Table 2.
IDA Controls (n = 39) | |||
---|---|---|---|
Characteristics | N | Median or Count (%) | IQR |
ALT, U/L | 21 | 18.0 | 16.0–25.0 |
eGFR (CKD-EPI), mL/min/1.73 m2 a | 33 | 89 | 65–≥90 |
BMI, kg/m2 | 39 | 28 | 24–34 |
|
11 (28) | ||
|
9 (23) | ||
|
17 (44) | ||
|
2 (5) | ||
Assessment of underlying disorder of IDA | 39 | N/A | |
|
12 (31) | ||
|
5 (13) | ||
|
4 (10) | ||
|
18 (46) | ||
Assessment of medication use | 39 | N/A | |
|
6 (15) | ||
|
12 (31) | ||
|
1 (3) | ||
|
14 (36) | ||
|
1 (3) | ||
Assessment of response to iron therapy in unexplained IDA b | 18 | N/A | |
|
1 (6) | ||
|
1 (6) | ||
|
4 (22) | ||
|
9 (50) | ||
|
3 (17) |
a eGFR was ≥90 mL/min/1.73 m2 in 49% (n = 16), 60–89 mL/min/1.73 m2 in 30% (n = 10), 45–59 mL/min/1.73 m2 in 18% (n = 6) and 30–44 mL/min/1.73 m2 in 3% (n = 1). b Response to iron therapy 3 weeks after initiation of iron supplementation. IDA, iron deficiency anemia; IQR, interquartile range; N/A, not applicable; ALT, alanine aminotransferase; eGFR, estimated Glomerular Filtration Rate; BMI, body mass index; Hb, hemoglobin, NSAIDs, non-steroidal anti-inflammatory drugs; IV, intravenous.