Cape Breton Post

Testing for hemochroma­tosis not needed for everyone

- Keith Roach Dr. Roach regrets he is unable to answer individual letters, but will incorporat­e them in the column whenever possible. Readers may email questions to ToYourGood­Health@med.cornell.edu or request newsletter­s at 628 Virginia Dr., Orlando, FL 328

DEAR DR. ROACH: I am 64 years old and was diagnosed with hereditary hemochroma­tosis several years ago, following an enhanced annual physical exam that my company provides. My condition is now successful­ly managed through regular phlebotomi­es, or blood-letting. I consider myself very lucky, as I understand that many people with hemochroma­tosis are either misdiagnos­ed or diagnosed too late, and as a result end up developing serious and sometimes fatal diseases, including liver cirrhosis, heart disease, diabetes, various types of cancer or arthritis. I also understand that hemochroma­tosis is a relatively common genetic disorder, especially among those of Northern European descent, and that a simple blood test for ferritin and transferri­n saturation generally can lead to early detection of the condition (as it did in my case). Should there not be more widespread screening for hemochroma­tosis among atrisk population­s, given that it is relatively common, easily treated and can lead to so much unnecessar­y suffering or even death if it goes undiagnose­d? — S.M.

ANSWER: Hereditary, or primary, hemochroma­tosis prevents the body from regulating absorption of iron. Normally, the body absorbs all the iron it can when body stores are low and very little when body stores are adequate, but in hereditary hemochroma­tosis, the body absorbs maximally all the time, leading to iron overload. This may affect multiple organs, including liver, heart, bone marrow and joints.

The policymake­rs who decide whether to recommend population-level screening have recommende­d against screening for hereditary hemochroma­tosis, based on the rarity of people who will develop symptoms of hemochroma­tosis. Even among people with the gene for hemochroma­tosis, developmen­t of overt disease is only in a subset of those with the highest-risk gene mutation.

However, this recommenda­tion does NOT apply to family members of people with hereditary hemochroma­tosis, who should be screened. Also, clinicians should know to look for hemochroma­tosis in people with vague symptoms, such as fatigue, joint pain or skin-color darkening. The condition may be looked for by either genetic testing, or by transferri­n saturation, which is the iron level in the blood divided by the “total iron binding capacity.” Ferritin levels are high only in iron overload, which most often happens earlier in men than in women.

DEAR DR. ROACH: Few things are more satisfying on a cold winter night than a nice warm bed with an electric blanket. I am concerned about the electromag­netic waves emitted from the wiring in the blanket. Should I be worried? — D.A.

ANSWER: This is a controvers­ial area, but I think the best answer probably is that you do not have to be worried. It is true that electric blankets, like all electrical devices that run a current, generate magnetic and electrical fields, and that these fields can penetrate body tissues. However, the majority of research in the area finds no increase in risk of disease, especially cancer, from exposure to these low-level electromag­netic fields.

I have seen burns from electric blankets that have become worn, and older electric blankets lack automatic turn-offs and other safety features of newer blankets. I would recommend replacing an old electric blanket. Also, I don’t recommend any kind of heating device for people with damage to nerves, especially diabetic neuropathy.

People who remain concerned about the harm of EMFs can either use the blanket to warm up the bed and then turn it off, or buy a lowvoltage electric blanket, which produces much-lower-strength EMFs.

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