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Apathy in PD

Dr. Fernandez

Joined: 20 Jan 2007
Posts: 90

Posted: Sun Sep 20, 2009 7:01 pm Post subject: Post of the Week: Apathy in PD

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How is apathy different from depression?

Apathy is characterized by “diminished motivation, a lack or absence of feeling, emotion, interest or concern”. Technically, it has three components: cognitive (loss of interest in new experiences, lack of concern for one’s problems), behavioral (lack of effort and productivity, dependence on others for structuring daily activities) and affective (flattened affect and lack of response to positive and negative events). Thus, there is some overlap with the symptoms of depression. However, while the symptoms of apathy can also be seen in depression, they differ in the sense that depressed patients feel intrinsically “blue” or sad. They are very bothered by this condition. While apathetic patients do not feel sad, they are indifferent, and they simply “don’t care”. They are not bothered or worried by this condition, rather it is often their spouse who is irritated by their lack of concern or unwillingness to participate in activities. The incidence of apathy in Parkinson’s disease is approximately 45% (Isela et al, 2002). Apathy can therefore be a feature of depression or stand alone as a separate behavioral symptom.

Unfortunately, there have been no consistently reported effective treatments for apathy in Parkinson’s disease. Antidepressants may be tried, and improvement can be seen usually if apathy is a component of depression. But the best remedy is assurance and education. Caregivers need to be assured that their loved one’s “lack of care” does not mean lack of love, or sadness or frustration. Once the spouse is assured and the Parkinson’s patient confirms that this is indeed what he or she is feeling, tension in the household eases up significantly. There is a therapy called cognitive behavioral therapy that researchers are currently testing for treatment of apathy.
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Hubert H. Fernandez

Lloydtan-trust & Malaysia Parkinson’s Centre

Thank you sooo much for this link.  The care and compassion in the writings is very touching and so respectful to those who suffer with PD.  When I read the article on Parkinson’s Hero’s I was shocked to see it was written by a doctor.  He wrote more like a compassionate father then a physician.

To have someone write with so much respect and compassion made me feel like a person again not a “patient”.  Respect and compassion are powerful “medications” to a person who has an illness.  When treated and acknowledge this way you feel as if you can do and get through anything.

Thank you for showing me how I need to treat and perceive those how have chronic illnesses.

Tina

parkinson and B6-B12

Anonymous

Posted: Wed Jul 29, 2009 10:40 pm Post subject: parkinson and b-6-b12

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what is a good dosage of b-6 and b12 your help would gratly be of use to help i have had parkinson for 20 yrs plus. thanks

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Kathrynne Holden, MS

Joined: 22 Jan 2007
Posts: 94
Location: www.nutritionucanlivewith.com
Posted: Sun Aug 02, 2009 1:19 pm Post subject:

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Dear Friend,
That’s a very good question. Folks with PD need to be certain to get enough B vitamins, because studies have shown that long-time users of levodopa can develop elevated homocysteine – a substance in the blood that is normally cleared by a combination of the vitamins B6, B12, and folate.

If you are using levodopa, you should be able to take 10 mg of B6 daily, possibly as much as 25 mg; very high amounts can interfere with levodopa absorption, however, so you will need to be cautious. The daily requirement for adults is 1.3 mg per day, and the upper safe limit is 100 mg/day.

Regarding vitamin B12, the minimum for adults is 2.4 mcg per day, with a safe upper limit not determined. B12 does not interfere with levodopa absorption.

I will separately post an article I wrote on B vitamins and Parkinson’s disease that may be helpful. Let me know if you have other questions.

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_________________
Best regards,
Kathrynne Holden, MS

For a Parkinson Tip of the Day visit:
http://www.nutritionucanlivewith.com/

NPF Forum:My Book

Joined: 03 Mar 2007
Posts: 157
Location: Malaysia
Posted: Sat Sep 19, 2009 6:10 pm Post subject: My Book

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http://www.heroteo.com/heroteo_book.pdf
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to help the PD patients aware the diseases and encourage to set up support groups to educate the patients and their immediate families

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Rogerstar1

Joined: 14 Mar 2007
Posts: 463

Posted: Sat Sep 19, 2009 7:19 pm Post subject:

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Teo- I know a very little about Parkinsons Disease but can recognize superb translating by a professional a mile away. You’ve brought on a talented one. Congratulations and best wishes with your book.

Rogerstar

http://www.patientslikeme.com/forum/show/54379

NPF Dis: Secret Recipe behind the Mask

teokimhoe

Joined: 03 Mar 2007
Posts: 155
Location: Malaysia
Posted: Fri Sep 18, 2009 8:17 am Post subject: secret recipe behind the mask

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Secret recipe behind the mask

I often smiled as I watched the video recording of my kick-boxing exercise which I have uploaded to YouTube a few weeks ago. My trainers and videographer told me the same thing – “You do not look like a Parkinson’s patient at all”. Even my doctor shook his head in disbelief and said, “This is shocking. I can’t imagine a 70-year-old Parkinson’s patient doing such a strenuous exercise such as kickboxing. I am sure that you are the only Parkinson’s patient in Malaysia who is doing the kickboxing exercise.”

As early as 1998, I already had both the motor and non-motor symptoms. Since my diagnosis in 2002, I went through a period of depression, anxiety, denial and anger. Subsequently, I bounced back after discovering a secret recipe for fighting Parkinson’s, which consisted of: knowledge (is power), exercise, medications, nutrition / supplements and prayer. In my quest for knowledge, I browsed various Parkinson’s websites, raining them with questions, questions and questions. I even started the first Parkinson’s blog in Malaysia (www.heroteo.com). I tried to learn everything about Parkinson’s in order to overcome all complications - the Chinese heroes won their battles by understanding their enemies first.
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Animal experiments showed that exercises may be neuroprotective. Rats which were forced to exercise had a lesser degree of brain damage after they were exposed to poison. In mice which were made to undergo treadmill exercises, there was increased production of dopamine.

Parkinson’s patients are comparable to the car. The medications are needed to help patients to start walking, while fuel or battery is needed to help start the car engine. Exercises are needed to improve the patients’ physical mobility and endurance, while driving helps to recharge the battery. Thus, exercises help our “engines” warm up before leaving home and keep the “cars” going everyday. Even healthy people such as Bruce Lee, the Chinese kungfu master, know that exercises are beneficial.

As such, since 2005, I decided to “get physical”. I am spending 3-4 hours everyday at the California Fitness gym, doing a wide range of “heavy” exercises such as kick-boxing, weight-training and spinning (indoor cycling). Twice a week, I do yoga exercises at home with the guidance of a trainer.

Since this year, my physical condition has drastically improved. I sleep and eat well (I eat to live a healthy and good life). I enjoy driving around the Kuala Lumpur city with my wife everyday and going overseas for holiday. I managed to reduce the daily dose of Parkinson’s medications recently. Sometimes, I wonder whether I am just a “normal person” behind the mask.

Am I a Parkinson’s patient? – Try taking my “killer” punch and you’d wonder whether I really have Parkinson’s.

I know that it is technically difficult to prove that exercise has neuroprotective effect in Parkinson’s patients. Despite this, I believe that exercise has slowed down my disease progression. I hope that my video recording will bring hope and happiness to all Parkinson’s patients in this world, by reminding them that they can still live a physically active life.

Mr. Hero Teo, Kuala Lumpur, Malaysia
10th July 2009.
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to help the PD patients aware the diseases and encourage to set up support groups to educate the patients and their immediate families

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Stargazer

Joined: 26 Dec 2007
Posts: 276
Location: Eastern Washington
Posted: Fri Sep 18, 2009 2:31 pm Post subject:

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Mr. Hero Teo I have followed your posts since around 2,007 or shortly there after. I can fully agree from reading your posts that you have come along way from day one. You have every right to be proud of your accomplishments.

I pray that the newly dx and younger people will heed your advice, being an older person my limitations to a great deal of excercise is limited but none the less even I can notice the difference in how I feel a good day w/exercise versus one with out. 100% on the knowledge part the more I read the more I get inspired and grow more content.

Keep it up Teo you have done well and am sure your wife and that little one are proud of you also.
Deeann

NPFAsk about Nutrition:Complimentary and Alernative medicine

Anonymous

Posted: Fri Sep 18, 2009 4:15 am Post subject: complimentary and alternative medicine

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Due to sideeffect of the medication there are growing interest for parkinson’s patients in alternative and complementary medicine or therapies who will live with disease for a longer peroid of time.

The CAM offers helpful information related to non motor and motor symptoms i.e proper diet, exercise, constipation, fatigue, insomina, massage, pain managment, Tai chi, rehabilation,speech therapy,acupuncture,spa treatment & etc.

As the result they try the above therapy to minimize their usage of medication they take to increase comfort or minimize effect of the physical or mental on them.

There are some doctors who do not agree for the above therapies as they are yet medical proven? Besides there are potential risks for the complementary/ alterative therapies

Sometimes the best treatment plans involve a wide range of interventions with their usage of the medications.

Over prescription on certain supplements interaction with medication have effect on each other i.e vitamin B6,iron and mineral .

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Kathrynne Holden, MS

Joined: 22 Jan 2007
Posts: 94
Location: www.nutritionucanlivewith.com
Posted: Fri Sep 18, 2009 7:09 am Post subject:

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Dear Friend,
I believe that many complementary and alternative therapies are most beneficial for people with PD. Although I’m not aware of any that slow progression of PD, there are other benefits. Tai Chi is an excellent exercise for improving balance; acupuncture and reflexology can help to relax muscles, improve digestion, and relieve some types of pain. Some herbs, such as chamomile tea, can help promote sleep.

I also know physicians who recommend such treatments, although not all are aware of the possible benefits.

However, one must also be aware of the many fraudulent schemes that are available – pills, juices, and other treatments designed to make money for the sellers rather than to provide relief for illnesses. These are expensive and useless, and in a few cases, even dangerous. It’s best to seek licensed practitioners for treatment and counseling.

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Best regards,
Kathrynne Holden, MS

For a Parkinson Tip of the Day visit:
http://www.nutritionucanlivewith.com/

Major nutritional issues in the management of PD

Kathrynne Holden, MS

Joined: 22 Jan 2007
Posts: 94
Location: www.nutritionucanlivewith.com
Posted: Wed Aug 26, 2009 7:37 am Post subject: News: Major nutritional issues in the management of PD Kathrynne Holden, MS

Joined: 22 Jan 2007
Posts: 94
Location: www.nutritionucanlivewith.com
Posted: Wed Aug 26, 2009 7:37 am Post subject: News: Major nutritional issues in the management of PD

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Dear Friends,
As long-time members know, I firmly believe that everyone with PD should see a registered dietitian on a regular basis, as nutritional concerns can occur, and can change, throughout the stages of PD. Best, Kathrynne

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Mov Disord. 2009 Aug 18.

Major nutritional issues in the management of Parkinson’s disease.

Barichella M, Cereda E, Pezzoli G.

Parkinson Institute, Istituti Clinici di Perfezionamento, Milano, Italy.

As with other neurodegenerative diseases, neurologic and nutritional elements may interact affecting each other in Parkinson’s disease (PD). However, the long-term effects of such interactions on prognosis and outcome have not been given much attention and are poorly addressed by current research.

Factors contributing to the clinical conditions of patients with PD are not only the basic features of PD, progression of disease, and the therapeutic approach but also fiber and nutrient intakes (in terms of both energy and protein content), fluid and micronutrient balance, and pharmaconutrient interactions (protein and levodopa).

During the course of PD nutritional requirements frequently change. Accordingly, both body weight gain and loss may occur and, despite controversy, it seems that both changes in energy expenditure and food intake contribute.

Nonmotor symptoms play a significant role and dysphagia may be responsible for the impairment of nutritional status and fluid balance. Constipation, gastroparesis, and gastro-oesophageal reflux significantly affect quality of life. Finally, any micronutrient deficiencies should be taken into account.

Nutritional assessments should be performed routinely. Optimization of pharmacologic treatment for both motor and nonmotor symptoms is essential, but nutritional interventions and counseling could and should also be planned with regard to nutritional balance designed to prevent weight loss or gain; optimization of levodopa pharmacokinetics and avoidance of interaction with proteins; improvement in gastrointestinal dysfunction (e.g., dysphagia and constipation); prevention and treatment of nutritional deficiencies (micronutrients or vitamins).

A balanced Mediterranean-like dietary regimen should be recommended before the introduction of levodopa; afterward, patients with advanced disease may benefit considerably from protein redistribution and low-protein regimens. (c) 2009 Movement Disorder Society.

PMID: 19691125 [PubMed - as supplied by publisher]

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_________________
Best regards,
Kathrynne Holden, MS

For a Parkinson Tip of the Day visit:

Suicide and PD

Dr. Okun

Joined: 19 Jan 2007
Posts: 251
Location: University of Florida
Posted: Thu Sep 10, 2009 10:57 am Post subject: New Study: Suicide and PD

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Dear forum members,

There is a new study out looking at suicide in PD. It has long been suspected by many authors it is actually slightly lower than in the general population. There is also debate as to whether it is higher in those receiving DBS. It is important to keep these numbers in mind and remember—PD patients commonly report having thought about suicide. Further, depression is treatable!!

Here is the abstract:

J Neurol Sci. 2009 Sep 7. [Epub ahead of print]
Suicide and suicidal ideation in Parkinson’s disease.

Kostić VS, Pekmezović T, Tomić A, Ječmenica-Lukić M, Stojković T, Spica V, Svetel M, Stefanova E, Petrović I, Džoljić E.
Institute of Neurology CCS, School of Medicine, Belgrade, Serbia.
Little is known about the prevalence and correlates of suicidal behavior in Parkinson’s disease (PD). In the first part of the study, we followed a cohort of 102 consecutive PD patients for 8years and found that the suicide-specific mortality was 5.3 (95% CI 2.1-12.7) times higher than expected. In the second part, we tested 128 PD patients for death and suicidal ideation and administered an extensive neurological, neuropsychological and psychiatric battery. Current death and/or suicidal ideation was registered in 22.7%. On univariate logistic regression analysis, psychiatric symptoms (depression, but also anxiety and hopelessness), but not the PD-related variables, were associated with such ideation. On multivariate logistic regression analysis this association held for major depression (odds ratio=4.6; 95% CI 2.2-9.4; p<0.001), psychosis (odds ratio=19.2; 95% CI 1.4-27.3; p=0.026), and increasing score of the Beck Hopelessness Scale (odds ratio=1.2; 95% CI 1.0-1.4; p=0.008). In conclusion, the suicide risk in PD may not be as high as it is expected, but it is certainly not trivial. According to our data almost a quarter of PD patients had death and/or suicidal ideation, that may significantly influence their quality of life.
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Michael S. Okun, M.D.

Lloydtan-trust & Malaysia Parkinson’s Centre

teokimhoe

Joined: 03 Mar 2007
Posts: 154
Location: Malaysia
Posted: Wed Sep 09, 2009 3:46 am Post subject: lloydtan-trust & Malaysia Parkinson’s Information centre

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http://www.lloydtan-trust.com/index.php?page=home
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to help the PD patients aware the diseases and encourage to set up support groups to educate the patients and their immediate families

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Stargazer

Joined: 26 Dec 2007
Posts: 267
Location: Eastern Washington
Posted: Thu Sep 10, 2009 2:29 pm Post subject:

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Thank you Teo that was an interesting article Mr. Loyd Tan was most certainly a devoted man to his religion, Family and the Parkinson group in Malaysia.

Teo you are also a busy man helping your friends and doing what you can to educate your people about Parkinson, I am sure you are appreciated.

The best of Health to you and your Family,

Deeann

parkinson’s,B6,B12 and Folate

Sun Aug 02, 2009 1:22 pm Post subject: Parkinson’s, B6, B12, and Folate - What’s the Connection?

. Parkinson’s, B6, B12, and Folate - What’s the Connection? Kathrynne Holden, MS, RD Copyright 2008 Ms. Holden is a nutritionist specializing in Parkinson’s disease. She has published research, books, articles, and manuals on nutrition and PD, including “Eat well, stay well with Parkinson’s disease.” She moderates the NPF forum Ask About Nutrition at: www.parkinson.org In the past decade, there has been increasing interest among researchers about the effects of three B vitamins - B6, B12, and folate. We now know that deficiencies occur with greater frequency than ever suspected previously, particularly in older adults. We also now know that deficiencies, if not corrected, can result in irreversible damage in some people. Some health professionals are beginning to suspect that these three vitamins may be significant factors in Parkinson’s disease. What are B6, B12, and folate, and what do they do? These are essential nutrients, meaning that they are vital to life. These three vitamins work both independently and together in many of the body’s systems. Vitamin B6 assists in making hormones, new proteins, and neurotransmitters (”messengers” between nerve cells) for the body’s use. It also helps release stored sugar when we need it for fuel. It works together with B12 and folate to remove homocysteine from the blood. Homocysteine is a substance increasingly associated with a number of diseases; more about this later. Vitamin B12 plays a role in the synthesis of DNA, needed for formation of new red blood cells. It takes part in the manufacture of the myelin sheath - the protective coating that surrounds nerve cells. With B6 and folate it removes homocysteine from the blood. Folate, also called folacin or folic acid, is a partner with B12 in DNA synthesis and in removal of homocysteine, and is required in many other vital processes. Without folate, B12 would be unable to complete many of its functions, and vice versa. Folate is the form found in foods, folic acid is the form in dietary supplements. How much do we need of these vitamins? Nutrient needs are broken down by gender, age group, pregnancy, and lactation. New guidelines have also established a Tolerable Upper Intake Level. So, for example, while the RDA for vitamin B6 for males and females age 19-30 years is 1.3 mg/day, the Tolerable Upper Intake Level for both is 100 mg/day, making it easier to provide recommended amounts. RDA* Tolerable Upper Intake Level ** + Vitamin B6*** + 1.7 mg/day 100 mg/day (age 19 and older) Vitamin B12 + 2.4 mcg/day Not Determined Folate + 400 mcg/day 1000 mcg/day * Recommended Dietary Allowance ** The Tolerable Upper Intake Level is the maximum level of daily nutrient intake that is likely to pose no risk of adverse effects, and represents the total intake from food, water, and supplements. *** Adults age 51 and older + not applicable if pregnant or lactating Why do deficiencies occur, and what are signs of deficiencies? Vitamin B6. Mild deficiencies of B6 are fairly common in the U.S., mostly because of dietary deficiencies, but sometimes due to use of certain medications which interfere with B6, including hydralazine, isoniazid, MAO inhibitors, penicillamine, and theophylline. (Conversely, large amounts of B6 can interfere with the absorption of levodopa, an important medication for Parkinson’s disease. Current use of the combinations of carbidopa-levodopa or benserazide-levodopa offset this interaction for the most part; but use of supplements containing more than 15 mg of B6 can overwhelm the protective effects of the carbidopa and benserazide.) Good food sources of B6 include chicken, fish, eggs, nuts and seeds, dried beans and peas, soybeans, wheat germ, bananas, avocados, and brewer’s yeast. Also, some foods, including a number of breakfast cereals, are fortified with B6. Signs of B6 deficiency include irritability, depression, and confusion; sore tongue, sores or ulcers of the mouth, and ulcers of the skin at the corners of the mouth. Vitamin B12. The human body stores this vitamin so well that it can take a long time to deplete, sometimes several years. Nevertheless, there are several reasons why people sometimes do experience deficiency. Animal foods are the only source of B12, therefore people who eat few or no animal products (meat, fish, poultry, eggs, milk) are at risk unless they use vitamin supplements. Another problem is that B12 in foods cannot be absorbed by the body until it is freed from the proteins in the food; the stomach produces an acid that removes this protein. However, with age, we produce less and less of this stomach acid. Many older adults don’t produce enough acid to allow them to absorb B12. Further, people who have acid reflux often use medications that reduce stomach acid, which unfortunately also decreases absorption of B12. Vitamin B12 is one of the few nutrients that is better absorbed in pill form than from dietary sources. Signs of B12 deficiency include numbness or a tingling “pins and needles” sensation, or a burning feeling; a red, sore, or burning tongue; loss of appetite; gait abnormalities, personality changes, an Alzheimer-like dementia, psychosis, depression, and agitation, particularly in older adults. Other signs are megaloblastic anemia, and elevated serum homocysteine, in people of all ages. Researchers believe that as many as 42% of people aged 65 and older may have some degree of B12 deficiency. Many people with PD are age 65 or older, and should be considered at risk and tested for B12 deficiency. Folate. Folate is available in many foods: lima beans, brewer’s yeast, orange juice, dried beans, green peas, asparagus, beets, Brussels sprouts, broccoli, corn, spinach and other dark green leafy vegetables, soybeans, nuts and seeds. Further, the U.S. government requires that food manufacturers fortify processed grain products with folic acid. Yet, deficiencies of folate are not uncommon. This could be in part because folate is another of the few nutrients in which the synthetic form is absorbed much better (about 40 percent better) than the natural form. Because of the possibility of deficiency, women, including women with PD, who are pregnant or wish to become pregnant are advised to take supplements of folic acid; deficiencies can result in neural tube defects in the unborn child. Deficiencies of folate are also being increasingly studied for a possible role in other diseases: . A low intake of folic acid is associated with risk for colon cancer. Chronic constipation, experienced by many people with PD, also increases risk for colon cancer; it is prudent for those with PD to control constipation and to be sure the diet is adequate in folate. . A low level of folic acid in the blood is associated with higher levels of serum homocysteine, a substance in the blood that may contribute to heart disease, stroke, and dementias. . Animal studies point to a link between low levels of folic acid and Alzheimer’s disease; and people with Alzheimer’s are often found to have low levels of folic acid. Some people with PD develop an Alzheimer-type dementia. Again, prudence dictates consumption of adequate folate. . Another study using mice found that folic acid deficiency led to increased levels of homocysteine and symptoms of Parkinson’s disease. Researchers speculate that homocysteine may damage DNA in the substantia nigra, the area of the brain affected in Parkinson’s disease. . There are reports of improvement in restless leg syndrome (RLS) with use of folate supplements; this has not as yet been studied thoroughly, so it is too early to say whether there is a definite link. However, people with PD often complain of RLS, and physicians should rule out the possibility of folic acid deficiency. Signs of folic acid deficiency include appetite loss, weight loss, burning tongue, fatigue, weakness, shortness of breach, memory loss, irritability, megaloblastic anemia, and increased levels of serum homocysteine. Should people with PD be concerned about these vitamins? Although there are concerns, as mentioned above, that deserve further study, it’s too early to say definitely that these three vitamins are of significance to people with PD. However, if you are over age 50 these vitamins are of importance independently of PD. Furthermore, studies have demonstrated that some people who use levodopa, considered the best medication for PD, develop elevated levels of serum homocysteine, due to the way in which the medication is metabolized. It is certainly a good idea to ask your doctor to test levels of serum homocysteine annually, and to check for signs of B vitamin deficiencies. Should you take supplements? There is growing agreement that older adults are at risk for nutrient deficiency, whether PD is present or not, and that supplements can help. . One study of older adults found that a multivitamin containing 100% of the Daily Value improved low levels of several nutrients, including vitamins B6, B12, and folate. . A recent study in the United Kingdom suggests that folic acid intake should be about three times that of the current recommendation for elderly people. . Other studies indicate that up to 10% of older adults with low-normal levels of B12 are actually deficient and could benefit from supplements. Because folate supplements can mask a B12 deficiency, it becomes extra important to get enough B12 daily. . The American Heart Association recommends a folate-rich diet to lower homocysteine levels, and supplements of 2 mg B6, 400 mcg folic acid, and 6 mcg of B12 if dietary means are not sufficient to lower the homocysteine. For people with PD who use a medication that contains levodopa (such as Sinemet, Madopar, Syndopa, Larodopa, etc.), you should be aware that large amounts of vitamin B6 (more than 15 mg) can affect the absorption of levodopa, by converting levodopa to dopamine in the stomach and bloodstream. Dopamine cannot cross the blood-brain barrier, so it is effectively blocked from its purpose. Sinemet and Madopar contain either carbidopa or benserazide, which “protect” the levodopa from B6; so ordinary supplements of B6 should not be a problem for most people. However, very large amounts of B6, greater than 15 mg (and in sensitive persons, possibly as low as 10 mg), could overwhelm the protective effects of the carbidopa or benserazide. Such a supplement should be taken at bedtime with a light snack, or with meals at least two hours separately from levodopa. In summary, older adults are acknowledged to be at increased risk for B vitamin deficiencies. People with PD who are age 50 and over, therefore, are at increased risk also. Whether younger people with PD should be concerned about such deficiencies remains to be seen. A prudent and rational approach for all those with PD is to: . Discuss the possibility with their physicians, and to request tests for B vitamin deficiencies . Be aware of the signs of B vitamin deficiency . Take a multivitamin/mineral supplement daily. Unless anemic, choose a supplement that does not contain iron . Take a B complex supplement if deficiencies occur; and take the supplement separately from levodopa by at least two hours, preferably with meals or a snack. Knowledge is strength; awareness of dietary needs can prevent illness, malnutrition, suffering, and hospitalization. If you have questions about B vitamins or other nutrition or dietary needs, please visit the National Parkinson Foundation website: http://www.nutritionucanlivewith.com/
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