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Betreff: Essex Study |
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Von: Mast Sanity |
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Datum: Tue, 24 Jul 2007 22:49:01 +0100 |
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Dr George Carlo has released the following comments as his reaction to theEssex EHS study in absence of the results findings: He has suggested that we circulate these comments widely prior to the releaseof the study at 10.30am in London, UK on 25.7.07. 'The following comments relate to the interpretation of the results of theEssex study.1. Based on what we have learned from our clinical experiences and thesymptoms reported by patients in our registry, a key to the integrity of theEssex study is in how a 'sensitive' person was defined at the outset. Webelieve that the pathology of these sensitivities is cell membrane based,but that the same pathology is present in conditions including multiplechemical sensitivities, alcoholism, drug addiction, and neuro-behavioralsyndromes like ADHD and Autism. In addition, there appears to be a familialpredisposition component that involves inability to clear metals from thesystem through methylation and an inability to adapt to oxidative stress. Thus, the definition of patients selected in the Essex study is a keypoint. And, in the analyses, it would be important to categorize thepatients on the severity scale in terms of these other conditions that havesimilar underlying pathology. The point is that there is a continuum we areseeing in terms of severity of effects, and the level of hypersensitivity tothe various types of EMR also scales along that continuum. Thus, withouteither controlling for these other conditions statistically or throughsubject category restriction, it is likely that associations that arepresent would not be identified.....false negative findings because ofimprecision in the measurement of the dependent variables. That is one ofthe main difficulty with the majority of provocation studies that have beendone. Measurement imprecision and bias toward the null.2. The other key is that depending on the severity of thehypersensitivity...and that in large part is related to the points raisedabove....different EMR effect windows will have varying effects on thepersons being provoked with EMR. Thus, the EMR that is used in the exposurescenario needs to be precisely defined as well. We know, for example, thatELF operates through a field intensity dependent mechanism that exertsdirect magnetic effect on tissue (including disruption of gap-junctionintercellular communication) and thus the ensuing pathology. But there is athreshold for ELF effects. RF has two different pathology mechanismcomponents: raw microwaves or RFR act through thermal mechanisms dependenton field intensity -- there is a thermal effects threshold; microwaves thatcarry information from wireless devices act through a biological mechanismthat is triggered as a protective cellular response -- for this response,there is no threshold. Thus, in the Essex study, the provocation exposureswould have needed to be defined along these effect windows, otherwise thereis a likely bias also toward false negative findings because of the lack ofprecison in the measurement of the independent variables. For example, fromwhat they define, the question of base station 'on or off' is key. For theeffect windows of ELF and raw microwaves, 'on or off' would have an effectif there was adequate field intensity to provoke the mechanistic pathways --in other words to go above the threshold. However, for the informationcarrying radio waves, there would have to be talking on the signal or therewould be no biological protective pathway triggered. It is the modulationassociated with the carried information that we now know triggers thenon-thermal effect pathways. So, without talking on the signal,the biological pathway would not be triggered. The result in the studywould be a false-negative finding.3. Overall, the electrohypersensitivity response is dependent then on theseverity of the patients cellular pathology -- and that from all sourcesincluding the conditions detailed in Number 1 above. The observed responseis also dependent on the mechanism that the EMR exposure provocation likelywill act through. At this point, we don't believe that a precise enoughdefinition of the conditions in the patients recruited to allow for propercontrolling. We don't believe that the exposure provocations were definedwell enough in terms of EMR effect windows and the likely pathologicalpathways triggered by the provocations. Because of the imprecision in the measurements in the Essex study, anyfindings showing 'no effect' are likely false negative or the result of thestudy not being able to pick up the real underlying pathology. Any findingshowing an 'effect' is likely an underestimation of the actual effectbecause the study is biased toward the null or 'no effect' finding.'___________________Dr. George L. CarloScience and Public Policy Institute1101 Pennsylvania Ave. NW -- 7th FloorWashington, D.C. 20004www.sppionline.org
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