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      Probiotic and Oxytocin Combination Therapy in Patients with Autism Spectrum Disorder: A Randomized, Double-Blinded, Placebo-Controlled Pilot Trial

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          Abstract

          Autism spectrum disorder (ASD) is a rapidly growing neurodevelopmental disorder. Both probiotics and oxytocin were reported to have therapeutic potential; however, the combination therapy has not yet been studied. We conducted a randomized, double-blinded, placebo-controlled, 2-stage pilot trial in 35 individuals with ASD aged 3–20 years (median = 10.30 years). Subjects were randomly assigned to receive daily Lactobacillus plantarum PS128 probiotic (6 × 10 10 CFUs) or a placebo for 28 weeks; starting on week 16, both groups received oxytocin. The primary outcomes measure socio-behavioral severity using the Social Responsiveness Scale (SRS) and Aberrant Behavior Checklist (ABC). The secondary outcomes include measures of the Clinical Global Impression (CGI) scale, fecal microbiome, blood serum inflammatory markers, and oxytocin. All outcomes were compared between the two groups at baseline, 16 weeks, and 28 weeks into treatment. We observed improvements in ABC and SRS scores and significant improvements in CGI-improvement between those receiving probiotics and oxytocin combination therapy compared to those receiving placebo ( p < 0.05). A significant number of favorable gut microbiome network hubs were also identified after combination therapy ( p < 0.05). The favorable social cognition response of the combination regimen is highly correlated with the abundance of the Eubacterium hallii group. Our findings suggest synergic effects between probiotics PS128 and oxytocin in ASD patients, although further investigation is warranted.

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          Most cited references72

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          Reproducible, interactive, scalable and extensible microbiome data science using QIIME 2

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            Prevalence of Autism Spectrum Disorder Among Children Aged 8 Years — Autism and Developmental Disabilities Monitoring Network, 11 Sites, United States, 2016

            Problem/Condition Autism spectrum disorder (ASD). Period Covered 2016. Description of System The Autism and Developmental Disabilities Monitoring (ADDM) Network is an active surveillance program that provides estimates of the prevalence of ASD among children aged 8 years whose parents or guardians live in 11 ADDM Network sites in the United States (Arizona, Arkansas, Colorado, Georgia, Maryland, Minnesota, Missouri, New Jersey, North Carolina, Tennessee, and Wisconsin). Surveillance is conducted in two phases. The first phase involves review and abstraction of comprehensive evaluations that were completed by medical and educational service providers in the community. In the second phase, experienced clinicians who systematically review all abstracted information determine ASD case status. The case definition is based on ASD criteria described in the Diagnostic and Statistical Manual of Mental Disorders, Fifth Edition. Results For 2016, across all 11 sites, ASD prevalence was 18.5 per 1,000 (one in 54) children aged 8 years, and ASD was 4.3 times as prevalent among boys as among girls. ASD prevalence varied by site, ranging from 13.1 (Colorado) to 31.4 (New Jersey). Prevalence estimates were approximately identical for non-Hispanic white (white), non-Hispanic black (black), and Asian/Pacific Islander children (18.5, 18.3, and 17.9, respectively) but lower for Hispanic children (15.4). Among children with ASD for whom data on intellectual or cognitive functioning were available, 33% were classified as having intellectual disability (intelligence quotient [IQ] ≤70); this percentage was higher among girls than boys (40% versus 32%) and among black and Hispanic than white children (47%, 36%, and 27%, respectively). Black children with ASD were less likely to have a first evaluation by age 36 months than were white children with ASD (40% versus 45%). The overall median age at earliest known ASD diagnosis (51 months) was similar by sex and racial and ethnic groups; however, black children with IQ ≤70 had a later median age at ASD diagnosis than white children with IQ ≤70 (48 months versus 42 months). Interpretation The prevalence of ASD varied considerably across sites and was higher than previous estimates since 2014. Although no overall difference in ASD prevalence between black and white children aged 8 years was observed, the disparities for black children persisted in early evaluation and diagnosis of ASD. Hispanic children also continue to be identified as having ASD less frequently than white or black children. Public Health Action These findings highlight the variability in the evaluation and detection of ASD across communities and between sociodemographic groups. Continued efforts are needed for early and equitable identification of ASD and timely enrollment in services.
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              Microbiota modulate behavioral and physiological abnormalities associated with neurodevelopmental disorders.

              Neurodevelopmental disorders, including autism spectrum disorder (ASD), are defined by core behavioral impairments; however, subsets of individuals display a spectrum of gastrointestinal (GI) abnormalities. We demonstrate GI barrier defects and microbiota alterations in the maternal immune activation (MIA) mouse model that is known to display features of ASD. Oral treatment of MIA offspring with the human commensal Bacteroides fragilis corrects gut permeability, alters microbial composition, and ameliorates defects in communicative, stereotypic, anxiety-like and sensorimotor behaviors. MIA offspring display an altered serum metabolomic profile, and B. fragilis modulates levels of several metabolites. Treating naive mice with a metabolite that is increased by MIA and restored by B. fragilis causes certain behavioral abnormalities, suggesting that gut bacterial effects on the host metabolome impact behavior. Taken together, these findings support a gut-microbiome-brain connection in a mouse model of ASD and identify a potential probiotic therapy for GI and particular behavioral symptoms in human neurodevelopmental disorders. Copyright © 2013 Elsevier Inc. All rights reserved.
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                Author and article information

                Journal
                Nutrients
                Nutrients
                nutrients
                Nutrients
                MDPI
                2072-6643
                05 May 2021
                May 2021
                : 13
                : 5
                : 1552
                Affiliations
                [1 ]Athinoula A. Martinos Center, Massachusetts General Hospital, Charlestown, MA 02129, USA; Jun_Liu@ 123456hms.harvard.edu (J.L.); kliu16@ 123456mgh.harvard.edu (K.L.); mkoh@ 123456mgh.harvard.edu (M.K.); htsherman@ 123456mgh.harvard.edu (H.S.); SLIU41@ 123456mgh.harvard.edu (S.L.); RTIAN2@ 123456mgh.harvard.edu (R.T.); Jwang106@ 123456mgh.harvard.edu (J.W.); Michelle_Fong@ 123456DFCI.HARVARD.EDU (M.F.); CCLAIRMONT1@ 123456mgh.harvard.edu (C.C.); msjeong@ 123456mgh.harvard.edu (M.-S.J.); CLI36@ 123456mgh.harvard.edu (A.L.); MLOPES6@ 123456mgh.harvard.edu (M.L.); VHAGAN@ 123456mgh.harvard.edu (V.H.); tdutton1@ 123456bwh.harvard.edu (T.D.); stchan@ 123456mgh.harvard.edu (S.-T.C.); alkendall@ 123456mgh.harvard.edu (A.K.); KKWONG@ 123456mgh.harvard.edu (K.K.)
                [2 ]Department of Psychiatry, Beth Israel Deaconess Medical Center, Boston, MA 02215, USA
                [3 ]Harvard Medical School, Boston, MA 02115, USA; Piyawat_Sukijthamapan@ 123456DFCI.harvard.edu (P.S.); lei@ 123456steele.mgh.harvard.edu (L.X.); hlee5@ 123456mgh.harvard.edu (H.L.)
                [4 ]Department of Radiation Oncology, Massachusetts General Hospital, Boston, MA 02114, USA
                [5 ]MGH Biostatistics Center, Massachusetts General Hospital, Boston, MA 02114, USA
                [6 ]Department of Epidemiology, Indiana University, Richard M. Fairbanks School of Public Health, Indianapolis, IN 46202, USA; yiqsong@ 123456iu.edu
                Author notes
                [* ]Correspondence: xkong1@ 123456mgh.harvard.edu ; Tel.: +1-(617)-726-9439
                Author information
                https://orcid.org/0000-0001-8551-8877
                https://orcid.org/0000-0002-8754-3504
                https://orcid.org/0000-0002-9654-690X
                https://orcid.org/0000-0002-2097-7332
                Article
                nutrients-13-01552
                10.3390/nu13051552
                8147925
                34062986
                f7c03947-eaaf-4b07-94ed-7bf3091886f1
                © 2021 by the authors.

                Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license ( https://creativecommons.org/licenses/by/4.0/).

                History
                : 09 April 2021
                : 02 May 2021
                Categories
                Article

                Nutrition & Dietetics
                autism spectrum disorder (asd),probiotics,oxytocin,microbiome,inflammation markers

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