Difference between revisions of "Medical Research"
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| − | + | == 2002 International Symposium == | |
| − | + | I am currently reading the book "Prader Willi Syndrome as a Model of Obesity" | |
| − | + | edited by Eiholzer, l'allemand, and Zipf ([http://www.amazon.com/exec/obidos/tg/detail/-/3805575742/dankohn available] from Amazon). This is the summary of the 2002 | |
| + | International Symposium held in Zurich. It is expensive ($120), but well worth | ||
| + | it if you like to read the science stuff. | ||
| + | |||
| + | Dr. Lee has an article in there where he proposes that the metabolic problem | ||
| + | is not actually a problem with the hypothalamus, but rather is a problem in the | ||
| + | periphery. I found his arguments quite convincing. "The peripheral model | ||
| + | relies on disordered regulation of substrate- or tissue-generated signaling, an | ||
| + | area which is even more poorly understood than central appetite regulation." | ||
| + | |||
| + | Also, some quotes from the Eiholzer article that I found interesting: | ||
| + | "From this viewpoint, the onset of obesity represents the external | ||
| + | manifestation of insufficient satiety and, at the same time, is an expression of | ||
| + | increasing physical strength, health an the children's ability to get their way." | ||
| + | (p.2) Does that make sense to any of you? Once the child becomes strong | ||
| + | enough to eat well, then they keep eating and gaining weight?? | ||
| + | "... children with PWS had decreased muscle mass in absolute terms (as | ||
| + | opposed to children with nonsyndromal obesity, who had an increased | ||
| + | muscle mass)..." | ||
| + | |||
| + | "Even after long-term growth hormone treatment, muscle mass remained | ||
| + | distinctly decreased and fat mass was increased." While I doubt this sentence | ||
| + | incorporates any data about infants given GH, it still underscores to me that | ||
| + | while GH seems to be able to fix the problem (at least partly) it does not really | ||
| + | get at the underlying cause. | ||
| + | |||
| + | In one spot he refers to hypoactivity as insufficient muscle mass. Does that | ||
| + | mean that once our kids get enough muscle mass they become more active? | ||
| + | Is there something wrong with their muscle or is it just that they don't have | ||
| + | enough muscle? Is it a quality problem or just a quantity problem? Why are | ||
| + | they low tone? Is it because their muscle to fat ratio is off? But that ratio stays | ||
| + | off throughout their life and yet their tone improves with time. | ||
| + | |||
| + | Also, I've discussed PWS and diabetes and the value of a | ||
| + | low glycemic index diet for our kids? Eiholzer writes: "The insulin levels, | ||
| + | however, are low, at least in children and adolescents. In the periphery, | ||
| + | insulin sensitivity is increased, in contrast to most individuals with non- | ||
| + | syndromal obesity. Whether the low insulin levels centrally play a role in | ||
| + | energy regulation is open." | ||
| + | |||
| + | Also, Eiholzer makes reference to daily training programme's to augment GH | ||
| + | therapy in the effort to achieve normal muscle mass. Does anyone know | ||
| + | anything about this? He seems to discount it by saying: "The downside of a | ||
| + | daily training programme, however, is that it requires an additional time | ||
| + | investment on part of the parents and other caretakers." | ||
| + | |||
| + | == Starvation or Obesity? == | ||
| + | |||
| + | This interesting article [[Paradox of Prader-Willi]] syndrome: a genetic model of starvation argues that PWS is more a model of starvation than it is a model of obesity. | ||
== Current studies == | == Current studies == | ||
Revision as of 00:48, 28 November 2004
2002 International Symposium
I am currently reading the book "Prader Willi Syndrome as a Model of Obesity" edited by Eiholzer, l'allemand, and Zipf (available from Amazon). This is the summary of the 2002 International Symposium held in Zurich. It is expensive ($120), but well worth it if you like to read the science stuff.
Dr. Lee has an article in there where he proposes that the metabolic problem is not actually a problem with the hypothalamus, but rather is a problem in the periphery. I found his arguments quite convincing. "The peripheral model relies on disordered regulation of substrate- or tissue-generated signaling, an area which is even more poorly understood than central appetite regulation."
Also, some quotes from the Eiholzer article that I found interesting: "From this viewpoint, the onset of obesity represents the external manifestation of insufficient satiety and, at the same time, is an expression of increasing physical strength, health an the children's ability to get their way." (p.2) Does that make sense to any of you? Once the child becomes strong enough to eat well, then they keep eating and gaining weight?? "... children with PWS had decreased muscle mass in absolute terms (as opposed to children with nonsyndromal obesity, who had an increased muscle mass)..."
"Even after long-term growth hormone treatment, muscle mass remained distinctly decreased and fat mass was increased." While I doubt this sentence incorporates any data about infants given GH, it still underscores to me that while GH seems to be able to fix the problem (at least partly) it does not really get at the underlying cause.
In one spot he refers to hypoactivity as insufficient muscle mass. Does that mean that once our kids get enough muscle mass they become more active? Is there something wrong with their muscle or is it just that they don't have enough muscle? Is it a quality problem or just a quantity problem? Why are they low tone? Is it because their muscle to fat ratio is off? But that ratio stays off throughout their life and yet their tone improves with time.
Also, I've discussed PWS and diabetes and the value of a low glycemic index diet for our kids? Eiholzer writes: "The insulin levels, however, are low, at least in children and adolescents. In the periphery, insulin sensitivity is increased, in contrast to most individuals with non- syndromal obesity. Whether the low insulin levels centrally play a role in energy regulation is open."
Also, Eiholzer makes reference to daily training programme's to augment GH therapy in the effort to achieve normal muscle mass. Does anyone know anything about this? He seems to discount it by saying: "The downside of a daily training programme, however, is that it requires an additional time investment on part of the parents and other caretakers."
Starvation or Obesity?
This interesting article Paradox of Prader-Willi syndrome: a genetic model of starvation argues that PWS is more a model of starvation than it is a model of obesity.
Current studies
- RESEARCH ON BEHAVIOR DIFFERENCES WHEN RELATED TO FOOD - University of North Carolina graduate student is conducting a parental survey-based research project on behavior differences between the three types of Prader-Willi syndrome when related to food versus non-food items. Your participation will be greatly appreciated!
- Genetics and Behavior: Compulsive Behavior in Prader-Willi Syndrome Researchers at the University of Kansas Medical Center and the Division of Genetics and Molecular Medicine at Children’s Mercy Hospital have embarked on a study to better understand compulsive behavior in individuals with Prader‑Willi syndrome (PWS).
- Research On Behavior And Development In Prader-Willi Syndrome - Dr. Elisabeth Dykens. Seeking persons with Prader-Willi syndrome aged 4 years through adulthood, and their families to come participate at the Kennedy Center at Vanderbilt University in Nashville, TN.
- Understanding childhood obesity and specifically, the mechanism of development of obesity -Andrea Haqq, MD, pediatric endocrinologist at Duke University Medical Center is conducting a study and needs your help.
- Summary of work being funded by the Foundation for Prader-Willi Research
