Guest guest Posted March 16, 2004 Report Share Posted March 16, 2004 ANA (anti-nuclear antibodies) tests .. confusing .. aren't they? Let me try to explain the process so it is easier to understand. When the lab tests your blood sample for ANA cells, they start by taking a couple of droplets of blood and dilute them with another liquid, usually alcohol. A result of 1:20 reads 1 to 20 .. or 1 drop of blood to 20 drops of alcohol. If they see ANA cells, then they dilute it again .. doubling the amount of alcohol each time.. then they read the results again .. and if they see more cells, then they dilute it again .. and again .. and again .. until they see a minuscule amount to no more cells. So .. 1:20 is usually where they start (remember to read it as 1 to 20) For some reason only known to the phlebotomists (smiles .. the vampires who draw our blood), on the higher readings such as 1:160 they will leave off the zero. Not always, but sometimes. So a reading of 1:16 is really 1:160 .. (1 to 160 = 1 drop of blood to 160 drops of alcohol). There were so many cells in your blood that it took a whole lot more alcohol to dilute the sample enough where no cells showed up. The cells that are " captured " are also put on a slide and stained with a special concoction of antigens. After the cells have been stained, they are washed and are then viewed under a fluorescent lighted microscope. The cells will glow in different stain patterns. The patterns have been divided into four to six groups (depending on the testing facility) and determine what kind of disease correlates to each pattern. Example: a reading of 1:160 with a Homogeneous pattern is almost a definite diagnosis of SLE (lupus). From a low reading to a high reading: 1:20 = negative 1:40 = very low positive 1:80 = low positive 1:160 = medium positive 1:320 = high positive 1:640 = very high positive I hope this helped you some. " Rion " http://www.itzarion.com/lupusgroup.html Quote Link to comment Share on other sites More sharing options...
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