Effect of pioglitazone treatment on behavioral symptoms in autistic children

被引:88
作者
Boris, Marvin
Kaiser, Claudia C.
Goldblatt, Allan
Elice, Michael W.
Edelson, Stephen M.
Adams, James B.
Feinstein, Douglas L.
机构
[1] Univ Illinois, Dept Anesthesiol, Chicago, IL 60612 USA
[2] Autism Res Inst, San Diego, CA 92116 USA
[3] Arizona State Univ, Tempe, AZ 85287 USA
来源
JOURNAL OF NEUROINFLAMMATION | 2007年 / 4卷
关键词
PERVASIVE DEVELOPMENTAL DISORDERS; EXPERIMENTAL AUTOIMMUNE ENCEPHALOMYELITIS; INFLAMMATORY-BOWEL-DISEASE; OPEN-LABEL TRIAL; PPAR-GAMMA; SPECTRUM DISORDERS; T-CELLS; 15-DEOXY-DELTA(12,14)-PROSTAGLANDIN J(2); THIAZOLIDINEDIONE AGONISTS; ULCERATIVE-COLITIS;
D O I
10.1186/1742-2094-4-3
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Introduction: Autism is complex neuro-developmental disorder which has a symptomatic diagnosis in patients characterized by disorders in language/communication, behavior, and social interactions. The exact causes for autism are largely unknown, but is has been speculated that immune and inflammatory responses, particularly those of Th2 type, may be involved. Thiazolidinediones (TZDs) are agonists of the peroxisome proliferator activated receptor gamma ( PPAR gamma), a nuclear hormone receptor which modulates insulin sensitivity, and have been shown to induce apoptosis in activated T-lymphocytes and exert anti-inflammatory effects in glial cells. The TZD pioglitazone ( Actos) is an FDA-approved PPAR gamma agonist used to treat type 2 diabetes, with a good safety profile, currently being tested in clinical trials of other neurological diseases including AD and MS. We therefore tested the safety and therapeutic potential of oral pioglitazone in a small cohort of children with diagnosed autism. Case description: The rationale and risks of taking pioglitazone were explained to the parents, consent was obtained, and treatment was initiated at either 30 or 60 mg per day p.o. A total of 25 children ( average age 7.9 +/- 0.7 year old) were enrolled. Safety was assessed by measurements of metabolic profiles and blood pressure; effects on behavioral symptoms were assessed by the Aberrant Behavior Checklist (ABC), which measures hyperactivity, inappropriate speech, irritability, lethargy, and stereotypy, done at baseline and after 3-4 months of treatment. Discussion and evaluation: In a small cohort of autistic children, daily treatment with 30 or 60 mg p.o. pioglitazone for 3-4 months induced apparent clinical improvement without adverse events. There were no adverse effects noted and behavioral measurements revealed a significant decrease in 4 out of 5 subcategories ( irritability, lethargy, stereotypy, and hyperactivity). Improved behaviors were inversely correlated with patient age, indicating stronger effects on the younger patients. Conclusion: Pioglitazone should be considered for further testing of therapeutic potential in autistic patients.
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页数:7
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共 61 条
  • [1] Atomoxetine for hyperactivity in autism spectrum disorders: Placebo-controlled crossover pilot trial
    Arnold, L. Eugene
    Aman, Michael G.
    Cook, Amelia M.
    Witwer, Andrea N.
    Hall, Kristy L.
    Thompson, Susan
    Ramadan, Yaser
    [J]. JOURNAL OF THE AMERICAN ACADEMY OF CHILD AND ADOLESCENT PSYCHIATRY, 2006, 45 (10) : 1196 - 1205
  • [2] Berger Joel, 2002, Diabetes Technol Ther, V4, P163, DOI 10.1089/15209150260007381
  • [3] Treatment of active psoriatic arthritis with the PPARγ ligand pioglitazone:: an open-label pilot study
    Bongartz, T
    Coras, B
    Vogt, T
    Schölmerich, J
    Müller-Ladner, U
    [J]. RHEUMATOLOGY, 2005, 44 (01) : 126 - 129
  • [4] Familial clustering of autoimmune disorders and evaluation of medical risk factors in autism
    Comi, AM
    Zimmerman, AW
    Frye, VH
    Law, PA
    Peeden, JN
    [J]. JOURNAL OF CHILD NEUROLOGY, 1999, 14 (06) : 388 - 394
  • [5] Peroxisome proliferator-activated receptor γ thiazolidinedione agonists increase glucose metabolism in astrocytes
    Dello Russo, C
    Gavrilyuk, V
    Weinberg, G
    Almeida, A
    Bolanos, JP
    Palmer, J
    Pelligrino, D
    Galea, E
    Feinstein, DL
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 2003, 278 (08) : 5828 - 5836
  • [6] Lymphocyte subsets and interleukin-2 receptors in autistic children
    Denney, DR
    Frei, BW
    Gaffney, GR
    [J]. JOURNAL OF AUTISM AND DEVELOPMENTAL DISORDERS, 1996, 26 (01) : 87 - 97
  • [7] Peroxisome proliferator-activated receptor-γ agonist 15-deoxy-Δ12,14-prostaglandin J2 ameliorates experimental autoimmune encephalomyelitis
    Diab, A
    Deng, CS
    Smith, JD
    Hussain, RZ
    Phanavanh, B
    Lovett-Racke, AE
    Drew, PD
    Racke, MK
    [J]. JOURNAL OF IMMUNOLOGY, 2002, 168 (05) : 2508 - 2515
  • [8] The role of PPARs in atherosclerosis
    Duval, C
    Chinetti, G
    Trottein, F
    Fruchart, JC
    Staels, B
    [J]. TRENDS IN MOLECULAR MEDICINE, 2002, 8 (09) : 422 - 430
  • [9] Receptor-independent actions of PPAR thiazolidinedione agonists: Is mitochondrial function the key?
    Feinstein, DL
    Spagnolo, A
    Akar, C
    Weinberg, G
    Murphy, P
    Gavrilyuk, V
    Dello Russo, C
    [J]. BIOCHEMICAL PHARMACOLOGY, 2005, 70 (02) : 177 - 188
  • [10] Feinstein Douglas L, 2003, Diabetes Technol Ther, V5, P67, DOI 10.1089/152091503763816481