1. Introduction: Unveiling LED Light Therapy for Skin Health
Light Emitting Diode (LED) therapy has emerged as a popular non-invasive treatment modality within dermatology and aesthetic medicine, utilized for addressing a variety of skin conditions and concerns. Its application spans from managing acne and signs of aging to potentially aiding in wound healing and reducing inflammation. The technology’s origins are often traced back to research conducted by NASA in the 1990s, initially exploring the use of LEDs to promote plant growth in space and subsequently observing accelerated wound healing in astronauts. This report aims to critically evaluate the scientific evidence regarding the efficacy of LED light therapy for various dermatological applications, with a particular focus on the common wavelengths employed and the performance of increasingly popular at-home LED face masks, based on analysis of available research findings.
It is important to distinguish between the two primary therapeutic approaches that utilize LED light in dermatology. Photodynamic Therapy (PDT) involves the application of a photosensitizing agent to the target tissue, which is then activated by specific wavelengths of light (often blue or red LED light) to generate reactive oxygen species that selectively destroy abnormal cells, such as in certain skin cancers or precancerous lesions. In contrast, Photobiomodulation Therapy (PBMT or PBM), the main focus of this report, utilizes low-level light exposure withoutan exogenous photosensitizer to stimulate cellular repair, modulate inflammation, and promote tissue regeneration.PBM is also frequently referred to in the literature as Low-Level Light Therapy or Low-Level Laser Therapy (LLLT), reflecting its historical development and the use of both laser and LED sources to achieve similar biological effects at low energy levels.
2. The Science of Light: How LED Therapy Interacts with Skin Cells
2.1 Photobiomodulation (PBM): The Core Mechanism
Photobiomodulation is defined as a non-thermal process employing non-ionizing electromagnetic energy, typically from light sources such as LEDs or low-level lasers, within the visible (approximately 400–700 nm) and near-infrared (NIR, approximately 700–1100 nm or even up to 1440 nm) spectrum. This light energy interacts with endogenous chromophores (light-absorbing molecules) within cells to elicit photophysical and photochemical events, ultimately modulating cellular functions and biological processes. PBM is characterized by its non-invasive nature and is generally associated with a favorable safety profile, offering a potential alternative or adjunct to traditional pharmacological therapies.
The primary proposed mechanism underlying PBM involves the absorption of photons by specific photoacceptors within the mitochondria, the powerhouses of the cell. Considerable evidence points to cytochrome c oxidase (CcO, also known as Complex IV), a key enzyme in the mitochondrial electron transport chain located in the inner mitochondrial membrane, as the principal chromophore responsible for absorbing red and NIR light.
This absorption of light energy by CcO is thought to stimulate the mitochondrial respiratory chain, enhancing electron transport and leading to an increase in the production of adenosine triphosphate (ATP), the cell’s primary energy currency. In tissues that are impaired, damaged, or stressed, ATP production may be compromised; PBM appears to help restore this crucial oxidative process, thereby normalizing cellular metabolism and energy balance. The consistent identification of mitochondria, specifically CcO, as the primary photoacceptor underscores the fundamental role of cellular energy metabolism in PBM’s effects. This focus on mitochondrial function provides a biological rationale for PBM’s observed benefits across diverse conditions potentially linked to mitochondrial dysfunction, such as aspects of skin aging, certain inflammatory states, and impaired wound healing.
Beyond boosting ATP production, mitochondrial activation by PBM triggers a cascade of downstream signaling events. This includes a transient increase in reactive oxygen species (ROS). While often associated with cellular damage, these PBM-induced ROS appear to function as crucial signaling molecules. This phenomenon relates to the concept of redox signaling or mitohormesis, where a mild, controlled stressor (like the transient ROS increase) activates adaptive cellular responses. Indeed, while PBM can generate ROS in normal cells, studies indicate that in oxidatively stressed cells or disease models, PBM can actually lower overall ROS levels and up-regulate the cell’s own antioxidant defenses. This suggests PBM actively modulates the cellular redox state rather than simply acting as an antioxidant, with its net effect potentially depending on the baseline stress level of the cell. This nuanced mechanism may contribute to the widely reported anti-inflammatory effects of PBM, possibly by re-balancing cellular stress responses and promoting inflammation resolution pathways.
Other significant signaling events include the light-induced dissociation or release of nitric oxide (NO) from CcO, where it can act as an inhibitor of respiration. This NO release may contribute to increased enzyme activity, enhanced blood flow (vasodilation), and further downstream signaling. Furthermore, PBM can activate various transcription factors, such as AP-1 (via the Jun/Fos pathway), leading to changes in gene expression. Ultimately, these interconnected events modulate numerous cellular pathways involved in proliferation, migration, survival, inflammation control, and the synthesis of growth factors, collectively contributing to tissue repair and regeneration.
2.2 Key Wavelengths and Their Cutaneous Targets
The therapeutic effects of LED light therapy are highly dependent on the specific wavelength (color) of light used. Different wavelengths penetrate the skin to varying depths and are preferentially absorbed by different molecular chromophores, initiating distinct biological responses. The concept of the “optical window” in biological tissue, typically cited as roughly 600 nm to 900-1100 nm, describes the range where light achieves maximum penetration depth due to relatively lower absorption by major tissue components like melanin, hemoglobin (blood), and water. This principle underpins the common use of red and NIR light for targeting deeper structures.
- Blue Light (approx. 405–470 nm): Blue light has the shortest wavelength among the commonly used therapeutic options and consequently exhibits the shallowest penetration, primarily affecting the epidermis, the uppermost layer of the skin. Its primary mechanism of action in dermatology relates to the treatment of acne vulgaris. Cutibacterium acnes (the bacterium implicated in inflammatory acne) naturally produces endogenous porphyrins, mainly coproporphyrin III and protoporphyrin IX. Blue light, particularly around 415 nm, is strongly absorbed by these porphyrins. This photo-excitation leads to the generation of cytotoxic reactive oxygen species (ROS), such as singlet oxygen, which effectively destroys the bacteria. Some evidence also suggests blue light may possess anti-inflammatory properties and potentially influence sebum production. Therefore, the main claimed benefit for blue light PBM is the treatment of acne. It is also used in PDT for certain skin cancers and precancerous actinic keratoses.
- Red Light (approx. 620–700 nm, often 630–660 nm): Red light possesses longer wavelengths than blue light, allowing it to penetrate deeper into the skin, reaching the dermis. Like NIR light, red light is primarily absorbed by the mitochondrial chromophore CcO. This interaction is believed to stimulate dermal fibroblasts, leading to increased production of collagen and elastin—key structural proteins for skin elasticity and firmness.Additionally, red light is reported to reduce inflammation , improve blood circulation , and accelerate wound healing processes. Consequently, red light therapy is primarily utilized for skin rejuvenation (addressing wrinkles, fine lines, skin texture, firmness, and elasticity), promoting wound healing, reducing inflammation (as seen in conditions like rosacea), and potentially stimulating hair growth. It is also frequently used in combination with blue light for acne management.
- Near-Infrared (NIR) Light (approx. 700–1200 nm, often 810–830 nm): NIR light has the longest wavelengths commonly used in PBM and thus penetrates most deeply into biological tissues, potentially reaching underlying muscle and even bone. Similar to red light, its primary target chromophore is mitochondrial CcO. NIR light is recognized for its potent effects on reducing inflammation, accelerating wound healing, promoting tissue repair, and providing pain relief. Due to its deeper penetration, it may influence processes in deeper tissues beyond the skin, although its dermatological applications often overlap with red light, focusing on wound healing, inflammation reduction, and skin rejuvenation, frequently in combination with red light.
- Yellow/Amber Light (approx. 570–590 nm): Yellow or amber light penetrates deeper than blue light, potentially reaching the superficial dermis. Its mechanism of action is less clearly defined compared to red, blue, or NIR light. Some sources attribute effects on reducing redness, swelling, improving pigmentation issues, stimulating lymphatic flow, and enhancing cellular metabolism. Absorption by mitochondrial protoporphyrin IX influencing ATP production has been suggested. One clinical trial found amber light (590 nm) to be as effective as red light (660 nm) for reducing periocular wrinkle volume when delivered at the same dose. Claimed benefits center around reducing redness, swelling, and pigmentation, with some potential for wrinkle reduction. However, the overall evidence base for yellow/amber light appears less robust than for red, blue, or NIR light based on the available literature.
- Other Wavelengths (Green, Purple): Green light (approx. 500–565 nm) and purple/violet light (often a combination of blue and red, or a specific violet wavelength) are occasionally mentioned in device marketing or some studies. Green light is sometimes linked to improving hyperpigmentation or skin tone , although some research raises concerns about its potential to worsen pigmentation. Purple light is often associated with acne treatment, leveraging the effects of its blue and red components. Generally, the scientific evidence supporting distinct benefits for green or purple wavelengths appears weaker or less developed compared to the primary therapeutic wavelengths.
The distinct penetration depths and target chromophores for different wavelengths underscore the importance of selecting the appropriate light color for the specific skin condition being addressed. A superficial blue light, targeting bacterial porphyrins in the epidermis, is unlikely to stimulate deep dermal collagen production effectively. Conversely, deep-penetrating NIR light is not the optimal choice for targeting surface bacteria. This inherent specificity means that effective LED therapy requires careful matching of the wavelength to the condition’s pathology and location within the skin layers. The frequent use of combination wavelengths, such as red plus NIR for skin rejuvenation (targeting CcO at slightly different depths for broader dermal stimulation) or blue plus red for acne (targeting both bacteria and inflammation) , reflects this principle. Consequently, marketing claims for devices using less-studied wavelengths (like yellow, green, or purple) or suggesting a single wavelength can treat all conditions should be approached with caution, pending robust, independent clinical validation. The “optical window” concept further reinforces the rationale for using red and NIR light when aiming for effects within the dermis or deeper tissues.
3. Evaluating the Evidence: LED Therapy for Dermatological Conditions
While the proposed mechanisms of photobiomodulation are biologically plausible, rigorous clinical evidence is necessary to confirm the efficacy of LED therapy for specific dermatological conditions. Evaluating this evidence is complicated by significant variability across studies in terms of the parameters used—including wavelength, fluence (total energy dose), irradiance (power density), treatment duration, and frequency of sessions. Furthermore, differences in study design, quality, sample sizes, and outcome measures make direct comparisons and definitive conclusions challenging. This section synthesizes the available evidence from the provided research for key conditions, prioritizing findings from systematic reviews and meta-analyses where possible.
3.1 Acne Vulgaris
The rationale for using LED therapy in acne involves blue light’s bactericidal action against C. acnes through porphyrin excitation and ROS generation and red light’s potential anti-inflammatory effects and influence on sebum production.
- Evidence for Blue Light: Numerous studies have investigated blue light (often 405–420 nm) for acne. Several trials report significant reductions in inflammatory acne lesions (papules and pustules). Reductions in the range of 60%–70% have been reported with protocols like twice-weekly treatments for four weeks. One in vitro study suggested a dose-dependent effect, finding 75 J/cm² potentially optimal for bactericidal activity per unit time.However, the evidence is not uniformly positive. Systematic reviews have yielded mixed conclusions, with some finding moderate evidence for efficacy , while others conclude there is limited evidence, non-significant overall effects on lesion counts, or low certainty due to methodological limitations of the primary studies (e.g., small sample sizes, short durations, high risk of bias). The effect on non-inflammatory lesions (comedones, blackheads, whiteheads) is generally reported as less significant or inconsistent , although one study did report a reduction.
- Evidence for Red Light: Red light alone is less commonly studied for acne compared to blue light. One trial showed a substantially smaller reduction in inflammatory lesions with red light (19.5%) compared to blue light (71.4%) in the same study. Another review analyzing red light specifically for acne found no significant difference compared to control groups. Despite this, its potential anti-inflammatory role and effects on sebum keep it relevant, often in combination therapy.
- Evidence for Combination Blue + Red Light: This combination is frequently reported to be more effective than blue light alone. Studies have demonstrated significant reductions in inflammatory lesions, with figures like 76–77% cited. Some studies also show improvement in non-inflammatory lesions (e.g., 54% reduction). A meta-analysis found statistically significant effects for both red and blue light (overall SMD -2.42). Network meta-analyses (NMAs) suggest that LED therapy (presumed blue/red combination) ranks well among treatments for inflammatory lesions, potentially serving as an alternative when drug resistance is a concern. A recent systematic review focusing on at-home devices concluded that red and/or blue light devices were effective for mild-to-moderate acne.
- Overall Assessment: The evidence for LED therapy in acne is mixed but leans towards supporting the use of blue light or, more commonly, a combination of blue and red light, particularly for reducing inflammatory lesions in mild-to-moderate acne vulgaris. The efficacy for non-inflammatory acne (comedones) is less convincing.Significant heterogeneity and methodological limitations persist in the available research, warranting cautious interpretation.
The pattern of evidence strongly suggests a specificity for inflammatory acne. The most consistent findings point towards reductions in papules and pustules, aligning well with the proposed mechanisms: blue light targeting the inflammation-driving bacteria (C. acnes) and red light potentially modulating the inflammatory response itself. Since comedones are primarily follicular plugs rather than lesions defined by acute inflammation or bacterial overgrowth in the same manner, it is biologically consistent that LED therapy shows less effect on them. This implies that LED therapy should not be considered a primary treatment for individuals with predominantly comedonal acne. Its main utility appears to be in managing the inflammatory component of the condition, suggesting that patient selection based on acne type is important for optimizing outcomes and managing expectations. For comprehensive acne management, combination with treatments targeting comedones, such as topical retinoids, may often be necessary.
3.2 Skin Aging and Wrinkles (Photorejuvenation)
The use of LED therapy for skin aging and wrinkle reduction is primarily based on the effects of red (approx. 630–660 nm) and NIR (often around 830 nm) light. The proposed mechanism involves PBM stimulating dermal fibroblasts to increase the synthesis of collagen and elastin, enhancing mitochondrial energy production, improving microcirculation, and potentially reducing low-grade chronic inflammation associated with aging.
The evidence supporting these claims includes:
- In vitro and ex vivo studies demonstrating increased gene expression and protein levels of collagen (Type I and III) and elastin following irradiation with red or red+NIR light. One study also noted increased hyaluronic acid synthase expression.
- Clinical studies using objective measures like ultrasonography have shown increases in intradermal collagen density after treatment courses. Similar findings were reported using advanced imaging like reflectance confocal microscopy (RCM) and dynamic optical coherence tomography (D-OCT).
- Multiple clinical trials and case studies report statistically significant improvements in various signs of photoaging, as assessed by both clinicians and patients. These include reductions in fine lines and wrinkles (particularly crow’s feet, with reported depth reductions around 30–38%), improved skin texture and smoothness (reduced roughness, smaller pore diameter), increased skin firmness and elasticity, more even skin tone, and lightening of dark spots/pigmentation. High patient satisfaction is often reported.
- Effective protocols often involve red light alone (e.g., 630 nm or 660 nm) or combinations of red and NIR light (e.g., 633/830 nm, 640/830 nm). One study comparing broadband polychromatic light to red light alone found no additional benefit from the broader spectrum. Another interesting trial found that amber light (590 nm) produced a similar reduction in wrinkle volume (~30%) as red light (660 nm) when the same energy dose was applied.
- Systematic reviews generally support a role for low-energy red/NIR light in skin rejuvenation, although the quality of evidence can vary, and some assign a moderate grade (e.g., Grade C in one review).
- Overall Assessment: There is a substantial body of evidence suggesting that red and/or NIR LED therapy can lead to measurable improvements in several signs of skin aging, including wrinkle reduction, increased collagen density, and enhanced skin texture and firmness. However, the effects are often described as subtle rather than dramatic and typically require consistent treatment over several months to become apparent.
The nature of the results observed points towards a cumulative effect. Studies demonstrate progressive improvements over weeks and months of regular use (e.g., 1, 2, and 3 months) , with some evidence suggesting that the benefits, such as increased dermal density and wrinkle reduction, can persist for a period (e.g., up to one month) even after treatment cessation. Dermatologists often counsel patients that visible improvements may take 3 to 6 months of regular application. This temporal pattern suggests that PBM is inducing genuine biological remodeling—stimulating structural components like collagen and elastin—rather than providing merely a temporary plumping effect. This supports the potential for “lasting structural and functional rejuvenation”. However, it also implies that LED therapy for anti-aging is a long-term commitment requiring patience and consistent adherence to the treatment schedule (often multiple times per week). Consequently, it may be best positioned as a maintenance or preventative strategy, or as an adjunct to other treatments, rather than a substitute for procedures offering more immediate or dramatic results like injectable fillers or ablative laser resurfacing.
3.3 Wound Healing
PBM, primarily using red and NIR wavelengths, is proposed to positively influence all phases of the wound healing cascade. Mechanisms include enhancing the proliferation and migration of key cells like fibroblasts and keratinocytes, stimulating stem cells, promoting angiogenesis (new blood vessel formation), increasing collagen deposition for tissue scaffolding, modulating the inflammatory response (reducing excessive inflammation while potentially supporting necessary early stages), and mitigating oxidative stress.
The evidence supporting LED/laser therapy for wound healing includes:
- Numerous positive results in preclinical animal models of various wound types, including burns, dermal abrasions, and excisional wounds. Studies often highlight the effectiveness of red light (approx. 630–680 nm) and NIR light (especially 810–830 nm, but also 904 nm). One study comparing multiple wavelengths in a mouse abrasion model found 810 nm to be maximally effective and 635 nm partially effective, while 730 nm and 980 nm showed no benefit, suggesting wavelength specificity is critical.
- Systematic reviews and meta-analyses provide clinical support:
- A Grade B recommendation was given for LED therapy in acute wound healing in one systematic review.
- A meta-analysis focusing on diabetic foot ulcers (DFUs) found that adjunctive treatment with red and infrared light significantly increased the ulcer healing rate (RR=1.93), shortened the healing time (MD=18.52 days), and improved local blood flow compared to conventional care alone, with no difference in adverse events. Other sources also note PBM as a promising adjunctive therapy for DFUs.
- A recent meta-analysis on LLLT for various human skin wounds (including surgical wounds, ulcers, burns) demonstrated a significantly greater rate of wound healing and significantly lower pain scores in the LLLT groups compared to controls.
- In contrast, a Cochrane review on phototherapy for pressure ulcers concluded there was insufficient evidence from the few small, low-quality trials available to support its routine use, although two trials using UV light did suggest faster healing.
- A Cochrane protocol exists for evaluating LLLT for venous leg ulcers, acknowledging the potential but highlighting the need for rigorous evidence.
- Studies comparing LED and low-level laser sources suggest they can promote similar biological effects relevant to healing, such as reduced inflammation, increased fibroblast proliferation, enhanced collagen synthesis, and angiogenesis stimulation. A dose of 4 J/cm² is frequently cited as effective in wound healing studies.
- Evidence for blue light in wound healing is generally lacking or negative , although one study mentioned its potential role via nitric oxide release, which is involved in early wound healing phases.
- Overall Assessment: There is strong preclinical rationale and accumulating clinical evidence, particularly from meta-analyses on DFUs and general skin wounds, supporting the use of red and NIR LED or laser therapy as an effective modality to accelerate wound healing and modulate associated inflammation. Its role in treating pressure ulcers requires further investigation.
3.4 Inflammatory Conditions (Psoriasis, Rosacea, Dermatitis)
A key proposed benefit of PBM, especially with red and NIR light, is its ability to exert anti-inflammatory effects. This is thought to involve modulation of various immune cells (e.g., macrophages, T-cells), reduction of pro-inflammatory cytokines (like TNF-α, IFN-γ), increases in anti-inflammatory cytokines (like IL-4, IL-10), mitigation of oxidative stress, and effects on inflammatory mediators such as nitric oxide and prostaglandins.
- Psoriasis: LED therapy is mentioned as a potential treatment for this chronic inflammatory skin condition.However, the specific evidence for LED therapy appears limited and somewhat confusing based on the available data. One systematic review focusing solely on LED for psoriasis identified only five relevant original articles.Notably, this review assigned a Grade B recommendation (suggesting moderate support) for LED-Blue light, but only a Grade C recommendation (low support) for LED-UVB, LED-Red light, and combination LED-NIR/Red light. This finding is somewhat counterintuitive, as psoriasis is primarily an inflammatory autoimmune disease, not bacterial, and red/NIR light are generally considered the primary anti-inflammatory wavelengths in PBM.Blue light’s main established role is antibacterial. This discrepancy might reflect the paucity of high-quality research specifically investigating different LED wavelengths for psoriasis, potential methodological issues in the included studies, or perhaps an under-recognized mechanism for blue light in this condition. Other reviews acknowledge that established phototherapies like UVB, PUVA, and excimer laser are mainstays for psoriasis treatment , while LLLT (which includes red/NIR LED/laser) shows promise but trials remain small. Another review noted mixed evidence for home UVB phototherapy versus clinic-based treatment. Overall, the evidence base specifically for LED therapy in psoriasis seems underdeveloped compared to its application in other areas or compared to established UV phototherapies. Patients considering LED for psoriasis should be aware of this uncertainty and the conflicting signals regarding optimal wavelengths.
- Rosacea: This condition, characterized by facial redness, inflammation, and sometimes papules and pustules, is mentioned as a potential target for red light therapy due to its anti-inflammatory properties. One report described positive outcomes in two patients treated with LED therapy, noting reductions in subjective symptoms (burning, itching) and objective signs (erythema, papules) after 5–10 sessions. The evidence appears emerging but limited based on the snippets provided.
- Dermatitis (Eczema, Radiation Dermatitis):
- Atopic Dermatitis (Eczema): LED therapy is mentioned as a possible treatment. However, a meta-analysis reported significant heterogeneity (I²=90%) in study results for LED treatment of AD, making conclusions difficult. Established dermatology guidelines heavily feature UV phototherapy (particularly Narrowband UVB) as an effective treatment for AD. Specific evidence supporting LED for eczema seems less robust in the provided material.
- Radiation Dermatitis (RD): PBM using red/NIR light has been investigated for both prevention and treatment of skin reactions caused by radiotherapy. Multiple systematic reviews and meta-analyses indicate that PBM can significantly decrease the severity, progressive worsening, and pain associated with RD.Controlled trials support its use as a protective treatment against severe RD. One review found that the majority of included studies (85.71%) reported positive outcomes for PBM in managing RD, with no adverse effects noted.
- General Inflammation: Beyond specific diagnoses, PBM using red and NIR light consistently demonstrates anti-inflammatory effects across a wide range of preclinical models, including inflammation in joints, wounds, the brain, abdominal fat, lungs, and spinal cord.
- Overall Assessment: Strong evidence supports the use of PBM (red/NIR light) for reducing inflammation in general and specifically for preventing and treating radiation dermatitis. Evidence for treating rosacea with LED is emerging but currently limited. The evidence specifically for LED therapy in psoriasis and atopic dermatitis appears less robust, more mixed, or less developed compared to established UV phototherapies or the application of PBM in wound healing or RD.
The following table summarizes the clinical evidence discussed for various conditions:
Table 1: Summary of Clinical Evidence for LED Photobiomodulation (PBM) in Dermatological Conditions (Based on Provided Snippets)
Condition | Wavelength(s) Studied | Key Findings Summary | Evidence Level/Grade (if available) | Key Supporting Sources |
---|---|---|---|---|
Acne Vulgaris (Inflammatory) | Blue, Red, Blue+Red | Blue or Blue+Red reduces inflammatory lesions (papules, pustules) in mild-moderate acne. Blue+Red often better than Blue alone. NMAs rank LED well. Evidence mixed overall. | Moderate support (Grade B for Blue/Red devices in some reviews). Low certainty in others due to study limitations. NMAs suggest effectiveness. | |
Acne Vulgaris (Non-inflammatory) | Blue, Red, Blue+Red | Effect on comedones (blackheads, whiteheads) is less consistent or significant compared to inflammatory lesions. Some studies show no effect. | Generally low/insufficient evidence. | |
Skin Aging/Wrinkles | Red, NIR, Red+NIR, Amber | Increases collagen/elastin/density. Improves wrinkles, texture, firmness, tone. Results often subtle, require consistent use over months. Red & Amber found equally effective in one study. | Good support from multiple trials and reviews (Grade C in one review). High patient satisfaction reported. | |
Wound Healing (General/DFU) | Red, NIR | Accelerates healing rate, shortens healing time (esp. DFUs), increases blood flow, modulates inflammation. Affects all healing phases. 4 J/cm² often cited. | Strong preclinical evidence. Strong clinical support from meta-analyses (DFUs, general skin wounds). Grade B for acute wounds. | |
Wound Healing (Pressure Ulcers) | UV (in some studies), Laser | Cochrane review found insufficient evidence for phototherapy (including laser) due to few, small, low-quality studies. | Insufficient evidence (Cochrane review). | |
Psoriasis | Blue, Red, NIR, UVB | Evidence specifically for LED is limited and conflicting (Blue Grade B vs Red/NIR Grade C in one review). LLLT shows promise but trials small. UV phototherapy is established. | Limited/Insufficient/Conflicting for LED (Grade B for Blue, C for Red/NIR/UVB in one review). Strong evidence for UV phototherapy. | |
Rosacea | Red | Potential benefit due to anti-inflammatory effects. One report showed reduced symptoms/signs. | Emerging/Limited evidence. | |
Radiation Dermatitis (RD) | Red, NIR | Prevents/reduces severity, progression, and pain of acute RD. Supported by multiple trials and systematic reviews/meta-analyses. | Strong support (Level IA evidence cited in one source based on controlled trials). | |
Atopic Dermatitis (Eczema) | LED (unspecified), UVB | Meta-analysis showed high heterogeneity for LED. UV phototherapy is established. | Insufficient/Heterogeneous for LED. Strong evidence for UV phototherapy. |