Brief Report: A Double-Blind, Placebo-Controlled, Crossover, Proof-of-Concept Study of Minocycline in Autism Spectrum Disorder

被引:3
作者
Erickson, Craig A. [1 ,2 ]
Shaffer, Rebecca C. [3 ,4 ]
Will, Meredith [3 ,4 ]
Schmitt, Lauren M. [3 ,4 ]
Horn, Paul [3 ,5 ]
Hirst, Kathy [6 ]
Pedapati, Ernest V. [1 ,2 ,5 ]
Ober, Nicole [7 ]
Tumuluru, Rameshwari V. [7 ]
Handen, Benjamin L. [8 ,9 ,10 ,11 ]
Beversdorf, David Q. [6 ,12 ]
机构
[1] Cincinnati Childrens Hosp Med Ctr, Div Child & Adolescent Psychiat, 3333 Burnet Ave MLC 4002, Cincinnati, OH 45229 USA
[2] Univ Cincinnati, Coll Med, Dept Psychiat & Behav Neurosci, Cincinnati, OH 45267 USA
[3] Univ Cincinnati, Coll Med, Dept Pediat, Cincinnati, OH USA
[4] Cincinnati Childrens Hosp Med Ctr, Div Behav Med & Clin Psychol, Cincinnati, OH USA
[5] Cincinnati Childrens Hosp Med Ctr, Div Neurol, Cincinnati, OH USA
[6] Univ Missouri, Thompson Ctr Autism & Neurodev Disorders, Columbia, MO USA
[7] Univ Pittsburgh, Sch Med, Psychiat, Pittsburgh, PA USA
[8] Univ Pittsburgh, Psychiat Dept, Pittsburgh, PA USA
[9] Univ Pittsburgh, Pediat Dept, Pittsburgh, PA USA
[10] Univ Pittsburgh, Psychol Dept, Pittsburgh, PA USA
[11] Univ Pittsburgh, Educ Dept, Pittsburgh, PA USA
[12] Univ Missouri, William & Nancy Thompson Endowed Chair Radiol, Radiol Neurol & Psychol Sci, Columbia, MO USA
关键词
Autism; Autism spectrum disorder; Minocycline; Clinical trial; FRAGILE-X-SYNDROME; VALPROIC ACID; MOUSE MODEL; BRAIN; ACTIVATION; BEHAVIOR; INDIVIDUALS; CHILDREN; INJURY; MEMORY;
D O I
10.1007/s10803-023-06132-1
中图分类号
B844 [发展心理学(人类心理学)];
学科分类号
040202 ;
摘要
Neuroinflammatory mechanisms have been implicated in the pathophysiology of autism spectrum disorder (ASD). Minocycline is a matrix metalloproteinase inhibitor 9 (MMP9) inhibitor tetracycline antibiotic with known anti-inflammatory properties. In preclinical animal models of ASD, minocycline has demonstrated potential positive effects on phenotypes that may have relevance to ASD. We conducted the first placebo-controlled study of minocycline in ASD. This double-blind, placebo-controlled crossover trial employed four week treatment periods with a two week washout period. Twenty-four 12-22 year olds (mean age 17.4 years; range 12.9-22.5 years) with ASD were enrolled. Overall minocycline was well tolerated. No minocycline-associated clinical changes were noted with treatment on any performance or clinician or caregiver completed measures were noted. We hypothesize that either minocycline does not have potential therapeutic effects in ASD or our project was underpowered to define potential subject subgroups who may potentially respond positively to this drug.
引用
收藏
页码:3387 / 3394
页数:8
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