Robert J. Thiel, Ph.D., N.M.D.
American Naturopathic Medical Association Monitor, Vol. 7, No. 1
  Reprinted with the permission of the author

Abstract

There is no standard medical treatment for Down syndrome (trisomy 21). However nutritional therapy has been used to a limited degree for this population since Turkel pioneered it in 1940. In the 1980s, Warner modified Turkel's approach and continues to innovate. Others, such as Lawrence, Leichtman, and Thiel, have built on the foundation laid by Turkel and Warner. Although the use of nutrition is not considered as standard therapy by most in the medical community, this may be because practitioners have not sufficiently reviewed the literature which supports nutritional approaches as well as the fact that results are sometimes inconsistent. This paper points out some of the nutrients which may be different in the Down syndrome population such as vitamins A, B1, B6, B8, B12, C, D, and E; minerals such as calcium, copper, iron, magnesium, manganese, selenium, and zinc; and amino acids and other substances such as carnitine, carnosine, choline, cysteine, dimethylglycine, inositol, omega 6 fatty acids, phenylalanine, serine, superoxide-dismutase, and tryptophan. In addition, it reports that height and various aspects of facial appearance seem to improve for children with Down syndrome who try nutritional therapy. This paper also provides some rationale for why food nutrients are preferred for this population.

Introduction

Trisomy 21, more commonly referred to as Down syndrome (DS), is a genetic disorder which is present in approximately 1 out of every 700 live births. It results in three number 21 chromosomes, as opposed to the normal two [1]. "The diagnostic clinical features of this condition are usually readily evident, even at birth. The flat facial profile, oblique palpebral fissures... Down syndrome is a leading cause of mental retardation. The mental retardation is severe... Virtually all patients with trisomy 21 older than 40 years of age develop neuropathologic changes characteristic of Alzheimer's disease, a degenerative disorder of the brain. Patients with Down syndrome have abnormal immune responses that predispose them to serious infections, particularly of the lungs, and to thyroid autoimmunity" [1]. Down's patients tend to be short since at age 18 the median average female with Down Syndrome grows to approximately 4' 9½", and the average male grows to approximately 5' ½" [2]. "These patients also have immune defects and an increased susceptibility to leukemia... Essentially nothing is known about how one extra chromosome 21 could have such profound effects" [3].
While there is no effective medical intervention for trisomy 21, there are treatments for complications such as cardiovascular disorders, hypothyroidism, and infections. Though some recommend nutrition as part of a program for those with trisomy disorders therapy (sometimes referred to as orthomolecular medicine), the prevalent medical opinion appears to be that nutritional is ineffective [4,5].
In 1940, Dr. Henry Turkel (M.D.) began experimenting with nutrition for Down syndrome [4]. Due to problems with the US FDA, he ended up basically being confined to practicing only in Michigan (as well as Japan). In the mid 1970s, Dr. F. Jack Warner (M.D.) began to communicate with Turkel. In a meeting in California in 1984, Turkel asked Warner to take over his work. Since that time, Warner began to specialize in seeing patients with trisomy 21. Warner has probably seen more people with Down syndrome than any doctor currently living. The mother of one of his patients, Dixie Lawrence, did additional research and developed another formula, originally similar to that which Warner uses, but without iron and L-glutamine, but including certain amino acids. Dr. Lawrence Leichtman (M.D.), with others (including Lawrence), has been working to modify/expand Lawrence's formula. This researcher (Thiel) has made modifications to previous approaches by attempting to better individualize nutritional therapy for those with Down syndrome, advocating more natural vitamins/minerals, supporting suspected hypothyroidism nutritionally, and correlating some of the nutritional connections between Down syndrome and epilepsy [6,7]. This paper discusses some nutrients used in nutritional therapy and some of the results that Warner has attained. The clinical portion of this paper was pre-approved by a review board of the American Naturopathic Medical Association.

Selected Nutrients

There are any number of nutrients which could be looked into; those shown below are some of those thought to be of interest for this paper.
Vitamin A
Based on a review of several published studies, Baer et al concluded, "Serum vitamin A levels have been reported to be lower in individuals with Down syndrome... possibly due to malabsorption... However other workers have failed to confirm these findings" [8]; it appears that beta-carotene levels may be high [8]. It has been speculated that the alteration of the conjunctival epithelium in patients with Down syndrome may be due to altered metabolism of vitamin A [9]. A five month study involving 23 children with Down syndrome tested supplementation with vitamin A and concluded that it significantly reduced the incidence of infection and improved plasma vitamin A levels [10].
Vitamin B1 (Thiamin)
A blood study of 90 children up to 16 years old with Down syndrome found that marginal thiamin deficiency seemed to exist in this population at higher rates than the general public [11]. A smaller study found that non-institutionalized children with Down syndrome tended to consume thiamin below the recommended daily allowance [12].
Vitamin B6
It appears that vitamin B6 metabolism may be abnormal in those with Down syndrome [13-14]. A three year double-blind placebo controlled longitudinal study involving those with Down syndrome found that vitamin B6 supplementation helped normalize brain function by reducing elevated cortical auditory evoked potentials to a more normal level [15].
Folate (once known as vitamin B8)
Children with Down syndrome often have below normal levels of folate [16-18]. Erythrocyte macrocytotis is more common in children and adults with Down syndrome and may be due to an alteration of the folate remethylation pathway [16]. As those with Down syndrome age, further declines in folate levels seem to occur [19].
Vitamin B12
Some reports suggest that serum vitamin B12 levels are reduced for those with Down syndrome [20] while others have not found that [16].
Vitamin C
One study found that many children with Down syndrome had a deficiency of vitamin C according to serum tests which correlated to dietary intakes [21]. A case report [22] found the same result, yet a small study [12] found that institutionalized children with Down syndrome tended to consume more vitamin C than the recommended daily allowance.
Vitamin D
Disorders of vitamin D metabolism have also been speculated for Down's patients [4,23]. Not only have poor dietary intakes of vitamin D been found in those with Down syndrome [24], low levels have been found even in cases of high exposure to sunlight [23].
Vitamin E
A recent study found that children with Down syndrome have significantly less vitamin E levels than those without it [25]. Down syndrome patients with dementia appear to have lower plasma levels of vitamin E than those that do not [26].
Calcium
Turkel & Nusbaum speculated that those with Down syndrome often have disorders of calcium metabolism [4]. A small study found that children with Down syndrome tended to consume more calcium than the recommended daily allowance [12]. Decreased intracellular calcium levels have been found in those with Down syndrome [27]. Decreased hair levels of calcium have also been noted in the Down syndrome population [28].
Copper
Down syndrome patients have often been found to have elevated levels of copper. These elevations have been found in erythrocytes, neutrophils, platelets, and serum [26,29-31]. Interestingly, one study found normal copper levels in those with Down syndrome who had poor dietary intakes of copper [24], which may suggest that some metabolic disturbance increases copper retention in this population.
Iron
Anneren et al found that median levels of iron in erythrocytes and neutrophils were significantly lower in those with Down syndrome than in controls without it [31]. A small study found that children with Down syndrome tended to consume less iron than the recommended daily allowance [12].
Magnesium
One study found that magnesium levels in erythrocytes and thrombocytes, but not neutrophils were lower in children with Down syndrome [31]. Another found lower red blood cell levels of magnesium lower in the Down's group as compared to the non-Down's group [32].
Manganese
One study found that manganese levels in erythrocytes and thrombocytes were lower in children with Down's [31]. Another study found that hair levels of manganese seems to be lower in those with Down syndrome [33].
Selenium
Down's patients may have below normal plasma levels of selenium (31,32,34,35). As selenium does affect thyroid metabolism by helping convert T4 to T3 [36], it is possible that supplementing with it would have some benefit. Hamilton reports that one study found that supplementation with selenium reduced (by 50%) elevated mononuclear cell copper content in Down syndrome [35].
Zinc
Several reports suggest that Down's patients have below normal plasma levels of zinc [29,30,34,35,37]. Stabile et al. found that supplementation with zinc has been shown to increase DNA synthesis in Down's patients with low zinc levels [38]. A study by Bucci et al found that zinc reduced TSH by 34% for hypothyroid Down syndrome patients [39]. In addition, it has been found that children with Down syndrome become deficient in a zinc-containing insulin-like growth factor type 1 (IGF-1) after one year of age [40]. Even though zinc is a constituent in cytoplasmic superoxide dismutase, zinc supplementation was reported by Abdalla & Samman to reduce superoxide dismutase levels in non-Down's female subjects [41].
Carnitine
Deficient blood levels of carnitine are much more common in children with Down syndrome than in children without it [26].
Carnosine
No studies on carnosine levels have been found for this population.
Choline
Down syndrome is associated with a presynaptic cortical cholinergic deficit involving an extensive loss of choline acetyltransferase [42]. A case report showed that the EEG pattern of a 2½ year with DS improved after phosphatidyl choline supplementation [43].
Cysteine
People with Down syndrome have been found to have abnormally high levels of cysteine [44]. As an attempt to compensate, this may be why abnormally high levels of cathepsin S (a lysosomal cysteine protease) have been found, post-mortem, in those with Down's and Alzheimer's [45].
Dimethylglycine/Trimethylglycine
Dimethylglycine (DMG) is a precursor of glycine, which is a neuroinhibitory amino acid [46]. "Children with Down syndrome usually have particular difficulties with, and delays in, language development" [47]. Warner believes that DMG can improve speech and affect behavior for Down syndrome patients [48]. Leichtman, however, told this researcher that he prefers trimethylglycine (TMG) to DMG for those with Down syndrome. Rimland told this researcher that although TMG has certain theoretical advantages over DMG, that he felt that it seemed that, to date, DMG was still better clinically.
Inositol
People with Down syndrome tend to have abnormally high levels of myo-inositol [49-51]. This has also been confirmed in animal models [52].
Omega-6 Fatty Acids
Hamilton reported that long-chain omega-6 polyunsaturated fatty acid concentrations appear to be higher in Down syndrome patients [53].
Phenylalanine
Excess phenylalanine is often present in those with Down's [54]. There seems to be a difficulty in converting phenylalanine into tyrosine in Down's, probably because the activity of phenylalanine hydroxylase is impaired in the liver of those with Down syndrome [55].
Serine
One study found a significant plasma deficit of serine for those with Down syndrome compared those with non-Down's mental retardation [44].
Superoxide Dismutase
It is well recognized that superoxide dismutase levels are abnormally high in those with Down syndrome [8,32,41,56].
Tryptophan
"There appears to be an abnormality of tryptophan metabolism in Down's syndrome" [14,26]. Infants with Down syndrome have been shown to improve muscle tone by taking tryptophan supplementation [57].

Results

Dr. F. Jack Warner (M.D.) employs primarily nutritional therapy for children with DS. Warner's protocol includes a multivitamin/mineral/glandular supplement, flaxseed oil, dimethylglycine, and sometimes selected herbs and amino acids. This researcher conducted an investigation of a randomly-selected sample of Warner's Down syndrome patient files. Height, weight, facial swelling, nose bridge development, and epicanthal eye fold was examined. The brief results are shown in the tables below (study details are part of two papers [58-59]):

Table 1 Height
Gender    N    Attribute  Initial Mean Final Mean
 as Percentile on Down's Grid 
Female 36 Height 63.1% 73.6%
Male 48 Height 63.6% 77.8%
Total 84 Height 63.4% 76.0%

Table 2 Weight
Gender    N    Attribute  Initial Mean Final Mean
 as Percentile on Down's Grid 
Female 40 Weight 60.9% 59.3%
Male 50 Weight 45.2% 53.7%
Total 90 Weight 52.2% 56.2%

For facial appearance, a comparison was made of before and after photographs in Warner's files. A ten point scale was developed with zero signifying normal for children without Down syndrome and to a maximum of ten signifying an appearance consistent with the more pronounced presentation of this feature. For example, a lack of any noticeable (or completely flat) nose bridge would receive a score of 10, whereas a completely normal appearing nose bridge would receive a score of zero. Some data was excluded if it was unclear from the photographs.

Table 3 Facial Swelling (excessive = 10)
Gender    N   Attibute  Initial Mean   Final Mean  Percent
 Improvement 
on 10 Point Scale
Female 39   Facial Swelling   5.9 4.2 28.8%
Male 46 Facial Swelling 6.6 2.8 57.6%
Total 85 Facial Swelling 6.3 3.4 46.0%

Table 4 Nose Bridge (lack of = 10)
Gender    N   Attibute  Initial Mean   Final Mean  Percent
 Improvement 
on 10 Point Scale
Female 37   Nose Bridge   7.8 5.1 34.6%
Male 45 Nose Bridge 7.5 5.2 30.7%
Total 82 Nose Bridge 7.6 5.1 32.9%

Table 5 Epicanthal Fold (highly discernible = 10)
Gender    N   Attibute  Initial Mean   Final Mean  Percent
 Improvement 
on 10 Point Scale
Female 38   Epicanthal Fold   5.4 3.8 29.6%
Male 43 Epicanthal Fold 6.1 4.0 34.4%
Total 81 Epicanthal Fold 5.8 3.9 32.8%

Discussion

In spite of apparent nutritional differences and clinical results, the use of nutritional therapy for persons with Down syndrome has been repeatedly challenged [5,60,61]. However, even some mainstream researchers have recommended vitamin and mineral supplementation for those with Down syndrome [62,63]. Early work, done by Turkel [4] as well as a study by Harrell et al [64] concluded that nutritional intervention did raise intelligence of persons with Down syndrome. Others, including the American Academy of Pediatrics, have criticized these researchers and have concluded that nutritional interventions are not effective [5,59,65]. Yet, Dr. Bernard Rimland (Ph.D.) investigated the work of some of the critics and found that they do not in fact properly duplicate with the Turkel or Harrell work; furthermore Rimland has written that the position of the American Academy of Pediatrics is "inaccurate, biased, and inept" [66]. Turkel, Warner, and others have shown before and after photographs to demonstrate that nutritional therapy can improve the appearance of those with Down syndrome [4,48]. This researcher, as shown above, has found that height, as well as facial features, appear to respond to nutritional therapy, specifically the Warner protocol [58,59]. Napolitano et al found that zinc supplementation increased growth in 15 of 22 children with Down syndrome [40].
Why might nutritional therapy play a role? Aside from the obvious nutritional differences previously mentioned in this paper, there are several possible reasons.
Down syndrome patients have increased incident of thyroid disorders [1,67,68]. Most nutritional interventions for it contain iodine which has been shown to be helpful for some thyroid problems [69] as well as the amino acid tyrosine (the primary thyroid hormone is composed of iodine and tyrosine [70]) and the minerals zinc and selenium. Bucci speculated that zinc deficiency may be one cause of subclinical hypothyroidism in children with Down syndrome [39], while a study by Kanavin et al found that thyroid hypofunction in Down syndrome appeared to be partially related to low selenium levels [71]. Feeding the thyroid through nutrition, instead of treating it through medications, seems to make clinical sense when dealing with this population [6].
Phenylketonuria, which can also cause mental retardation, is caused by a deficiency of hepatic phenylalanine hydroxylase and reduces the conversion of phenylalanine into tyrosine, and is often controlled by reducing consumption of high phenylalanine foods [72]; there is a case report where a improvements were noted in a Down's patient who went on a low phenylalanine diet [73]. Since those with Down's tend to have a problem converting phenylalanine into tyrosine [55], it is possible that DYRK (dual-specificity tyrosine-regulated kinase) may have some involvement. DYRK1A, which is located in the Down syndrome critical region of chromosome 21, catalyzes tyrosine directed autophosphorylation as well as the phosphorylation of serine residues—it is suspected that DYRK1A may be involved in causing mental retardation in Down syndrome [74,75]. It should be added that DYRK1A only affects certain tyrosine forms [76]. DYRK1A may not have anything to do directly with the development of hypothyroidism or any other specific tyrosine abnormality currently recognized as being part of Down syndrome, but its impact does show that there are metabolic differences in Down syndrome that affect nutrients somewhat differently than occur in the non-Down's population.
Oxygen radical-induced damage appears to be important in Down's, Alzheimer's, and other illnesses with a neuropsychiatric components [56,77]. Biomarkers of oxidative stress have been found to be significantly elevated in patients with Down syndrome [78,79]. Warner has clinical findings which support his position that ingestion of antioxidant nutrients have the effect of lowering the DS person's body's excessive levels of superoxide dismutase [79]—others involved with natural health have suggested that antioxidant nutrients such as vitamin C, beta carotene, flavonoids, zinc, selenium, and vitamin E may reduce free radical damage and possibly slow the accelerated aging associated with DS [77,80]. Some believe that the impaired viability of Down syndrome neurons can be amended by antioxidants, such as vitamin E [78].
Since vitamin C as found in foods can have 3.2 times the antioxidant of ascorbic acid [81], selenium in foods can have 17.6 times the antioxidant effect of seleniomethionine [82], and natural vitamin E can have 4.0 times the free radical scavenging strength than synthetic vitamin E [83], it appears that food nutrients may be the most helpful type for this population. Also, because most food vitamins and food minerals are better absorbed and/or retained by the body [81-88], food vitamins and food minerals are the preferable form for this population for more than just antioxidant reasons [84-86].
Furthermore, an in vitro study concluded that food vitamin C had negative ORP (oxidative reductive potential), whereas regular ascorbic acid had positive ORP (negative ORP is much better as it helps 'clean up' oxidative damage, whereas items with positive ORP do not) [87]. It may be of interest to note that it has been written, "that an 'overdose' of natural food complex {vitamins} is not harmful, whereas an overdose of a chemically pure vitamin or other isolated 'nutrient' can be. Science is beginning to concur" [86].
Accelerated brain glycation (and the resulting brain damage) occurs early in the life of those with Down syndrome [89] and probably leads to dementia. Carnosine is an antiglycation agent [90,91] that might prove helpful. Since selenium rich yeast has been shown to have 123.01 times the antiglycation effect as sodium selenite for diabetics [88] and food vitamin C has greater antiglycation effects than ascorbic acid [84,88], this is another reason that food nutrients may be the preferred form to use when Down syndrome is present.
Carnosine is also an efficient chelating agent for copper [92] which is of interest as many with DS have abnormally high copper levels [26,29,30]. Carnosine and related compounds such as homocarnosine have been found to have protective effects against hydrogen peroxide-mediated Cu,Zn-superoxide dismutase fragmentation [93] and Cu,Zn-superoxide mutants [94].
Supplementation with acetyl-l-carnitine has been shown to improve memory and attention in patients with Down syndrome [95]. N,n-dimethylglycine (DMG), an amino acid derivative, is naturally found in the human body and supports transmethylation processes [96]. There is a report of a Korean study which used DMG for autistic children which found that it improved verbal communications and behavior, while a report of a Taiwanese study suggests that DMG reduced lethargy in autistic children, but did not improve speech [97]—Warner has found that it does improve speech in those with Down syndrome [48].
Down children are especially prone to bacterial respiratory infections [1]. One study found that supplementation with selenium rich yeast tablets significantly stimulated serum concentrations of IgG2 and IgG4 antibodies (which are frequently low in Down syndrome patients) [34]. IgG2 is known to be directed against the bacterial polysaccharide antigens of encapsulated bacteria such as streptococcus pneumoniae and hemophilus influenza [34]. An Italian study, however, found that low levels of vitamin C consumption was correlated with increased infection rates for children with Down syndrome [21]. Warner reports a reduced incidence of infections for those undergoing his treatment [48].
Dietary restrictions may also be advisable. A study involving Dutch children with Down syndrome concluded that those children were more prone to have celiac disease than other Dutch children, but not more likely to have a cow's milk intolerance [98]. Celiac disease seems to increase IgA and IgG in Down's patients [99,100]. A German study concluded that children with Down syndrome had higher bovine serum albumin antibody levels than others [101]. Warner, Thiel, and Leichtman often advise against the consumption of cow's milk for those with Down syndrome, but Turkel did not.

Conclusion

Whether or not specifically due to the presence of a third 21st chromosome, metabolic disturbances are involved with Down syndrome. The nutritional profiles of the Down syndrome population do in certain significant ways, differ from those of the general public. Various signs and symptoms associated with Down syndrome have been reported to improve when certain nutritional protocols have been tried (which is of profound interest as there is no accepted medical treatment currently in existence for Down syndrome). Nutritional therapy has safely been treating people with Down syndrome for over sixty years. Nutrition, especially involving food nutrients, is a logical therapy to consider when Down syndrome is present.

References

[1] Cotran RS, Kumar V, Collins T. Pathologic Basis of Disease, 6th ed. WB Saunders, Phil., 1999
[2] Van Dyke DC, Lang DJ, Heide F, van Duyne S, Soucek MJ, editors. Standardized anthropometric techniques. In Clinical Perspectives in the Management of Down Syndrome. Springer-Verlag, NY, 1990:230-237
[3] Kissane JM. Anderson's Pathology, 9th ed. CV Mosby Co., St. Louis, 1990
[4] Turkel H, Nusbaum I. Medical Treatment of Down Syndrome and Genetic Diseases, 4th ed. Ubiotica, Southfield (MI), 1985
[5] Sacks BI, Buckley RF. Multi-nutrient formulas and other substances as therapies for Down syndrome: an overview. Down Syndrome News and Update 1(2):70-83, 1998
[6] Cohen B, Thiel RJ. What to do about borderline elevated TSH levels? Presentation at the Down Syndrome Medical Interest Group, San Diego, July 8, 2001
[7] Thiel RJ, Fowkes SW. Down syndrome and epilepsy: A nutritional connection? Accepted for review, Medical Hypotheses, December 2002
[8] Baer MT, Waldron J, Gumm H, Van Dyke DC, Chang H. Nutrition assessment of the child with Down syndrome. In Clinical Perspectives in the Management of Down Syndrome. Springer-Verlag, NY, 1990:107-125
[9] Filippello M, Cascone G, Zagami A, Scimone G. Impression cytology in Down's syndrome. Br J Opthalmol,1997;81(8):683-685
[10] Palmer S. Influence of vitamin A nutriture on the immune response: findings in children with Down's syndrome. Int J Vitam Nutr Res 1978;48(2):188-216
[11] Schmid F, Christeller S, Rehm W. Studies on the state of vitamins B1, B2 and B6 in Down's syndrome. Fortschr Med 1975;93(25):1170-1172
[12] Chad K, Jobling A, Frail H. Metabolic rate: a factor of developing obesity in children with Down syndrome? Am J Ment Retard 1990;95(2):228-235
[13] McCoy EE, Columbini C, Ebadi M. The metabolism in vitamin B6 in Down's syndrome. Ann NY Scie 1969;166(1):116-125
[14] Tu JB, Zellweger H. Blood serotinin deficiency in Down's syndrome. Lancet 1965;2(415):715-716
[15] Frager J, Barnet A, Weiss I, Coleman M. A double blind study of vitamin B6 in Down's syndrome infants. J Ment Def Res 1985;29(Pt3):241-246
[16] David O, Fiorucci GC, Tosi MT, Altare F, Valori A, Saracco P, Asinardi P, Ramenghi U, Gabutti V. Hematological studies in children with Down syndrome. Pediatr Hematol Oncol 1996;13(3):271-275
[17] Ibarra B, Rivas F, Medina C, Franco ME, Romero-Garcia F, Enrique C, Galarza M, Hernandez-Cordova A, Hernandez T. Hematological and biochemical studies in children with Down syndrome. Ann Genet 1990;33(2):84-87
[18] Wachtel TJ, Pueschel SM. Macrocytosis in Down syndrome. Am J Ment Retard 1991;95(4):417-420
[19] Gericke GS, Hesseling PB, Birnk S, Tiedt FC. Leukocyte ultrastructure and folate metabolism in Down's syndrome. S Afr Med J 1977;51(12):369-374
[20] Hestnes A, Stovner LJ, Husoy O, Folling I, Fougner KJ, Sjaastad O. Hormonal and biochemical studies in children with Down's syndrome. J Ment Defic Res 1991;35 (Pt 3):179-193
[21] Colombo MI, Girdardo E, Incarbone E, Conti R, Ricci BM, Maina D. Vitamin C in children with trisomy 21. Minerva Pediatr,1989;41(4):189-192
[22] Hilty N, Sepp N, Rammal E, Pechlaner C, Hintner H, Fritsch P. Scurvy in trisomy 21. Hautarzt 1991;42(7):464-466
[23] Center J, Beange H, McElduff A. People with mental retardation have an increased prevalence of osteoporosis. Am J Ment Retard,1998;103(1):19-28
[24] Molteno C, Smit I, Mills J, Huskisson J. Nutritional status of patients in a long-stay hospital for people with mental handicap. S Afr Med J 2000;90(11):1135-1140
[25] Cengiz M, Seven M. Vitamin and mineral status in Down syndrome. Trace Elem Elec 2000;17(3):156-160
[26] Werbach M. Down syndrome. In Textbook of Nutritional Medicine. Third Line Press, Tarzana (CA), 1999:340-348
[27] McCoy EE, Sneddon JM. Decreased calcium content and 45Ca2+ uptake in Down's syndrome blood platelets. Pediatr Res 1984;18(9):914-916
[28] Barlow PJ, Sylvestrer PE, Dickerson JW. Hair trace metal levels in Down syndrome patients. J Ment Def Res 1981;25(Pt 3):161-168
[29] Purice M, Maximillan C, Dumitru I, Ioan D. Zinc and copper in plasma and erythrocytes of Down's syndrome children. Endocrinologie 1988;26(2):113-117
[30] Kadrobova J, Madaric A, Sustrova M, Ginter E. Changed serum element profile in Down's syndrome. Biol Trace Elem Res 1996;54(3):201-206
[31] Anneren G, Johansson E, Lindu U. Trace element profiles in individual blood cells from patients with Down's syndrome. Acta Paediatr Scand 1985;74(2):259-263
[32] Monteiro CP, Varela A, Pinto M, Neves J, Felisberto GM, Vaz C, Bicho MP, Laires MJ. Effects of an aerobic training program on magnesium, trace elements and antioxidant systems in Down syndrome population. Magnes Res 1997;10(1):65-71
[33] Barlow PJ, Sylvestrer PE, Dickerson JW. Hair trace metal levels in Down syndrome patients. J Ment Def Res 1981;25(Pt 3):161-168
[34] Anneren G, Magnusson CG, Nordvall SL. Increase in serum concentrations of IgG2 and IgG4 by selenium supplementation in children with Down's syndrome. Arch Dis Child 1990;65(12):1353-1355
[35] Hamilton K. Down's syndrome: selenium supplementation and trace elements. CP Currents 1994;4(3):46
[36] Kralik A, et al. Influence of zinc and selenium deficiency on parameters related to thyroid metabolism. Hormone Metabol Res 1996;28:223-226
[37] Sherman AR. Zinc, copper and iron nutriture and immunity. J Nutr,1992;122:604-609
[38] Stabile A, et al. Immunodeficiency and plasma zinc levels in children with Down's syndrome: a long-term follow-up of oral zinc supplementation. Clin Immunolog Immunopath, 1991;58:207:216
[39] Bucci I, Napolitano G, Giuliani C, Lio S, Minnucci A, Di Giacomo F, Calabrese G, Sabatino G, Palka G, Monocao F. Zinc sulphate supplementation improves thyroid hypofunction in hypozincemic Down children. Biol Trace Elem Res 1999;67:257-268
[40] Napolitano G, Plaka G, Grimaldi S, Guilani C, Laglia G, Calabreese G, Satta MA, Neri G, Monaco F. Growth delay in Down syndrome and zinc sulphate supplementation. Amer J Med Genetics 1990;S7:63
[41] Abdallah SM, Samman S. The effect of increasing dietary zinc on the activity of superoxide and dismutase and zinc concentrations in healthy female subjects. Eur J Clin Nutr 1993;47:327-332
[42] Perry EK, Perry RH, Smith CJ, Purohit D, Bonham J, Dick DJ, Candy JM, Edwardson JA, Fairbairn A. Cholinergic receptors in cognitive disorders. Can J Neurol Sci 1986;13(S4):521-527
[43] Cantor DS, et al. A report on phosphatidylcholine therapy in a Down's syndrome child. Psychol Rep 1986;58:207-217
[44] Lejeune J, Rethore MO, de Blois MC, Peeters M, Naffah J, Megarbane A, Cattaneo F, Mircher O, Rabier D, Parvey P, et al. Amino acids and trisomy 21. Ann Genet 1992;35(1):8-13
[45] Lemere CA, et al. The lysomal cysteine protease, cathepsin S, is increased in Alzheimer's disease and Down syndrome brain. An imunocytochemical study. Am J Pathol 1995,146(4):848-860
[46] Werbach M. Epilepsy. In Textbook of Nutritional Medicine. Third Line Press, Tarzana (CA), 1999:363-375
[47] Meyers LF. Language development and intervention. In Clinical Perspectives in the Management of Down Syndrome. Springer-Verlag, NY, 1990:153-164
[48] Warner FJ. Nutrition and Down syndrome. Presentation at the Third Annual Convention of the California State Naturopathic Medical Association, Buena Park, February 11, 2001
[49] Shetty HU, Siarey RJ, Galdzicki Z, Stoll J, Rapoport SI. Ts65Dn mouse, a Down syndrome model, exhibits elevated myo-inositol in selected brain regions and regional and peripheral tissues. Neuochem Res 2000;25(4):431-435
[50] Huang W, Alexander GE, Daly EM, Shetty HU, Krasuski JS, Rapoport SI, Schapiro MB. High brain myo-inositol levels in the predementia phase of Alzheimer's disease in adult's with Down's syndrome. Am J Psychiatry 1999;156(12):1879-1886
[51] Shonk T, Ross BD. Role of increased cerebral myo-inositol I the dementia of Down syndrome. Magn Reson Med 1995;33(6):858-861
[52] Shetty HU, Schapiro MB, Holloway HW, Rapaport SI. Polyol profiles in Down syndrome: myo-inositol, specifically is elevated in the cerebrospinal fluid. J Clin Invest 1995;95(2):542-546
[53] Hamilton K. Down's syndrome. In Clinical Pearls in Nutrition and Preventative Medicine. ITServices, Sacramento, 1998:204
[54] Watkins SE, Thomas DE, Clifford M, Tidmarsh SF, Sweeney AE. Ah-Sing E, Dickerson JW, Cowie VA, Shaw DM. Plasma amino acids in patients with senile dementia and in subjects with Down's syndrome at an age vulnerable to Alzheimer's changes. J Ment Defic Res 1989;33(Pt 2):159-166
[55] Shaposhnikov AM, Khal'chitskii SE, Shvarts EI. Disorders of phenylalanine and tyrosine metabolism in Down's syndrome. Vopr Med Khim 1979;25(1):15-19
[56] Leichtman LG. Targeted nutritional intervention (TNI) in the treatment of children and adults with Down syndrome. 1998 NDSC Meeting.
[57] Airaksinen EM. Tryptophan treatment of infants with Down's syndrome. Ann Clin Res 1974;6(1):33-39
[58] Thiel RJ. Growth effects of Warner protocol for children with Down syndrome. J Orthomol Med, 2002, 17(1):42-48
[59] Thiel RJ. Facial effects of Warner protocol for children with Down syndrome. J Orthomol Med, 2002, 17(2):111-116
[60] Dwyer J. Fertile fields for fads and frauds: questionable nutritional therapies. NY State J Med, 1993:105-108
[61] Barness LA, Dallman PR, Anderson H, Collipp PJ, Nichols BL, Walker WA, Woodruff CW. Megavitamins and mental retardation. American Academy of Pediatrics Policy Statement, August 1981
[62] Luke A, Sutton M, Schoeller DA, Roizen NJ. Nutrient intake and obesity in prepubescent children with Down syndrome. J Am Diet Assoc,1996;96(12):1262-1267
[63] Reading CM. Down's syndrome: nutritional interventions. Nutr Health,1984;3(1-2):91-111
[64] Harrell RF, Capp RH, Davis DR, Peerless J, Ravitz LR. Can nutritional supplementation help mentally retarded children? an exploratory study. Proc Natl Acad Sci U S A,1981;78(1):574-578
[65] Weathers C. Effects of nutritional supplementation on IQ and certain other variables associated with Down syndrome. Am J Ment Defic, 1983;88(2):214-217
[66] Rimland B. Vitamin and mineral supplementation as a treatment for autistic and mentally retarded persons. Presentation to the President's Committee on Mental Retardation, Washington (D.C.), September 20, 1984
[67] Prasher VP. Down syndrome and thyroid disorders: a review. Downs Syndr Res Pract,1999;6(1):25-42
[68] Karlsson B, et al. Thyroid dysfunction in Down's syndrome: relation to age and thyroid antibody. Arch Dis Childhood 1998;79:242-245
[69] Hetzel BS, Clugston GA. Iodine. In Modern Nutrition in Health and Disease, 9th ed. Williams & Wilkins, Balt.,1999:253-264
[70] Guyton AC, Hall JE. Textbook of Medical Physiology, 9th ed. WB Saunders, Phil.,1996
[71] Kanavin OJ, Aaseth J, Birketvedt GS. Thyroid hypofunction in Down's syndrome: is it related to oxidative stress? Biol Trace Elem Res 2000;78(1-3):35-42
[72] Pietz J. Neurological aspects of adult phenylketonuria. Curr Opin Neurol 1998;11(6):679-688
[73] Marsh RW, Cabaret JJ. Down's syndrome treated with a low phenylalanine diet: case report. N Z Med J 1972;75(481):364-365
[74] Becker W, Joost HG. Structural and functional characteristics of Dyrk, a novel subfamily of protein kinases with dual specificity. Prog Nucleic Acid Mol Biol 1999;62:1-17
[75] Kentrup H, Joost HG, Heimann G, Becker W. Midbrain/DYRK1A gene: a candidate for mental retardation in Down syndrome? Klin Padiatr 2000;212(2):60-63
[76] Himpel S, Panxer P, Eirmbter K, Czajkowska H, Sayed M, Packman L, Blundell T, Kentrup H, Grotzinger J, Joost HG, Becker W. Identification of the autophosphorylation sites and characterization of their effects in the protein kinase DYRK1A. Biochem J 2001;359(Pt3):497-505
[77] Lohr JB. Oxygen radicals and neuropsychiatric illness: some speculations. Arch Gen Psychiat,1991;48:1097-1106
[78] Jovanoic SV, Clements D, MacLeod K. Biomarkers of oxidative stress are significantly elevated in Down syndrome. Free Radic Biol Med,1998;25(9):1044-1048
[79] Warner FJ, Stephens C. Metabolic supplementation for correction of raging free radicals in trisomy 21. Presentation at the International Down's Conference. Madrid, Spain, 1997
[80] Murray M, Pizzorno J. Alzheimer's disease. In Encyclopedia of Natural Medicine. Prima Publishing, Rocklin (CA), 1991:128-135
[81] Vinson JA, Jang J. In Vitro and In Vivo antioxidant effect of a citrus extract and ascorbic acid on normal and hypercholesterolemic human subjects. J Med Food, 2001:4(4):187-192
[82] Vinson J, Stella J, Flanagan T. Selenium yeast is an effective in vitro and in vivo antioxidant and hypolipemic agent in hamsters. Nutr Res,1998;18:735-742
[83] Traber MG. Vitamin E. In Modern Nutrition in Health and Disease, 9th ed. Williams & Wilkins, 1999:347-362
[84] Thiel RJ. Natural vitamins may be superior to synthetic ones. Med Hypo 2000, 55(6):461-469
[85] Thiel RJ. Mineral salts are for plants, food complexed minerals are for humans. ANMA Monitor, 1999;3(2):5-10
[86] DeCava JA. The Lee Philosophy—Part II. Nutrition News and Views, 2003;7(1):1-6
[87] Thiel RJ. The Truth About Vitamins in Supplements. ANMA Monitor, in press 2003
[88] Vinson J, Howard TB. Inhibition of protein glycation and advanced glycation end products by ascorbic acid and other nutrients. Nutr Biochem 1996;7:659-663
[89] Odetti P, Angelini G, Dapino D, Zaccheo D, Garibaldi S, Dagna-Brica F, Piomba G, Perry G, Smith M, Traverso N, Tabaton M. Early glycation damage in the brains from Down's syndrome. Biochem Biophys Res Commun 1998;243(3):849-851
[90] Brownson C, Hipkiss AR. Carnosine reacts with a glycated protein. Free Radic Biol Med 2000;28(10):1564-1570
[91] Seidler NW. Carnosine prevents glycation-induced changes in electrophoretic of aspartate aminotransferase. J Biochem Mol Toxicol 2000;14(4):215-220
[92] Kohen R, Misgav R, Ginsburg I. The SOD like activity of copper: carnosine, copper: anserine copper: homocarnosine complexes. Free Radic Res Commun 1991;12-13, pt1:179-185
[93] Choi SY, Kwon HY, Kwon OB, Kang JH. Hydrogen peroxide-mediated Cu,ZN-superoxide dismutase fragmentation: protection by carnosine, homocarnosine and anserine. Biochim Biophys Acta 1999;1472(3):651-657
[94] Kang JH, Eum WS. Enhanced oxidative damage by the familial amyotrophic lateral sclerosis-associated Cu,Zn-superoxide dismutase mutants. Biochim Biophys Acta 2000;1524(2-3):162-170
[95] De Falco FA D'Angelo E, Grimaldi G, Scafuro F, Sachez F, Caruso G. Effect of the chronic treatment with L-acetylcarnitine in Down's syndrome. Clin Ter 1994;144(2):123-127
[96] Laryea MD, Steinhagen F, Pawliczek S, Wendel U. Simple method for the routine determination of betaine and N,N-dimethylglycine in blood and urine. Clin Chem,1998;44(9):1937-1941
[97] Kendall RV, Lawson JW. Recent findings on N,N-dimethylglycine (DMG): a nutrient for the new millenium. Townsend Letter,2000;202:75-85
[98] Hamilton K. Nutritional aspects of children with Down syndrome. In Clinical Pearls 1999. ITServices, Sacramento, 1999:256
[99] Storm W. Prevalence and diagnostic significance of gliaden antibodies in children with Down's syndrome. Eur J Ped, 1990;149:833-834
[100] Dorfman K. Exploring the casein-free, gluten-free diet. New Developments;1(2):4
[101] Fuchtenbusch M, Karges W, Standl E, Dosch HM, Ziegler AG. Antibodies to bovine serum albumin in type 1 diabetes and other autoimmune disorders. Exp Clin Endocrinol Diabetes,1997;105(2):86-91