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2020 | 80 | 1 |
Tytuł artykułu

A ten year longitudinal examination of the incidence rate and age of childhood encephalopathy diagnoses in an autism spectrum disorder diagnosed cohort

Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
Autism spectrum disorder (ASD) is defined by persistent deficits in social communication/interaction and stereotypic behaviors with many diagnosed persons experiencing a developmental regression at >1 year‑old. It was hypothesized that progressive childhood encephalopathy is an important etiological factor in ASD pathogenesis. This hypothesis‑testing study examined the relationship between diagnosed childhood encephalopathy and ASD. The Independent Healthcare Research Database is composed of de‑identified linked eligibility and claim healthcare records prospectively generated from the Florida Medicaid system. A cohort of 101,736 persons eligible for Florida Medicaid from 1990‑2009 and continuously eligible with ≥10 outpatient office visits during the 120 month period following birth were examined using SAS software. There were 1,397 persons (7,223 person‑years) in the ASD diagnosed cohort and 100,339 persons (980,786 person‑years) in the undiagnosed cohort. The incidence rate of encephalopathy was examined using Cox proportional hazards ratio models. In the ASD cohort relative to the undiagnosed cohort, a significantly increased incidence rate of diagnosed encephalopathy was observed in the unadjusted and adjusted models. The risk for an encephalopathy diagnosed at >1 year‑old was greater than for an encephalopathy diagnosed at <1 year‑old. This study provides important new evidence supporting the hypothesis that a significant number of children with an eventual ASD diagnosis experience a progressive childhood encephalopathy diagnosed at >1 year‑old.
Słowa kluczowe
Wydawca
-
Rocznik
Tom
80
Numer
1
Opis fizyczny
p.66-75,fig.,ref.
Twórcy
autor
  • Institute of Chronic Illnesses, Inc, Silver Spring, MD, USA
  • CoMeD, Inc, Silver Spring, MD, USA
autor
  • Institute of Chronic Illnesses, Inc, Silver Spring, MD, USA
  • CoMeD, Inc, Silver Spring, MD, USA
autor
  • International Academy of Oral Medicine and Toxicology, Champions Gate, FL, USA
autor
  • Institute of Chronic Illnesses, Inc, Silver Spring, MD, USA
Bibliografia
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  • Bjorklund G, Saad K, Chirumbolo S, Kern JK, Geier DA, Geier MR, Urbina MA (2016) Immune dysfunction and neuroinflammation in autism spectrum disorder. Acta Neurobiol Exp 76: 257–268.
  • Bjorklund G, Kern JK, Urina MA, Saad K, El‑Houfey AA, Geier DA, Chirumbolo S, Geier MR, Mehta JA, Aaseth J (2018) Cerebral hypoperfu‑ sion in autism spectrum disorder. Acta Neurobiol Exp 78: 21–29.
  • Dheen ST, Kaur C, Ling EA (2007) Microglial activation and its implications in the brain diseases. Curr Med Chem 14: 1189–1197.
  • Geier DA, Hooker BS, Kern JK, King PG, Sykes LK, Geier MR (2013) A two‑phase study evaluating the relationship between Thimerosal‑contain‑ ing vaccine administration and the risk for an autism spectrum disorder diagnosis in the United States. Transl Neurodegener 2: 25.
  • Geier DA, Kern JK, Geier MR (2012) A prospective cross‑sectional cohort assessment of health, physical, and behavioral problems in autism spectrum disorders. Maedica 7: 193–200.
  • Geier D, Kern J, Geier M (2018) Neonatal factors among subjects diagnosed with a pervasive developmental disorder in the US. J Matern Fetal Neo‑ ntal Med 31: 1709–1714.
  • Geier DA, Kern JK, Sykes LK, Geier MR (2016) Examining genotypic variation in autism spectrum disorder and its relationship to parental age and phenotype. Appl Clin Genet 9: 121–129.
  • Kern JK, Geier DA, Audhya T, King PG, Sykes LK, Geier MR (2012) Evidence of parallels between mercury intoxication and the brain pathology in autism. Acta Neurobiol Exp 72: 113–153.
  • Kern JK, Geier DA, Geier MR (2014b) Evaluation of regression in autism spectrum disorder based on parental reports. N Am J Med Sci 6: 41–47.
  • Kern JK, Geier DA, Homme KG, King PG, Bjorklund G, Chirumbolo S, Geier  MR (2017) Developmental neurotoxicants and the vulnerable male brain: a systematic review of suspected neurotoxicants that disproportionally affect males. Acta Neurobiol Exp 77: 269–296.
  • Kern JK, Geier DA, King PG, Sykes LK, Mehta JA, Geier MR (2015) Shared brain connectivity issues, symptoms, and comorbidities in autism spectrum disorder, attention deficit/hyperactivity disorder, and Tourette syndrome. Brain Connect 5: 321–335.
  • Kern JK, Geier DA, Sykes LK, Geier, MR (2013) Evidence of neurodegeneration in autism spectrum disorder. Transl Neurodegener 2: 17.
  • Kern JK, Geier DA, Sykes LK, Homme KG, Geier MR (2014a) Medical condi‑ tions in autism and events associated with initial onset of autism. OA Autism 2: 9.
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Typ dokumentu
Bibliografia
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Identyfikator YADDA
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