Posts Tagged ‘Disease’

Wheat And Gluten Intolerance: An Introduction To Celiac Disease

Monday, December 14th, 2009

Celiac disease, or celiac sprue, officially known as “gluten intolerant enteropathy” is a genetic auto-immune disorder, this means that a gene carries a physical trait, and that trait can be passed down from one family member to another.


“Auto-immune” describes the way that the disease does damage; “auto” means “to oneself” so it is saying that the immune system of a celiac mistakenly does damage to the celiac rather than to the supposed invader. What happens is that the immune system believes that a portion of the food eaten needs to be attacked, and as a side-effect of the attack, the lining of the small intestine gets damaged.


It appears as though the gene for celiac disease may ride on the same gene as diabetes, and like diabetes, you can carry the gene but not have the disease. It takes some “triggering event” to start up the process (little is known about this mechanism, but suspected “events” include physical or emotional stress, pregnancy, over-exposure to wheat, other diseases, and even antibiotics); and, of course, the celiac must be exposed to wheat in the first place.


Dermatitis herpetiformis (DH) is another form of celiac disease. Anyone who has DH is a celiac. In this form of the disease, lesions that look like a herpes sore appear on the skin, usually in very symmetrical ways: on the hands, arms, head, elbows, knees, buttocks, etc. They are often extremely itchy. (Please note that the name of this disease is misleading, it has absolutely nothing to do with herpes.


A very common wheat allergy happens when your body sees wheat as an invader and attacks it. Symptoms of a wheat allergy could be eczema (different from dermatitis herpetiformis), sneezing, increased acne, or if you have a very serious allergy to wheat, you might have an anaphylactic reaction in which your throat can swell up to the point where you can no longer breath. However, these are not typical symptoms of celiac disease.


The main effect of celiac disease is the damage that is done to the small intestine; if you have symptoms that are caused by damage to the small intestine (for example, flattened villi as seen in a biopsy, or any form of malnutrition that is caused by the damaged villi) then what you have is not a wheat allergy, but rather celiac disease.


Traditionally, experts have seen very few people with a simple “wheat allergy”, and many more with celiac disease, so many experts predict that celiac disease is more common than wheat allergies. If you have problems with wheat, you should visit with a gastroenterologist and get tested for celiac disease.


Unfortunately, at this time, there is no cure, and no hope for a cure any time soon. Once the disease has been triggered there is no way to turn it off, though in the far future there might be hope for gene therapies or other mechanisms which might work; none of these are likely in the near future. However, while there is no actual cure, a gluten-free diet solves most of the problems associated with the disease.


“Gluten-free” is another slight misnomer, since it’s probable that “gluten” isn’t the problem, and it certainly isn’t the whole problem, however this term has come to represent the celiac diet and so we define what we eat, or what we don’t eat, by this term. A gluten-free diet just means strict avoidance of wheat, rye, barley and oats, even in the tiniest of amounts. This is more easily said than done, but once one becomes familiar with the diet it becomes routine.


According to experts, celiac disease is known as “The Great Mimic” because patients who ultimately end up diagnosed with the disease come to the doctor’s office with such a wide variety of symptoms that it can be very hard to diagnose. What this means is that there is no typical set of symptoms. There is a classic set of symptoms (diarrhea, thinness, malnutrition, pot belly) that is associated with the disease, but classic is not the same as typical. People with celiac disease who are not following a gluten-free diet may have just one symptom (maybe just anemia, or feeling run down, or behavioral problems) or they may have several.


That said, here is a list of possible symptoms which can include short term symptoms such as: diarrhea, constipation, steatorrhea (fatty stools that float rather than sink), abdominal pain, excessive gas, fuzzy-mindedness after gluten ingestion, burning sensations in the throat, irritability, inability to concentrate, pale, malodorous, bulky stools, frequent, foamy diarrhea, and an itchy rash (in dermatitis herpetiformis).


Longer term symptoms can include: any problem associated with vitamin deficiencies such as; iron deficiency (anemia), chronic fatigue, weakness, weight loss, bone pain, easily fractured bones, abnormal or impaired skin sensation (paresthesia), including burning, prickling, itching or tingling, and edema, as well as, white flecks on the fingernails, failure to thrive (in infants and children), paleness, wasted buttocks, pot belly with or without painful bloating, and persistent itchy rashes (in dermatitis herpetiformis).


Celiacs who are not following a gluten-free diet will suffer from damage to the lining of their small intestines (specifically, to the “villi” the little hair-like growth that helps process food in the small intestine). This damage slows and even prevents the digestion of food, which can lead to malnutrition (anemia, osteoporosis, vitamin deficiencies, and more).


Over the long term, the constant damage to the small intestine can cause enough wear to lead to intestinal cancers. In the short run, many annoying symptoms can also make life downright uncomfortable. Following a gluten-free diet reduces the risk of cancer down to that of the general population, and will improve digestion enough to sustain the body normally, as well as getting rid of the usual short-term side effects.


The primary indicator test for celiac disease involves three biopsies (one before going on a gluten-free diet, showing damage to the villi; one during a gluten-free diet, showing healed villi; one after going back to eating gluten, again showing damage), but many knowledgeable physicians now accept one biopsy, an antibody blood test, and improvement of symptoms while on a gluten-free diet (the biopsy showing damage to the villi prior to a gluten-free diet; the antibody test showing elevated antibodies to gluten while still eating a gluten-filled diet). A less formal diagnostic process would just involve the blood tests, and improvement on a gluten-free diet.


It should be noted that the blood tests look for elevated IgA antibodies as an immune response to gluten, but a fair percentage of people with celiac disease are IgA deficient, and so their tests would give a false negative. There is another test now being manufactured (Tissue Transglutaminase Testing or tTG) which looks at IgG antibodies, instead of IgA antibodies, that is proving very reliable for diagnosing celiac disease.


Although the disease itself has been around for quite some time, it gets the name “sprue” from the similarity of symptoms to “tropical sprue” which is an older known disease, the cause of the disease was not recognized until the middle of this century, when war-time limited supplies of wheat to local populations, and a physician noticed after the war, that several of his “sprue” patients who had improved during the war, were now ill again. It was not long before he realized that wheat was the culprit.


From that point, continued investigation added rye, barley, and oats to the list of grains that made celiac sprue patients sick. Still, for quite a while it was thought of as a childhood disease that would be outgrown, so it was not that long ago that the medical community recognized that adults suffered from the disease as well. Until very recently, it was thought of as a “rare” disease in the United States, and most medical practitioners are still unaware of the growing evidence that celiac disease is actually quite common.

Alzheimer?s Disease

Thursday, December 10th, 2009

Along with the development of modern technologies, going to the moon and other exciting developments humans face the threat of diseases that affect the process of life and can be lethal in some cases. One of the illnesses that have a great affect on people’s behavior is Alzheimer’s disease (AD). Alzheimer’s disease is the degenerative disease of the brain among old people from which there is no recovery. Slowly the disease attacks the brain cells in all parts of the brain and some surrounding structures, so the an ill person loses the previous abilities to govern emotions, understand mistakes, coordinate his movements and finally a person loses all of his memory and ability to mentally function (B. Heights 2002).

AD is named after German doctor Alois Alzheimer. Dr. Alzheimer noticed changes in the brain tissue of a woman that died of an unusual mental illness. He found abnormal clumps (now called amyloid plaques) and tangled bundles of fibers (now called neurofibrillary tangles). Today, these plaques and tangles in the brain are considered hallmarks of AD. Many scientists have found other brain changes in people with AD. There is a loss of nerve cells in areas of the brain that are vital to memory and other mental abilities. There also are lower levels of chemicals in the brain that carry complex messages back and forth between nerve cells. AD may disrupt normal thinking and memory by blocking these messages between nerve cells (H. Simon).

Scientists are finding specific biologic factors (Peter, Konrad, and Ballenger 2000) involved with the AD. Different environmental and genetic aspects take part in causing AD. However, the actual cause of the disease is still unknown. The greatest known risk factors for late-onset Alzheimer’s are increasing age and a family history of AD. Researches all over the world are trying to find other factors that can cause AD.

AD is nowadays the fourth leading cause of death among the adults. Nearly four million Americans have it. The number doubles every five years in people over sixty five years old. By the age of eighty five almost half of Americans have AD. Some studies show that women have much higher risk of being affected by the AD than men (most of these studies were conducted on European and Asian populations, the U.S. studies, however, found no major differences). If there is a gender difference, then it is because of estrogen which is the main female’s hormone that is responsible for protecting against memory losses and normal mental functioning as compared to normal age. When a female gets older, the drop of estrogen level takes place after menopause and that could explain the higher risk of AD for older women than for men. From the other side, some of testosterone, male hormone, converts into estrogen and that could protect men. People that have a family history of the disease are above the average risk level for AD. Researchers have found that ApoE4 gene could be responsible for late and early onset cases. Some studies discovered that African Americans and Hispanics are at higher risk than Caucasian Americans, AD happens less often in Native Americans Crees and Cherokees and in Asians than in regular American population. Genes may have dissimilar effects in different populations (Tanzi and Ann B. 2000).

High blood pressure and high cholesterol levels can be in fact even more risky than ApoE4. At a very high risk are also people that inherit the Down syndrome. Some other risk factors are: 1) lower education and economic groups, 2) small head size, 3) Depression, 4) head injury.

A very dangerous thing about AD is that brain is being damaged for years before even the symptoms appear. The early symptoms that appear might be so mild that people could hardly notice them. The first one could be forgetfulness. People with AD may have troubles with recalling names of people that they know or remember latest events or solve simple math problems. As the disease progresses people may face

• Unreasonable weight losses

• Incontinence

• Changes in sexuality

• Difficulties in walking

• Depression, apathy, irritability

Half of all patients that have AD face the psychotic problems that can include hallucinations, visions. It is a complex form of the disease that is probably based in the genetic level. Many other medical conditions have similar to Alzheimer’s symptoms. It is crucially important to identify the right disease to succeed in future treatments of it. However, we have not yet developed a test that would diagnose AD with the hundred percent guarantee. So, right now diagnosis involves ruling out other disorders the following questions about the state of a patient:

• Do psychologist tests indicate dementia?

• Does the patient have problems with using language, walking, perception?

• Has memory gotten greatly worse?

• Is the patient over 40?

• Does his/her behavior changes daily?

• Does the patient have a family history of AD?

• Are there other symptoms like depression, weight loss, hallucinations?

Other steps that are involved in making a decision involve laboratory tests (EEG and tests to rule out other diseases) and psychological testing to determine the presence of dementia.

There is no guarantee that some life styles will prevent AD, however, studies show that particular life styles can play very important role in preventing AD. It is crucial to prevent heart diseases. Calcium – Channel Blocker and other Anti – Hypertensive Agents can be used to protect the heart and consequently the brain. Statins which are the common drugs to lower the cholesterol level can also be used to lower the risk for AD. Another method that is used to prevent AD is the Hormone Replacement Therapy. Because of the difference in AD rates among different populations, researches are looking at dietary factors as a protection. In China and Nigeria where fat consumption is much lower than in the U.S. the risk for AD at the age of sixty five is only 1% compared to 5% in the U.S. Studies in Netherlands reported the relationship between dementia and cholesterol levels. Eating a lot of dark colored fruits and vegetables may slow the brain degradation. Blueberries are found to be the most helpful. In any case dark colored fruits and vegetables are good for health. Other studies showed that soy has estrogen which is thought to protect the memory. Some reported that small consumption of alcohol can be effective in stopping the brain aging. Not everybody agrees though. Caffeine has a good effect on women in terms of mental functioning. Much research on AD has showed that oxidation may have an impact in the disease process. Vitamin E may protect from mental decline. Other health behaviors like aerobic exercises or jogging are important in stopping the mental decline. The more person exercise the better. Another aspects that play role in the prevention of mental decline is lifelong learning and stress reduction.

Unfortunately, today we can only try to prevent AD and have no cures. However, there are drugs under investigation that are aimed to slow the progression of the AD. The bad thing is that improvements from some of these drugs can so little that a patient or his/her family would not even notice. The good thing is that even these drugs will help to postpone the necessity of taking a patient to a nursing home (Alzheimer’s Association). The only agents that are approved called selective Acetylcholinesterase inhibitors. They are designed to protect the cholinergic system which is responsible for memory and learning and is destroyed in AD. We have the following:

• Donepezil. Donepezil (Aricept) is taken once a day and has only modest benefits but it helps to slow loss of function and reduce caregiver burden. It works equally in patients with or without ApoE4. It may even have some advantage for patients with moderate to severe Alzheimer’s disease.

• Rivastigmine. Rivastigmine (Exelon) targets two enzymes (the major one, acetylcholinesterase, and butyrylcholinesterase). It is taken twice a day. This agent may be particularly beneficial for patients with rapidly progressing disease. This drug has slowed or slightly improved disease status even in patients with advanced disease. (Rivastigmine may cause significantly more side effects than donepezil, including nausea, vomiting, and headache.) As with all anticholinergics, the drug is not a cure.

• Galantamine (Reminyl). Galantamine not only protects the cholinergic system but also acts on nicotine receptors, which are also depleted during Alzheimer’s Studies report that it improves daily living, behavior, and mental functioning, including in patients with mild to advanced?moderate Alzheimer’s disease and those with a mix of Alzheimer’s disease and vascular dementia. Some studies have suggested that the effects of galantamine may persist for a year or longer and even strengthen over time.

• Tacrine. Tacrine (Cognex) was the first cholinergic protective drug. It needs to be taken four times a day, has only modest benefits, and has no benefits for patients who carry the ApoE4 gene. In high doses, it can also injure the liver. In general, newer cholinergic protective drugs that do not pose as great a risk for the liver are now used for Alzheimer’s (Castleman, Gallagher-Thompson, and Naythons 2000).

Half of the patients that have mild to moderate disease show sight improvement. Latest studies, however, show little difference in effectiveness among them. All these drugs have gastrointestinal side effects, including nausea. Anyway, these drugs still have some effect. Some researchers found that some patient could have no reactions to one particular drug, in this case the drug should be switched and there is actually a chance that it will work. There are also some alternative treatments that are being studied right now. One of them is Gingko Biloba. It is a common herb that increases blood flow to the brain. Its extract Egb 761 may slightly improve the memory of patients that have mild to moderate AD. Gingko Biloba has only minimal side effects. Turmeric also has properties that may protect from AD. Turmeric is a spice that has curcumin as one of its components which is thought to protect from AD. Studies have also found that melatonin, the natural hormone that has to do with sleep regulation, could break down beta amyloid, and it is able to pass through the blood – brain barrier. Studies reported that melatonin improves the sleep, and in some cases even slows the mental regression (H. Simon).

A number of other medical treatments are being investigated and show promise in early or late trials. Researches are focusing on agents that can prevent the build-up of beta amyloid, its toxic effects on nerve cells, or other mechanisms of the disease process. Among them are the following:

• N?methyl?D?aspartate (NMDA) blockers. NMDA blockers, such as memantine (Ebixa), bind to glutamate, an amino acid that excites nerves and, in excess, is a powerful nerve?cell killer. Memantine has shown some to be somewhat effective in improving symptoms and is being considered for approval in Europe and the US.

• Growth factors that stimulate nerve activity in the brain. Cerebrolysin (Cere) is an example of such drugs and is showing promise in clinical trials in improving mental function and other symptoms, with sustained effects even after the drug has been stopped. Leteprinim potassium (Neotrofin) activates genes that produce nerve?growth factor in the brain. Early human trials are suggesting that it may have positive effects on memory and behavior. Insulin and insulin growth factors may prevent beta amyloid accumulation.

• Antioxidants. Indole?3?propionic acid, or IPA (Oxigon), is a natural agent that may interfere with enzymes that contribute to the Alzheimer’s disease process.

• Huperzine alpha, another acetylcholinesterase inhibitor, improved mental function, behavior, and mood in Alzheimer’s disease patients in one Chinese study. Other research also suggests some benefits.

• Piracetam is a nerve protective agent called a nootropic. It has undergone a number of small studies, with few significant results. More research is needed to determine any benefits.

• Researchers are investigating immunotherapies that include vaccines, which use molecules in beta amyloid as targets for the body’s immune system, and antibodies that block proteins called CD40?CD40L, which are involved in amyloid deposition.

• Tetracyclines. Antibiotics known as tetracyclines, such as tetracycline itself, doxycycline, and minocycline, have anti?inflammatory properties that are now being investigated in a number of chronic inflammatory conditions (such as periodontal disease). They also may have activity against beta amyloid in the brain (H. Simon).

The worst thing about Alzheimer’s disease is that it is not fully investigated yet. None of the doctors can surely diagnose it. And what is even worse none can cure it. The worst thing is that AD lethal in all case. Using all the treatments that have been or are still being studied can only postpone the need for the nursing home (Terry, Katzman, Bick, Sisodia 1999).

The issue of Alzheimer’s disease is crucially important to me and should be to everyone. Mainly, because nobody is insured from getting AD and there is no certain way to escape it. Our modern medicine has been developing through ages and now it cures many dangerous diseases; however, it is simply helpless against the Alzheimer’s. If scholars completely investigate AD it will help to understand the brain and its impact on people’s behavior. Using that knowledge it would be possible to impact the brain and its functions. Unfortunately, all the studies that were conducted about AD and were presented above can not state something about AD with a hundred percent certainty. All the medications that are listed above do not stop AD; they can even hardly slow it. It is very unpleasing fact that mankind has greatly developed ways to make the brain progress but have not yet found any way to stop the regression of the brain.

Introduction And Definition Of Disease

Wednesday, December 2nd, 2009

Disease is the term used for any condition or tendency that hampers the normal functioning of the body. In general, human beings refer the term ‘disease’ to any condition that causes uneasiness, dysfunction etc. The study of diseases is called pathology. Also, the classification of diseases is called Nosology.

Diseases can be classified based on the cause or the mechanism by which the disease is caused.

There are various factors that cause disease. They are classified as:

 Intrinsic factor – Disease caused due to the abnormalities existing within the body. They include genetic defects, stress-related diseases, autoimmune disorders, nutritional defects etc.

 Extrinsic factor – Disease caused due to environmental conditions. An example for extrinsic factor may be passive smoking.

There are also other factors that cause diseases they are social, psychological, chemical and biological. These factors may fall into intrinsic or extrinsic factors. For example, when it comes to cigarette smoking the smoke released contains chemical substances that causes diseases to the smoker as well as the neighboring person. This is called either chemical factor or extrinsic factor.

When harmful germs or microbes (like bacteria, viruses and protozoa) enter the human body, they multiply and cause diseases, the human body is said to have an infection.

Infections are classified as

 Infectious disease
 Non-infectious disease

Infectious diseases are those diseases that transmit from one person to another. These diseases are transmitted through air, insect bites, infected injections, contaminated water or food and sometimes through blood transfusion. These diseases can also be called as contagious or communicable diseases. To avoid spreading of this type of disease it is advised to take the appropriate medicines that fight the germs that cause them. Also, it is better to stay away from person during the time when the disease can be spread.

Non-infectious diseases are those diseases that do not transmit from one person to another. Examples of non-infectious disease are diabetes, stress-related disease etc.

The nine most expensive diseases in the US according to an article in Forbes, based on the research performed by Agency for Health Care Research and Quality (AHRQ) are:

Diseases Annual Cost
Heart Conditions (this excludes hypertension and elevated cholesterol) $68 billion
Trauma $56 billion
Cancer $48 billion
Mental Illness $48 billion
Respiratory Ailments $45 billion
Hypertension $32.5 billion
Arthritis And Joint Disorders $32 billion
Diabetes $28 billion
Back Problems $23 billion

The research further provides with the fast growing diseases in the US. Some of the diseases listed in the research are:

 Esophageal Disorders

The cost per patients has come down whereas the number of people diagnosed with heartburn and related disorders have increased by 509% to 10 million between 1997 and 1996-2002.

 High Cholesterol

The number of people diagnosed with High Cholesterol has increased by 145% to 19 million.

 Hemorrhoids

The number of people increased by only 23% to 1.2 million.

 Anxiety Disorders

The number of patients treated for anxiety has doubled to 12 million over five years.

 Breast Cancer

The number of cases rose 65% to 1.2 million.

Hashimoto’s Disease – Causes, Symptoms and Treatment Methods

Friday, November 20th, 2009

Hashimoto’s disease is a disease characterized by the immune system attacking the thyroid gland. . A family history of thyroid disorders is common, with the HLADR5 gene most strongly implicated conferring a relative risk of 3 in the UK. The person may experience symptoms of hyperthyroidism at first when the thyroid may actually produce too much thyroid hormones. It is caused by a reaction of the immune system against the thyroid gland. Hashimoto’s disease is the most common cause of hypothyroidism in the United States. Hashimoto’s disease, also known as chronic lymphocytic thyroiditis, causes inflammation of your thyroid gland that often leads to underactive thyroid (hypothyroidism). Lymphocytic thyroiditis may also occur as a self-limited condition which lasts 2-6 months, resolving spontaneously, and leaving most patients with normal thyroid function. Chronic thyroiditis or Hashimoto’s disease is a common thyroid gland disorder that can occur at any age, but it is most often seen in middle aged women. It is more prevalent in women than in men (8:1), and its incidence increases with age Blood tests of thyroid function are used to detect Hashimoto’s disease. Patients with this form of thyroiditis sometimes exhibit so few symptoms that the disease may go unnoticed for many years, but eventually it may destroy so much thyroid tissue that hypothyroidism develops.

Many people with this disease have no symptoms. Hashimoto’s Disease is often referred to as Hashimoto’s thyroiditis, autoimmune thyroiditis, lymphadenoid goiter, struma lymphomatosa, and chronic lymphocytic thyroiditis. Hashimoto’s Thyroiditis is not uncommon. Many people with Hashimoto’s thyroiditis have other endocrine disorders, such as diabetes, an underactive adrenal gland, or underactive parathyroid glands, and other autoimmune diseases, such as pernicious anemia, rheumatoid arthritis, Sjögren’s syndrome, or systemic lupus erythematosus (lupus). In many cases, Hashimoto’s thyroiditis usually results in hypothyroidism, although in its acute phase, it can cause a transient thyrotoxic state. Hashimoto’s disease progresses slowly over a number of years and causes chronic thyroid damage, leading to a drop in thyroid hormone levels in your blood. Less commonly, Hashimoto’s disease occurs with hypoparathyroidism, adrenal insufficiency, and fungal infections of the mouth and nails in a condition called type 1 polyglandular autoimmune syndrome. The thyroid gland typically becomes and the antibodies the body normally produces to protect the body and fight foreign substances such as bacteria, are found to ‘attack’ their own thyroid tissue. Treatment with synthetic thyroid hormone replacement medication usually is simple and effective. Natural treatment options also exist.

Causes of Hashimoto’s disease

The common causes and risk factor’s of Hashimoto’s disease include the following:

The exact cause of Hashimoto’s disease is unknown.

A reaction of the immune system against the thyroid gland.

If someone in your family has had thyroid disease, you may have an increased risk for Hashimoto’s disease.

Hashimoto’s thyroiditis is most common among women, particularly older women, and tends to run in families.

It may rarely be associated with other endocrine disorders caused by the immune system.

A combination of factors including heredity, and age may determine your likelihood of developing the disorder.

Hashimoto’s Thyroiditis is seen more frequently in people taking extra iodine in their diets.

Symptoms of Hashimoto’s disease

Some sign and symptoms related to Hashimoto’s disease are as follows:

Fatigue.

Enlarged neck or presence of goiter.

Small or atrophic thyroid gland.

Dry skin.

Joint stiffness.

Excessive sleepiness.

Dry, coarse hair.

Facial swelling.

Hair loss.

Heavy and irregular menses.

Hoarse voice.

An elevated blood cholesterol level.

Intolerance to cold.

Most often, people with Hashimoto’s Thyroiditis suffer from symptoms of Hypothyroidism (fatigue, lethargy, decreased metabolic rate).

Treatment of Hashimoto’s disease

Here is list of the methods for treating Hashimoto’s disease:

Iron supplements.

If Hashimoto’s disease causes thyroid hormone deficiency, you may need replacement therapy with thyroid hormone.

Antibiotics to fight infection.

Hormones to suppress or replace thyroid function.

Sucralfate, an ulcer medication.

Long-term prognosis is very good. Most people with the disease can be easily treated.

Cholestyramine (Questran), a medication used to lower blood cholesterol levels.

Replacement therapy with thyroid hormone is given if the hormone is deficient or may be given if there is evidence of mild thyroid failure.