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Fast Fact
A fasting blood sugar at or above 126 mg/dL or a random blood sugar at or above 200 mg/dL is diagnostic of diabetes, according to the official American Diabetes Association definition.
A fasting blood sugar of 100 to 125 mg/dL or a random blood sugar between 140 to 199 mg/dL is diagnostic of prediabetes, according to this same definition.
Prediabetes occurs when a person's blood glucose levels are higher than normal but not high enough to be diagnosed with type 2 diabetes.
The name, diabetes mellitus, comes from the Greek words for "to flow through" and "sweet." The Greek physicians used to diagnose the condition by actually tasting the urine. (That's dedication!)
Normally, a hormone called insulin pushes sugar from the blood into the body's cells where it can be used for fuel. The concentration of sugar in the blood remains within a fairly narrow range. If the body stops making insulin (type 1 diabetes), then adequate sugar doesn't get into the cells.
Until June 23, 1997, type 1 diabetes was also called insulin-dependent diabetes mellitus (IDDM).
Without insulin, muscle and fat begin to be burned for fuel (evidence of this -- ketones -- shows up in the urine). The person feels hungry all the time, but loses weight in spite of increased eating. Without replacement insulin, the person would eventually starve to death. Meanwhile, the concentration of sugar in the blood begins to increase. When the level reaches around 180 mg/dL, the sugar begins to spill over into the urine. This causes the person to make more urine and then to get thirstier, creating an accelerating cycle.
The classic symptoms of type 1 diabetes are increased urination (polyuria), increased thirst (polydipsia), increased eating (polyphagia) and weight loss. Anyone with the classic symptoms should have a blood sugar test as well as a urine test.
Occasionally people also report fatigue, blurred vision, vomiting, abdominal pain, or frequent skin infections.
If the disease remains undiagnosed, symptoms progress to include labored breathing, coma, and death.
People who get type 1 diabetes were born with a genetic predisposition to it. Not everyone born with this predisposition gets diabetes, however. In fact, if an identical twin has diabetes, the other twin gets it only about half the time.
Along the way, some of the predisposed individuals are exposed to something in the environment that triggers the diabetes. This is usually a viral infection. The virus misleads the body's immune system into making antibodies against its own pancreas cells that make insulin. (This is why type 1 diabetes is now also called immune-mediated diabetes.) The insulin-producing cells of the pancreas are gradually destroyed over time. When 90% of them have been destroyed, the person suddenly begins to develop symptoms.
Immune-mediated or type 1 diabetes most often strikes young people, especially between the ages of 5 and 7 (when viruses run through the schools), or at the time of puberty (when so many hormones change). For this reason, it used to be called juvenile-onset diabetes.
About 0.4% of the general public (or one out of 250) will eventually develop type 1 diabetes.
According to the National Diabetes Information Clearinghouse, just over 175,000 children under age 20 in the United States have diabetes.
About 800,000 people in the United States now have type 1 diabetes.
About 30,000 people develop type 1 diabetes each year.
Type 2 diabetes is caused, not by the absence of insulin, but by insulin's not working properly. It is much more frequent in overweight adults over the age of 45, but can occur at any age and weight. There are often no symptoms.
The National Institutes of Health estimates that more than 7 million adults in the United States have undiagnosed type 2 diabetes.
As obesity becomes more common among children, the number of children with prediabetes and with type 2 diabetes has been rising dramatically in recent years.
The American Academy of Pediatrics recommends that if you can answer "yes" to any of the following questions a blood test to check for lead should be considered.
Does your child live in or regularly visit a house that was built before 1950? This includes a home child care center or the home of a relative.
Does your child live in or regularly visit a house built before 1978 that has been remodeled in the last 6 months? Are there any plans to remodel?
Does your child have a brother, sister, housemate, or playmate who is being treated for lead poisoning?
Additionally, if you can answer “yes” to any of the following questions, your child may need to be screened for lead.
Have you ever been told that your child has high levels of lead in his or her blood or lead poisoning?
Does your child live with an adult whose job or hobby involves exposure to lead?
Does your child live near an active lead smelter, battery recycling plant, or other industry likely to release lead into the environment?
Does your child live within one block of a major highway or busy street?
Do you use hot tap water for cooking or drinking?
Has your child ever been given home remedies (azarcon, greta, pay looah)?
Has your child ever lived outside the United States?
Does your family use pottery or ceramics for cooking, eating, or drinking?
The Centers for Disease Control and Prevention also recommends universal screening (testing all children) in areas defined by zip codes where at least 27 percent of the housing was built before 1950 and in which the percentage of 1- and 2-year-olds with elevated blood lead levels is at least 12 percent.
In addition, recent studies have found that older furniture and toys found in antique shops and secondhand stores may have lead-containing paint (Journal of Environmental Health, 70(10):80, 86, 2008). If your home contains these items, your child may benefit from lead screening.
Talk to your pediatrician about lead screening for your child.
Infections can be avoided both by decreasing the exposure to germs and by boosting your child’s immunity. Click here for 6 powerful ways to decrease germ exposure.
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