TREATING ADD/ADHD 

 

 

 NATURALLY

Presented by:

Debbie Markel, CH, CNHP

Certified Herbalist, Certified Natural Health Professional

APOTHECARIAN HERBALS, LLC

3430-D Anderson Hwy. (Rt. 60)

Powhatan, VA  23139

Ph: (804) 598-5352

www.herbalconsultant.com

  

COPYRIGHT 2003 and 2005, Apothecarian Herbals, LLC, All rights reserved.

 

WHAT ARE ADD & ADHD?

Attention Deficit Hyperactivity Disorder (ADHD) and Attention Deficit Disorder (ADD) are the most commonly diagnosed neurobehavioral disorders affecting children, although many adults have it, too.  Core symptoms include hyperactivity, impulsivity, distractibility and inattentiveness.  Usually, ADD/ADHD people have other symptoms like insomnia, fluctuating emotions (emotional lability), disorganization in activities and/or problem solving and conduct disorder.  Ear infections are more frequent in hyperactive children.  Other conditions can mimic ADD/ADHD such as epilepsy, fetal alcohol syndrome, lead poisoning, sleep apnea and thyroid abnormalities.  It is VERY important that all other causes of erratic behavior be eliminated through tests before a diagnosis of ADD/ADHD is made.

To diagnose ADD/ADHD, symptoms present themselves before the age of 7 and cause impairment in social, academic or occupational functioning, and must be present in two or more settings (i.e., at school and at home).  For the Inattentive Type, at least six of the following symptoms must have persisted for at least 6 months: lack of attention ot details/careless mistakes; lack of sustained attention; poor listener; failure to follow through on tasks; poor organization; avoids tasks requiring sustained mental effort; loses things; easily distracted; forgetful.  For the Hyperactive-Impulsive Type, at least six of the following symptoms must have persisted for at least 6 months: fidgeting/squirming; leaving sea; inappropriate running/climbing; difficulty with quiet activities; “on the go;” excessive talking; blurting answers; can’t wait turn; intrusive.  The Combined Types requires both inattentive and hyperactive-impulsive criteria to be met.  (Source: The attachment to the FDA Approval Letter for NDA 21-284 (Ritalin LA)

Recently, besides well-known medications like Ritalin and Adderall, anti-depressants have been prescribed to treat ADD/ADHD.  Adverse affects include excessive sedation and rebound hypertension during withdrawal of the therapy.

NOTABLE QUOTES

“Adverse drug reactions (ADRs) are believed to be the leading cause of death in the United States...”  (Lasser et al, Journal of the American Medical Association, 287(17):2215-2220.  May 1, 2002.)

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“We feed our children nutritionless pseudo-foods, artificial colors, preservatives and allergens (wheat, dairy, etc.).  We sit them in front of the constant[ly] changing and stimulating images of television and video games.  Then we expect them to sit quietly throughout the school day.  Everything is tightly scheduled; never enough time for sleep, unregulated play, real relaxation and time to be human.”  (David Winston, Herbalist, Ethnobotanist, Co-founder of the American Herbalists Guild)

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 “The results indicate that people, especially children, can easily consume enough caffeine to leave them jittery and anxious.  And because foods and drinks are not required to list how much caffeine they contain, it can be hard to gauge how much you or your kids are getting.” [Results from conducting a recent analysis of the caffeine content of 25 products]  (“Caffeinated Kids,” Consumer Reports, July, 2003, p. 28.)

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“The U.S. produces and uses 80% of the world’s stimulants such at Ritalin – ten times more than Europe and industrialized Asia….Virginia has the highest per capita use of Ritalin among the states, with rates six times higher than that of the lowest state, Hawaii.” [from www.stayfreemagazine.org/archives/ with demographic information from Running on Ritalin by Lawrence Diller and Attention-Deficit Hyperactivity Disorder by Russell Barkley.]

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“More than 75% of primary care doctors surveyed said that had prescribed children selective serotonin reuptake inhibitors (SSRIs), such as Prozac, even though these drugs have not been approved for use in children.  On the basis of the survey, which included 557 primary care doctors, about 500,000 prescriptions for SSRIs are prescribed annually for adolescents and children under age 18.” [Presented at a Pediatrics Academic Societies annual meeting in San Francisco, CA, May 8, 1999.]

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The number of preschoolers in the United States being prescribed antidepressants and stimulants soared in the mid-1990s, despite limited knowledge about the effects of such drugs on young children, according to a study published Tuesday.  The number of 2- to 4-year-olds on psychiatric drugs including Ritalin and anti-depressants like Prozac soared 50 percent between 1991 and 1995. The number of 2- to 4-year-olds on psychiatric drugs including Ritalin and antidepressants like Prozac jumped 50 percent between 1991 and 1995, researchers reported in the Journal of the American Medical Association….With an increasing number of children attending day care, parents may feel pressured to have their children conform in their behavior, Julie Magno Zito, the lead author and an assistant professor of pharmacy and medicine at the University of Maryland, suggested. She also said there is a much greater acceptance in the 1990s of psychoactive drugs.”  [From MSNBC News Services, 2/3/00, and published on www.rense.com, accessed 07/19/03. 

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IDEA (Individuals with Disabilities Education Act):

Part B, Sec. 602 (3)(A); 300.7(c(9)) adds “attention deficit disorder” and “attention deficit hyperactivity disorder” to the list of conditions that could render a child eligible under “other health impaired.”

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“In 1990, Supplemental Security Income, SSI, a Federal Government welfare program, was opened to allow low income parents whose children were labeled with ADHD to be eligible for a cash benefit under the SSI program.  This allowed some families to receive more that $450 a month per child from the Federal Government…

Then, in 1991, the Department of Education made hundreds of special education dollars available every year for children labeled with ADHD and also those in need of special education.  After that, modification schools could receive more than $400 per student under IDEA for each child diagnosed with ADHD and in need of special education.

Now both SSI and ADHD changes coincide with a dramatic rise in the number of children said to have DHD.  Between 1990 and 1992, the number of ADHD diagnoses jumped from approximately one million to over three million and the production of one drug, Ritalin, increased from 2,000 kilos to over 8,000 kilos in that time period.”  - Opening Statement of Congressman Bob Schaffer, Subcommittee on Oversight and Investigations, Committee on Education and the Workforce, Washington, DC, September 29, 2000.  

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Virginia has the highest per capital use of Ritalin among the states, with rates six times higher than that of the lowerst state, Hawaii.    After Virginia, the next four states are South Carolina, Delaware, Indiana, and Michigan.   www.stayfreemagazine.org

 

COMMON ADD/ADHD PRESCRIPTION DRUGS: RITALIN, ADDERALL & STRATTERA

Drugs merely mask symptoms.  They’re not getting to the causes of the problems!

ADDERALL XR CAPSULES

[Excerpts from the attachment to the FDA Approval Letter for NDA 21-303/S-001]

“AMPHETAMINES FOR PROLONGED PERIODS OF TIME MAY LEAD TO DRUG DEPENDENCE”

“The mode of therapeutic action in Attention Deficit Hyperactivity Disorder (ADHD) is not known.”

The clinical trial conducted in children aged 6 – 12 lasted only three weeks!

“The effectiveness of ADDERALL XR for long-term use, i.e., for more than 3 weeks, (author’s emphasis) has not been systematically evaluated in controlled trials.”

WARNINGS:  Psychosis and Long-Term Suppression of Growth

DRUG INTERACTIONS include: Gastrointestinal alkalinizing agents (like sodium bicarbonate – simple baking soda), tricyclic antidepressants, MAO antidepressants.

Adderall XR has “anorectic” effects.                                                                                      

ADVERSE EVENTS:  14% of patients report abdominal pain, 22% report loss of appetite, 17% report insomnia.  Other adverse reactions include palpitations, psychotic episodes, dizziness, anorexia and impotence.

“Toxic symptoms may occur idiosyncratically at low doses.”

ANIMAL TOXICOLOGY: “Acute administration of high doses of amphetamine (d- or d,l-) has been shown to produce long-lasting neurotoxic effects, including irreversible nerve fiber damage, in rodents.  The significance of these findings to humans is unknown (author’s emphasis).

RITALIN LA & SR, CONCERTA, Metadate, Methylin

[Excerpts from the attachment to the FDA Approval Letter for NDA 21-284]

“The mode of therapeutic action in Attention Deficit Hyperactivity Disorder (ADHD) is not known.”

“The pharmacokinetics of Ritalin LA was examined in 18 children with ADHD between 7 and 12 years of age.  Fifteen of these children were between 10 and 12 years of age.”

“Ritalin LA … was evaluated in a randomized, double-blind, placebo-controlled, parallel group clinical study in which 134 children, ages 6 to 12 … for up to 2 weeks.” (Author’s emphasis)

“The effectiveness of Ritalin LA for long-term use, i.e., for more than 2 weeks, has not been systematically evaluated in controlled trials.”  “There is no body of evidence available from controlled trials to indicate how long the patient with DHD should be treated with Ritalin LA.”

“Ritalin LA … is contraindicated in marked anxiety, tension, and agitation, since the drug may aggravate these symptoms.”

WARNINGS, ADVERSE EVENTS and DRUG INTERACTIONS are all similar to Adderall XR.

ADDITIONAL ADVERSE EVENTS: “Difficulties with accommodation and blurring of vision have been reported with methylphenidate [the active ingredient in Ritalin LA].”  “Abnormal liver function…”  “Scalp/hair loss.”

“Ritalin LA … should not be used in children under six years of age, since safety and efficacy in this age group have not been established.”  

STRATTERA

[Excerpts from the FDA’s Strattera consumer website: www. http://www.fda.gov/cder/consumerinfo/druginfo/strattera.HTM]

 “Strattera may make it difficult to urinate.”

 “Some people may lose weight while taking Strattera. It is not known if growth will be slowed in children who use Strattera for a long time. Height and weight will be watched in children who are taking Strattera.”

 “The most common side effects of Strattera in children and adolescents are: upset stomach, decreased appetite, nausea or vomiting, dizziness, tiredness, mood swings.”

 “The pharmacokinetics of atomoxetine have not been evaluated in children under 6 years of age.”

The studies on Strattera lasted 8 weeks, 6 weeks and 9 weeks.  None were long-term.

 “The effectiveness of STRATTERA for long-term use, i.e., for more than 9 weeks in child and adolescent patients and 10 weeks in adult patients, has not been systematically evaluated in controlled trials.”

ALTERNATIVES TO DRUGS – AN INTEGRATIVE APPROACH

Regardless of the causes of ADD/ADHD (environmental, chemical, behavioral, genetic), various holistic treatments have been shown to regulate neurotransmitter activity, resulting in calmer, more focused behavior in children (and adults with the disorder, too).  None can be utilized alone.  The combinations of therapies may vary from person to person with differing results, but all are reasonable, harmless and in many, many documented cases, very effective.

NUTRITION

First is food

NO SUGAR!  NO SUGAR!  NO SUGAR!  NO SUGAR!  NO SUGAR!  NO SUGAR!  NO SUGAR!  NO SUGAR!

NO SODAS!  NO SODAS!  NO SODAS!  NO SODAS!  NO SODAS!  NO SODAS!  NO SODAS!  NO SODAS!

NO JUNK!  NO JUNK!  NO JUNK!  NO JUNK!  NO JUNK!  NO JUNK!  NO JUNK!  NO JUNK!  NO JUNK! 

NOTHING ARTIFICIAL!  NOTHING ARTIFICIAL!  NOTHING ARTIFICIAL!  NOTHING ARTIFICIAL! 

Did I make myself clear?  This may look like an exaggeration, but it isn’t.  There’s an old saying, “You are what you eat.”  It’s true.  Do you want to be refined sugar?  Or artificial colors, preservatives, additives & flavorings?  How about caffeine?  And certainly not junk!  What we eat affects our health and mental well-being more than any other factor except heredity.  Stimulants like Ritalin and Adderall suppress appetites, which leads to fewer vitamins and minerals being ingested.  This aggravates the nutrition dilemma.

ADD/ADHD is a combination of factors that contribute to the symptoms.  Often, food sensitivities are major factors.  Food sensitivities or allergies affect our brain’s neurotransmitters, resulting in behavior abnormalities.  Following are some of the foods that should be eliminated immediately from anyone’s diet who has been diagnosed with ADD/ADHD.  Once these foods have been completely eliminated, observe the person’s behavior in about 2 – 3 weeks and see what changes have occurred.  Also notice that the dark circles around their eyes will probably go away, indicating they were sensitive to those foods.  If you want to be certain which food caused the behavior change, add back only one food at a time for a period of 2 weeks and observe behavior changes.  It will become readily apparent which food or foods contributed to the ADD/ADHD symptoms.  This process takes some work and makes eating at fast food establishments off-limits.  Label reading is mandatory.  The results will be worth it, however.  Charles Gant, M.D., Ph.D. in Syracuse, New York claims a 95% success rate using diets and supplements.  Dr. Gant wrote ADD and ADHD: Complementary Medicine Solutions, and feels that ADD/ADHD patients are the easiest to treat nutritionally.  These recommendations are based on the famous “Feingold Diet,” which has been around for over 30 years (www.feingold.org) and has a substantial list of studies on its website.

Dairy products – Causes mucous, earaches, gastro-intestinal distress.  Many ADD/ADHD people suffered from continual ear infections as children.

White flour & white rice products – All of the essential nutrients have been eliminated from white flours & rice.  What’s left is a nutrition-less, glutinous, empty carbohydrate that becomes glucose when ingested.

Sodas – Sodas are full of phosphates which leach calcium from our bodies.  Most people with ADD/ADHD need larger quantities of calcium, a mineral that has a calming effect.  They also contain caffeine, sugars or artificial sweeteners, which are like poison to ADD/ADHD sufferers.

Artificial sweeteners – These are nothing but chemicals.  Of all food additives, artificial sweeteners produce the most side-effects.  They can result in irritability, sleep and memory loss, headaches, stomachaches, muscle weakness, seizures and other conditions.  Stevia is an herb that’s very, very sweet.  It’s sold in powdered or liquid form and can be easily substituted for sugar or artificial sweeteners.  It also contains vitamins and minerals, something sugar or artificial sweeteners lack.  Information about how to use it can be found at www.stevia.com.

Corn, soy, wheat, eggs, citrus – These are common food allergens.  Any food allergen will aggravate ADD/ADHD symptoms.  Read labels carefully.

Foods containing high amounts of salicylate (a chemical shown to aggravate hyperactivity in several studies) - These include: plums (canned), raspberries (fresh), peppers, almonds, peppermint tea, prunes (canned), strawberries (fresh), tomatoes, peanuts, honey, and some spices: cardamom, cinnamon, cloves, curry, oregano, paprika, pepper, rosemary, sage, turmeric.

WHAT CAN THIS POOR PERSON EAT???? – GOOD STUFF!                           

Fresh, whole fruits and vegetables not on the above list

Brown rice, oats and other whole grains other than wheat, corn or soy

Lean meats (in small quantities)

Stevia as a sweetener

Herbs & spices not on the above list

Beans, legumes

Nuts not on the above list

Seeds – pumpkin, sunflower, etc.

Sprouts

Rice milk

Carob (instead of chocolate)

Raisins & other dried fruits

Be creative!  Search the Internet for recipes.  Good sources are www.allrecipes.com or www.recipesource.com.  Search by ingredients. 

Next are vitamins & supplements

Many studies have been done showing common nutritional deficiencies among people with ADD/ADHD.  These deficiencies affect the brain’s neurotransmitter activity (the “wiring routes”, if you will) and deprive the body of essential nutrients that provide calmness and focus.  Poor nutritional habits in children lead to low concentrations of water-soluble vitamins in the blood, impair brain function and subsequently cause violence and other antisocial behavior.  After correcting the nutrient intake through diet and/or supplementation, brain function and resulting behavior improves.  Some of these studies have been reported in the American Journal of Clinical Nutrition (1994), Biological Psychiatry (1996) and Magnesium Research (1997).  In 1999, the Center for Science in the Public Interest published a report that cited 17 controlled studies on artificial colors, milk, corn and other adverse effects on children’s behavior (“Diet, ADHD, and Behavior”).  Supplementing the diet with these nutrients should produce profound results if combined with dietary changes.

Zinc – 5 to 10 mg daily (never exceed 50 mg of zinc).  There is a theory that yellow food dyes bind to zinc & prevent its absorption into the bloodstream.  Zinc is a common deficiency among ADD/ADHD people.  Zinc also helps nails, skin disorders and hair.

B-complex – 50 to 100 mg daily (cannot overdose as the body expels what isn’t used).  B6 in particular has a positive effect on the body’s regulation of dopamine, adrenaline and serotonin, all of which affect brain activity.  B vitamins are also good as anti-stress supplements, and vegetarians should supplement with B-12, a vitamin only found in animal products.

Magnesium – 200 – 400 mg daily (higher doses may cause diarrhea).  Almost all patients in all nutritional studies show a marked deficiency of magnesium (as do most of us!).  It’s also good for

Calcium –800 - 1000 mg daily.  Produces a calming effect.  Needs magnesium to be absorbed.

Omega 3 Essential Fatty Acids (DHA, in particular, found in fish & flax oils) – 100 – 500 mg DHA daily.  Low levels of DHA are associated with depression, memory loss, dementia and visual problems.  It also is responsible for abnormal behavior of children with ADHD (from a study at Purdue University).  DHA is high in breast milk.  There are theories that one reason ADD/ADHD is so prevalent today is because (a) mothers don’t breast feed as often or as long as in the past and (2) most of us rarely eat fish.  Flax can be taken as ground seeds, but must be ground fresh every day to ensure potency.  It has a nutty flavor & can be sprinkled on oatmeal or other foods.

Multivitamin – Essential for all of us!  Even the government recommends them, but they don’t usually have enough of the above nutrients (or any, like DHA), to make a difference.

Other supplements have been studied, but not as extensively.  These include digestive enzymes to help with proper food digestion and assimilation of nutrients; grape seed extract or pine bark extract, which contain proanthocyanidins, powerful antioxidants; GABA, a neurotransmitter amino acid that promotes relaxation; and Vitamin C, another strong antioxidant and anti-stress vitamin.  Positive results have been reported using the amino acids L-glutamine and L-tyrosine.

 

 

HERBAL SUPPORT

Nature usually has the answer to whatever ails you!  There are numerous herbs that have calming effects on children without harmful effects.  Some companies have created formulas specifically for ADD/ADHD that have shown to be effective.  Only experimentation can show which herb or herbs will work for your child (or you).

Valerian root – Increases concentration, calms

Hops – Calms the nervous system

Skullcap – A natural sedative

Ginkgo – Helps forgetfulness, increases concentration and focus.  Has a positive effect on brain neurotransmitters.

Chamomile – Soothing, calming

Lemon balm – Soothing, calming

Hawthorn – Supports circulation to the brain

If herbs are purchased singly, the amounts may vary.  Use the following as a dosage guide:

The standard adult dose is based on a 150 pound person.  Take the patient’s weight & divide by 150.  Use that percentage to determine dose.  Example: Bottle says take 2 capsules 3 times daily.  Child is 90 pounds.

90 / 150 = .60; 6 x .60 = 3.6 (round to 4).  A 90 lb. Child should take a total of 4 capsules in a day in divided doses.

If herbs are administered as teas (which most of the above except valerian can be), use 2 tablespoons to 8 oz of water & steep for at least 15 minutes.  A small child would drink 2 cups daily, an adolescent 3 cups daily & teen-agers and adults would drink 4 cups daily.

OTHER APPROACHES

AROMATHERAPY

The scent of certain essential oils will produce a calming effect in hyperactive people.  Lavender and orange are soothing and peppermint clears the mind.  Other aromas may work.  Contact a trained aromatherapist for guidance.

FLOWER ESSENCES

Flower essences are homeopathic dilutions made from flowers.  Extensive research has shown that flower essences have a strong effect on people’s emotional states.  Usually a lengthy test is given to the client before a formula is recommended.  Following are a few flower essences that have proven helpful with ADD/ADHD in children:

For repeating the same mistakes – Chestnut bud

For “daydreaming” – Clematis                                                                

For the one who constantly gives up easily – Gentian

For those lacking confidence – Larch

For persistent unwanted thoughts – White Chestnut

For those lacking motivation – Wild Rose

For stress in general – Rescue Remedy (a combination formula)

HOMEOPATHIC FORMULAS

Homeopathy is the science of similars.  This means that homeopathic practitioners believe that by giving the patient highly diluted amounts of the very thing they’re suffering from, their bodies will build up immunity to the condition and cure itself.  It’s a little like getting a vaccination against a disease.  Homeopathic remedies are difficult to recommend because they’re very symptom-specific.  For example, one remedy commonly used for teething, Calcarea Carbonica, is also used for sore throat, earache, acid stomach, constipation or diarrhea, mental disorders, anxiety, depression, old sprains, excessive menstruation.  It is indicated when the patient is shy, sensitive, fair in color, flabby, with tendency towards overweight.  Conditions may be due to overexertion, mental strain or poor nutrition.  Symptoms are worse with wet, cold, mental or physical exertion, full moon and when standing.  Symptoms are better with dry weather & lying on the painful side.  It is best to consult a trained homeopath to determine the correct formula for your specific needs.  (There’s a trained M.D. in Charlottesville, Dr. George Guess, who practices homeopathic medicine.)

BEHAVIOR CHANGES

Dr. John Rosemond, a family psychologist with a regular syndicated column in the Richmond Times-Dispatch, believes that combining powerful love and powerful discipline (not harsh) from a child’s earliest years can help children learn focus and self-control, two of the most prevalent symptoms in ADD/ADHD.  Saying “no” and meaning it will NOT cause your children irreversible harm.

Getting outside and playing hard enough to become worn out also helps.  Most children today have structured activities, spend lots of time in the car, watch too much TV or play video games for hours.  They rarely expend a lot of physical energy.  Kids need to get their “YA YA’s” out!

IN CONCLUSION

There are many other opinions, theories and treatment methods for handling ADD/ADHD.  There isn’t a “one size fits all” approach.  Only you can determine the best method for your child or yourself.  Just be aware of the options and consider using narcotics as your last resort when all else fails.  Good luck!!!


APPENDIX

 PUBLICATIONS AND STUDIES FROM THE NATIONAL LIBRARY OF MEDICINE, NATIONAL INSTITUTES OF HEALTH at www.ncbi.nlm.nih.gov/

Assessment of magnesium levels in children with attention deficit hyperactivity disorder (ADHD).

Kozielec T, Starobrat-Hermelin B.

Department of Family Medicine, Pomeranian Medical Academy, Szczecin, Poland.

A positive influence of magnesium in the prevention and treatment of hyperactivity in children is more and more frequently raised in the literature. The aim of our work was to estimate magnesium contents in children with attention deficit hyperactivity disorder, (ADHD). The investigations comprised 116 children (94 boys and 20 girls), aged 9-12 years, with recognized ADHD. In 68 out of 116 patients examined ADHD occurred with other coexisting disorders specific to the developmental age and in the remaining 48 patients it occurred together with disruptive behaviour. Magnesium levels have been determined in blood serum, red blood cells and in hair with the aid of atomic absorption spectroscopy. Magnesium deficiency was found in 95 per cent of those examined, most frequently in hair (77.6 per cent), in red blood cells (58.6 per cent) and in blood serum (33.6 per cent) of children with ADHD. The conclusion from the investigations is that magnesium deficiency in children with ADHD occurs more frequently than in healthy children. Analysis of the material indicated the correlation between levels of magnesium and the quotient of development to freedom from distractibility.

Publication Types:

Clinical Trial

Controlled Clinical Trial

PMID: 9368235 [PubMed - indexed for MEDLINE]

 

Food dyes impair performance of hyperactive children on a laboratory learning test.

Swanson JM, Kinsbourne M.

Forty children were given a diet free of artificial food dyes and other additives for 5 days. Twenty of the children had been classified as hyperactive by scores on the Conners Rating Scale and were reported to have favorable responses to stimulant medication. A diagnosis of hyperactivity had been rejected in the other 20 children. Oral challenges with large doses (100 or 150 milligrams) of a blend of FD & C approved food dyes or placebo were administered on days 4 and 5 of the experiment. The performance of the hyperactive children on paired-associate learning tests on the day they received the dye blend was impaired relative to their performance after they received the placebo, but the performance of the nonhyperactive group was not affected by the challenge with the food dye blend.

Publication Types:

Clinical Trial

Controlled Clinical Trial

Substances:

Food Coloring Agents

PMID: 7361102 [PubMed - indexed for MEDLINE]

 

Foods and additives are common causes of the attention deficit hyperactive disorder in children.

Boris M, Mandel FS.

North Shore Hospital-Cornell Medical Center, Manhasset, New York.

The attention deficit hyperactive disorder (ADHD) is a neurophysiologic problem that is detrimental to children and their parents. Despite previous studies on the role of foods, preservatives and artificial colorings in ADHD this issue remains controversial. This investigation evaluated 26 children who meet the criteria for ADHD. Treatment with a multiple item elimination diet showed 19 children (73%) responded favorably, P < .001. On open challenge, all 19 children reacted to many foods, dyes, and/or preservatives. A double-blind placebo controlled food challenge (DBPCFC) was completed in 16 children. There was a significant improvement on placebo days compared with challenge days (P = .003). Atopic children with ADHD had a significantly higher response rate than the nonatopic group. This study demonstrates a beneficial effect of eliminating reactive foods and artificial colors in children with ADHD. Dietary factors may play a significant role in the etiology of the majority of children with ADHD.

Publication Types:

Clinical Trial

Controlled Clinical Trial

Randomized Controlled Trial

Review

Review of Reported Cases

Substances:

Placebos

Food Additives

PMID: 8179235 [PubMed - indexed for MEDLINE]

 

 BIASED RESEARCH – FUNDED BY PEOPLE IN THE FOOD ADDITIVE, DRUG & SUGAR INDUSTRIES

From www.cspinet.org (Center for Science in the Public Interest)

 Eugene L. Arnold, M.D., Professor Emeritus of Psychiatry, Nisonger Center for Mental Retardation and Developmental Disabilities, Ohio State University, Columbus.  In February 2003, received $4,764 from Eli Lilly for research conducted for a safety study of Strattera (tomoxetine) in adolescents. Received $22,558 from MDS Pharma Services to evaluate the safety and efficacy of the supplement ALCAR (acetyl-1-carnitine) in pediatric patients with attention deficit hyperactivity disorder. In March 2003, received $44,686 from Noven Pharmaceuticals for research involving methylphenidate transdermal system in pediatric patients with attention deficit disorder. In March 2003, received $6,368 from Endpoint Research Ltd. to compare the efficacy of immediate release of Ritalin (methylphenidate) and modified release methylphenidate in children with ADHD. In April 2003, received $50,000 from Sigma-Tau HealthSciences S.P.A. to study the safety and efficacy of dietary supplement SH90011 in pediatric patients with ADHD. Received $16,000 from Novartis Pharmaceuticals to study the efficacy, safety and tolerability of methylphenidate in female adolescents diagnosed with ADHD. ( Ohio State University , Monthly Details of Research Awards; http://www.rf.osu.edu/pubrpt/awardsdetail.cfm; accessed 3/7/04)

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Joseph Biederman, M.D., Professor, Department of Psychiatry, Harvard University Medical School; Chief of the Program in Pediatric Psychopharmacology, Massachusetts General Hospital, Boston, MA.  Research support from Shire, Eli Lilly, Wyeth, Pfizer, Cephalon, Janssen, and Noven. Speakers bureau for GlaxoSmithKline, Eli Lilly, Pfizer, Wyeth, Shire, Alza, and Cephalon. Scientific Advisory Board for Eli Lilly, Celltech, Shire, Noven, and Alza/McNeil. (J. Clin. Psychiatry 2002;63:s12)   Research on the effect of long-release Adderall on children with attention-deficit hyperactivity disorder funded by Shire Pharmaceuticals, the maker of Adderall. (Pediatrics 2002;110:258-66)

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David L. Clark, Ph.D., Associate Professor of Neuroscience, Department of Anatomy and Medical Education, Ohio State University, Columbus.  In June 2003, received $179,228 from Passive Motion Therapeutics, Inc., to study the eighth nerve stimulation for the treatment of ADHD. (Ohio State University Research Foundation, Monthly Details of Research Awards; http://www.rf.osu.edu/pubrpy/awardsdetail.cfm; accessed 2/7/04)

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Josephine Elia, M.D., Department of Child and Adolescent Psychiatry, Children's Hospital of Philadelphia, and the Department of Psychiatry, University of Pennsylvania School of Medicine, Philadelphia. "Received grant support from Celegene," according to a New England Journal of Medicine review of "Drug Therapy" article authors who have ties to industry. (N. Engl. J. Med. 2000;342:586-7)

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John M. Kane, M.D., Investigator, Director, NIMH Intervention Research Center in Schizophrenia, Zucker Hillside Hospital, Glenn Oaks, NY. Received financial support from Abbott Laboratories, AstraZeneca Pharmaceuticals, Bristol-Myers Squibb, Pfizer Inc., Janssen Pharmaceutica, Eli Lilly, Novartis Pharmaceuticals, Aventis Organon, and Lundbeck. (Am J Psychiatry. 2004;161:1334-49.) Consultant for and has received honoraria from Abbott, Aventis, Janssen, Novartis, Eli Lilly, Lundbeck, Pfizer, Bristol-Myers Squibb, AstraZeneca, and Organon. (J Clin Psychiatry. 2003;64 Suppl 16:41-6.)

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 Cynthia L. Leibson, Ph.D., Department of Health Sciences Research, Mayo Clinic, Rochester , MN . Research on attention-deficit/hyperactivity disorder supported in part by Eli Lilly. (JAMA 2001;285:60-6)

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Frank A. Lopez, M.D., Children’s Developmental Center , Maitland, FL. Research on the effect of long-release Adderall on children with attention-deficit hyperactivity disorder was funded by Shire Pharmaceuticals, the makers of Adderall. (Pediatrics 2002;110:258-66)

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 James J. McGough, M.D., Associate Professor of Clinical Psychiatry, Division of Child and Adolescent Psychiatry, David Geffen School of Medicine, University of California, Los Angeles.  Research on the efficacy of Adderall XR(R) on children with attention-deficit/hyperactivity disorder was funded by the drug’s manufacturer, Shire Pharmaceuticals. (J. Am. Acad. Child Adolesc. Psychiatry 2003;42:6)  Grant/research support from Boston Life Sciences, Eli Lilly, Janssen Pharmaceutica, McNeil Consumer Healthcare, Novartis, and Shire US ; consultant to McNeil Consumer Healthcare and Shire US ; and speakers bureau for Eli Lilly, McNeil Consumer Healthcare, and Shire US. (http://ccoe.umdnj.edu/rwjms/self%20study/monographs/MC_PediatricADHD.pdf, pg.3; accessed 01/30/04)

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 Steven P. Shon, M.D., Medical Director, Texas Department of Mental Health and Mental Retardation, Austin, TX. “Clinician Adherence to a Major Depressive Disorder Algorithm in the Texas Public Mental Health Sector” supported in part by Forest Laboratories. (http://www.nimh.nih.gov/ncdeu/abstracts2002/ncdeu3086.cfm; accessed 3/4/05) Co-author on “The Factor Structure of the Brief Psychiatric Rating Scale Expanded Version in a Large Diverse Sample of Psychiatric Patients” which was sponsored in part by Bristol-Myers Squibb, Eli Lilly, Glaxo-Wellcome, Janssen Pharmaceutica, Novartis, Pfizer and Wyeth-Ayerst Laboratories. (http://www.nimh.nih.gov/ncdeu/abstracts2002/ncdeu2048.cfm; accessed 3/4/05) According to the New York Times, "Janssen paid twice for Dr. Shon to fly to Pennsylvania....Janssen made the grant covering Dr. Shon's travel expenses 'to expand atypical [schizophrenia medication] usage'," through the Texas Medication Algorithm Project (TMAP). Dr. Shon was also paid a $1,500 honoraria to fly to Washington State to talk to state legislators about the TMAP guidelines. (Melody Petersen. Making Drugs, Shaping the Rules, 2/1/04, Section 3, pg.1) Research on the Texas Medication Algorithm Project Schizophrenia Algorithms partially supported by Abbott Laboratories, Bristol-Myers Squibb, Eli Lilly, Forest Laboratories, Glaxo-Wellcome, Janssen Pharmaceutica, Novartis, Pfizer, SmithKline Beecham, Wyeth-Ayerst Laboratories (pharmaceutical division of American Home Products), and AstraZeneca. (J Clin Psychiatry. 1999;60:649-657.)

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 Mary V. Solanto, Ph.D., Albert Einstein College of Medicine, Bronx , NY . Paper on sugar and hyperactivity received funding from Sugar Association. (Pediatrics, 1991;88:960-6)

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 Trisha M. Suppes, M.D., Ph.D., Associate Professor and Director of Bipolar Disorder Clinic and Research Program, Department of Psychiatry, University of Texas Southwestern Medical Center, Dallas. Co-author on “Olanzapine Versus Divalproex in the Treatment of Acute Mania” which was sponsored by Lilly Research Laboratories. (Am J Psychiatry. 2002;159:1011-7.) Received financial and/or research funding support from Abbott, Zeneca, Eli Lilly, Pfizer, Janssen, Novartis, SmithKline Beecham, Parke-Davis, Glaxo-Wellcome, Bristol-Myers Squibb, Forest Laboratories, Scios, Wyeth-Ayerst, Organon, and Pharmacia Upjohn. (Ann Intern Med. 2001;134:47-60.)

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 James Swanson, Ph.D., Professor, Department of Pediatrics, Child Development Center , University of California , Irvine .   Honoraria/grants/research support from Alza, Novartis, Shire, Celltech, Cephalon, and Eli Lilly; consultant to Alza, Novartis, Shire, Cephalon, and Celltech; and member of the speakers bureau for Alza, Shire, and Celltech. (Conference disclosure notes: 41st Annual Meeting of the American College of Neuropsychopharmacology, December 2002, San Juan , Puerto Rico ; on file with CSPI)

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 Esther H. Wender, M.D., Schneider Children’s Hospital, Long Island Jewish Medical Center, New Hyde Park, NY. Paper on sugar and hyperactivity received funding from the Sugar Association. (Pediatrics. 1991;88:960-6)

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 George M. Anderson, Ph.D., Yale University School of Medicine. Study on aspartame and behavior of ADD children received funding from NutraSweet Co. (Pediatrics 1994;93:70-5).

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 Graham J. Emslie, M.D., Professor and Chair, Division of Child and Adolescent Psychiatry, University of Texas Southwestern Medical Center and Director, Bob Smith Center for Research in Pediatric Psychiatry, Dallas, TX. Consultant and member of speakers bureaus for Bristol-Myers Squibb, Eli Lilly, McNeil, Otsuka, and Wyeth-Ayerst. Receives grant/research support from Novartis. (Preliminary Report of the Task Force on SSRIs and Suicidal Behavior in Youth, American College of Neuropsychopharmacology, 1/21/04, p.16; on file with CSPI)  Consultant to GlaxoSmithKline, Forest , and Pfizer.   Receives research support from Eli Lilly, Organon, RepliGen, and Wyeth-Ayerst. Member of the speakers bureau for McNeil. ("Experience in the use of SSRIs and other antidepressants in children and teens"; conference disclosure notes: Child & Adolescent Psychiatry, convened by The College of Physicians and Surgeons of Columbia University, April 2003, Washington, DC. On file at CSPI)   Serves on the Corporate Contributions and Research Committee for the American Academy of Child and Adolescent Psychiatry. (http://www3.utsouthwestern.edu/psychiatry/facbios/emslie.htm; accessed 6/16/03)

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 Sheila M. Gillespie, MSN Yale University School of Medicine. Study on aspartame and behavior of ADD children received funding from NutraSweet Co. (Pediatrics 1994;93:70- 5).

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Ronald L. Lindsay, M.D., Medical Director, Nisonger Center for Mental Retardation and Developmental Disabilities, Ohio State University, Columbus. Between January and May 2003, received $28,301 from EndPoint Research Ltd. for research comparing the efficacy of immediate release of methylphenidate and modified release methylphenidate in children with attention deficit hyperactivity disorder. In March 2003, received a total of $44,686 from Noven Pharmaceuticals for an efficacy study of Ritalin (methylphenidate) transdermal system in pediatric patients with attention deficit disorder. Received $16,000 from Novartis Pharmaceuticals to study the efficacy, safety, and tolerability of methylphenidate in female adolescents diagnosed with ADHD. ( Ohio State University , Monthly Details of Research Awards; http://www.rf.osu.edu/pubrpt/awardsdetail.cfm; accessed 3/7/04)

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 Bennett A. Shaywitz, M.D., Department of Pediatrics, Yale University School of Medicine. Study on aspartame and behavior of ADD children received funding from NutraSweet Co. (Pediatrics 1994;93:70-5)

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 Sally E. Shaywitz, M.D., Yale University School of Medicine. Study on aspartame and behavior of ADD children received funding from NutraSweet Co. (Pediatrics 1994;93:70- 5)

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 Barbara Sullivan, MSN, Yale University School of Medicine. Study on aspartame and behavior of ADD children received funding from NutraSweet Co. (Pediatrics. 1994;93:70-5.)

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 Colleen M. Sullivan, MSN, Yale University School of Medicine. Study on aspartame and behavior of ADD children received funding from NutraSweet Co. (Pediatrics. 1994;93:70-5.)

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Gabrielle A. Carlson, M.D., Participating Physician, Stony Brook Psychiatric Associates, P.C., Stony Brook University Hospital , Stony Brook , NY . Consultant to GlaxoSmithKline, Johnson & Johnson, Eli Lilly, Novartis, and Pfizer. Receives research support from Johnson & Johnson, Eli Lilly, Novartis, Pfizer, and Shire. Member of the speakers bureaus for Johnson & Johnson and Eli Lilly. ("The differential diagnosis of ADHD and bipolar illness": conference disclosure notes, Child & Adolescent Psychiatry, convened by The College of Physicians and Surgeons of Columbia University, April 2003, Washington, DC. On file at CSPI)

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 Sam Goldstein, Ph.D., University of Utah , board-certified psychologist. Wrote the pamphlet “7 Guidelines for managing ADHD” for Mallinckrodt, Inc., which markets methylphenidate and pemoline drugs to treat ADHD. (pamphlet, undated)

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 Laurence L. Greenhill, M.D., Professor of Clinical Psychiatry, Columbia University; Medical Director, Disruptive Behavior Disorders Clinic, Columbia Presbyterian Medical Center, New York, NY. Consultant to Eli Lilly, Shire, Noven, Novartis, McNeil, Celltech, Sigma-Tau, Pfizer and Janssen-Cilag. Receives research support from McNeil, Shire and Novartis. ("Effective Treatment of ADHD: Methylphenidate, the tricyclics, SSRIs, atomoxetine, and sustained release formulations": conference disclosure notes: Child and Adolescent Psychiatry, convened by The College of Physicians and Surgeons of Columbia University, April 2003, Washington, DC. On file at CSPI)

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 Christopher J. Kratochvil, M.D., Associate Professor, Department of Psychiatry, University of Nebraska Medical Center, Omaha, NE. Consultant to Eli Lilly and Shire Pharmaceuticals. Receives research support from Eli Lilly, McNeil, and GlaxoSmithKline. Member of speakers bureaus for Lilly and Novartis. ("Treatment of ADHD with non-stimulants": conference disclosure notes; Child and Adolescent Psychiatry, convened by The College of Physicians and Surgeons of Columbia University, April 2003, Washington, DC. On file at CSPI.)


REFERENCES

Adderall XR Capsules. Attachment to FDA Approval Letter for NDA 21-303/S-001. www.fda.gov/ , accessed July 19, 2003.

Anderson, Nina and Howard Peiper, A.D.D. – The Natural Approach.  Safe Goods/New Century Publishing, Markham, ON, Canada, September, 2001.

“Aspartame Warnings.”  321recipes.com, accessed July 26, 2003.

“Behavioral Drugs in Schools: Questions and Concerns.”  Hearing before the Subcommittee on Oversight and Investigations of the Committee on Education and the Workforce, House of Representatives, 106th Congress, Second Session, Washington, D.C., September 29, 2000.  Serial No. 106-130.

Brown, Donald, N.D., “Attention Deficit Hyperactivity Disorder” (Excerpted from Herbal Prescriptions for Better Health: Your Everyday Guide to Prevention, Treatment, and Care).  www.healthy.net, accessed July 19, 2003.

“Cancer Risks Linked to Ritalin.”  Mercola website, www.mercola.com, accessed July 21, 2005.

Center for Science in the Public Interest website, www.cpsinet.org, accessed September 22, 2005.

Cushman, Tom and Johnson, Thomas.  “Nutritional, Medical and Ecological Sources of Inattention,” National Association of School Psychologists, www.nasponline.org/publications/cq293Attentionpt3.html, accessed September 22, 2005.

Catalog of Federal Domestic Assistance. Office of Special Education and Rehabilitative Services, U.S. Department of Education, Section 84.027: Special Education – Grants to States.

Feingold Organization, www.feingold.org, accessed September 21, 2005.

Individuals with Disabilities Education Act, Part B – Assistance for Education of All Children With Disabilities.  Section 611. Authorization; Allotment; Use of Funds; Authorization of Appropriations

Individuals with Disabilities Education Act, Section 602(3)(A); 300.7(c(9)), Definitions (“Other Health Impaired, Attention Deficit Disorder, Attention Deficit Hyperactivity Disorder).

Khosh, Farhand, N.D. and Deena Beneda, N.D., “Attention Deficit/Hyperactivity Disorder.”  Townsend Letter for Doctors & Patients, January, 2003, pp. 68 – 71.

Lombard, Dr. Jay,  “An Integrative Approach to Treating Attention Deficit Disorder.” www.nutraceuticalsworld.com/Sept011.htm, accessed May 31, 2003.

Lyon, Michael R., M.D., Clines, John C., M.D., Totosy de Zepetnek, Joanne, PhD, Jie Shan, Jacqueline, PhD, DSc, Pang, Peter, PhD, DSc, Benishin, Christina, PhD.  2001. “Effect of the herbal extract combination Panax quinquefolium and Ginkgo biloba on attention-deficit hyperactivity disorder: a pilot study.”  Journal of Psychiatry & Neuroscience, Vol. 26, No. 3, 2001, pp. 221 – 228.

Optimal Wellness Center interview with Dr. Lendon Smith, author of 15 books, including: Improving Your Child’s Behavior Chemistry (1976), Hyper Kids Workbook (1990) How to Raise a Healthy Child (1996) and more.  (Visit www.smithsez.com for more information and links to some excellent articles by Dr. Smith, including http://www.smithsez.com/ADHDandADD.html).  

Package inserts for Ritalin, Adderall and Strattera from the FDA, www.fda.gov

Ritalin LA Extended Release Capsules.  Attachment to FDA Approval Letter for NDA 21-284.  www.fda.gov/, accessed July 19, 2003.  

Rosemond, John.  2003.  “Is ADHD the price paid for way we raise kids?”  Richmond Times-Dispatch, May 18, 2003

Traylor, Polly Schneider, “Kicking the Ritalin Habit.”  Alternative Medicine Magazine, September, 2002, pp. 62 – 68 and pp. 118 – 129.

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