Key result
A combination of four Coulter parameters including RDW and MCV can distinguish nonanemic, macrocytic alcohol abusers from macrocytic patients with early, nonanemic pernicious anemia in 94% of cases.
Why the study?
Can automated blood cell count parameters (RDW and MCV) distinguish between alcohol abuse and pernicious anemia?
Can automated blood cell count parameters (RDW and MCV) distinguish between alcohol abuse and pernicious anemia?
Answers are grounded in this paper and cite their sources.
A combination of automated blood cell count parameters including RDW and MCV may help distinguish macrocytic alcohol abusers from patients with early pernicious anemia.
To the Editor. —According to Bessman and McClure,1automated blood cell count, when it includes the red cell distribution width (RDW), is sufficient to detect iron deficiency in an ambulatory population. This seems to be true, especially with a mean corpuscular volume (MCV) of 99 fL or less. We have also found that a high RDW is frequently connected with alcohol abuse. The combination of a high MCV and a high RDW may indicate immune hemolytic anemia or a deficiency of folate or vitamin B12.2Our previously reported results3using a Coulter Counter S-Plus IV (Coulter Electronics Inc, Hialeah, Fla) showed that this combination may, however, also indicate alcohol abuse among male patients, even though the combination is seen more often with pernicious anemia. A combination of four Coulter parameters can distinguish nonanemic, macrocytic alcohol abusers from macrocytic patients with early, nonanemic pernicious anemia; 94%
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Pekka Sillanaukee (1992) conducted a letter in Alcohol abuse and iron deficiency anemia. Red cell distribution width (RDW) and mean corpuscular volume (MCV) was evaluated on Distinguishing nonanemic, macrocytic alcohol abusers from macrocytic patients with early, nonanemic pernicious anemia. A combination of four Coulter parameters including RDW and MCV can distinguish nonanemic, macrocytic alcohol abusers from macrocytic patients with early, nonanemic pernicious anemia in 94% of cases.
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