalp health and hair growth and quality.[17],[60],[61],[62],[63],[64],[65],[66],[67],[68],[69],[70],[71],[72],[73] Most of the published data are epidemiological in nature comparing hair obtained from individuals with dandruff or seborrheic dermatitis,[17],[60],[61],[62],[63],[64],[65] atopic dermatitis,[61],[66] and psoriasis[67],[68],[69],[70],[71],[72],[73] with that from a control group of healthy scalp individuals. The results are summarized in [Table 1].
Table 1: Observed impacts to hair in relation to scalp pathologies

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As can be seen from the summary of scalp abnormalities, the most common manifestation to hair emerged from an unhealthy scalp is an altered cuticle with evidence of surface pitting, roughness, cuticle rigidity, or breakage. In some cases, the impact is manifested as shine reduction. In addition to the physical changes, there are biochemical alterations observed in hair emerged from an unhealthy scalp, with both protein and lipid components affected, most commonly by oxidative damage.[17],[61],[66],[67]

Finally, a number of observations have found that premature hair loss may be caused by the poor scalp health associated with either dandruff and seborrheic dermatitis,[62],[63],[64] or psoriasis,[68],[69] indicating that the effect on the preemergent hair fiber may alter the anchoring force of the fiber with the follicle, as evidenced by an increased proportion both of catagen and telogen,[74],[75] and of dysplastic anagen hairs (anagen hairs devoid of hair root sheaths)[75],[76] in the trichogram (hair pluck).


   The Effect of Scalp Care on Hair Growth and Quality Top


Until the introduction of the first nonalkaline shampoos in 1933, soap was the only available cleanser for the hair and scalp.[77] Today, shampoos are expected to be more than mere cleansing agents. They are expected to improve the hair cosmetically while being tailored to the needs of various hair types, age, and scalp condition. Finally, with respect to product comfort, shampoos are expected to not dry out the hair, to produce lather in hard and soft water and, when applied to oily hair, to be nonirritating to skin and mucous membranes, to be chemically and physically stable, to be biodegradable, and affordable. Accordingly, shampoos have evolved into high-tech products consisting of ten to thirty ingredients that are combined in precise formulations to meet consumer demands.[78]

Ultimately, shampoo treatments are the most commonly used means of managing hair and scalp conditions and have proven to be effective for the treatment of dandruff and seborrheic dermatitis,[79],[80],[81],[82],[83] psoriasis,[84] and atopic dermatitis of the head-and-neck type.[85],[86] Today, it is understood that scalp care products for dandruff and seborrheic dermatitis, psoriasis, and atopic dermatitis exert their benefits by controlling scalp Malassezia levels.

Given the observations on the role of oxidative stress in premature hair loss and the part that Malassezia spp. play in generating oxidative stress, it is likely that products with Malassezia control active would exert some hair loss prevention benefits.

Originally, Piérard et al.[87] hypothesized on a microbial-driven inflammatory reaction abutting on the hair follicles and performed a pilot study with twenty males using an 0.25% octopirox leave-on product and demonstrated that the product improved the semi-quantitative self-assessment of hair loss over a 1.5-year treatment period. Subsequently, Piérard-Franchimont et al.[88] conducted a study to compare the effect of 2% ketoconazole shampoo to that of an unmedicated shampoo used in combination with or without 2% minoxidil therapy for male androgenetic alopecia and found that hair density and size and proportion of anagen follicles were improved almost similarly by both ketoconazole and minoxidil regimens, even in the absence of dandruff. The authors concluded that there may be a significant action of ketoconazole upon the course of androgenetic alopecia and that Malassezia spp. play a role in the inflammatory reaction.

Value of zinc pyrithione-based shampoo for normal hair growth and retention

Following the original studies of Piérard et al. and Piérard-Franchimont et al.,[87],[88] Berger et al.[89] performed a 6-month, randomized, investigator-blinded, parallel-group clinical study to assess the hair growth benefits of a 1% zinc pyrithione (ZPT)-based shampoo (Head & Shoulders®, Procter and Gamble Company) in males between the ages of 18 and 49 years exhibiting Hamilton–Norwood type III vertex or type IV baldness. The efficacy of the 1% ZPT-based shampoo (used daily) was compared with that of 5% minoxidil topical solution (applied twice daily), a placebo shampoo, and a combination of the 1% ZPT-based shampoo and the 5% minoxidil topical solution. Hair count results showed a significant net increase in total visible hair counts for the 1% ZPT shampoo, the 5% minoxidil topical solution, and the combination treatment groups relative to the placebo shampoo after 9 weeks of treatment. Finally, a placebo-controlled treatment study with a ZPT-based shampoo (Head & Shoulders®) was published demonstrating decreased oxidative stress in both scalp and preemergent hair for the ZPT leg. This provides support for the underlying mechanisms for hair loss reduction observations for the ZPT-based shampoo as well as other Malassezia-inhibiting shampoo actives.[17]


   Summary and Conclusions Top


The science of hair care not only addresses the esthetic problem of the condition of the hair fiber in terms of hair quality and color, but also the underlying biological problem of hair aging and pathologies. While the role of oxidative stress has been widely discussed in relation to the skin and aging, in comparison, little focus has been placed on its role in impacting scalp health, hair growth, and condition. There is a wealth of observational data on specific dermatological conditions, such as dandruff and seborrheic dermatitis, psoriasis, and atopic dermatitis, providing the evidence for the role of a healthy scalp in supporting the production of healthy hair. Oxidative stress, the inability of the body to sufficiently counteract sources of oxidative damage, is prevalent in all of these skin conditions, just as in normal skin aging. On the scalp, the hair appears to be impacted prior to emergence, and oxidative stress appears to play a role in premature hair loss. The scalp commensal organism, Malassezia, has been recognized to be a source of oxidative damage. Therefore, hair care products with active agents that reduce the population of Malassezia tend to reduce premature hair loss [Figure 2]. Since Malassezia is a source of oxidative stress, its presence, even in individuals not showing symptoms of scalp pathologies, likely enhances subclinical stress that could contribute to compromised hair quality and growth. Besides its known benefits in treating scalp pathologies, such as dandruff and seborrheic dermatitis, psoriasis, and atopic dermatitis of the scalp, a ZPT-based shampoo (Head & Shoulders) has demonstrated reduction in hair loss by several assessment methods, even in the absence of scalp pathologies. Considering the relationship between oxidative stress, Malassezia spp., and hair aging, it is therefore conceivable that regular use may contribute to hair loss prevention.
Figure 2: A 37-year-old man with seborrheic dermatitis and hair loss in the vertex (a) before, and (b) after 3 months successful treatment with anti-dandruff shampoo with antimycotic activity (personal observation)

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Declaration of patient consent

The authors certify that they have obtained all appropriate patient consent forms. In the form the patient(s) has/have given his/her/their consent for his/her/their images and other clinical information to be reported in the journal. The patients understand that their names and initials will not be published and due efforts will be made to conceal their identity, but anonymity cannot be guaranteed.

Financial support and sponsorship

Nil.

Conflicts of interest

R. M. Trüeb is an active member of the Healthy Hair and Scalp Alliance and in this function provides consulting activity for Procter and Gamble. J. R. Schwartz, M. G. Davis, and J. P. Henry are employees of Procter and Gamble. Parts of this article were orally presented by R. M. Trüeb on November 2nd 2017 on the occasion of the 10th World Congress of Hair Research Societies (WCHR) 2017 in Kyoto, Japan.



 
   References Top

1.
Trüeb RM; Swiss Trichology Study Group. The value of hair cosmetics and pharmaceuticals. Dermatology 2001;202:275-82.  Back to cited text no. 1
    
2.
Trüeb RM. Dermocosmetic aspects of hair and scalp. J Investig Dermatol Symp Proc 2005;10:289-92.  Back to cited text no. 2
    
3.
Schwartz JR, Henry JP, Kerr KM, Flagler MJ, Page SH, Redman-Furey N, et al. Incubatory environment of the scalp impacts pre-emergent hair to affect post-emergent hair cuticle integrity. J Cosmet Dermatol 2018;17:105-11.  Back to cited text no. 3
    
4.
Reichel M, Heisig P, Kampf G. Identification of variables for aerobic bacterial density at clinically relevant skin sites. J Hosp Infect 2011;78:5-10.  Back to cited text no. 4
    
5.
Bickers DR, Athar M. Oxidative stress in the pathogenesis of skin disease. J Invest Dermatol 2006;126:2565-75.  Back to cited text no. 5
    
6.
Niki E. Lipid peroxidation: Physiological levels and dual biological effects. Free Radic Biol Med 2009;47:469-84.  Back to cited text no. 6
    
7.
Niki E. Lipid oxidation in the skin. Free Radic Res 2015;49:827-34.  Back to cited text no. 7
    
8.
Niki E, Yoshida Y, Saito Y, Noguchi N. Lipid peroxidation: Mechanisms, inhibition, and biological effects. Biochem Biophys Res Commun 2005;338:668-76.  Back to cited text no. 8
    
9.
Ackerman AB, Kligman AM. Some observations on dandruff. J Soc Cosm Chem 1969;20:81-101.  Back to cited text no. 9
    
10.
DeAngelis YM, Gemmer CM, Kaczvinsky JR, Kenneally DC, Schwartz JR, Dawson TL Jr., et al. Three etiologic facets of dandruff and seborrheic dermatitis: Malassezia fungi, sebaceous lipids, and individual sensitivity. J Investig Dermatol Symp Proc 2005;10:295-7.  Back to cited text no. 10
    
11.
Xu Z, Wang Z, Yuan C, Liu X, Yang F, Wang T, et al. Dandruff is associated with the conjoined interactions between host and microorganisms. Sci Rep 2016;6:24877.  Back to cited text no. 11
    
12.
Ozturk P, Arican O, Belge Kurutas E, Karakas T, Kabakci B. Oxidative stress in patients with scalp seborrheic dermatitis. Acta Dermatovenerol Croat 2013;21:80-5.  Back to cited text no. 12
    
13.
Yile W, Yili W, Xunchun W. Oxidative stress level in patients with facial seborrheic dermatitis. Guongdong Med J 2013;34:3620-1.  Back to cited text no. 13
    
14.
Emre S, Metin A, Demirseren DD, Akoglu G, Oztekin A, Neselioglu S, et al. The association of oxidative stress and disease activity in seborrheic dermatitis. Arch Dermatol Res 2012;304:683-7.  Back to cited text no. 14
    
15.
Trznadel-Grodzka E, Kaczorowska A, Rotsztejn H. Oxygen metabolism in seborrhoeic dermatitis. Centr Europ J Immunol 2011;36:248-53.  Back to cited text no. 15
    
16.
Jourdain R, Moga A, Vingler P, El Rawadi C, Pouradier F, Souverain L, et al. Exploration of scalp surface lipids reveals squalene peroxide as a potential actor in dandruff condition. Arch Dermatol Res 2016;308:153-63.  Back to cited text no. 16
    
17.
Schwartz JR, Henry JP, Kerr KM, Mizoguchi H, Li L. The role of oxidative damage in poor scalp health: Ramifications to causality and associated hair growth. Int J Cosmet Sci 2015;37 Suppl 2:9-15.  Back to cited text no. 17
    
18.
El Shabrawi-Caelen L, La Placa M, Vincenzi C, Haidn T, Muellegger R, Tosti A, et al. Adalimumab-induced psoriasis of the scalp with diffuse alopecia: A severe potentially irreversible cutaneous side effect of TNF-alpha blockers. Inflamm Bowel Dis 2010;16:182-3.  Back to cited text no. 18
    
19.
Cullen G, Kroshinsky D, Cheifetz AS, Korzenik JR. Psoriasis associated with anti-tumour necrosis factor therapy in inflammatory bowel disease: A new series and a review of 120 cases from the literature. Aliment Pharmacol Ther 2011;34:1318-27.  Back to cited text no. 19
    
20.
Osório F, Magro F, Lisboa C, Lopes S, Macedo G, Bettencourt H, et al. Anti-TNF-alpha induced psoriasiform eruptions with severe scalp involvement and alopecia: Report of five cases and review of the literature. Dermatology 2012;225:163-7.  Back to cited text no. 20
    
21.
Gomez-Moyano E, Crespo-Erchiga V, Martínez-Pilar L, Godoy Diaz D, Martínez-García S, Lova Navarro M, et al. Do Malassezia species play a role in exacerbation of scalp psoriasis? J Mycol Med 2014;24:87-92.  Back to cited text no. 21
    
22.
Kadam DP, Suryakar AN, Ankush RD, Kadam CY, Deshpande KH. Role of oxidative stress in various stages of psoriasis. Indian J Clin Biochem 2010;25:388-92.  Back to cited text no. 22
    
23.
Yazici C, Köse K, Utaş S, Tanrikulu E, Taşlidere N. A novel approach in psoriasis:First usage of known protein oxidation markers to prove oxidative stress. Arch Dermatol Res 2016;308:207-12.  Back to cited text no. 23
    
24.
Dimon-Gadal S, Gerbaud P, Thérond P, Guibourdenche J, Anderson WB, Evain-Brion D, et al. Increased oxidative damage to fibroblasts in skin with and without lesions in psoriasis. J Invest Dermatol 2000;114:984-9.  Back to cited text no. 24
    
25.
Bayer M, Mosandl A, Thaçi D. Improved enantioselective analysis of polyunsaturated hydroxy fatty acids in psoriatic skin scales using high-performance liquid chromatography. J Chromatogr B Analyt Technol Biomed Life Sci 2005;819:323-8.  Back to cited text no. 25
    
26.
Waersted A, Hjorth N. Pityrosporum orbiculare – A pathogenic factor in atopic dermatitis of the face, scalp and neck? Acta Derm Venereol Suppl (Stockh) 1985;114:146-8.  Back to cited text no. 26
    
27.
Kim TY, Jang IG, Park YM, Kim HO, Kim CW. Head and neck dermatitis: The role of Malassezia furfur, topical steroid use and environmental factors in its causation. Clin Exp Dermatol 1999;24:226-31.  Back to cited text no. 27
    
28.
Bayrou O, Pecquet C, Flahault A, Artigou C, Abuaf N, Leynadier F, et al. Head and neck atopic dermatitis and Malassezia-furfur-specific IgE antibodies. Dermatology 2005;211:107-13.  Back to cited text no. 28
    
29.
Schmid-Grendelmeier P, Scheynius A, Crameri R. The role of sensitization to Malassezia sympodialis in atopic eczema. Chem Immunol Allergy 2006;91:98-109.  Back to cited text no. 29
    
30.
Darabi K, Hostetler SG, Bechtel MA, Zirwas M. The role of Malassezia in atopic dermatitis affecting the head and neck of adults. J Am Acad Dermatol 2009;60:125-36.  Back to cited text no. 30
    
31.
Brodská P, Panzner P, Pizinger K, Schmid-Grendelmeier P. IgE-mediated sensitization to Malassezia in atopic dermatitis: More common in male patients and in head and neck type. Dermatitis 2014;25:120-6.  Back to cited text no. 31
    
32.
Devos SA, van der Valk PG. The relevance of skin prick tests for Pityrosporum ovale in patients with head and neck dermatitis. Allergy 2000;55:1056-8.  Back to cited text no. 32
    
33.
Tsuboi H, Kouda K, Takeuchi H, Takigawa M, Masamoto Y, Takeuchi M, et al. 8-hydroxydeoxyguanosine in urine as an index of oxidative damage to DNA in the evaluation of atopic dermatitis. Br J Dermatol 1998;138:1033-5.  Back to cited text no. 33
    
34.
Nakai K, Yoneda K, Maeda R, Munehiro A, Fujita N, Yokoi I, et al. Urinary biomarker of oxidative stress in patients with psoriasis vulgaris and atopic dermatitis. J Eur Acad Dermatol Venereol 2009;23:1405-8.  Back to cited text no. 34
    
35.
Omata N, Tsukahara H, Ito S, Ohshima Y, Yasutomi M, Yamada A, et al. Increased oxidative stress in childhood atopic dermatitis. Life Sci 2001;69:223-8.  Back to cited text no. 35
    
36.
Niwa Y, Sumi H, Kawahira K, Terashima T, Nakamura T, Akamatsu H, et al. Protein oxidative damage in the stratum corneum: Evidence for a link between environmental oxidants and the changing prevalence and nature of atopic dermatitis in Japan. Br J Dermatol 2003;149:248-54.  Back to cited text no. 36
    
37.
Trüeb RM. Aging of hair. J Cosmet Dermatol 2005;4:60-72.  Back to cited text no. 37
    
38.
Piérard-Franchimont C, Uhoda I, Saint-Léger D, Piérard GE. Androgenetic alopecia and stress-induced premature senescence by cumulative ultraviolet light exposure. Exog Dermatol 2002;1:203-6.  Back to cited text no. 38
    
39.
Harman D. Aging: A theory based on free radical and radiation chemistry. J Gerontol 1956;11:298-300.  Back to cited text no. 39
    
40.
Nishimura EK, Granter SR, Fisher DE. Mechanisms of hair graying: Incomplete melanocyte stem cell maintenance in the niche. Science 2005;307:720-4.  Back to cited text no. 40
    
41.
Trüeb RM. The impact of oxidative stress on hair. Int J Cosmet Sci 2015;37 Suppl 2:25-30.  Back to cited text no. 41
    
42.
Bluhm AL, Weinstein J, Sousa JA. Free radicals in tobacco smoke. Nature 1971;229:500.  Back to cited text no. 42
    
43.
Trüeb RM. Association between smoking and hair loss: Another opportunity for health education against smoking? Dermatology 2003;206:189-91.  Back to cited text no. 43
    
44.
Trüeb RM. Is androgenetic alopecia a photoaggravated dermatosis? Dermatology 2003;207:343-8.  Back to cited text no. 44
    
45.
Trüeb RM. Molecular mechanisms of androgenetic alopecia. Exp Gerontol 2002;37:981-90.  Back to cited text no. 45
    
46.
Bahta AW, Farjo N, Farjo B, Philpott MP. Premature senescence of balding dermal papilla cells in vitro is associated with p16(INK4a) expression. J Invest Dermatol 2008;128:1088-94.  Back to cited text no. 46
    
47.
Upton JH, Hannen RF, Bahta AW, Farjo N, Farjo B, Philpott MP, et al. Oxidative stress-associated senescence in dermal papilla cells of men with androgenetic alopecia. J Invest Dermatol 2015;135:1244-52.  Back to cited text no. 47
    
48.
Huang WY, Huang YC, Huang KS, Chan CC, Chiu HY, Tsai RY, et al. Stress-induced premature senescence of dermal papilla cells compromises hair follicle epithelial-mesenchymal interaction. J Dermatol Sci 2017;86:114-22.  Back to cited text no. 48
    
49.
Akar A, Arca E, Erbil H, Akay C, Sayal A, Gür AR, et al. Antioxidant enzymes and lipid peroxidation in the scalp of patients with alopecia areata. J Dermatol Sci 2002;29:85-90.  Back to cited text no. 49
    
50.
Koca R, Armutcu F, Altinyazar C, Gürel A. Evaluation of lipid peroxidation, oxidant/antioxidant status, and serum nitric oxide levels in alopecia areata. Med Sci Monit 2005;11:CR296-299.  Back to cited text no. 50
    
51.
Abdel Fattah NS, Ebrahim AA, El Okda ES. Lipid peroxidation/antioxidant activity in patients with alopecia areata. J Eur Acad Dermatol Venereol 2011;25:403-8.  Back to cited text no. 51
    
52.
Bakry OA, Elshazly RM, Shoeib MA, Gooda A. Oxidative stress in alopecia areata: A case-control study. Am J Clin Dermatol 2014;15:57-64.  Back to cited text no. 52
    
53.
Motor S, Ozturk S, Ozcan O, Gurpinar AB, Can Y, Yuksel R, et al. Evaluation of total antioxidant status, total oxidant status and oxidative stress index in patients with alopecia areata. Int J Clin Exp Med 2014;7:1089-93.  Back to cited text no. 53
    
54.
Yenin JZ, Serarslan G, Yönden Z, Ulutaş KT. Investigation of oxidative stress in patients with alopecia areata and its relationship with disease severity, duration, recurrence and pattern. Clin Exp Dermatol 2015;40:617-21.  Back to cited text no. 54
    
55.
Naito A, Midorikawa T, Yoshino T, Ohdera M. Lipid peroxides induce early onset of catagen phase in murine hair cycles. Int J Mol Med 2008;22:725-9.  Back to cited text no. 55
    
56.
Niwa Y, Sumi H, Kawahira K, Terashima T, Nakamura T, Akamatsu H, et al. Protein oxidative damage in the stratum corneum: Evidence for a link between environmental oxidants and the changing prevalence and nature of atopic dermatitis in Japan. Br J Dermatol 2003;149:248-54.  Back to cited text no. 56
    
57.
Kurutas EB, Ozturk P. The evaluation of local oxidative/nitrosative stress in patients with pityriasis versicolor: A preliminary study. Mycoses 2016;59:720-5.  Back to cited text no. 57
    
58.
Nazzaro-Porro M, Passi S, Picardo M, Mercantini R, Breathnach AS. Lipoxygenase activity of Pityrosporum in vitro and in vivo. J Invest Dermatol 1986;87:108-12.  Back to cited text no. 58
    
59.
Später S, Hipler UC, Haustein UF, Nenoff P. Generation of reactive oxygen species in vitro by Malassezia yeasts. Hautarzt 2009;60:122-7.  Back to cited text no. 59
    
60.
Sinclair RD, Schwartz JR, Rocchetta HL, Dawson TL Jr., Fisher BK, Meinert K, et al. Dandruff and seborrheic dermatitis adversely affect hair quality. Eur J Dermatol 2009;19:410-1.  Back to cited text no. 60
    
61.
Kim KS, Shin MK, Park HK. Effects of scalp dermatitis on chemical property of hair keratin. Spectrochim Acta A Mol Biomol Spectrosc 2013;109:226-31.  Back to cited text no. 61
    
62.
Piérard-Franchimont C, Xhauflaire-Uhoda E, Loussouarn G, Saint Léger D, Piérard GE. Dandruff-associated smouldering alopecia: A chronobiological assessment over 5 years. Clin Exp Dermatol 2006;31:23-6.  Back to cited text no. 62
    
63.
Piérard-Franchimont C, Xhauflaire-Uhoda E, Piérard GE. Revisiting dandruff. Int J Cosmet Sci 2006;28:311-8.  Back to cited text no. 63
    
64.
Pitney L, Weedon D, Pitney M. Is seborrhoeic dermatitis associated with a diffuse, low-grade folliculitis and progressive cicatricial alopecia? Australas J Dermatol 2016;57:e105-7.  Back to cited text no. 64
    
65.
Kim KS, Shin MK, Ahn JJ, Haw CR, Park HK. Investigation of hair shaft in seborrheic dermatitis using atomic force microscopy. Skin Res Technol 2011;17:288-94.  Back to cited text no. 65
    
66.
Kim KS, Shin MK, Kim JH, Kim MH, Haw CR, Park HK, et al. Effects of atopic dermatitis on the morphology and water content of scalp hair. Microsc Res Tech 2012;75:620-5.  Back to cited text no. 66
    
67.
Kim KS, Shin MK, Ahn JJ, Haw CR, Park HK. A comparative study of hair shafts in scalp psoriasis and seborrheic dermatitis using atomic force microscopy. Skin Res Technol 2013;19:e60-4.  Back to cited text no. 67
    
68.
Shuster S. Psoriatic alopecia. Arch Dermatol 1990;126:397.  Back to cited text no. 68
    
69.
Runne U, Kroneisen-Wiersma P. Psoriatic alopecia: Acute and chronic hair loss in 47 patients with scalp psoriasis. Dermatology 1992;185:82-7.  Back to cited text no. 69
    
70.
Wyatt E, Bottoms E, Comaish S. Abnormal hair shafts in psoriasis on scanning electron microscopy. Br J Dermatol 1972;87:368-73.  Back to cited text no. 70
    
71.
Headington JT, Gupta AK, Goldfarb MT, Nickoloff BJ, Hamilton TA, Ellis CN, et al. A morphometric and histologic study of the scalp in psoriasis. Paradoxical sebaceous gland atrophy and decreased hair shaft diameters without alopecia. Arch Dermatol 1989;125:639-42.  Back to cited text no. 71
    
72.
Plozzer C, Coletti C, Kokelj F, Trevisan G. Scanning electron microscopy study of hair shaft disorders in psoriasis. Acta Derm Venereol Suppl (Stockh) 2000;211:9-11.  Back to cited text no. 72
    
73.
Kumar B, Soni A, Saraswat A, Kaur I, Dogra S. Hair in psoriasis: A prospective, blinded scanning electron microscopic study. Clin Exp Dermatol 2008;33:491-4.  Back to cited text no. 73
    
74.
Schoorl WJ, van Baar HJ, van de Kerkhof PC. The hair root pattern in psoriasis of the scalp. Acta Derm Venereol 1992;72:141-2.  Back to cited text no. 74
    
75.
Denizli H, Güler Özden M, Sentürk N, Bek Y. Trichogram findings in psoriasis and seborrheic dermatitis patients. Turk Klinikleri J Dermatol 2017;27:61-8.  Back to cited text no. 75
    
76.
Stanimirović A, Skerlev M, Stipić T, Beck T, Basta-Juzbasić A, Ivanković D, et al. Has psoriasis its own characteristic trichogram? J Dermatol Sci 1998;17:156-9.  Back to cited text no. 76
    
77.
Urbano CC. 50 years of hair care development. Cosmet Toiletries 1995;110:85-104.  Back to cited text no. 77
    
78.
Trüeb RM. Shampoos: Ingredients, efficacy and adverse effects. J Dtsch Dermatol Ges 2007;5:356-65.  Back to cited text no. 78
    
79.
Squire RA, Goode K. A randomised, single-blind, single-centre clinical trial to evaluate comparative clinical efficacy of shampoos containing ciclopirox olamine (1.5%) and salicylic acid (3%), or ketoconazole (2%, nizoral) for the treatment of dandruff/seborrhoeic dermatitis. J Dermatolog Treat 2002;13:51-60.  Back to cited text no. 79
    
80.
Piérard-Franchimont C, Goffin V, Decroix J, Piérard GE. A multicenter randomized trial of ketoconazole 2% and zinc pyrithione 1% shampoos in severe dandruff and seborrheic dermatitis. Skin Pharmacol Appl Skin Physiol 2002;15:434-41.  Back to cited text no. 80
    
81.
Schmidt-Rose T, Braren S, Fölster H, Hillemann T, Oltrogge B, Philipp P, et al. Efficacy of a piroctone olamine/climbazole shampoo in comparison with a zinc pyrithione shampoo in subjects with moderate to severe dandruff. Int J Cosmet Sci 2011;33:276-82.  Back to cited text no. 81
    
82.
Schwartz JR, Bacon RA, Shah R, Mizoguchi H, Tosti A. Therapeutic efficacy of anti-dandruff shampoos: A randomized clinical trial comparing products based on potentiated zinc pyrithione and zinc pyrithione/climbazole. Int J Cosmet Sci 2013;35:381-7.  Back to cited text no. 82
    
83.
Okokon EO, Verbeek JH, Ruotsalainen JH, Ojo OA, Bakhoya VN. Topical antifungals for seborrhoeic dermatitis. Cochrane Database Syst Rev 2015;5:CD008138.  Back to cited text no. 83
    
84.
van de Kerkhof PC, Franssen ME. Psoriasis of the scalp. Diagnosis and management. Am J Clin Dermatol 2001;2:159-65.  Back to cited text no. 84
    
85.
Broberg A, Faergemann J. Topical antimycotic treatment of atopic dermatitis in the head/neck area. A double-blind randomised study. Acta Derm Venereol 1995;75:46-9.  Back to cited text no. 85
    
86.
Mayser P, Kupfer J, Nemetz D, Schäfer U, Nilles M, Hort W, et al. Treatment of head and neck dermatitis with ciclopiroxolamine cream – Results of a double-blind, placebo-controlled study. Skin Pharmacol Physiol 2006;19:153-8.  Back to cited text no. 86
    
87.
Piérard GE, Piérard-Franchimont C, Nikkels-Tassoudji N. Improvement in the inflammatory aspect of androgenetic alopecia. A pilot study with an antimicrobial lotion. J Dermatol Treat 1996;7:153-7.  Back to cited text no. 87
    
88.
Piérard-Franchimont C, De Doncker P, Cauwenbergh G, Piérard GE. Ketoconazole shampoo: Effect of long-term use in androgenic alopecia. Dermatology 1998;196:474-7.  Back to cited text no. 88
    
89.
Berger RS, Fu JL, Smiles KA, Turner CB, Schnell BM, Werchowski KM, et al. The effects of minoxidil, 1% pyrithione zinc and a combination of both on hair density: A randomized controlled trial. Br J Dermatol 2003;149:354-62.  Back to cited text no. 89
    


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