Light Therapy & Kids with Autism

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Autism Spectrum Disorder (ASD)

Autism spectrum disorder (ASD) is a complicated syndrome of nervous system development characterized clinically by language impairment, dysfunction in social engagement, language, stereotypical movements and behaviors, and various cognitive deficits.

Light can have a deep influence on people. Different colored lighting can affect our moods, and a lack of natural light can cause depression. This especially applies to those with autism.

Children with autism are especially susceptible to mood changes due to lighting. Lights with mellow colors, like blue, can help a child relax and become creative. Flickering, humming, or harshly colored lights, on the other hand, can confuse and even hurt them. For this reason, it is important that lighting is controllable and monitored in the child’s rooms.

In addition to manufactured lighting, natural lighting also has its effects. Natural lighting has proven benefits for autistic children. Seasonal affective disorder, or SAD, caused by a lack of natural light during winter months, can foster behavioral issues and depression. Natural light has been shown to relieve these symptoms.

Light therapy has been used for more than to relieve these symptoms. Natural light can help regulate a child’s circadian rhythms. These rhythms govern our body’s “internal master clock.” For example, they tell us when it’s time to sleep. A lack of natural light can cause our rhythms to fall out of sync. Therefore, treatment can make a child with insomnia fall asleep without aids and become more alert during the day, among other benefits.

The best time for treatment is in the morning, soon after the child rises. Even spending just 30 minutes in the light can improve their mood and sleeping habits. 30 minutes might not be possible initially, so while building up to it, another session in the afternoon can help. But therapy at night can have negative effects, worsening a child’s routine and making it harder to fall asleep.

Clinical Study

A study examined the efficacy of low-level laser therapy, a form of photobiomodulation, to treat irritability associated with an autistic spectrum disorder in children and adolescents aged 5–17 years. Twenty-one of the 40 participants received eight 5-min procedures administered to the base of the skull and temporal areas across a 4-week period (test, i.e., active treatment participants). All the participants were evaluated with the Aberrant Behavior Checklist (ABC), with the global scale and five subscales (irritability/agitation, lethargy/social withdrawal, stereotypic behavior, hyperactivity/noncompliance, and inappropriate speech), and the Clinical Global Impressions (CGI) Scale including a severity-of-illness scale (CGI-S) and a global improvement/change scale (CGI-C). The evaluation took place at baseline, week 2 (interim), week 4 (endpoint), and week 8 (post-procedure) of the study. The adjusted mean difference in the baseline to study endpoint change in the ABC irritability subscale score between test and placebo participants was -15.17 in favor of the test procedure group. ANCOVA analysis found this difference statistically significant (F = 99.34, p < 0.0001) compared to the baseline ABC irritability subscale score. The study found that low-level laser therapy could be an effective tool for reducing irritability and other symptoms and behaviors associated with the autistic spectrum disorder in children and adolescents, with positive changes maintained and augmented over time.

A significant literature exists on Low-Level Laser Therapy (LLLT) ability, a form of photobiomodulation, to penetrate the skull in both diagnostic and therapeutic applications. Low energy laser passes the skull, and a therapeutic effect likely exists. Low energy laser systems employ the so-called quantum optical induced transparency (QIT)-effect. This effect, electromagnetically induced transparency (EIT), controls optical properties of dense media and can enhance transparency contrast by a factor of five. Therefore, the skull, spine, or joints can be penetrated even with moderate intensity light. Due to the QIT effect, the radiation should reach deep tissue layers in muscles, connective tissue, and even bone, enabling noninvasive transcranial treatments.

Conclusions

The study’s findings strongly illustrate that not only does the application of light therapy affect a sizable, statistically significant, and clinically meaningful improvement in all of the key evaluable behaviors characteristic of autism disorder in children and adolescents, but it continues to affect a progressive and meaningful improvement in symptoms for up to 6 months following completion of the procedure administration protocol.

LLLT can achieve a therapeutic effect by employing non-ionizing light, including lasers, light-emitting diodes, or broadband light in the visible red (600–700 nm) and near-infrared (780–1100 nm) spectra. LLLT is a non-thermal process beginning when a chromophore molecule is exposed to a suitable wavelength of light. Chromophores are responsible for the color associated with biological compounds such as hemoglobin, myoglobin, and cytochromes. When a chromophore absorbs a photon of light, an electron transits to an excited state. The physiologic effects of LLLT occur when photons dissociate the inhibitory signaling molecule, nitric oxide (NO), from cytochrome-C-oxidase, increasing: electron transport, mitochondrial membrane potentials production of mitochondrial products such as ATP, NADH, RNA, and cellular respiration. The leading hypothesis is that the photons dissociate inhibitory nitric oxide from the enzyme, leading to increased electron transport, mitochondrial membrane potential, and ATP production.

References

1. Abbott, A. E., A. C. Linke, A. Nair, A. Jahedi, L. A. Alba, C. L. Keown, I. Fishman, and R. A. Muller. 2018. 'Repetitive behaviors in autism are linked to imbalance of corticostriatal connectivity: a functional connectivity MRI study', Soc Cogn Affect Neurosci, 13: 32-42.
2. Batista-Garcia-Ramo, K., and C. I. Fernandez-Verdecia. 2018. 'What We Know About the Brain Structure-Function Relationship', Behav Sci (Basel), 8.
3. Brown, E. C., M. G. Aman, and S. M. Havercamp. 2002. 'Factor analysis and norms for parent ratings on the Aberrant Behavior Checklist-Community for young people in special education', Res Dev Disabil, 23: 45-60.
4. de Freitas, L. F., and M. R. Hamblin. 2016. 'Proposed Mechanisms of Photobiomodulation or Low-Level Light Therapy', IEEE J Sel Top Quantum Electron, 22.
5. Demirtas-Tatlidede, A., A. M. Vahabzadeh-Hagh, M. Bernabeu, J. M. Tormos, and A. Pascual-Leone. 2012. 'Noninvasive brain stimulation in traumatic brain injury', J Head Trauma Rehabil, 27: 274-92.
6. Emelyanov, A. N., and V. V. Kiryanova. 2015. 'Photomodulation of proliferation and differentiation of stem cells by the visible and infrared light', Photomed Laser Surg, 33: 164-74.
7. Freitas, L. F., M. R. Hamblin, F. Anzengruber, J. R. Perussi, A. O. Ribeiro, V. C. A. Martins, and A. M. G. Plepis. 2017. 'Zinc phthalocyanines attached to gold nanorods for simultaneous hyperthermic and photodynamic therapies against melanoma in vitro', J Photochem Photobiol B, 173: 181-86.
8. Hamblin, M. R. 2018. 'Photobiomodulation for traumatic brain injury and stroke', J Neurosci Res, 96: 731-43.
9. Heiskanen, V., and M. R. Hamblin. 2018. 'Photobiomodulation: lasers vs. light emitting diodes?', Photochem Photobiol Sci, 17: 1003-17.
10. Henderson, T. A., and L. D. Morries. 2015. 'Near-infrared photonic energy penetration: can infrared phototherapy effectively reach the human brain?', Neuropsychiatr Dis Treat, 11: 2191-208.
11. Hiwaki, O., and H. Miyaguchi. 2018. 'Noninvasive measurement of dynamic brain signals using light penetrating the brain', PLoS One, 13: e0192095.
12. Huang, Y. Y., A. Gupta, D. Vecchio, V. J. de Arce, S. F. Huang, W. Xuan, and M. R. Hamblin. 2012. 'Transcranial low level laser (light) therapy for traumatic brain injury', J Biophotonics, 5: 827-37.
13. Jiang, P., V. Vuontela, M. Tokariev, H. Lin, E. T. Aronen, Y. Ma, and S. Carlson. 2018. 'Functional connectivity of intrinsic cognitive networks during resting state and task performance in preadolescent children', PLoS One, 13: e0205690.
14. Kaat, A. J., L. Lecavalier, and M. G. Aman. 2014. 'Validity of the aberrant behavior checklist in children with autism spectrum disorder', J Autism Dev Disord, 44: 1103-16.
15. Karabekiroglu, K., and M. G. Aman. 2009. 'Validity of the aberrant behavior checklist in a clinical sample of toddlers', Child Psychiatry Hum Dev, 40: 99-110.
16. Khuman, J., J. Zhang, J. Park, J. D. Carroll, C. Donahue, and M. J. Whalen. 2012. 'Low-level laser light therapy improves cognitive deficits and inhibits microglial activation after controlled cortical impact in mice', J Neurotrauma, 29: 408-17.
17. Kotkowski, E., L. R. Price, P. Mickle Fox, T. J. Vanasse, and P. T. Fox. 2018. 'The hippocampal network model: A transdiagnostic metaconnectomic approach', Neuroimage Clin, 18: 115-29.
18. Lapchak, P. A., and P. D. Boitano. 2016. 'Transcranial Near-Infrared Laser Therapy for Stroke: How to Recover from Futility in the NEST-3 Clinical Trial', Acta Neurochir Suppl, 121: 7-12.
19. Leisman, G., C. Machado, Y. Machado, and M. Chinchilla-Acosta. 2018. 'Effects of Low-Level Laser Therapy in Autism Spectrum Disorder', Adv Exp Med Biol.
20. Machado, C., M. Estevez, G. Leisman, R. Melillo, R. Rodriguez, P. DeFina, A. Hernandez, J. Perez-Nellar, R. Naranjo, M. Chinchilla, N. Garofalo, J. Vargas, and C. Beltran. 2015. 'QEEG spectral and coherence assessment of autistic children in three different experimental conditions', J Autism Dev Disord, 45: 406-24.
21. Machado, C., M. Estevez, R. Rodriguez, and G. Leisman. 2017. 'Letter re: The autism "epidemic": Ethical, legal, and social issues in a developmental spectrum disorder', Neurology, 89: 1310.
22. Machado, C. J., and J. Bachevalier. 2003. 'Non-human primate models of childhood psychopathology: the promise and the limitations', J Child Psychol Psychiatry, 44: 64-87.
23. Machado, C., R. Rodriguez, M. Estevez, G. Leisman, R. Melillo, M. Chinchilla, and L. Portela. 2015. 'Anatomic and Functional Connectivity Relationship in Autistic Children During Three Different Experimental Conditions', Brain Connect, 5: 487-96.
24. Moreira, M. S., I. T. Velasco, L. S. Ferreira, S. K. Ariga, F. Abatepaulo, L. T. Grinberg, and M. M. Marques. 2011. 'Effect of laser phototherapy on wound healing following cerebral ischemia by cryogenic injury', J Photochem Photobiol B, 105: 207-15.
25. Morries, L. D., P. Cassano, and T. A. Henderson. 2015. 'Treatments for traumatic brain injury with emphasis on transcranial near-infrared laser phototherapy', Neuropsychiatr Dis Treat, 11: 2159-75.
26. Naeser, M. A., P. I. Martin, M. D. Ho, M. H. Krengel, Y. Bogdanova, J. A. Knight, M. K. Yee, R. Zafonte, J. Frazier, M. R. Hamblin, and B. B. Koo. 2016. 'Transcranial, Red/Near-Infrared Light-Emitting Diode Therapy to Improve Cognition in Chronic Traumatic Brain Injury', Photomed Laser Surg, 34: 610-26.
27. Poiani, Gdcr, A. L. Zaninotto, A. M. C. Carneiro, R. A. Zangaro, A. S. I. Salgado, R. B. Parreira, A. F. de Andrade, M. J. Teixeira, and W. S. Paiva. 2018. 'Photobiomodulation using low-level laser therapy (LLLT) for patients with chronic traumatic brain injury: a randomized controlled trial study protocol', Trials, 19: 17.
28. Primo, F. L., M. B. da Costa Reis, M. A. Porcionatto, and A. C. Tedesco. 2011. 'In vitro evaluation of chloroaluminum phthalocyanine nanoemulsion and low-level laser therapy on human skin dermal equivalents and bone marrow mesenchymal stem cells', Curr Med Chem, 18: 3376-81.
29. Raj, A., and F. Powell. 2018. 'Models of Network Spread and Network Degeneration in Brain Disorders', Biol Psychiatry Cogn Neurosci Neuroimaging, 3: 788-97.
30. Ranasinghe, K. G., L. B. Hinkley, A. J. Beagle, D. Mizuiri, S. M. Honma, A. E. Welch, I. Hubbard, M. L. Mandelli, Z. A. Miller, C. Garrett, A. La, A. L. Boxer, J. F. Houde, B. L. Miller, K. A. Vossel, M. L. Gorno-Tempini, and S. S. Nagarajan. 2017. 'Distinct spatiotemporal patterns of neuronal functional connectivity in primary progressive aphasia variants', Brain, 140: 2737-51.
31. Rochkind, S., A. Shahar, M. Amon, and Z. Nevo. 2002. 'Transplantation of embryonal spinal cord nerve cells cultured on biodegradable microcarriers followed by low power laser irradiation for the treatment of traumatic paraplegia in rats', Neurol Res, 24: 355-60.
32. Rojahn, J., and W. J. Helsel. 1991. 'The Aberrant Behavior Checklist with children and adolescents with dual diagnosis', J Autism Dev Disord, 21: 17-28.
33. Salehpour, F., J. Mahmoudi, F. Kamari, S. Sadigh-Eteghad, S. H. Rasta, and M. R. Hamblin. 2018. 'Brain Photobiomodulation Therapy: a Narrative Review', Mol Neurobiol, 55: 6601-36.
34. Scherman, M., O. S. Mishina, P. Lombardi, E. Giacobino, and J. Laurat. 2012. 'Enhancing electromagnetically-induced transparency in a multilevel broadened medium', Opt Express, 20: 4346-51.
35. Shen, C. C., Y. C. Yang, T. B. Huang, S. C. Chan, and B. S. Liu. 2013. 'Neural regeneration in a novel nerve conduit across a large gap of the transected sciatic nerve in rats with low-level laser phototherapy', J Biomed Mater Res A, 101: 2763-77.
36. Shen, C. C., Y. C. Yang, and B. S. Liu. 2013. 'Effects of large-area irradiated laser phototherapy on peripheral nerve regeneration across a large gap in a biomaterial conduit', J Biomed Mater Res A, 101: 239-52.
37. Stevens, E. J., and D. R. Tomlinson. 1995. 'Effects of endothelin receptor antagonism with bosentan on peripheral nerve function in experimental diabetes', Br J Pharmacol, 115: 373-9.