Figure 1
Figure 1. Clinical conditions known to influence circulating hepcidin levels. Clinically relevant conditions include CKD,11,16 RBC transfusions,27 iron administration,28.29 replete iron stores,1 TMPRSS6 variants,30,31 infections/inflammatory disorders,32-34 ineffective erythropoiesis,3,49 hypoxia,35,36 administration of erythropoietic stimulating agents,37 chronic liver diseases,38 alcohol abuse,39 HCV,40 hemochromatosis-related mutations,1,28,41,42 and administration of the sex hormones testosterone43 and estrogens.44,45 CKD, chronic kidney disease; GFR, glomerular filtration rate; HCV, hepatitis C virus; HH, hereditary hemochromatosis; IDA, iron deficiency anemia; RBC, red blood cell; TMPRSS6 (transmembrane protease serine 6), the gene encoding for matriptase-2.

Clinical conditions known to influence circulating hepcidin levels. Clinically relevant conditions include CKD,11,16  RBC transfusions,27  iron administration,28.29  replete iron stores,TMPRSS6 variants,30,31  infections/inflammatory disorders,32-34  ineffective erythropoiesis,3,49  hypoxia,35,36  administration of erythropoietic stimulating agents,37  chronic liver diseases,38  alcohol abuse,39  HCV,40  hemochromatosis-related mutations,1,28,41,42  and administration of the sex hormones testosterone43  and estrogens.44,45  CKD, chronic kidney disease; GFR, glomerular filtration rate; HCV, hepatitis C virus; HH, hereditary hemochromatosis; IDA, iron deficiency anemia; RBC, red blood cell; TMPRSS6 (transmembrane protease serine 6), the gene encoding for matriptase-2.

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