Norway Baby Study Expected to Yield Insights Into Autism

Total Page:16

File Type:pdf, Size:1020Kb

Norway Baby Study Expected to Yield Insights Into Autism Spectrum | Autism Research News https://www.spectrumnews.org NEWS Norway baby study expected to yield insights into autism BY ANDREA ANDERSON 20 AUGUST 2010 1 / 6 Spectrum | Autism Research News https://www.spectrumnews.org 2 / 6 Spectrum | Autism Research News https://www.spectrumnews.org Baby steps: Participating families answer questions about the children's health, environmental exposures, and social and communicative behaviors between 6 months and 7 years of age. 3 / 6 Spectrum | Autism Research News https://www.spectrumnews.org Researchers in the United States and Norway are launching autism studies based on data from more than 100,000 Norwegian children and their families, collected over the past decade. The unusual project, called the Autism Birth Cohort, is intended to uncover genetic and environmental causes of the disorder and the interplay of these factors over time. The researchers are evaluating data on a variety of aspects, ranging from the participants' physical and mental health status to prescription drug history and environmental exposures, they explain in the July issue of Molecular Psychiatry1. "We really think of this as sort of a three-strikes hypothesis: It's genes, it's environmental exposures, but it's also the temporal context," says Mady Hornig, one of the project leaders and associate professor of epidemiology at Columbia University. The project, which began in 2005, relies in large part on data amassed for Norway's Mother and Child Birth Cohort2,3. That study, known as MoBa, includes questionnaires and biological samples — such as parental blood and cord blood, urine, rectal swabs and milk teeth — collected from more than 100,000 children and their parents over the past decade. A similar effort, the U.S. National Children's Study, is expected to grow into a resource for environmental and other analyses of roughly 100,000 children. But that project is still in its infancy, and began recruitment in 2009. Based on prevalence estimates, researchers from the Autism Birth Cohort expect to find at least 550 children with autism in MoBa. Other groups are using MoBa data for studies on conditions ranging from cerebral palsy to attention deficit hyperactivity disorder. For decades, researchers have been mining data from registries and prospective projects in Scandinavian countries, particularly Denmark and Norway, which have a long tradition of compiling large and comprehensive community datasets. More than 98 percent of Norwegian hospitals participated in MoBa, inviting pregnant women to enroll when they came in for an ultrasound at 17 weeks of pregnancy. Between 1999 and 2008, 90,700 mothers, 72,100 fathers and their 108,500 children enrolled in the study. The pregnant women answered questions about, among other things, their own diet and possible environmental exposures at home, work or school. Enrolled families continue to fill out questionnaires addressing the children's health, environmental exposures, and social and communicative behaviors at 6 and 18 months, and 3, 5 and 7 years of age. Early signs: Most autism studies are retrospective, forcing researchers to rely on medical histories and work 4 / 6 Spectrum | Autism Research News https://www.spectrumnews.org backwards to pinpoint environmental exposures. For instance, many studies have to make do with parents' memories of the first signs of autism-related behavior in their children. But memories are notoriously unreliable and can shift over time. Even ambitious efforts such as the Autism Genetic Resource Exchange — a repository of blood samples and cognitive data from 8,000 people in families with autism — provide limited information about environmental exposures, and do not include samples taken prior to autism diagnoses. In contrast, this study begins before the children have shown any signs of autism. Children who appear to have autism-related traits based on information from the MoBa questionnaire at age 3, along with their parents and randomly selected controls, are assessed in person at an Oslo clinic. Those diagnosed with autism will be asked to return for another assessment at age 7 or 8. The team is also identifying MoBa-enrolled children diagnosed with autism through the government's Norwegian Patient Registry, which tracks patient visits and diagnoses nationwide, and through community referrals. Experts are particularly optimistic about the new database's ability to identify reliable behavioral or physiological signatures that may help diagnose the disorder early. "Eventually we really want those biomarkers," says Catherine Lord, director of the University of Michigan's Autism and Communication Disorders Center, and a member of the project's scientific advisory board. For the scheme's pilot phase, researchers are looking for autism biomarkers in umbilical cord blood. Hornig says they have preliminary evidence for a risk factor that can be detected at birth in a subset of children who go on to develop autism. Genetic studies based on the project will focus on candidates identified in previous studies, Hornig says. But the scope is likely to expand as the cost of generating genetic data — particularly DNA sequencing — drops. The study could also help uncover environmental, genetic or biological ties between autism and other conditions, such as attention deficit hyperactivity disorder or preterm birth. Because researchers have access to reams of behavioral and other data from the families, they should be able to study how specific biological and environmental factors contribute to conditions on the autism spectrum, even if autism diagnostic criteria change, notes Camilla Stoltenberg, deputy director general at the Norwegian Institute of Public Health, who helped oversee MoBa from 2001 to 2008. 5 / 6 Spectrum | Autism Research News https://www.spectrumnews.org The clinical definition of the disorder is likely to change significantly in the next version of the American Psychiatric Association's Diagnostic and Statistical Manual of Mental Disorders, or DSM-5, scheduled to come out in 2013. "We can actually work on different definitions of the diagnosis within the same cohort and look at how that affects what we're studying," Stoltenberg says. "We're not stuck with one simple set of diagnostic criteria forever." References: 1. Stoltenberg C. et al. Mol. Psychiatry 15, 676-680 (2010) PubMed 2. Magnus P. et al. Int. J. Epidemiol. 35, 1146-1150 (2006) PubMed 3. Ronningen K.S. et al. Eur. J. Epidemiol. 21, 619-625 (2006) PubMed 6 / 6 Powered by TCPDF (www.tcpdf.org).
Recommended publications
  • Association Between Maternal Use of Folic Acid Supplements and Risk of Autism Spectrum Disorders in Children
    ORIGINAL CONTRIBUTION Association Between Maternal Use of Folic Acid Supplements and Risk of Autism Spectrum Disorders in Children ˚ ´ Pal Suren, MD, MPH Importance Prenatal folic acid supplements reduce the risk of neural tube defects Christine Roth, MSc in children, but it has not been determined whether they protect against other neu- Michaeline Bresnahan, PhD rodevelopmental disorders. Margaretha Haugen, PhD Objective To examine the association between maternal use of prenatal folic acid supplements and subsequent risk of autism spectrum disorders (ASDs) (autistic disor- Mady Hornig, MD der, Asperger syndrome, pervasive developmental disorder–not otherwise specified Deborah Hirtz, MD [PDD-NOS]) in children. Kari Kveim Lie, MD Design, Setting, and Patients The study sample of 85 176 children was derived from the population-based, prospective Norwegian Mother and Child Cohort Study W. Ian Lipkin, MD (MoBa). The children were born in 2002-2008; by the end of follow-up on March 31, Per Magnus, MD, PhD 2012, the age range was 3.3 through 10.2 years (mean, 6.4 years). The exposure of Ted Reichborn-Kjennerud, MD, PhD primary interest was use of folic acid from 4 weeks before to 8 weeks after the start of pregnancy, defined as the first day of the last menstrual period before conception. Synnve Schjølberg, MSc Relative risks of ASDs were estimated by odds ratios (ORs) with 95% CIs in a logistic George Davey Smith, MD, DSc regression analysis. Analyses were adjusted for maternal education level, year of birth, and parity. Anne-Siri Øyen, PhD Main Outcome Measure Specialist-confirmed diagnosis of ASDs. Ezra Susser, MD, DrPH Results At the end of follow-up, 270 children in the study sample had been diag- Camilla Stoltenberg, MD, PhD nosed with ASDs: 114 with autistic disorder, 56 with Asperger syndrome, and 100 with PDD-NOS.
    [Show full text]
  • Lower Autism Risk with Folic Acid Supplements in Pregnancy 12 February 2013
    Lower autism risk with folic acid supplements in pregnancy 12 February 2013 Women who took folic acid supplements in early of folic acid supplements in the mother during pregnancy almost halved the risk of having a child pregnancy and a reduced risk of childhood autism. with autism. Beginning to take folic acid supplements later in pregnancy did not reduce the "The study does not prove that folic acid risk. This is shown in new findings from the ABC supplements can prevent childhood autism. Study and Norwegian Mother and Child Cohort However, the findings are so apparent that they Study published in the Journal of The American constitute a good argument to further examine Medical Association (JAMA). possible causal mechanisms. It should also be ascertained whether folic acid is associated with a Women who took folic acid supplements from four reduced risk of other brain disorders in children," weeks before conception to eight weeks into says Surén. pregnancy had a 40 per cent lower risk of giving birth to children with childhood autism (classic Emphasises the importance of folic acid autism). Use of folic acid supplements midway supplements through pregnancy (week 22) had no effect. The results support the Norwegian Directorate of The findings only apply to a lower risk of childhood Health's recommendations for folic acid autism, the most severe form of autism. The supplements during pregnancy and emphasise the results show no reduction in the risk of atypical or importance of starting early—preferably before unspecific autism. The study also investigated the conception. prevalence of Asperger syndrome, but the number of examined children was too low to give a reliable Method result.
    [Show full text]
  • Environmental Health Issue
    FIFTH EDITION 2006, Volume 45 R5 Environmental Health and Autism In thIs Issue: Time To GeT a Grip By martha r. Herbert, m.D., ph.D. Beyond Behavior—Biomedical Diagnoses in Autism spectrum Disorders By Margaret L. Bauman, M.D. transforming the Public Debate on neurotoxicants By Elise Miller, M.Ed. ADVERTISEMENT ADVERTISEMENT Autism does not have to be a life sentence You’re not about to give up on your child. Neither Are We. Since , the Autism Treatment Center of America™ has provided innovative training programs for parents and professionals caringifor children challenged by Autism Spectrum Disorders and related developmental difficulties. • Practical Tools • Powerful Results • Limitless Hope c Help your child improve in all areas of over p learning, development, communication and hoto skill acquisition. : © W I Join us for our internationally-acclaimed ll T ERR Son-Rise Program® Start-Up, a y comprehensive weeklong training program for parents and professionals. We don’t put limits on the possibilities for your child. Free 25-Minute Initial Call 877-766-7473 We’ll give you the keys to unlock their world. HOME OF THE SON-RISE PROGRAM® SINCE 1983 South Undermountain Road Sheffield, MA - USA Telephone: -- • E-mail: [email protected] www.autismtreatment.com Copyright © 2006 by The Option Institute & Fellowship. All rights reserved. 02.06-6 CONTENTS December 2006 page 18 SpOTlIGHT Time to Get A Grip By marTHa r. HerBerT, m.D., pH.D. Does an environmental role in autism make sense? How do we decide? And if environment is involved in autism, what do we do about it? These are challenging questions.
    [Show full text]
  • Sensitivity and Specificity of Early Screening for Autism
    BJPsych Open (2019) 5, e41, 1–8. doi: 10.1192/bjo.2019.34 Sensitivity and specificity of early screening for autism Pål Surén, Alexandra Saasen-Havdahl, Michaeline Bresnahan, Deborah Hirtz, Mady Hornig, Catherine Lord, Ted Reichborn-Kjennerud, Synnve Schjølberg, Anne-Siri Øyen, Per Magnus, Ezra Susser, W. Ian Lipkin and Camilla Stoltenberg Background (95% CI 58–79) for ASD without phrase speech and 34% (95% CI – Early identification and diagnosis is beneficial for children with 29 40) for ASD with phrase speech. Specificity was then reduced – autism spectrum disorder (ASD). Universal early screening is to 89% (95% CI 89 90). recommended by many experts, but disputed because evidence is limited, and sensitivity and specificity in general populations Conclusions are largely unknown. Early ASD screening with a parent checklist had low sensitivity. It identified mainly individuals with ASD with significant develop- Aims mental delay and captured very few children with ASD with To estimate the sensitivity and specificity of early population- cognitive skills in the normal range. Increasing sensitivity was not based screening for ASDs. possible without severely compromising specificity. Method Declaration of interest The study was based on the Norwegian Mother and Child Cohort C.L. receives royalty for the Social Communication Study. The 36-month cohort questionnaire included the Social Questionnaire, which she has co-authored. Communication Questionnaire (SCQ), a 40-item screening instrument for ASD. Keywords Results Autistic spectrum disorders; developmental disorders; A total of 58 520 mothers (58%) responded to the questionnaire. epidemiology. By the end of follow-up on 31 December 2015, 385 (0.7%) indi- viduals with ASD had been identified among the responders’ Copyright and usage children.
    [Show full text]
  • Prenatal Exposure to Antipsychotic Medication Does Not Increase Odds of Autism, ADHD
    Spectrum | Autism Research News https://www.spectrumnews.org NEWS Prenatal exposure to antipsychotic medication does not increase odds of autism, ADHD BY PETER HESS 20 AUGUST 2021 Listen to this story: Children born to mothers who take antipsychotic medications during pregnancy do not have elevated odds of autism or attention deficit hyperactivity disorder (ADHD), nor are they more likely to be born preterm or underweight, according to a study released this past Monday in JAMA Internal Medicine. Some women with schizophrenia, Tourette syndrome or bipolar disorder take antipsychotic drugs, such as aripiprazole, haloperidol or risperidone. Clinicians have long debated whether women should discontinue these medications during pregnancy out of concern for the drugs’ effects on the developing fetus. But children born to mothers who take antipsychotics during pregnancy and to those who do not take them have similar outcomes, the new work shows. “Our findings do not support a recommendation for women to discontinue their regular antipsychotic treatment during pregnancy,” says senior investigator Kenneth Man, research fellow at the University College London School of Pharmacy in the United Kingdom. Prescribing antipsychotics during pregnancy can help prevent potentially dangerous psychotic episodes and ensure that an expectant mother can take care of herself, says Mady Hornig, associate professor of epidemiology at Columbia University, who was not involved in the study. “We certainly don’t want to be cavalier about the use of any medication during pregnancy, but one 1 / 2 Spectrum | Autism Research News https://www.spectrumnews.org also wants to balance out the implications of not treating.” Any apparent effects of antipsychotics on a developing fetus are likely due to the condition being treated, rather than the treatment, the study shows.
    [Show full text]
  • Read the Full Survey Report
    Evaluating a Proposed Name to Replace ‘ME/CFS’: A Community Survey Project Conducted by Lisa Petrison, Ph.D. Published by Paradigm Change (March 2015) Copyright 2015 www.paradigmchange.me 2 Table of Contents Executive Summary ...................................................................................................................................... 5 Part 1 – Results Overview .......................................................................................................................... 13 Part 2 - Implications ................................................................................................................................... 29 Part 3 – Survey Questions .......................................................................................................................... 49 Part 4 – Main Survey Results ..................................................................................................................... 66 Part 5 – ME vs. Non-ME Results ............................................................................................................... 110 Part 6 – US ME vs. Non-ME Results ......................................................................................................... 127 Part 7 – Related Illnesses Results ............................................................................................................ 161 Part 8 – US vs. Non-US Results ................................................................................................................. 181
    [Show full text]
  • Absence of Evidence for Bornavirus Infection in Schizophrenia, Bipolar
    Molecular Psychiatry (2012) 17, 486–493 & 2012 Macmillan Publishers Limited All rights reserved 1359-4184/12 www.nature.com/mp ORIGINAL ARTICLE Absence of evidence for bornavirus infection in schizophrenia, bipolar disorder and major depressive disorder M Hornig1,2, T Briese1,2, J Licinio3, RF Khabbaz4, LL Altshuler5, SG Potkin6, M Schwemmle7, U Siemetzki1, J Mintz5, K Honkavuori1, HC Kraemer8, MF Egan9, PC Whybrow5, WE Bunney6 and WI Lipkin1,2 1Center for Infection and Immunity, Columbia University Mailman School of Public Health, New York, NY, USA; 2Department of Epidemiology, Columbia University Mailman School of Public Health, New York, NY, USA; 3John Curtin School of Medical Research, The Australian National University, Canberra, ACT, Australia; 4Centers for Disease Control and Prevention, Atlanta, GA, USA; 5Department of Psychiatry and Biobehavioral Sciences, University of California Los Angeles, Los Angeles, CA, USA; 6University of California Irvine, Irvine, CA, USA; 7Department of Virology, Universita¨tsklinikum, Freiburg, Germany; 8Department of Psychiatry and Behavioral Sciences, Stanford University, Palo Alto, CA, USA and 9Clinical Neuroscience, Merck & Company, North Wales, PA, USA In 1983, reports of antibodies in subjects with major depressive disorder (MDD) to an as-yet uncharacterized infectious agent associated with meningoencephalitis in horses and sheep led to molecular cloning of the genome of a novel, negative-stranded neurotropic virus, Borna disease virus (BDV). This advance has enabled the development of new diagnostic assays, including in situ hybridization, PCR and serology based on recombinant proteins. Since these assays were first implemented in 1990, more than 80 studies have reported an association between BDV and a wide range of human illnesses that include MDD, bipolar disorder (BD), schizophrenia (SZ), anxiety disorder, chronic fatigue syndrome, multiple sclerosis, amyo- trophic lateral sclerosis, dementia and glioblastoma multiforme.
    [Show full text]
  • Doubt Greets Reports of Suramin's Promise for Treating Autism
    Spectrum | Autism Research News https://www.spectrumnews.org NEWS Doubt greets reports of suramin’s promise for treating autism BY HANNAH FURFARO 15 JUNE 2017 A drug normally used to treat African sleeping sickness had only mild side effects in a widely reported trial of 10 boys with autism. But many researchers question the trial’s rationale and caution that serious side effects may emerge in larger studies. Half the boys in the trial received a single low dose of the drug, called suramin, intravenously. All five developed a mild rash but experienced no other health problems, researchers reported in May in the Annals of Clinical and Translational Neurology1. But suramin is not a benign medication. In higher doses, it is known to cause anemia and problems with the adrenal gland, which makes hormones, including the stress hormone cortisol. “If I had someone with [autism] in my family, I would certainly not immediately jump to using this as a treatment,” says David Sulzer, professor of psychiatry, neurology and pharmacology at Columbia University. “It easily could be that a sizeable fraction of people who might take this in the future develop additional side effects, which could be bad side effects.” The boys who received the drug showed modest improvements in autism features relative to the five boys in the control group. However, the study was not designed to assess the drug’s effectiveness. The rash may have tipped off the parents as to whether their child was in the treatment or control group — and may have contributed to a placebo effect.
    [Show full text]
  • Center for Solutions for ME/CFS W
    Center for Solutions for ME/CFS W. Ian Lipkin, MD Director, Center for Infection and Immunity John Snow Professor of Epidemiology, Mailman School of Public Health Professor of Neurology and Pathology, Vagelos College of Physicians and Surgeons ME/CFS Population 21,736-65,000 ME/CFS patients in NYS (2.6% of US population) 836,000-2,500,000 ME/CFS patients in the US Estimated 84-91% have not yet been diagnosed Estimates of 17-24 million ME/CFS patients worldwide https://www.cdc.gov/me-cfs/about/index.html https://ammes.org/how-many-people-have-mecfs/ The Burden of ME/CFS DIAGNOSING AND TREATING MYALGIC ENCEPHALOMYELITIS/ CHRONIC FATIGUE SYNDROME (ME/CFS) - U.S. ME/CFS CLINICIAN COALITION - Version 2 ∙ July 2020 ME/CFS studies have shown one peak of onset between ages 11-19 and a second between 30-39. At least 25% of patients are bedbound or housebound and up to 75% are unable to work or attend school. Symptoms can persist for years, and most patients never regain their pre-disease functioning ME/CFS costs the US $17-$24 billion annually in lost productivity and direct medical costs. https://drive.google.com/file/d/1SG7hlJTCSDrDHqvioPMq-cX-rgRKXjfk/view What is Known About ME/CFS Prior Infections KEY FACTS ∙ FEBRUARY 2015 Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) Epstein-Barr virus What are the symptoms and other effects of ME/CFS? Ross River virus 11% develop ME/CFS symptoms • Reduction or impairment in ability to carry out normal daily activities, Coxiella burnetti accompanied by profound fatigue • Post-exertional malaise
    [Show full text]
  • Udell-Lecture.Pdf
    www.childdev.org www.theautismdoctor.com October 19, 2018 Brian D. Udell MD FAAP Medical Director Child Development Center of America Davie, FL 33314 954-873-8413 [email protected] Nutritional Evaluation of the Patient with Developmental Challenges • Understanding the scope of autism - Multiple causes and Multiple presentations • Evaluation of the medical status of the patient with developmental concerns • Treatment and documentation of progress • No disclosures • This presentation does not represent Nova University policies or recommendations. Autism Spectrum Disorders Autism Spectrum Disorders Individual susceptibility Environmental event(s) Phenotypic presentation ? Cause(s) Autism Spectrum Disorder DSM IV to DSM 5.0: Speech and Early and Language Significant Movement Social Movement Social Learning Cognition Reading Arithmetic Seizures Metabolic Environment, Hypotonia, Processing Intrinsic Repetitive Apraxia CNS Hyperactivity Sensory Genetic Restricted Skin Eczema AutoImmunity Inflammation Immune Infections Aggression Gut Constipation/Diarrhea microbiome, nutrition Focus/Attention Autism Spectrum Disorders Types Genetic – Fragile X, Rett’s S., Trisomy 21?, Copy number variations Syndromes – Metabolic disturbances, Unclassified Gastro-intestinal Most common in practice If a person acts like they have ‘ants in their pants’, sometimes they actually do! In 8/11 originally described ASD patients (Kanner), disturbances documented Immunologic – Asthma, eczema, food sensitivities, frequent ear infections, ?vaccination Microbiome alterations
    [Show full text]
  • Environmental Risks for Psychiatric Disorders: Exploring Biological Mechanisms March 21-22, 2017 Tuesday, March 21 • 9:00 A.M
    Environmental Risks for Psychiatric Disorders: Exploring Biological Mechanisms March 21-22, 2017 Tuesday, March 21 • 9:00 a.m. – 4:40 p.m. Wednesday, March 22 • 8:30 a.m. – 3:00 p.m. Building 101, Rodbell Auditorium Research Triangle Park, N.C. National Institutes of Health • U.S. Department of Health and Human Services Environmental Risks for Psychiatric Disorders: Exploring Biological Mechanisms March 21-22, 2017 Tuesday, March 21 • 9:00 a.m. – 4:40 p.m. Wednesday, March 22 • 8:30 a.m.– 3:00 p.m. Building 101, Rodbell Auditorium Research Triangle Park, N.C. National Institutes of Health U.S. Department of Health and Human Services Table of Contents Welcome ............................................................................................................................1 Agenda .............................................................................................................................. 2 Abstracts ........................................................................................................................... 5 Biographies .................................................................................................................... 16 Participants .................................................................................................................... 28 Environmental Risks for Psychiatric Disorders: Exploring Biological Mechanisms Welcome Message from Linda Birnbaum On behalf of the National Institute of Environmental Health Sciences (NIEHS), I am honored and delighted to welcome
    [Show full text]
  • Scientistspotlight
    ScientistSpotlight Mady Hornig: The battle against Chronic Fatigue Syndrome Introduction Chronic Fatigue Syndrome, known medically as myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS), is a debilitating disease that by some estimates affects as many as 4.5 million individuals in the US alone. Symptoms, which include extreme fatigue, difficulty concentrating, headaches, and muscle pain, typically begin in the aftermath of a viral-type infection and often last for years. There are no lab tests for ME/CFS. The disorder remains a mysterious and sometimes controversial illness. It is not yet part of any medical school curriculum; physicians as well as the general public have long disagreed about whether it qualifies as a biological disease or a psychological disorder. As a consequence, people with ME/CFS often feel stigmatized. A sharper understanding of ME/CFS has emerged. Researchers at the Center for Infection and Immunity (CII) at Columbia University’s Mailman School of Public Health recently published research findings that identify distinct immune changes in patients with ME/CFS. Showing distinct phases in the trajectory of the disease, this work provides perhaps the strongest support yet that chronic fatigue syndrome is a biological illness, not a psychological disorder. Mady Hornig, MD, Director of Translational Research at CII and an associate professor of Epidemiology at Columbia’s Mailman School, is the lead author of the research, published in Science Advances. Affymetrix: Why is ME/CFS getting more attention these days? Hornig: Renewed interest in studying ME/CFS began heating up around 2010 with a suggestion that one or more viruses might be implicated in the disease.
    [Show full text]