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Letters |
1
Dept. of Physiol.,
2
Cardiovasc. Res. Inst. (CARIM),
3
Dept. of Nephrol., Med. School of Bialystok, 15230 Bialystok, Poland, Univ. of Limburg, P.O. Box 616, 6200 MD Maastricht, The Netherlands
a Author for correspondence.
To the Editor:
The soluble cytoplasm of most cells contains low-molecular-mass
(1415 kDa) proteins able to bind long-chain unesterified fatty acids.
Of these so-called fatty acid-binding proteins (FABP), nine different
types have been identified (1)(2). Heart and
skeletal muscles contain the same type of FABP [referred to as
heart-type (H)-FABP] (1)(2), but its
concentration in the heart is severalfold higher than that in the
skeletal muscles (3). The concentration of FABP in the
plasma of healthy persons is relatively low (26
µg · L-1) (4). FABP is released from
the heart early after the onset of infarction, whereafter its plasma
concentration increases manyfold (3)(4)(5)(6). Increased
excretion of FABP in urine also occurs after infarction
(5)(7). Several recent studies indicate the
usefulness of the plasma FABP concentration as an early biochemical
marker for myocardial infarction diagnosis
(3)(5)(7). However, to interpret
properly the values of plasma FABP concentration, one has to take into
account not only its source and rate of release into plasma but also
its elimination from plasma. It is obvious that any change in the
clearance rate of FABP would affect its plasma concentration, and thus
may lead to erroneous interpretation. Kleine et al. (8)
reported a patient with acute myocardial infarction and severe renal
Acknowledgments
References
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