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. Author manuscript; available in PMC: 2022 Oct 1.
Published in final edited form as: Br J Haematol. 2021 Aug 16;195(1):123–132. doi: 10.1111/bjh.17723

Table 4:

Multivariable Model for Hyperfiltration at Baseline in Adults with Sickle Cell Disease

All Sickle Cell Disease HbSS/HbSβ° Thalassemia HbSC/HbSβ+ Thalassemia
Variable Odds Ratio (95% CI) p Odds Ratio (95% CI) p Odds Ratio (95% CI) p
Age 0.86 (0.82 – 0.90) < 0.0001 0.81 (0.75 – 0.87) <0.0001 0.93 (0.87 – 0.99) 0.03
Male Sex 0.16 (0.07 – 0.41) 0.0001 0.13 (0.04 – 0.50) 0.003 0.08 (0.02 – 0.46) 0.004
Hemoglobin 0.76 (0.61 – 0.94) 0.01
Weight 0.96 (0.93 – 0.99) 0.004 0.94 (0.89 – 0.99) 0.01
Hydroxyurea Therapy 2.99 (1.18 – 7.56) 0.02
Use of ACE-I/ARBs 0.08 (0.01 – 0.75) 0.03 0.07 (0.01 – 0.82) 0.03
Lactate Dehydrogenase 0.998 (0.997 – 1.000) 0.03

ACE-I = angiotensin-converting enzyme inhibitor; ARB = angiotensin receptor blocker

For continuous variables Odds Ratios (OR) are for a one unit change.

Results from multivariable logistic regression with backward elimination for variable selection. Variables initially assessed for inclusion in the model: white blood cell count, hemoglobin, reticulocyte count, lactate dehydrogenase, total bilirubin, hydroxyurea therapy, weight, systolic blood pressure, diastolic blood pressure, acute chest syndrome, and ACE inhibitor/ARB therapy. The model was adjusted for age and sex.