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Environment as important as genes in autism, study finds.
http://uk.reuters.com/article/2014/05/03/us-health-autism-idUKKBN0DJ0H020140503
Environment as important as genes in autism, study finds
BY KATE KELLAND
LONDON Sat May 3, 2014 9:41pm BST
(Reuters) - Environmental factors are more important than previously thought in leading to autism, as big a factor as genes, according to the largest analysis to date to look at how the brain disorder runs in families.
Sven Sandin, who worked on the study at King's College London and Sweden's Karolinska institute, said it was prompted "by a very basic question which parents often ask: 'If I have a child with autism, what is the risk my next child will too?'"
The findings, published in the Journal of the American Medical Association (JAMA), suggest heritability is only half the story, with the other 50 percent explained by environmental factors such as birth complications, socio-economic status, or parental health and lifestyle.
The study also found that children with a brother or sister with autism are 10 times more likely to develop the condition, three times if they have a half-brother or sister with autism, and twice as likely if they have a cousin with autism.
<>
Environment as important as genes in autism, study finds
BY KATE KELLAND
LONDON Sat May 3, 2014 9:41pm BST
(Reuters) - Environmental factors are more important than previously thought in leading to autism, as big a factor as genes, according to the largest analysis to date to look at how the brain disorder runs in families.
Sven Sandin, who worked on the study at King's College London and Sweden's Karolinska institute, said it was prompted "by a very basic question which parents often ask: 'If I have a child with autism, what is the risk my next child will too?'"
The findings, published in the Journal of the American Medical Association (JAMA), suggest heritability is only half the story, with the other 50 percent explained by environmental factors such as birth complications, socio-economic status, or parental health and lifestyle.
The study also found that children with a brother or sister with autism are 10 times more likely to develop the condition, three times if they have a half-brother or sister with autism, and twice as likely if they have a cousin with autism.
<>
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Environment as important as genes in autism, study finds. (Original Post)
proverbialwisdom
May 2014
OP
"Smoking causes the majority of lung cancers, both in smokers & in people exposed to 2nd-hand smoke'
proverbialwisdom
May 2014
#2
NEW: Mitochondrial Dysfunction as a Neurobiological Subtype of Autism Spectrum Disorder
proverbialwisdom
May 2014
#4
NEW: A key role for an impaired detoxification mechanism in the etiology and severity of ASD.
proverbialwisdom
May 2014
#5
That side issue buries the lead, i.e., which 'environmental factors' are involved & WHAT CAN WE DO?
proverbialwisdom
May 2014
#8
Yes you can - really! For example, non-genetic inheritance of behavioural disorders!
bananas
May 2014
#10
It's out TODAY! Purchase Options • Buy this article • Subscribe to the journal. Anyone?
proverbialwisdom
May 2014
#9
d_r
(6,907 posts)1. genes and environment
interact in complex ways. You can't partial them out really.
proverbialwisdom
(4,959 posts)2. "Smoking causes the majority of lung cancers, both in smokers & in people exposed to 2nd-hand smoke'
SOURCE: http://www.mayoclinic.org/diseases-conditions/lung-cancer/basics/causes/con-20025531
Of course, not all smokers develop lung cancer and not all lung cancers are caused by smoking. Historical overview (WITHOUT FURTHER COMMENT), here:
I beg to differ with your conclusion as evidenced in the case above and because autism researchers are already parsing out environmental causes.
Retweeted by Autism Revolution
Martha Herbert ?@marthaherbertmd 25 Jul 2012
Probably wont find a single enviro culprit for #autism many env agents, fewer physiological pathways. @AutismRevolutio @marthaherbertmd
Martha Herbert ?@marthaherbertmd 25 Jul 2012
Probably wont find a single enviro culprit for #autism many env agents, fewer physiological pathways. @AutismRevolutio @marthaherbertmd
Retweeted by Autism Revolution
Martha Herbert ?@marthaherbertmd 25 Jul 2012
Synapses, glial cells, brain energy & more: all highly environmentally vulnerableto many things. #ASD @marthaherbertmd @AutismRevolutio
Martha Herbert ?@marthaherbertmd 25 Jul 2012
Synapses, glial cells, brain energy & more: all highly environmentally vulnerableto many things. #ASD @marthaherbertmd @AutismRevolutio
Martha Herbert ?@marthaherbertmd Feb 20 2014
MT - Beyond Hopelessness: Autism as a complex, chronic, whole-body disorder (not a permanent, brain-based trait)
MT - Beyond Hopelessness: Autism as a complex, chronic, whole-body disorder (not a permanent, brain-based trait)
proverbialwisdom
(4,959 posts)4. NEW: Mitochondrial Dysfunction as a Neurobiological Subtype of Autism Spectrum Disorder
http://archpsyc.jamanetwork.com/article.aspx?articleid=1859135
JAMA Psychiatry
Original Investigation | April 09, 2014
Mitochondrial Dysfunction as a Neurobiological Subtype of Autism Spectrum Disorder
Evidence From Brain Imaging
Suzanne Goh, MD1; Zhengchao Dong, PhD1,3; Yudong Zhang, PhD1,2; Salvatore DiMauro, MD3; Bradley S. Peterson, MD1
[-] Author Affiliations
1Department of Psychiatry, Columbia University Medical Center, New York, New York
2New York State Psychiatric Institute, New York
3Department of Neurology, Columbia University Medical Center, New York, New York
JAMA Psychiatry. Published online April 09, 2014. doi:10.1001/jamapsychiatry.2014.179
JAMA Psychiatry
Original Investigation | April 09, 2014
Mitochondrial Dysfunction as a Neurobiological Subtype of Autism Spectrum Disorder
Evidence From Brain Imaging
Suzanne Goh, MD1; Zhengchao Dong, PhD1,3; Yudong Zhang, PhD1,2; Salvatore DiMauro, MD3; Bradley S. Peterson, MD1
[-] Author Affiliations
1Department of Psychiatry, Columbia University Medical Center, New York, New York
2New York State Psychiatric Institute, New York
3Department of Neurology, Columbia University Medical Center, New York, New York
JAMA Psychiatry. Published online April 09, 2014. doi:10.1001/jamapsychiatry.2014.179
Link from Generation Rescue Twitter.
____________________________
Near the conclusion of the latest IACC Full Committee Meeting on April 8, 2014, the topic of impaired mitochondrial function was briefly discussed + plans for follow-up at the next session in July. Watch here:
http://videocast.nih.gov/summary.asp?Live=13929&bhcp=1
IACC Full Committee Meeting, April 2014 Video
Air date: Tuesday, April 08, 2014, 8:45:00 AM
Views: Total views: 630, (471 Live, 159 On-demand)
Runtime: 06:48:21
Category: Interagency Autism Coordinating Committee
Description: The IACC will meet to discuss ASD research and services activities.
Author: Dr. Thomas Insel
IACC Full Committee Meeting, April 2014 Video
Air date: Tuesday, April 08, 2014, 8:45:00 AM
Views: Total views: 630, (471 Live, 159 On-demand)
Runtime: 06:48:21
Category: Interagency Autism Coordinating Committee
Description: The IACC will meet to discuss ASD research and services activities.
Author: Dr. Thomas Insel
Overview page: https://iacc.hhs.gov/events/index.shtml
____________________________
RECAP: Environmental insult with genetic susceptibility -> impaired mitochondria -> impaired cell energy -> impaired body function and health. Developing...
proverbialwisdom
(4,959 posts)5. NEW: A key role for an impaired detoxification mechanism in the etiology and severity of ASD.
http://www.behavioralandbrainfunctions.com/content/10/1/14/abstract
Research
A key role for an impaired detoxification mechanism in the etiology and severity of autism spectrum disorders
Altaf Alabdali, Laila Al-Ayadhi and Afaf El-Ansary
Behavioral and Brain Functions 2014, 10:14 doi:10.1186/1744-9081-10-14
Published: 28 April 2014
Abstract (provisional)
Background
Autism Spectrum Disorders (ASD) is a syndrome with a number of etiologies and different mechanisms that lead to abnormal development. The identification of autism biomarkers in patients with different degrees of clinical presentation (i.e., mild, moderate and severe) will give greater insight into the pathogenesis of this disease and will enable effective early diagnostic strategies and treatments for this disorder.
Methods
In this study, the concentration of two toxic heavy metals, lead (Pb) and mercury (Hg), were measured in red blood cells, while glutathione-s-transferase (GST) and vitamin E, as enzymatic and non-enzymatic antioxidants, respectively, were measured in the plasma of subgroups of autistic patients with different Social Responsiveness Scale (SRS) and Childhood Autism Rating Scale (CARS) scores. The results were compared to age- and gender-matched healthy controls.
Results
The obtained data showed that the patients with autism spectrum disorder had significantly higher Pb and Hg levels and lower GST activity and vitamin E concentrations compared with the controls. The levels of heavy metals (Hg and Pb), GST and vitamin E were correlated with the severity of the social and cognitive impairment measures (SRS and CARS). Receiver Operating Characteristics (ROC) analysis and predictiveness curves indicated that the four parameters show satisfactory sensitivity, very high specificity and excellent predictiveness. Multiple regression analyses confirmed that higher levels of Hg and Pb, together with lower levels of GST and vitamin E, can be used to predict social and cognitive impairment in patients with autism spectrum disorders.
Conclusion
This study confirms earlier studies that implicate toxic metal accumulation as a consequence of impaired detoxification in autism and provides insight into the etiological mechanism of autism.
The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production.
Research
A key role for an impaired detoxification mechanism in the etiology and severity of autism spectrum disorders
Altaf Alabdali, Laila Al-Ayadhi and Afaf El-Ansary
Behavioral and Brain Functions 2014, 10:14 doi:10.1186/1744-9081-10-14
Published: 28 April 2014
Abstract (provisional)
Background
Autism Spectrum Disorders (ASD) is a syndrome with a number of etiologies and different mechanisms that lead to abnormal development. The identification of autism biomarkers in patients with different degrees of clinical presentation (i.e., mild, moderate and severe) will give greater insight into the pathogenesis of this disease and will enable effective early diagnostic strategies and treatments for this disorder.
Methods
In this study, the concentration of two toxic heavy metals, lead (Pb) and mercury (Hg), were measured in red blood cells, while glutathione-s-transferase (GST) and vitamin E, as enzymatic and non-enzymatic antioxidants, respectively, were measured in the plasma of subgroups of autistic patients with different Social Responsiveness Scale (SRS) and Childhood Autism Rating Scale (CARS) scores. The results were compared to age- and gender-matched healthy controls.
Results
The obtained data showed that the patients with autism spectrum disorder had significantly higher Pb and Hg levels and lower GST activity and vitamin E concentrations compared with the controls. The levels of heavy metals (Hg and Pb), GST and vitamin E were correlated with the severity of the social and cognitive impairment measures (SRS and CARS). Receiver Operating Characteristics (ROC) analysis and predictiveness curves indicated that the four parameters show satisfactory sensitivity, very high specificity and excellent predictiveness. Multiple regression analyses confirmed that higher levels of Hg and Pb, together with lower levels of GST and vitamin E, can be used to predict social and cognitive impairment in patients with autism spectrum disorders.
Conclusion
This study confirms earlier studies that implicate toxic metal accumulation as a consequence of impaired detoxification in autism and provides insight into the etiological mechanism of autism.
The complete article is available as a provisional PDF. The fully formatted PDF and HTML versions are in production.
Provisional PDF: http://www.behavioralandbrainfunctions.com/content/pdf/1744-9081-10-14.pdf
Link from http://www.rescuepost.com/files/alabdali-et-al-2014-saudi-asd-study-on-hg-and-pb-in-blood-cells-of-3-12-yo.pdf via AOA.
d_r
(6,907 posts)6. genes and environment
interact in complex ways. You can't partial them out, really.
proverbialwisdom
(4,959 posts)8. That side issue buries the lead, i.e., which 'environmental factors' are involved & WHAT CAN WE DO?
FYI:
http://www.merriam-webster.com/dictionary/parse
Parse: to study (something) by looking at its parts closely.
Parse: to study (something) by looking at its parts closely.
bananas
(27,509 posts)10. Yes you can - really! For example, non-genetic inheritance of behavioural disorders!
Here, they "partialled them out" and found genes had nothing to do with it, it was all environment!
Good thing these scientists didn't say, "It's too complex, we're too stupid, let's go shopping!"
From last month: http://www.democraticunderground.com/101690675
http://medicalxpress.com/news/2014-04-scientists-unmask-piece-puzzle-inheritance.html
Scientists unmask a piece in the puzzle of how the inheritance of traumas is mediated
The phenomenon has long been known in psychology: traumatic experiences can induce behavioural disorders that are passed down from one generation to the next. It is only recently that scientists have begun to understand the physiological processes underlying hereditary trauma. "There are diseases such as bipolar disorder, that run in families but can't be traced back to a particular gene", explains Isabelle Mansuy, professor at ETH Zurich and the University of Zurich. With her research group at the Brain Research Institute of the University of Zurich, she has been studying the molecular processes involved in non-genetic inheritance of behavioural symptoms induced by traumatic experiences in early life.
<snip>
Small RNAs with a huge impact
The researchers studied the number and kind of microRNAs expressed by adult mice exposed to traumatic conditions in early life and compared them with non-traumatized mice. They discovered that traumatic stress alters the amount of several microRNAs in the blood, brain and sperm while some microRNAs were produced in excess, others were lower than in the corresponding tissues or cells of control animals. These alterations resulted in misregulation of cellular processes normally controlled by these microRNAs.
After traumatic experiences, the mice behaved markedly differently: they partly lost their natural aversion to open spaces and bright light and had depressive-like behaviours. These behavioural symptoms were also transferred to the next generation via sperm, even though the offspring were not exposed to any traumatic stress themselves.
Even passed on to the third generation
The metabolism of the offspring of stressed mice was also impaired: their insulin and blood-sugar levels were lower than in the offspring of non-traumatized parents. "We were able to demonstrate for the first time that traumatic experiences affect metabolism in the long-term and that these changes are hereditary", says Mansuy. The effects on metabolism and behaviour even persisted in the third generation.
<snip>
Scientists unmask a piece in the puzzle of how the inheritance of traumas is mediated
The consequences of traumatic experiences can be passed on from one generation to the next.
Credit: Isabelle Mansuy / UZH / ETH Zurich
The phenomenon has long been known in psychology: traumatic experiences can induce behavioural disorders that are passed down from one generation to the next. It is only recently that scientists have begun to understand the physiological processes underlying hereditary trauma. "There are diseases such as bipolar disorder, that run in families but can't be traced back to a particular gene", explains Isabelle Mansuy, professor at ETH Zurich and the University of Zurich. With her research group at the Brain Research Institute of the University of Zurich, she has been studying the molecular processes involved in non-genetic inheritance of behavioural symptoms induced by traumatic experiences in early life.
<snip>
Small RNAs with a huge impact
The researchers studied the number and kind of microRNAs expressed by adult mice exposed to traumatic conditions in early life and compared them with non-traumatized mice. They discovered that traumatic stress alters the amount of several microRNAs in the blood, brain and sperm while some microRNAs were produced in excess, others were lower than in the corresponding tissues or cells of control animals. These alterations resulted in misregulation of cellular processes normally controlled by these microRNAs.
After traumatic experiences, the mice behaved markedly differently: they partly lost their natural aversion to open spaces and bright light and had depressive-like behaviours. These behavioural symptoms were also transferred to the next generation via sperm, even though the offspring were not exposed to any traumatic stress themselves.
Even passed on to the third generation
The metabolism of the offspring of stressed mice was also impaired: their insulin and blood-sugar levels were lower than in the offspring of non-traumatized parents. "We were able to demonstrate for the first time that traumatic experiences affect metabolism in the long-term and that these changes are hereditary", says Mansuy. The effects on metabolism and behaviour even persisted in the third generation.
<snip>
proverbialwisdom
(4,959 posts)7. NEW: The Familial Risk of Autism
http://jama.jamanetwork.com/article.aspx?articleid=1866100
[img][/img]
Original Investigation | May 7, 2014
The Familial Risk of Autism
Sven Sandin, MSc1,2; Paul Lichtenstein, PhD1; Ralf Kuja-Halkola, MSc1; Henrik Larsson, PhD1; Christina M. Hultman, PhD1; Abraham Reichenberg, PhD3,4,5
JAMA. 2014;311(17):1770-1777. doi:10.1001/jama.2014.4144.
ABSTRACT:
Importance Autism spectrum disorder (ASD) aggregates in families, but the individual risk and to what extent this is caused by genetic factors or shared or nonshared environmental factors remains unresolved.
Objective To provide estimates of familial aggregation and heritability of ASD.
Design, Setting, and Participants A population-based cohort including 2?049?973 Swedish children born 1982 through 2006. We identified 37?570 twin pairs, 2?642?064 full sibling pairs, 432?281 maternal and 445?531 paternal half sibling pairs, and 5?799?875 cousin pairs. Diagnoses of ASD to December 31, 2009 were ascertained.
<>
Conclusions and Relevance Among children born in Sweden, the individual risk of ASD and autistic disorder increased with increasing genetic relatedness. Heritability of ASD and autistic disorder were estimated to be approximately 50%. These findings may inform the counseling of families with affected children.
[img][/img]
Original Investigation | May 7, 2014
The Familial Risk of Autism
Sven Sandin, MSc1,2; Paul Lichtenstein, PhD1; Ralf Kuja-Halkola, MSc1; Henrik Larsson, PhD1; Christina M. Hultman, PhD1; Abraham Reichenberg, PhD3,4,5
JAMA. 2014;311(17):1770-1777. doi:10.1001/jama.2014.4144.
ABSTRACT:
Importance Autism spectrum disorder (ASD) aggregates in families, but the individual risk and to what extent this is caused by genetic factors or shared or nonshared environmental factors remains unresolved.
Objective To provide estimates of familial aggregation and heritability of ASD.
Design, Setting, and Participants A population-based cohort including 2?049?973 Swedish children born 1982 through 2006. We identified 37?570 twin pairs, 2?642?064 full sibling pairs, 432?281 maternal and 445?531 paternal half sibling pairs, and 5?799?875 cousin pairs. Diagnoses of ASD to December 31, 2009 were ascertained.
<>
Conclusions and Relevance Among children born in Sweden, the individual risk of ASD and autistic disorder increased with increasing genetic relatedness. Heritability of ASD and autistic disorder were estimated to be approximately 50%. These findings may inform the counseling of families with affected children.
proverbialwisdom
(4,959 posts)9. It's out TODAY! Purchase Options • Buy this article • Subscribe to the journal. Anyone?
May 7, 2014, Vol 311, No. 17 > http://jama.jamanetwork.com/issue.aspx?journalid=67&issueid=930078
Current Issue
JAMA
May 7, 2014, Vol 311, No. 17PDF
Theme: Child Health
EDITORIAL
ORIGINAL INVESTIGATION
Current Issue
JAMA
May 7, 2014, Vol 311, No. 17PDF
Theme: Child Health
EDITORIAL
The Genetic and Environmental Contributions to Autism: Looking Beyond Twins
Diana E. Schendel, PhD; Therese K. Grønborg, MSc; Erik T. Parner, MSc, PhD
Topics: autistic disorder, twins, genetics
JAMA. 2014;311(17):1738-1739. doi:10.1001/jama.2014.3554.
ORIGINAL INVESTIGATION
The Familial Risk of Autism
Sven Sandin, MSc; Paul Lichtenstein, PhD; Ralf Kuja-Halkola, MSc; Henrik Larsson, PhD; Christina M. Hultman, PhD; Abraham Reichenberg, PhD
Includes: Supplemental Content, Author Interview
Topics: autistic disorder, relationship - sibling
JAMA. 2014;311(17):1770-1777. doi:10.1001/jama.2014.4144.