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Figure 1.
Blinded Ratings of Keratosis Pilaris (KP) Severity
Blinded Ratings of Keratosis Pilaris (KP) Severity

Blinded dermatologists assigned ratings of KP severity after 3 laser treatments. Severity was rated on a scale of 0 (least severe) to 3 (most severe). P values were calculated to assess differences between treatment and control sites.

Figure 2.
Patient Self-assessment of Keratosis Pilaris (KP) Severity
Patient Self-assessment of Keratosis Pilaris (KP) Severity

Patient self-assessment of KP severity was performed after 3 laser treatments. Severity was rated on a scale of 0 (least severe) to 3 (most severe). P values were calculated to assess differences between treatment and control sites.

Figure 3.
Representative Photographs of Keratosis Pilaris (KP) Treatment
Representative Photographs of Keratosis Pilaris (KP) Treatment

Photographs were obtained of a young woman with Fitzpatrick skin type II with KP on the upper extremities. A, Upper right arm at baseline. B, Upper right arm after 3 laser treatments.

Table.  
Demographics of Enrolled Patients
Demographics of Enrolled Patients
1.
Griffiths  WAD, Leigh  IM, Marks  R. Disorders of keratinization. In: Champion  RH, Burton  JL, Ebling  FJG, eds. Textbook of Dermatology.Vol 2. 5th ed. Oxford, England: Blackwell Scientific Publications Ltd; 1992:1352-1355.
2.
Fritsch  P. Follicular syndromes with inflammation and atrophy. In: Freedberg  IM, Eisen  AZ, Wolff  K, Austen  KF, Goldsmith  LA, Katz  SI, eds. Fitzpatrick's Dermatology in General Medicine.6th ed. New York, NY: McGraw-Hill Co; 2003:713-718.
3.
Poskitt  L, Wilkinson  JD.  Natural history of keratosis pilaris. Br J Dermatol. 1994;130(6):711-713.
PubMedArticle
4.
Lateef  A, Schwartz  RA.  Keratosis pilaris. Cutis. 1999;63(4):205-207.
PubMed
5.
Dawn  G, Urcelay  M, Patel  M, Strong  AM.  Keratosis rubra pilaris responding to potassium titanyl phosphate laser. Br J Dermatol. 2002;147(4):822-824.
PubMedArticle
6.
Clark  SM, Mills  CM, Lanigan  SW.  Treatment of keratosis pilaris atrophicans with the pulsed tunable dye laser. J Cutan Laser Ther. 2000;2(3):151-156.
PubMedArticle
7.
Kaune  KM, Haas  E, Emmert  S, Schön  MP, Zutt  M.  Successful treatment of severe keratosis pilaris rubra with a 595-nm pulsed dye laser. Dermatol Surg. 2009;35(10):1592-1595.
PubMedArticle
8.
Alcántara González  J, Boixeda  P, Truchuelo Díez  MT, Fleta Asín  B.  Keratosis pilaris rubra and keratosis pilaris atrophicans faciei treated with pulsed dye laser: report of 10 cases. J Eur Acad Dermatol Venereol. 2011;25(6):710-714.
PubMedArticle
9.
Marqueling  AL, Gilliam  AE, Prendiville  J,  et al.  Keratosis pilaris rubra: a common but underrecognized condition. Arch Dermatol. 2006;142(12):1611-1616.
PubMedArticle
10.
Voss  M.  Keratosis follicularis: new genetic aspects [in German]. Hautarzt. 1991;42(5):319-321.
PubMed
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Original Investigation
February 2015

Treatment of Keratosis Pilaris With 810-nm Diode LaserA Randomized Clinical Trial

Author Affiliations
  • 1Department of Dermatology, Cleveland Clinic Foundation, Cleveland, Ohio
  • 2Department of Dermatology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois
  • 3Section of Dermatology, University of Chicago, Chicago, Illinois
  • 4Department of Dermatology, Washington Hospital Center, Georgetown University, Washington, DC
  • 5Department of Medicine, Emory University School of Medicine, Atlanta, Georgia
  • 6Department of Medicine, Baptist Health South Florida, Miami
  • 7Department of Otolaryngology, Feinberg School of Medicine, Northwestern University, Chicago, Illinois
  • 8Department of Surgery, Feinberg School of Medicine, Northwestern University, Chicago, Illinois
JAMA Dermatol. 2015;151(2):187-191. doi:10.1001/jamadermatol.2014.2211
Abstract

Importance  Keratosis pilaris (KP) is a common skin disorder of follicular prominence and erythema that typically affects the proximal extremities, can be disfiguring, and is often resistant to treatment. Shorter-wavelength vascular lasers have been used to reduce the associated erythema but not the textural irregularity.

Objective  To determine whether the longer-wavelength 810-nm diode laser may be effective for treatment of KP, particularly the associated skin roughness/bumpiness and textural irregularity.

Design, Setting, and Participants  We performed a split-body, rater-blinded, parallel-group, balanced (1:1), placebo-controlled randomized clinical trial at a dermatology outpatient practice of an urban academic medical center from March 1 to October 1, 2011. We included all patients diagnosed as having KP on both arms and Fitzpatrick skin types I through III. Of the 26 patients who underwent screening, 23 met our enrollment criteria. Of these, 18 patients completed the study, 3 were lost to or unavailable for follow-up, and 2 withdrew owing to inflammatory hyperpigmentation after the laser treatment.

Interventions  Patients were randomized to receive laser treatment on the right or left arm. Each patient received treatment with the 810-nm pulsed diode laser to the arm randomized to be the treatment site. Treatments were repeated twice, for a total of 3 treatment visits spaced 4 to 5 weeks apart.

Main Outcomes and Measures  The primary outcome measure was the difference in disease severity score, including redness and roughness/bumpiness, with each graded on a scale of 0 (least severe) to 3 (most severe), between the treated and control sites. Two blinded dermatologists rated the sites at 12 weeks after the initial visit.

Results  At follow-up, the median redness score reported by the 2 blinded raters for the treatment and control sides was 2.0 (interquartile range [IQR], 1-2; P = .11). The median roughness/bumpiness score was 1.0 (IQR, 1-2) for the treatment sides and 2.0 (IQR, 1-2) for the control sides, a difference of 1 (P = .004). The median overall score combining erythema and roughness/bumpiness was 3.0 (IQR, 2-4) for the treatment sides and 4.0 (IQR, 3-5) for the control sides, a difference of 1 (P = .005).

Conclusions and Relevance  Three treatments with the 810-nm diode laser may induce significant improvements in skin texture and roughness/bumpiness in KP patients with Fitzpatrick skin types I through III, but baseline erythema is not improved. Complete treatment of erythema and texture in KP may require diode laser treatment combined with other laser or medical modalities that address redness.

Trial Registration  clinicaltrials.gov Identifier: NCT01281644

Introduction

Keratosis pilaris (KP) is a common hereditary, benign disorder of unknown etiology1 that is frequently seen in conjunction with atopy. The hereditary pattern of this skin disorder is thought to be autosomal dominant without a known predisposition based on race or sex.2 Keratinaceous plugging of follicles results in markedly visible papules, often involving the lateral and extensor aspects of the proximal extremities but sometimes also the face, buttocks, and trunk.3 Perifollicular erythema is routinely notable.4 Topical treatments for KP include emollients, exfoliants, and anti-inflammatory agents, such as urea, salicylic acid, lactic acid, topical corticosteroids, topical retinoids, and cholecalciferol. Because most patients obtain limited benefit from these treatments, less conventional treatments, including phototherapy and lasers, have been explored. Among lasers, the 532-, 585-, and 595-nm vascular devices have been used with modest success, particularly in reducing redness.58 Longer-wavelength lasers have not been studied for the treatment of KP, and lasers have not been shown to be successful for treating the textural components of KP. Our study investigates the effectiveness of the longer-wavelength 810-nm diode laser for color and texture of upper extremity KP.

Methods
Study Design

We performed a split-body, parallel-group, placebo-controlled randomized clinical trial with an allocation ratio of 1:1 and a block size of 2 at an urban academic medical center. The unit of randomization was the individual unilateral upper extremity. The study was approved by the institutional review board of Northwestern University. All participants provided written informed consent.

Patient Selection

Patients were recruited from a dermatology practice at Feinberg School of Medicine, Northwestern University, and the surrounding community. Inclusion criteria consisted of age 18 to 65 years, good health, Fitzpatrick skin types I to III, and a diagnosis of KP on both upper extremities. We excluded patients who had received any laser therapy to the arms in the 12 months before recruitment, with a concurrent diagnosis of another skin condition or malignant neoplasm, with a tan or sunburn over the upper arms in the month before recruitment, with open ulcers or infections at any skin site, or who were using topical or oral photosensitizing medications.

Study Procedures

When potential participants called or e-mailed the clinic for possible inclusion in the study, they underwent prescreening (performed by O.I.) over the telephone using the aforementioned inclusion and exclusion criteria. Once enrollment criteria were met, patients were scheduled for a total of 4 visits, 4 to 5 weeks apart, in the Department of Dermatology, Feinberg School of Medicine.

On the patient’s first visit, one of us (O.I.) reviewed the inclusion and exclusion criteria. After the patients provided written informed consent, they separately rated redness and roughness/bumpiness on each arm using a scale of 0 (least severe) to 3 (most severe) for a total maximum score of 6 per patient per arm. Next, patients were randomized into 2 groups as described below, and baseline standardized digital photographs were obtained. Each patient received treatment using the 810-nm pulsed diode laser to the arm randomized to be the treatment site. After laser treatment, both sides were treated with topical petrolatum. Treatments were repeated twice for a total of 3 treatment visits, with visits spaced 4 to 5 weeks apart. At the fourth and final visit, 12 to 15 weeks after the initial visit, the patients again rated disease severity as previously described. At this last visit, 2 blinded dermatologists (S.Y. and M.A.) also rated the roughness/bumpiness and redness of the treatment and control arms separately using the same scales, and digital photographs were again obtained.

Patient Randomization

Patient screening and enrollment were performed by one of us (M.D.), as were random sequence generation and concealment (R.K.), which were conducted by coin toss of the same fair coin, with the outcomes (1 or 2) recorded separately on individual paper cards then placed in sealed, opaque, consecutively numbered envelopes. Each patient was assigned to one of 2 groups (by W.D.). Patients in group 1 were designated to receive laser therapy on the right arm, and those in group 2 were assigned to receive laser therapy on the left arm. All study treatments were delivered by the same clinician (D.B.).

Laser Treatments

All study treatments used the 810-nm pulsed diode laser. A lidocaine and prilocaine–based cream was applied to the arms 30 to 60 minutes before treatment and washed off before treatment. Laser therapy was performed on the treatment side at a fluence of 45 to 60 J/cm2 (to convert to gray, multiply by 1) (depending on Fitzpatrick skin type) and a pulse duration of 30 to 100 milliseconds, with precise settings selected to be just below the patient’s threshold for purpura. Each treatment session entailed 2 nonoverlapping passes separated by a 1-minute delay. The patient was then instructed to minimize sun exposure and apply sunscreen with a sun protection factor of 50 to the treatment area daily until the next visit.

Outcome Measures

The primary outcome measure was the difference in disease severity score, including redness and roughness/bumpiness, between the treated site and the control site as rated by the blinded dermatologists at 12 weeks after the initial visit. This scale was not validated because no relevant validated scale was available. However, raters were trained on the use of the study scale, and before the review of study images, they were asked to rate archival skin images on the same 4-point qualitative subscales used in the study. Raters reviewed and rated archival images separately and then reconciled their ratings through face-to-face forced agreement, with the process repeated until concordance was achieved between raters and their separately rated scores were consistently equivalent.

During the evaluation of study data, forced agreement was used to reconcile blinded ratings. The secondary outcome measure was the change from baseline in disease severity of each arm as rated by the patients.

Power Analysis and Sample Size

Assuming an SD of change of 0.84, a sample of 20 patients had 80% power to detect median differences (or median changes) in severity scores of 0.5. We assumed a 2-sided test and type I error rate of 5%.

Statistical Analysis

We used the Wilcoxon signed rank test to compare the magnitude of change from baseline between treatment and control for all patient ratings (redness, roughness/bumpiness, and overall score). Blinded dermatologists’ ratings of the treatment and control sides were also compared using the Wilcoxon signed rank test.

Results
Patient Baseline Demographic Characteristics

The study was conducted during a 7-month period from March 1 to October 1, 2011. A total of 26 patients underwent screening for our study, and 23 of those patients (46 arms) met our criteria and were enrolled in the study. Of these 23 patients, 18 (36 arms) completed the study and underwent analysis, 3 were lost to or unavailable for follow-up, and 2 voluntarily withdrew owing to inflammatory hyperpigmentation after the laser treatment. The demographic characteristics of our patients are presented in the Table. At baseline, patients rated the severity of the roughness/bumpiness in the texture of their arm test sites at a median score of 1.5 (interquarile range [IQR], 1-2) and the severity of the erythema of their arm test sites at a median score of 2.0 (IQR, 1-2). (The maximum score for both ratings was 3.0.)

Blinded Raters’ Scores

At follow-up, the median redness score assigned by the blinded raters for the treatment and control sides was 2.0 (IQR, 1-2), a null difference (Figure 1). The median roughness/bumpiness score was 1.0 (IQR, 1-2) for the treatment sides and 2.0 (IQR, 1-2) for the control sides, a difference of 1 (P = .004) (Figure 1). The median overall score combining erythema and roughness/bumpiness was 3.0 (IQR, 2-4) for the treatment sides and 4.0 (IQR, 3-5) for the control sides, a difference of 1 (P = .005) (Figure 1).

Patient Self-assessment Scores

At follow-up, patients’ self-reported median erythema rating for the control sides did not change from the baseline score of 2.0 (IQR, 1-2), but the self-reported median erythema score for the treatment side decreased from 2.0 to 1.5 (IQR, 1-2), a nominal difference that was not statistically significant (P = .13) (Figure 2). The median roughness/bumpiness score for the control sides increased from 1.5 to 2.0 (IQR, 1-2) and for the treatment sides decreased from 1.5 to 1.0 (IQR, 1-2). The 1-point decrease in roughness/bumpiness in the treatment arm compared with the control arm was significant (P = .008) (Figure 2). The overall score (erythema and roughness/bumpiness) for the control sides increased from 3.5 to 4.0 (IQR, 3-4), and for the treatment arm decreased from 3.5 to 2.5 (IQR, 2-4), with the cumulative difference of 1.5 points being significant (P = .005) (Figure 2).

Adverse Events

We found no unexpected adverse events associated with laser treatment. Two participants developed inflammatory hyperpigmentation after laser treatment and chose to withdraw from the study. These patients were instructed to continue sun-protective measures to their affected extremities, and in both cases hyperpigmentation completely resolved within 3 months.

Discussion

We investigated the effectiveness of the 810-nm diode laser in the treatment of KP. After 3 treatments spaced 4 to 5 weeks apart, blinded dermatologist ratings and patient self-report indicated significant improvements in skin texture and roughness/bumpiness when compared with baseline (Figure 3). However, neither raters nor patients detected a significant change in erythema.

Most topical treatments for KP, including emollients, corticosteroids, and retinoids, are of limited effectiveness.9 Light-based treatments have typically entailed use of vascular lasers, like the application of a 532-nm potassium titanyl phosphate laser to treat a case of resistant facial KP by Dawn et al.5 Repeated treatments resulted in a marked improvement in erythema and some clearance of papules. A study of 12 patients using the 585-nm pulsed-dye laser6 found improvement in erythema but not in roughness/bumpiness. A similar report7 described a case in which multiple treatments with a 595-nm pulsed-dye laser induced marked improvements in facial erythema, patient satisfaction, and quality of life. A study of 10 patients treated with a 595-nm pulsed-dye laser8 confirmed these results.

To our knowledge, our study is the first of its kind to investigate the use of a longer-wavelength laser, the diode laser, in the treatment of KP. More important, our results are the first from a clinical trial that demonstrate the effectiveness of laser treatment of the textural abnormality and roughness/bumpiness associated with KP. The data from our investigation suggest that the 810-nm diode laser is a particularly promising and effective treatment for the nonerythematous variants of KP. The variant of KP known as keratosis pilaris alba, which presents mostly as follicular papules, may be highly responsive to this laser modality.10 The variant that includes perifollicular erythema with follicular papules, keratosis pilaris rubra,9,10 may best respond to joint treatment with diode and vascular lasers, with the former improving texture and the latter addressing erythema.

We have theoretical reasons for selecting the 810-nm diode laser and the settings used in this study. Specifically, KP is an inflammatory condition of vellus hair follicles. Compared with terminal hair, vellus hair is relatively deficient in melanin (ie, has less chromophore) and smaller in diameter (ie, has shorter thermal relaxation time). Based on the theory of selective photothermolysis, these features would be consistent with a thermal relaxation time of approximately 50 milliseconds, which means that a pulse duration of less than 50 milliseconds, such as the 30 milliseconds used in this study, would be appropriate for treatment. Because of a substantial lack of chromophore, the fluence required for photothermal destruction of a vellus hair follicle is 40 to 45 J/cm2, greater than that for a terminal hair. Ideally a highly absorbing wavelength such as 695 nm would be the best to treat vellus follicles, but this wavelength is absorbed by epidermal pigment in darker skinned individuals before it can reach deeper targets, such as the stem cells in the bulge region of the follicles. Similarly, 1064 nm is not highly selective for melanin, and we know that the vellus follicle has little melanin to begin with. As a consequence, the 810-nm wavelength appears to be the best choice because its depth of penetration is sufficient, it has selectivity for melanin, and it is compatible with a pulse duration of 30 milliseconds.

In terms of adverse events, our study found that treatment with the 810-nm diode laser was safe and not associated with any serious or unexpected adverse events. Although 2 patients (9%) developed bothersome inflammatory hyperpigmentation after laser treatment, resulting in their withdrawal from the study, these sequelae resolved completely in the medium term. Further counseling about the need for sun protection and avoidance of tanning during the period of laser treatment may mitigate the risk for posttreatment inflammatory hyperpigmentation in the future.

A limitation of our study is that enrollment was restricted to participants with Fitzpatrick skin types I to III. The exclusion of darker skin types was not incidental but rather designed to minimize the risk for posttreatment inflammatory hyperpigmentation, which is more common after laser procedures in patients with Fitzpatrick skin types IV to VI. That posttreatment inflammatory hyperpigmentation was observed in this study despite careful patient selection suggests that this precaution was appropriate. Regardless, patients with darker skin types can indeed be treated safely with the diode laser if gentle settings are used. Once this treatment paradigm is optimized, such broader application will likely be appropriate and feasible. One protective benefit of the current treatment settings was that they were deliberately below the threshold for purpura and thus designed to avoid bruising, which can resolve with tan pigmentation, particularly in darker skin. To the extent that the 810-nm diode laser has hair-removing activity, this treatment may be inappropriate for patients who do not want hair loss at the site of their KP. Finally, although incidental reports from some participants previously in this study have indicated that they have maintained textural benefits for more than a year, it remains to be seen to what extent these improvements are maintained over the longer term. To the extent that laser treatment may significantly modify hair growth in abnormal vellus hair follicles initially induced by genetic predisposition, improvement may be long lasting. This result would then be parallel to the case of traditional hair removal, in which posttreatment long-term remission of coarse terminal hairs and the corresponding pseudofolliculitis is often observed.

However, this study was not designed to assess long-term improvement, and additional studies would need to be performed to systematically measure the duration and likelihood of persistent benefits. The present study only provides proof of concept and indicates that improvement of the textural abnormalities associated with KP is possible after treatment with an 810-nm diode laser.

Conclusions

By objective and subjective measures, we found that, among lighter-skinned persons, serial treatment with a long-pulsed 810-nm diode laser at subpurpuric levels provided medium-term improvement in KP, particularly for the associated roughness/bumpiness and textural irregularity. Combined with preexisting data about the utility of vascular lasers for the reduction of KP-associated erythema, this finding suggests that laser treatment may comprehensively address the clinical manifestations of KP in selected patients. Future studies may assess the durability of these responses and the comparative effectiveness of different long-wavelength lasers.

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Article Information

Accepted for Publication: July 7, 2014.

Corresponding Author: Murad Alam, MD, MSCI, Department of Dermatology, Feinberg School of Medicine, Northwestern University, 676 N St Clair St, Ste 1600, Chicago, IL 60611 (m-alam@northwestern.edu).

Published Online: November 5, 2014. doi:10.1001/jamadermatol.2014.2211.

Author Contributions: Dr Alam had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis.

Study concept and design: Ibrahim, Khan, Dubina, Yoo, West, Alam.

Acquisition, analysis, or interpretation of data: Ibrahim, Khan, Bolotin, Nodzenski, Disphanurat, Kakar, Whiting, Poon, Veledar, Alam.

Drafting of the manuscript: Ibrahim, Alam.

Critical revision of the manuscript for important intellectual content: All authors.

Statistical analysis: Nodzenski, Veledar.

Obtained funding: Alam.

Administrative, technical, or material support: Dubina, Disphanurat, Kakar, Whiting, West.

Study supervision: Khan, Bolotin, Alam.

Conflict of Interest Disclosures: Dr Alam is employed at Northwestern University and has been a consultant for Amway and Leo Pharma, both unrelated to this research. Northwestern University has a clinical trials unit that receives grants from many corporate and governmental entities to perform clinical research; Dr Alam has been principal investigator on studies funded in part by Allergan, Bioform, Medicis, and Ulthera. In all cases, grants and gifts in kind have been provided to Northwestern University and not to Dr Alam directly, and Dr Alam has not received any salary support from these grants. Dr Alam receives royalties (<$5000 per year) from Elsevier for technical books he has edited. No other disclosures were reported.

Funding/Support: This study was supported by Departmental Research Funds, Department of Dermatology, Northwestern University.

Role of the Funder/Sponsor: The funding source had a role in the design and conduct of the study; collection, management, analysis, and interpretation of the data; preparation, review, or approval of the manuscript; and decision to submit the manuscript for publication.

References
1.
Griffiths  WAD, Leigh  IM, Marks  R. Disorders of keratinization. In: Champion  RH, Burton  JL, Ebling  FJG, eds. Textbook of Dermatology.Vol 2. 5th ed. Oxford, England: Blackwell Scientific Publications Ltd; 1992:1352-1355.
2.
Fritsch  P. Follicular syndromes with inflammation and atrophy. In: Freedberg  IM, Eisen  AZ, Wolff  K, Austen  KF, Goldsmith  LA, Katz  SI, eds. Fitzpatrick's Dermatology in General Medicine.6th ed. New York, NY: McGraw-Hill Co; 2003:713-718.
3.
Poskitt  L, Wilkinson  JD.  Natural history of keratosis pilaris. Br J Dermatol. 1994;130(6):711-713.
PubMedArticle
4.
Lateef  A, Schwartz  RA.  Keratosis pilaris. Cutis. 1999;63(4):205-207.
PubMed
5.
Dawn  G, Urcelay  M, Patel  M, Strong  AM.  Keratosis rubra pilaris responding to potassium titanyl phosphate laser. Br J Dermatol. 2002;147(4):822-824.
PubMedArticle
6.
Clark  SM, Mills  CM, Lanigan  SW.  Treatment of keratosis pilaris atrophicans with the pulsed tunable dye laser. J Cutan Laser Ther. 2000;2(3):151-156.
PubMedArticle
7.
Kaune  KM, Haas  E, Emmert  S, Schön  MP, Zutt  M.  Successful treatment of severe keratosis pilaris rubra with a 595-nm pulsed dye laser. Dermatol Surg. 2009;35(10):1592-1595.
PubMedArticle
8.
Alcántara González  J, Boixeda  P, Truchuelo Díez  MT, Fleta Asín  B.  Keratosis pilaris rubra and keratosis pilaris atrophicans faciei treated with pulsed dye laser: report of 10 cases. J Eur Acad Dermatol Venereol. 2011;25(6):710-714.
PubMedArticle
9.
Marqueling  AL, Gilliam  AE, Prendiville  J,  et al.  Keratosis pilaris rubra: a common but underrecognized condition. Arch Dermatol. 2006;142(12):1611-1616.
PubMedArticle
10.
Voss  M.  Keratosis follicularis: new genetic aspects [in German]. Hautarzt. 1991;42(5):319-321.
PubMed
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