Basis for and Nutritional Replacement Therapy€¦ · Trace Minerals Intern./Blaurock-Busch...
Transcript of Basis for and Nutritional Replacement Therapy€¦ · Trace Minerals Intern./Blaurock-Busch...
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Biomonitoring of Metal Intoxication
Basis for
successful Detoxification
and Nutritional Replacement Therapy
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What we need to know about
metal testing
Each test reflects a specific biochemical pathway
No test tells all No test is ‘the best’
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I. Blood Mineral Analysis
Blood is transport medium for nutrient and toxic metals to and from cells
Blood values reflect mineral concentration in circulating blood stream
Note - use metal-free vacutainers
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1. Intake and Circulation
Every element has its own unique distribution in body fluids, tissues and organs
Concentrations fluctuate throughout the day in body fluids, and over longer periods in solid body tissues
Acute exposures have different effects than exposures over longer periods
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Specifics of Blood Minerals Analysis
Allows detection of immediate and acute Toxic Metal exposure within maximal 72hrs after exposure.
Thereafter, metals have been deposited in target storage tissue or have been elimated
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What type of blood for mineral analysis?
Whole blood reflects extra- and intracellular levels
95% of cadmium is bound to erythrocytes- thus whole blood analysis recommended
For heavy metal evaluation use special, metal-free tubes
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Sikorski R, Paszkowski T, Slawinski P, Szkoda J, Zmudzki J, Skawinski S.
The intrapartum content of toxic metals in maternal blood and umbilical cord
blood.PMID: 2806969 [PubMed - indexed for MEDLINE]
Cadmium and mercury levels measured on both sides of placenta did not differ significantly while lead levels in maternal blood were significantly higher than its cord blood values. In all three metals studied, the concentrations in maternal blood strongly correlated with the corresponding cord blood values. A significant, positive correlation was established between the parity of the examined women and the umbilical cord blood contents of lead and mercury. The obtained results support the opinion that human placenta does not form an effective barrier to toxic metal intake by the fetus.
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Cd und Hg in Blut und Urin deutscher Kinder 1990-1992 Quelle: Schulz,Becker. Bundesumweltamt
Parameter Deutschland West Ost
N GM N GM N GM
Cadmium in blood (µg/l) 713 0.14 512 0.13 201 0.17 ***
Cadmium in urine (µg/l) 732 0.09 525 0.077 208 0.12 ***
Mercury in blood (µg/l) 712 0.33 509 0.26 202 0.59 ***
Mercury in urine (µg/l) 732 0.54 525 0.43 208 0.99 ***
Mercury in urine (µg/g Crea) 731 0.39 524 0.31 208 0.69 ***
N= Testpersonen GM = Geometric mean
*** statistisch signifikanter Unterschied (P 0.001)
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Blood evaluation Rumanian school children 95percentile 3µg/l CDC Ref.Range <1µg/l
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Hongkong children: average level 14µg/l
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II: Urine Metal Analysis (UMA)
• Assessment of renal clearance of essential and toxic elements
• Monitors chelation efficacy (not all chelated patients are able (genetically or otherwise) to detoxify
• Allows physician to ‚individualize‘ chelation therapy
• Provides ‚proof‘ of treatment progress
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TMI Logic for Reference Ranges
TMI Baseline urine evaluation of 120healthy people plus <300 patients with no signs of metal toxicity
Present evaluation in progreess at TMI:
typical mean value for each chelating agent
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Sampling before Provocation
Collect 10ml of first morning urine. Best to urinate directly in cup or tube to prevent contamination
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Post Urine collection
Patient must empty bladder before start of treatment
After treatment has started, collect for 2 to 6 hr – depending on chelating agent used
Fluid intake (2-3 cups) should be constant
Food intake: best to stay fasting
Do not take supplements or algae during chelation
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Lead and Arsenic in Algae products
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Evaluation of mean Urine creatinine (g/L)
in pre and post urines of children and adults
# of tested persons:
Baseline urines:
N = 977 adults
N = 355 children
Post urines:
N = 4018 adults
N = 101 children 0
0.2
0.4
0.6
0.8
1
1.2
pre post
children <12
adults
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Limitations of 24-hr urine collection
Main problem:
Patient compliance
Factors influencing urine excretion results
Food and drink (coffee, tea)
Smoking or smoke exposure
Medication
Cosmetics
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III. Hair Mineral Analysis
Internationally researched at recognized universities and institutions
Largely Misunderstood
Often Misrepresented
Instruments do not know how to
differentiate between specimen.
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Hair sample preparation –
Key to reliable results
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Hair is Body Tissue
Hair follicle receives nutrients and toxins from circulating blood
What has been stored will remain ‚locked‘ in this inert tissue and thus hair can be stored indefinitely. In fact, hair has been used as an ideal forensic tissue for decades
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Hair mineral analysis provides a record of past exposure or nutritional inadequacies reflecting the specific growth period (i.e. Hair growth is 1mm/day or 3cm/months. If taken close to scalp now, we evaluate the mineral exposure of last month)
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Al -Aluminum MTM Study 1997-98 N=10000 random collection
0-6 7-
1415-
2122-
3031-
4041-
5051
and
up
Germany
United States
Brazil
0.0%
10.0%
20.0%
30.0%
40.0%
50.0%
60.0%
70.0%
80.0%
% o
f p
ati
en
ts s
ho
win
g h
igh
va
lue
s
Germany
United States
Brazil
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Mercury Distribution in Body Tissues
0
0,5
1
1,5
2
2,5
3
3,5
4
4,5
Bon
e
Brain
Skin
Hair
Mus
cle
Hea
rt
Colon
Live
r
Kidne
ys
Source: Thomas L. Labor & Diagnose, Med.Verlag pg 430
mc
g/k
g
Mercury
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Physiological Distribution of Lead in Human Tissue
0
10
20
30
40
Bon
e
Brain
Skin
Hair
Mus
cle
Heart
Colon
Live
r
Kidne
ys
Source: Thomas L., Labor & Diagnose, Med.Verlag
Marburg
mcg/k
g
Lead
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Pb - Lead - Chumbo - Blei
0-6 7-14 15-21 22-30 31-40 41-50 51 and up
Germany
United States
Brazil
0
1
2
3
4
5
6
7
8
9
Av
era
ge
Le
ve
l (p
pm
)
Germany
United States
Brazil
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Case of Oliver Sch.
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What about problem patients?
Consideration:
Reduce toxic exposure (lifestyle changes etc)
Evaluate nutritional status (and supplement accordingly)
Evaluate toxic status (hair analysis)
Change chelating agent or combine chelating agents
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Enzyme systems needed for
detoxification
Glutathione –S-TransferaseM1 (GSTM1)
Glutathione –S-Transferase T1 (GSTT1)
Glutathione –S-Transferase P1 (GSTP1)
Superoxide dismutase 2 (SODs)
Manganese and/or Copper-dependant for functioning
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GSTM1 deletion genotype-
common in Asians
Groups such as Pacific Islanders and Malaysians have a reported frequency of no enzyme activity of 62%-100% .
Other Asian populations have high-reported frequencies of the deletion genotype ranging from 48%-50% for Japanese and 35%-63% for Chinese.
A population-based study conducted among Chinese reported a frequency of 51% for the GSTM1 deletion genotype.
Two Korean case-control studies found frequencies of 53% and 56% for the GSTM1 deletion genotype
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Genetic testing
once in a lifetime
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Why testing?
Individuals with homozygous deletions of either the GSTM1 or the GSTT1 locus have no enzymatic functional activity of the respective enzyme.
This population has to be made aware of lifestyle risks
Chelation treatment is more often needed then by those who do have proper enzyme function
Greater nutritional support is needed
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Presence of GSTM1 0/0 Polymorphisms at
certain diseases
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Summary:
Diagnostic Screening for difficult cases
1. Metal screening -hair and/or blood
2. Detoxification treatment with chelator of choice, depending on metal exposure
including pre and post urine
3. If insignificant metal excretion, resume treatment
using different chelating agent and/or use combination of chelating agents. Record doses used. and repeat post urine (pre not necessary)
4. Consider genetic test panel GSTM1, GSTT1, GSTP1 and SODs
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Thank you!