Addressing racial disparity in autism outcomes
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ASPartOfMe
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Joined: 25 Aug 2013
Age: 68
Gender: Male
Posts: 39,637
Location: Long Island, New York
Washington University seeks to improve diagnosis and intervention for black children
Quote:
Historically, African-American children have been identified with autism spectrum disorder at a significantly lower rate than Caucasian children, but this gap has narrowed: across all network monitoring sites, autism remains about 7 percent more likely to be identified in Caucasian children than African-American children, and there is no evidence that this disorder is more common in any one race than another.
A serious residual disparity revealed by the CDC’s most recent network report is that African-American children who were identified with an autism spectrum disorder were twice as likely as Caucasian children to be co-diagnosed with an intellectual disability (44 percent compared to 22 percent). In other words, when an African-American child has this common condition, he/she is much more likely to suffer also from intellectual disability.
Researchers at the Washington University School of Medicine have recently been awarded funding by the National Institute of Mental Health (NIMH) to address this disparity, which may be caused by delays in the timing of diagnosis and access to high-quality intervention.
Despite the fact that autism can often be reliably diagnosed by the age of 2 years old, most children, irrespective of race, do not receive a diagnosis until the age of 4 years. For African-American children in greater St. Louis, the average age of diagnosis is 66 months. This delay exists even though African-American parents report having concerns about their child’s development, and reporting these concerns to professionals at roughly the same time as Caucasian families.
The new NIMH research initiative will help expand capacity and opportunity for early diagnosis for African-American families seeking to participate. The goal is to identify children under age three suspected of having autism spectrum disorder, establish eligibility for intervention as early in life as possible, and to determine whether outcomes are better when diagnosis occurs earlier.
The research team will work collaboratively with intervention specialists in the community to develop treatment plans individually tailored to the developmental needs of each child.
Importantly, the program will control for genetic factors affecting the severity of autism and simultaneously contribute to the national gene discovery effort to identify causes and new approaches to higher-impact treatment.
A serious residual disparity revealed by the CDC’s most recent network report is that African-American children who were identified with an autism spectrum disorder were twice as likely as Caucasian children to be co-diagnosed with an intellectual disability (44 percent compared to 22 percent). In other words, when an African-American child has this common condition, he/she is much more likely to suffer also from intellectual disability.
Researchers at the Washington University School of Medicine have recently been awarded funding by the National Institute of Mental Health (NIMH) to address this disparity, which may be caused by delays in the timing of diagnosis and access to high-quality intervention.
Despite the fact that autism can often be reliably diagnosed by the age of 2 years old, most children, irrespective of race, do not receive a diagnosis until the age of 4 years. For African-American children in greater St. Louis, the average age of diagnosis is 66 months. This delay exists even though African-American parents report having concerns about their child’s development, and reporting these concerns to professionals at roughly the same time as Caucasian families.
The new NIMH research initiative will help expand capacity and opportunity for early diagnosis for African-American families seeking to participate. The goal is to identify children under age three suspected of having autism spectrum disorder, establish eligibility for intervention as early in life as possible, and to determine whether outcomes are better when diagnosis occurs earlier.
The research team will work collaboratively with intervention specialists in the community to develop treatment plans individually tailored to the developmental needs of each child.
Importantly, the program will control for genetic factors affecting the severity of autism and simultaneously contribute to the national gene discovery effort to identify causes and new approaches to higher-impact treatment.
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“Self Acceptance is a process not a performance”
“You are autistic enough. And you always have been”
Professionally Identified and joined WP August 26, 2013
DSM 5: Autism Spectrum Disorder, DSM IV: Aspergers Moderate Severity.
Kraichgauer
Veteran
Joined: 12 Apr 2010
Gender: Male
Posts: 49,751
Location: Spokane area, Washington state.
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