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How does one get tested for mitochondrial dysfunction?

Thanks for any info!

On Feb 3, 2011, at 7:55 AM, jeannne buesser <jbmistletoe@...> wrote:

> Mitochondrial Dysfunction Linked to Autism

>

>

>

> January 31, 2011 — Mitochondrial dysfunction (MD) is more common in children

with autism and autism spectrum disorder (ASD) than the general population, a

comprehensive systematic review and meta-analysis of relevant research confirms.

>

> Mitochondrial dysfunction " may play a significant role in contributing to the

symptoms of autism and is generally underrecognized in these children, "

A. Rossignol, MD, of the International Child Development Resource Center,

Melbourne, Florida, told Medscape Medical News.

>

> " Testing for mitochondrial dysfunction is available, and early treatment might

lead to better long-term developmental outcomes, " said Dr. Rossignol, who

coauthored the review with E. Frye, MD, PhD, of the University of Texas

in Houston.

>

> The report was published online January 25 in Molecular Psychiatry.

>

> Commenting on the study Cecilia Giulivi, PhD, professor of biochemistry and

metabolic regulation, at the University of California, , who was not

involved in the analysis, said, " At this point, it looks like there is a higher

incidence of mitochondrial disease in autism, much higher than we suspected. "

>

> She noted, however, that testing for MD " is not a trivial task [and] we need

more research to come up with a consensus of diagnostic tests to run. In

addition, maybe other metabolic syndromes should be looked into, " Dr. Giulivi

said.

>

> The primary objectives of the analysis were to identify features of MD in the

general population of children with ASD and compare characteristics of MD in

children with ASD and concomitant significant and severe MD with that of ASD

children without MD and non-ASD children with MD.

>

> They included 68 relevant published articles in a qualitative synthesis,

including 18 studies with a total of 112 children with ASD and MD.

>

> Genetics Not the Culprit

>

> The results showed the prevalence of MD in the general population of children

with ASD is approximately 5% (95% confidence interval [CI], 3.2% – 6.9%),

which is 500% higher than the general population prevalence of 0.01%. For a

variety of reasons, " this 5% value is most likely an underestimation, " Dr.

Rossignol said.

>

> It also appears that one-third or more of children with autism may have some

type of dysfunction in their mitochondria. On the basis of laboratory testing,

the prevalence of abnormal biomarker values of MD, including lactate, pyruvate,

carnitine, and ubiquinone, was high in children with ASD, much higher than the

prevalence of MD. Some of these markers correlated with the severity of ASD.

>

> Most of the 112 children with ASD and MD (79%) had no an identifiable genetic

abnormality that could account for the MD.

>

> " The mitochondrial dysfunction and disease reported in autism are related to a

genetic abnormality in only 1 out of 5 children; meaning that a majority of

these children have something else contributing to this dysfunction, which might

include multiple environmental factors, such as toxins, oxidative stress,

inflammation, and decreased levels of antioxidants, " said Dr. Rossignol.

>

> " Clearly, mitochondrial function is a ripe area of research when investigating

the biological mechanism(s) of action of environmental toxicant exposures and

indigenous abnormalities associated with ASD, " the study authors write.

>

> Loss of Social Skills

>

> Children with ASD and MD had some distinct characteristics compared with the

general population of children with ASD. In 12 studies, " children with autism

and mitochondrial problems were more likely to lose acquired skills compared to

children with autism in general, " said Dr. Rossignol. However, it was not clear

whether MD contributed to or caused the reported regression.

>

> In addition to a higher prevalence of developmental regression (52%), seizures

(41%), motor delay (51%), and gastrointestinal abnormalities (74%), such as

reflux and constipation, also appear to be significantly more common in children

with ASD and MD relative to children with just ASD.

>

> Currently, " testing for mitochondrial problems in children with autism is

rarely done, and we feel that testing should be routine, especially in children

with regression or loss of skills, " said Dr. Rossignol. " This is important

because early recognition of mitochondrial problems in autism might lead to

better outcomes in children with autism. "

>

> Dr. Rossignol and Dr. Frye note in their report that published studies looking

at treatment for ASD and MD are limited. However, some studies have suggested

that treatment with mitochondrial cofactor supplementation, including

antioxidants, carnitine, coenzyme Q10, and B vitamins, may improve mitochondrial

function and behavior in some children with ASD.

>

> " A therapeutic trial of mitochondrial cofactors and antioxidants may be

reasonable in children with ASD/MD, " the study authors conclude. Carnitine, they

say, may be particularly helpful in children with ASD because carnitine

deficiency has been implicated in ASD, and some studies have reported

improvements with the use of carnitine in ASD.

>

> The researchers emphasize, however, that systematic studies documenting the

efficacy of this and other potential treatments for MD in children with ASD are

generally lacking.

>

> Need for Longitudinal Studies

>

> A small study by Dr. Giulivi and colleagues showed that impaired mitochondrial

function and mitochondrial DNA abnormalities, including overreplication and

deletions, were more common in children with autism than in typically developing

children (Giulivi et al. JAMA. 2010;304:2389-2396).

>

> " According to our study and those of others, there is evidence for MD in

typical autism and ASD, " Dr. Giulivi said. " However, I don't think that we know

the role of this MD, meaning if it is related to the etiology (cause) or

consequence of another underlying altered pathway.

>

> " In any case [cause or consequence], a decline in mitochondrial function

[below the threshold for a given tissue] and especially in highly aerobic

tissues, such as brain, will have an impact on cellular energy and, in addition,

maybe on other mitochondria-dependent pathways, such as heme metabolism, " Dr.

Giulivi noted.

>

> She also made the point that most studies to date have been cross-sectional

and therefore, " unless it is a longitudinal one, we cannot assess the role of MD

in ASD and autism. "

>

> Dr. Rossignol and Dr. Frye point out that many of the studies they reviewed

had a number of limitations, including " small sample sizes, referral or

publication biases, and variability in protocols for selecting children for MD

workup, collecting mitochondrial biomarkers, and defining MD. " Only 39% of the

ASD/MD studies reviewed noted the criterion used for diagnosing MD.

>

> They agree with Dr. Giulivi that further studies are needed to further define

the role of MD in ASD.

>

> This research was funded in part by the Autism Research Institute and the Jane

Botsford Foundation. Dr. Rossignol has 2 children with ASD and is a

practicing primary care physician who treats ASD children with standard and

integrative treatments. Dr. Frye provides expert testimony for children with MDs

who may have been injured from vaccines. Funds from such testimony are used to

support research on the biological basis of neurodevelopmental disorders. Dr.

Giulivi has disclosed no relevant financial relationships.

>

> Mol Psychiatry. Published online January 25, 2011.

>

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Hey ,

 

I just wanted to say how much I find your blog info so informative. Thanks so

much for all the great info !!

Demi

From: kiddietalk <kiddietalk@...>

Subject: [ ] Re: Mitochondrial Dysfunction Linked to Autism

Date: Thursday, February 3, 2011, 4:30 PM

 

I do have a blog on mitochondrial dysfunction including video which provides

much of the information as to what can help and hurt the mitochondria.

http://pursuitofresearch.org/2010/12/10/mitochondrial-dysfunction-in-autism-and-\

other-disorders-can-diet-help/

=====

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Wow that study was co-authored by our neurologist. Too cool!

From:

[mailto: ] On Behalf Of HD

Sent: Thursday, February 03, 2011 10:07 AM

Subject: Re: [ ] Mitochondrial Dysfunction Linked to Autism

How does one get tested for mitochondrial dysfunction?

Thanks for any info!

On Feb 3, 2011, at 7:55 AM, jeannne buesser <jbmistletoe@...

<mailto:jbmistletoe%40optonline.net> > wrote:

> Mitochondrial Dysfunction Linked to Autism

>

>

>

> January 31, 2011 — Mitochondrial dysfunction (MD) is more common in children

with autism and autism spectrum disorder (ASD) than the general population, a

comprehensive systematic review and meta-analysis of relevant research confirms.

>

> Mitochondrial dysfunction " may play a significant role in contributing to the

symptoms of autism and is generally underrecognized in these children, "

A. Rossignol, MD, of the International Child Development Resource Center,

Melbourne, Florida, told Medscape Medical News.

>

> " Testing for mitochondrial dysfunction is available, and early treatment might

lead to better long-term developmental outcomes, " said Dr. Rossignol, who

coauthored the review with E. Frye, MD, PhD, of the University of Texas

in Houston.

>

> The report was published online January 25 in Molecular Psychiatry.

>

> Commenting on the study Cecilia Giulivi, PhD, professor of biochemistry and

metabolic regulation, at the University of California, , who was not

involved in the analysis, said, " At this point, it looks like there is a higher

incidence of mitochondrial disease in autism, much higher than we suspected. "

>

> She noted, however, that testing for MD " is not a trivial task [and] we need

more research to come up with a consensus of diagnostic tests to run. In

addition, maybe other metabolic syndromes should be looked into, " Dr. Giulivi

said.

>

> The primary objectives of the analysis were to identify features of MD in the

general population of children with ASD and compare characteristics of MD in

children with ASD and concomitant significant and severe MD with that of ASD

children without MD and non-ASD children with MD.

>

> They included 68 relevant published articles in a qualitative synthesis,

including 18 studies with a total of 112 children with ASD and MD.

>

> Genetics Not the Culprit

>

> The results showed the prevalence of MD in the general population of children

with ASD is approximately 5% (95% confidence interval [CI], 3.2% – 6.9%),

which is 500% higher than the general population prevalence of 0.01%. For a

variety of reasons, " this 5% value is most likely an underestimation, " Dr.

Rossignol said.

>

> It also appears that one-third or more of children with autism may have some

type of dysfunction in their mitochondria. On the basis of laboratory testing,

the prevalence of abnormal biomarker values of MD, including lactate, pyruvate,

carnitine, and ubiquinone, was high in children with ASD, much higher than the

prevalence of MD. Some of these markers correlated with the severity of ASD.

>

> Most of the 112 children with ASD and MD (79%) had no an identifiable genetic

abnormality that could account for the MD.

>

> " The mitochondrial dysfunction and disease reported in autism are related to a

genetic abnormality in only 1 out of 5 children; meaning that a majority of

these children have something else contributing to this dysfunction, which might

include multiple environmental factors, such as toxins, oxidative stress,

inflammation, and decreased levels of antioxidants, " said Dr. Rossignol.

>

> " Clearly, mitochondrial function is a ripe area of research when investigating

the biological mechanism(s) of action of environmental toxicant exposures and

indigenous abnormalities associated with ASD, " the study authors write.

>

> Loss of Social Skills

>

> Children with ASD and MD had some distinct characteristics compared with the

general population of children with ASD. In 12 studies, " children with autism

and mitochondrial problems were more likely to lose acquired skills compared to

children with autism in general, " said Dr. Rossignol. However, it was not clear

whether MD contributed to or caused the reported regression.

>

> In addition to a higher prevalence of developmental regression (52%), seizures

(41%), motor delay (51%), and gastrointestinal abnormalities (74%), such as

reflux and constipation, also appear to be significantly more common in children

with ASD and MD relative to children with just ASD.

>

> Currently, " testing for mitochondrial problems in children with autism is

rarely done, and we feel that testing should be routine, especially in children

with regression or loss of skills, " said Dr. Rossignol. " This is important

because early recognition of mitochondrial problems in autism might lead to

better outcomes in children with autism. "

>

> Dr. Rossignol and Dr. Frye note in their report that published studies looking

at treatment for ASD and MD are limited. However, some studies have suggested

that treatment with mitochondrial cofactor supplementation, including

antioxidants, carnitine, coenzyme Q10, and B vitamins, may improve mitochondrial

function and behavior in some children with ASD.

>

> " A therapeutic trial of mitochondrial cofactors and antioxidants may be

reasonable in children with ASD/MD, " the study authors conclude. Carnitine, they

say, may be particularly helpful in children with ASD because carnitine

deficiency has been implicated in ASD, and some studies have reported

improvements with the use of carnitine in ASD.

>

> The researchers emphasize, however, that systematic studies documenting the

efficacy of this and other potential treatments for MD in children with ASD are

generally lacking.

>

> Need for Longitudinal Studies

>

> A small study by Dr. Giulivi and colleagues showed that impaired mitochondrial

function and mitochondrial DNA abnormalities, including overreplication and

deletions, were more common in children with autism than in typically developing

children (Giulivi et al. JAMA. 2010;304:2389-2396).

>

> " According to our study and those of others, there is evidence for MD in

typical autism and ASD, " Dr. Giulivi said. " However, I don't think that we know

the role of this MD, meaning if it is related to the etiology (cause) or

consequence of another underlying altered pathway.

>

> " In any case [cause or consequence], a decline in mitochondrial function

[below the threshold for a given tissue] and especially in highly aerobic

tissues, such as brain, will have an impact on cellular energy and, in addition,

maybe on other mitochondria-dependent pathways, such as heme metabolism, " Dr.

Giulivi noted.

>

> She also made the point that most studies to date have been cross-sectional

and therefore, " unless it is a longitudinal one, we cannot assess the role of MD

in ASD and autism. "

>

> Dr. Rossignol and Dr. Frye point out that many of the studies they reviewed

had a number of limitations, including " small sample sizes, referral or

publication biases, and variability in protocols for selecting children for MD

workup, collecting mitochondrial biomarkers, and defining MD. " Only 39% of the

ASD/MD studies reviewed noted the criterion used for diagnosing MD.

>

> They agree with Dr. Giulivi that further studies are needed to further define

the role of MD in ASD.

>

> This research was funded in part by the Autism Research Institute and the Jane

Botsford Foundation. Dr. Rossignol has 2 children with ASD and is a

practicing primary care physician who treats ASD children with standard and

integrative treatments. Dr. Frye provides expert testimony for children with MDs

who may have been injured from vaccines. Funds from such testimony are used to

support research on the biological basis of neurodevelopmental disorders. Dr.

Giulivi has disclosed no relevant financial relationships.

>

> Mol Psychiatry. Published online January 25, 2011.

>

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Share on other sites

 

Mitochondrial Dysfunction Linked to Autism

http://www.medscape.com/viewarticle/736560?src=mpnews & spon=12

January 31, 2011 — Mitochondrial dysfunction

(MD) is more common in children with autism and autism spectrum disorder (ASD)

than the general population, a comprehensive systematic review and meta-analysis

of relevant research confirms.

Mitochondrial dysfunction " may play a

significant role in contributing to the symptoms of autism and is generally

underrecognized in these children, " A. Rossignol, MD, of the

International Child Development Resource Center, Melbourne, Florida, told

Medscape Medical News.

 

Dr. A. Rossignol

" Testing for mitochondrial dysfunction is available, and early

treatment might lead to better long-term developmental outcomes, " said Dr.

Rossignol, who coauthored the review with E. Frye, MD, PhD, of the

University of Texas in Houston.

The report was published online January 25 in

Molecular Psychiatry.

Commenting on the study Cecilia Giulivi, PhD, professor of biochemistry

and metabolic regulation, at the University of California, , who was not

involved in the analysis, said, " At this point, it looks like there is a higher

incidence of mitochondrial disease in autism, much higher than we

suspected. "

She noted, however, that testing for MD " is not a trivial task [and] we

need more research to come up with a consensus of diagnostic tests to run. In

addition, maybe other metabolic syndromes should be looked into, " Dr. Giulivi

said.

The primary objectives of the analysis were to identify features of MD

in the general population of children with ASD and compare characteristics of MD

in children with ASD and concomitant significant and severe MD with that of ASD

children without MD and non-ASD children with MD.

They included 68 relevant published articles in a qualitative

synthesis, including 18 studies with a total of 112 children with ASD and

MD.

Genetics Not the Culprit

The results showed the prevalence of MD in the general population of

children with ASD is approximately 5% (95% confidence interval [CI], 3.2% –

6.9%), which is 500% higher than the general population prevalence of 0.01%. For

a variety of reasons, " this 5% value is most likely an underestimation, " Dr.

Rossignol said.

It also appears that one-third or more of children with autism may have

some type of dysfunction in their mitochondria. On the basis of laboratory

testing, the prevalence of abnormal biomarker values of MD, including lactate,

pyruvate, carnitine, and ubiquinone, was high in children with ASD, much higher

than the prevalence of MD. Some of these markers correlated with the severity of

ASD.

Most of the 112 children with ASD and MD (79%) had no an identifiable

genetic abnormality that could account for the MD.

" The mitochondrial

dysfunction and disease reported in autism are related to a genetic abnormality

in only 1 out of 5 children; meaning that a majority of these children have

something else contributing to this dysfunction, which might include multiple

environmental factors, such as toxins, oxidative stress, inflammation, and

decreased levels of antioxidants, " said Dr. Rossignol.

" Clearly,

mitochondrial function is a ripe area of research when investigating the

biological mechanism(s) of action of environmental toxicant exposures and

indigenous abnormalities associated with ASD, " the study authors write.

Loss of Social Skills

Children with ASD and MD had some distinct characteristics compared

with the general population of children with ASD. In 12 studies, " children with

autism and mitochondrial problems were more likely to lose acquired skills

compared to children with autism in general, " said Dr. Rossignol. However, it

was not clear whether MD contributed to or caused the reported

regression.

In addition to a higher prevalence of developmental regression (52%),

seizures (41%), motor delay (51%), and gastrointestinal abnormalities (74%),

such as reflux and constipation, also appear to be significantly more common in

children with ASD and MD relative to children with just ASD.

Currently, " testing for mitochondrial problems in children with autism

is rarely done, and we feel that testing should be routine, especially in

children with regression or loss of skills, " said Dr. Rossignol. " This is

important because early recognition of mitochondrial problems in autism might

lead to better outcomes in children with autism. "

Dr. Rossignol and Dr. Frye note in their report that published studies

looking at treatment for ASD and MD are limited. However, some studies have

suggested that treatment with mitochondrial cofactor supplementation, including

antioxidants, carnitine, coenzyme Q10, and B vitamins, may improve mitochondrial

function and behavior in some children with ASD.

" A therapeutic trial of mitochondrial cofactors and antioxidants may be

reasonable in children with ASD/MD, " the study authors conclude. Carnitine, they

say, may be particularly helpful in children with ASD because carnitine

deficiency has been implicated in ASD, and some studies have reported

improvements with the use of carnitine in ASD.

The researchers emphasize, however, that systematic studies documenting

the efficacy of this and other potential treatments for MD in children with ASD

are generally lacking.

Need for Longitudinal Studies

A small study by Dr. Giulivi and colleagues showed that impaired

mitochondrial function and mitochondrial DNA abnormalities, including

overreplication and deletions, were more common in children with autism than in

typically developing children (Giulivi et al. JAMA. 2010;304:2389-2396).

" According to our study and those of others, there is evidence for MD

in typical autism and ASD, " Dr. Giulivi said. " However, I don't think that we

know the role of this MD, meaning if it is related to the etiology (cause) or

consequence of another underlying altered pathway.

" In any case [cause or consequence], a decline in mitochondrial

function [below the threshold for a given tissue] and especially in highly

aerobic tissues, such as brain, will have an impact on cellular energy and, in

addition, maybe on other mitochondria-dependent pathways, such as heme

metabolism, " Dr. Giulivi noted.

She also made the point that most studies to date have been

cross-sectional and therefore, " unless it is a longitudinal one, we cannot

assess the role of MD in ASD and autism. "

Dr. Rossignol and Dr. Frye point out that many of the studies they

reviewed had a number of limitations, including " small sample sizes, referral or

publication biases, and variability in protocols for selecting children for MD

workup, collecting mitochondrial biomarkers, and defining MD. " Only 39% of the

ASD/MD studies reviewed noted the criterion used for diagnosing MD.

They

agree with Dr. Giulivi that further studies are needed to further define the

role of MD in ASD.

This research was funded in part by the Autism Research Institute and

the Jane Botsford Foundation. Dr. Rossignol has 2 children with ASD and

is a practicing primary care physician who treats ASD children with standard and

integrative treatments. Dr. Frye provides expert testimony for children with MDs

who may have been injured from vaccines. Funds from such testimony are used to

support research on the biological basis of neurodevelopmental disorders. Dr.

Giulivi has disclosed no relevant financial relationships.

Mol Psychiatry. Published online January 25, 2011.

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