Abstract
Taurine is a sulfur-containing amino acid which is not incorporated into protein. However, taurine has various critical physiological functions including development of the eye and brain, reproduction, osmoregulation, and immune functions including anti-inflammatory as well as anti-oxidant activity. The causes of autistic spectrum disorder (ASD) are not clear but a high heritability implicates an important role for genetic factors. Reports also implicate oxidative stress and inflammation in the etiology of ASD. Thus, taurine, a well-known antioxidant and regulator of inflammation, was investigated here using the sera from both girls and boys with ASD as well as their siblings and parents. Previous reports regarding taurine serum concentrations in ASD from various laboratories have been controversial. To address the potential role of taurine in ASD, we collected sera from 66 children with ASD (males: 45; females: 21, age 1.5–11.5 years, average age 5.2 ± 1.6) as well as their unaffected siblings (brothers: 24; sisters: 32, age 1.5–17 years, average age 7.0 ± 2.0) as controls of the children with ASD along with parents (fathers: 49; mothers: 54, age 28–45 years). The sera from normal adult controls (males: 47; females: 51, age 28–48 years) were used as controls for the parents. Taurine concentrations in all sera samples were measured using high performance liquid chromatography (HPLC) using a phenylisothiocyanate labeling technique. Taurine concentrations from female and male children with ASD were 123.8 ± 15.2 and 145.8 ± 8.1 μM, respectively, and those from their unaffected brothers and sisters were 142.6 ± 10.4 and 150.8 ± 8.4 μM, respectively. There was no significant difference in taurine concentration between autistic children and their unaffected siblings. Taurine concentrations in children with ASD were also not significantly different from their parents (mothers: 139.6 ± 7.7 μM, fathers: 147.4 ± 7.5 μM). No significant difference was observed between adult controls and parents of ASD children (control females: 164.8 ± 4.8 μM, control males: 163.0 ± 7.0 μM). However, 21 out of 66 children with ASD had low taurine concentrations (<106 μM). Since taurine has anti-oxidant activity, children with ASD with low taurine concentrations will be examined for abnormal mitochondrial function. Our data imply that taurine may be a valid biomarker in a subgroup of ASD.
Access this chapter
Tax calculation will be finalised at checkout
Purchases are for personal use only
Abbreviations
- ASD:
-
Autistic spectrum disorder
- PITC:
-
Phenylisothiocyanate
- HPLC:
-
High performance liquid chromatography
References
Aldred S, Moore KM, Fitzgerald M, Waring RH (2003) Plasma amino acid levels in children with autism and their families. J Autism Dev Disord 33(1):93–97
American Psychiatric Association (2013) Diagnostic and statistical manual of mental disorders: DM5, 5th edn. Washington, DC
Arnold GL, Hyman SL, Mooney RA, Kirby RS (2003) Plasma amino acids profiles in children with autism: potential risk of nutritional deficiencies. J Autism Dev Disord 33(4):449–454
Ashwood P, Willis S, Van De Water J (2006) The immune response in autism: a new frontier for autism research. J Leukoc Biol 80:1–15
Bolte S, Poustka F (2002) The relation between general cognitive level and adaptive behavior domains in individuals with autism with and without co-morbid mental retardation. Child Psychiatry Hum Dev 33(2):165–172
Bourgeron T (2016) Current knowledge on the genetics of autism and propositions for future research. C R Biol 339(7–8):300–307. doi:10.1016/j.crvi.2016.05.004
CDC (2014) Community report on autism, https:\\www.cdc.gov/ncbddd/autism/states/comm_report_autism_2014.pdf
Chauhan A, Chauhan V (2006) Oxidative stress in autism. Pathophysiology 13:171–181
Chawarska K, Shic F, Macari S, Campbell DJ, Brian J, Landa R, Hutman T, Nelson CA, Oznoff S, Tager-Flusberg H, Young GS (2014) 18-month predictors of later outcomes in younger siblings of children with autism spectrum disorder: a baby siblings research consortium study. J Am Acad Child Adolesc Psychiatry 53(12):1317–1327
Cohen IL (2003) Criterion-related validity of the PDD Behavior Inventory. J Autism Dev Disord 33(1):47–53
Cohen IL, Schmidt-Lackner S, Romanczyk R, Sudhalter V (2003) The PDD Behavior Inventory: a rating scale for assessing response to intervention in children with pervasive developmental disorder. J Autism Dev Disord 33(1):31–45
Cohen IL, Liu X, Hudson M, Gillis J, Cavalari RNS, Romanczyk RG, Karmel BZ, Gardner JM (2016) Using the PDD Behavior Inventory as a level 2 screener: a classification and regression trees analysis. J Autism Dev Disord 46:3006–3022
Erickson CA, Early M, Stigler KA, Wink LK, Mullett JE, McDougle CJ (2011) An open-label naturalistic pilot study of acamprosate in youth with autistic disorder. J Child Adolesc Psychopharmacol 21(6):565–569
Frye RE, Rossignol DA (2011) Mitochondrial dysfunction can connect the diverse medical symptoms associated with autism spectrum disorders. Pediatr Res 69(5):41R–47R
Gaugler T, Klei L, Sanders S, Bodea C, Goldberg AP, Lee AB, Mahajan M, Manaa D, Pawitan Y, Reicher J, Ripke S, Sandin S, Sklar P, Svantesson O, Reichenberg A, Hultman CM, Devlin B, Roeder K, Buxbaum JD (2014) Most genetic risk for autism resides with common variation. Nat Genet 46:881–885
Geier DA, Kern JK, Garver CR, Adams JB, Audhya T, Geier MR (2009) A prospective study of transsulfuration biomarkers in autistic disorders. Neurochem Res 34:386–393
Geschwind DH, State MW (2015) Gene hunting in autism spectrum disorder: on the path to precision medicine. Lancet Neurol 14(11):1109–1120
Ghabizadeh A (2013) Increased glutamate and homocysteine and decreased glutamine levels in autism: a review and strategies for future studies of amino acids in autism. Dis Markers 35(5):281–186
Giulivi C, Zhang YF, Omanska-Klusek A, Ross-Inta C, Wong S, Herts-picciotto I, Tassone F, Pessah IN (2011) Mitochondrial dysfunction in autism. JAMA 304(21):2389–2396
Hampson DR, Blatt GJ (2015) Autism spectrum disorders and neuropathology of the cerebellum. Front Neurosci 9:1–16
Huxtable R (1999) Expanding the circle 1975–1999: Sulfur biochemistry and insight on the biological functions of taurine. Adv Exp Med Biol 483:1–25
Jong CJ, Azuma J, Schaffer SW (2012) Mechanism underlying the antioxidant activity of taurine: prevention of mitochondrial oxidant production. Amino Acids 42:2223–2232
Junyent F, Utrera J, Romero R, Pallas M, Camins A, Duque D, Auladell C (2009) Prevention of epilepsy by taurine treatment in mice experimental model. J Neurosci Res 87:1500–1508
Kern JK, Geier DA, Adams JB, Garver CR, Audhya T, Geier MR (2011) A clinical trial of glutathione supplementation in autism spectrum disorders. Med Sci Monit 17(12):CR677–CR682
Lord C, Rutter M, Le Couteur A (1994) Autism diagnostic interview-a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord 24:659–685
Lord C, Risi S, Lambrecht L, Cook EH, Leventhal BL, DiLavore PC, Pickeles A, Rutter M (2000) The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord 30:205–223
Mavel S, Nadal-Desbarats L, Blasco H, Bonnet-Brilhault F, Barthelemy C, Montigny F, Sarda P, Laumonnier F, Vourc’h P, Andres CR, Emond P (2013) 1H-13C NMR-based urine metabolic profiling in autism spectrum disorders. Talanta 114:95–102
Ming X, Stein TP, Barnes V, Rhodes N, Guo L (2012) Metabolic perturbance in autism spectrum disorders: a metabolomics study. J Preteome Res 11(12):5856–5862
Moreno H, Borjas L, Arrieta A, Saez L, Prassad A, Estevez J, Bonilla E (1992) Clinical heterogeneity of the autistic syndrome: a study of 60 families. Investig Clin 33(1):13–31
Moreno-Fuenmayer H, Borjas L, Arrieta A, Valera V, Socorro-Candanoza L (1996) Plasma excitatory amino acids in autism. Investig Clin 37(2):113–128
Nakagawa Y, Chiba K (2016) Involvement of neuroinflammation during brain development in social cognitive deficits in autism spectrum disorder and schizophrenia. J Pharmacol Exp Ther 358(3):504–515
Naviaux JC, Schuchbauer MA, Li K, Wang L, Robrough VB, Powell SB, Naviaux RK (2014) Reversal of autism-like behaviors and metabolism in adult mice with single-dose antipuinergic therapy. Transl Psychiatry 4:e400
Oliveira G, Diogo L, Ganzina M, Garcia P, Ataide A, Marques C, Miguel T, Borges L, Omcemte AM, Oliveira CR (2005) Mitochondrial dysfunction in autism spectrum disorders: a population-based study. Dev Med Child Neurol 47:185–189
Onore C, Careaga M, Ashwood P (2012) The role of immune dysfunction in the pathophysiology of autism. Brain Behav Immun 26:383–392
Ozonoff S, Young GS, Carter A et al (2011) Recurrence risk for autism spectrum disorders: a baby siblings research consortium study. Pediatrics 128:e488–e495
Park E, Quinn MR, Wright CE, Schuller-Levis GB (1993) Taurine chloramine inhibits the synthesis of nitric oxide and the release of tumor factor in activated RAW 264.7 cells. J Leukoc Biol 54:119–124
Park E, Schuller-Levis GB, Quinn MR (1995) Taurine chloramine inhibits production of nitric oxide and TNF-α in activated RAW 264.7 cells by mechanisms that induce transcriptional and translational events. J Immunol 154:4778–4784
Park E, Alberti J, Quinn MR, Schuller-Levis GB (1998) Taurine chloramine inhibits the production of superoxide anion, IL-6 and IL-8 in activated human polymorphonuclear leukocytes. In: Schaffer S, Lombardini JB, Huxtable RJ (eds) Taurine 3 cellular and regulatory mechanisms. Plenum Press, New York, pp 177–182
Park E, Jia J, Quinn MR, Schuller-Levis G (2002) Taurine chloramine inhibits lymphocyte proliferation and decreases cytokine production in activated human leukocytes. Clin Immunol 102:179–184
Park E, Park SY, Dobkin C, Schuller-Levis G (2014) Development of a novel cysteine sulfinic acid decarboxylase knockout mouse: dietary taurine reduces neonatal mortality. J Amino Acids 2014:346809
Parvez S, Tabassum H, Banerjee BD, Raisuddin S (2008) Taurine prevents tamoxifen-induced mitochondrial oxidative damage in mice. Basic Clin Pharmacol Toxicol 102:382–387
Patterson PH (2011) Maternal infection and immune involvement in autism. Trends Mol Med 17:389–394
Rossignol DA, Frye RE (2012) Mitochondrial dysfunction in autism spectrum disorders: a systematic review and meta-analysis. Mol Psychiatry 17(3):290–314
Sandin S, Lichtenstein P, Kuja-Halkola R, Larsson H, Hultman CM, Reichenberg A (2014) The familial risk of autism. JAMA 311(17):1770–1777
Schuller-Levis GB, Park E (2003) Taurine: new implications for an old amino acid. FEMS Microbiol Lett 226:195–202
Schuller-Levis G, Park E (2006) Is taurine a biomarker? Adv Clin Chem 41:1–21
Schuller-Levis G, Gordon RE, Park E, Pendino KJ, Laskin D (1995) Taurine protects rat bronchioles from acute ozone-induced lung inflammation and hyperplasia. Exp Lung Res 21:877–888
Schuller-Levis G, Gordon R, Wang C, Park S, Park E (2009) Protection of bleomycin-induced fibrosis and inflammation by taurine. Int Immunopharmacol 9:971–977
Sealey LA, Hughes BW, Sriskanda AN, Guest JR, Gibson AD, Johnson-William L, Pace DG, Bagasra O (2016) Environmental factors in the development of autism spectrum disorders. Environ Int 88:288–298
Shetewy A, Shimada-Takaura K, Warner D, Jong CJ, Mehdi AB, Alexeyev M, Takahashi K, Schaffer SW (2016) Mitochondrial defects associated with β-alanine toxicity: relevance to hyper-beta-alaninemia. Mol Cell Biochem 416(1–2):11–22
Shimada K, Jong CJ, Takhashi K, Schaffer SW (2014) Role of ROS production and turnover in the antioxidant acidity of taurine. Adv Exp Med Biol 803:581–596
Singh K, Connors SL, Macklin EA, Smith KD, Fahey JW, Talalay P, Zimmerman AW (2014) Sulforaphane treatment of autism spectrum disorder (ASD). Proc Natl Acad Sci U S A 111(43):15550–15555
Sturman J (1993) Taurine in development. Physiol Rev 73(1):119–147
Sweeten TL, Bowyer SL, Posey DJ et al (2003) Increased prevalence of familial autoimmunity in probands with pervasive developmental disorders. Pediatrics 112(5):e420
Tu WJ, Chen H, He J (2012) Application of LC/MS/MS analysis of plasma amino acids profiles in children with autism. J Clin Biochem Nutr 51(3):248–249
Vargas DL, Nascimbene C, Krishnan C, Zimmerman AW, Pardo CA (2005) Neuroglial activation and neuroinflammation in the brain of patient with autism. Ann Neurol 57:67–81
Wegiel J, Flory M, Kuchna I, Norwicki K, Ma SY, Wegiel J, Frackowiak J, Mazur-Kolecka B, Wierzba-Bobrowicz T, London E, Wisniewski T, Hof PR, Brown WT (2015) Neuronal nucleus and cytoplasm volume deficit in children with autism and volume increase in adolescents and adults. Acta Neuropathol Commun 3:2
White JF (2003) Intestinal pathophysiology in Autism. Exp Biol Med (Maywood) 228(6):639–649
Wink LK, Adams R, Wang Z, Klaunig JE, Plawecki MH, Posey DJ, McDougle CJ, Erickson CA (2016) A randomized placebo-controlled pilot study of N-acetylcysteine in youth with autism spectrum disorder. Mol Autism 7:26. doi:10.1186/s13229-016-0088-6. Ecollection 2016
Yap IK, Angley M, Veselkov KA, Holmes E, London JC, Nicholson JK (2010) Uninary metabolic phenotyping differentiates children with autism from their unaffected siblings and age-matched controls. J Proteome Res 9(6):3996–4004
Acknowledgement
This work was supported by the Office for People with Developmental Disabilities, Albany, NY. We are thankful to Dr. William Levis for discussing the research and reviewing this manuscript.
Author information
Authors and Affiliations
Corresponding author
Editor information
Editors and Affiliations
Rights and permissions
Copyright information
© 2017 Springer Science+Business Media B.V.
About this paper
Cite this paper
Park, E. et al. (2017). Is Taurine a Biomarker in Autistic Spectrum Disorder?. In: Lee, DH., Schaffer, S.W., Park, E., Kim, H.W. (eds) Taurine 10. Advances in Experimental Medicine and Biology, vol 975. Springer, Dordrecht. https://doi.org/10.1007/978-94-024-1079-2_1
Download citation
DOI: https://doi.org/10.1007/978-94-024-1079-2_1
Publisher Name: Springer, Dordrecht
Print ISBN: 978-94-024-1077-8
Online ISBN: 978-94-024-1079-2
eBook Packages: Biomedical and Life SciencesBiomedical and Life Sciences (R0)