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. 2017 Oct 9;12(11):1795–1803. doi: 10.2215/CJN.03950417

Table 2.

Associations of baseline fibroblast growth factor 23 with prevalent anemia

Number of Patients, Total N Per 1 SD ln FGF23 FGF23 Quartiles, RU/ml P Value for Trend
Quartile 1: ≤96.0, N=969 Quartile 2: 96.1–145.6, N=966 Quartile 3: 145.7–239.2, N=967 Quartile 4: ≥239.3, N=967
Prevalence
 1872 48 26 46 55 67
 3869
Unadjusted odds ratio (95% CI)
 1872 1.88 (1.75 to 2.03) Reference 2.37 (1.96 to 2.87) 3.34 (2.76 to 4.04) 5.58 (4.59 to 6.79) <0.001
 3869
Plus demographic factorsa
 1872 1.85 (1.71 to 2.00) Reference 2.31 (1.90 to 2.82) 3.30 (2.71 to 4.02) 5.34 (4.36 to 6.55) <0.001
 3869
Plus cardiovascular risk factorsb
 1871 1.75 (1.61 to 1.90) Reference 2.14 (1.74 to 2.62) 2.77 (2.25 to 3.41) 4.65 (3.73 to 5.79) <0.001
 3866
Plus CKD-specific factorsc
 1871 1.41 (1.30 to 1.54) Reference 1.78 (1.44 to 2.20) 1.85 (1.48 to 2.30) 2.62 (2.06 to 3.34) <0.001
 3866
Plus markers of mineral metabolismd
 1817 1.39 (1.26 to 1.52) Reference 1.76 (1.42 to 2.18) 1.80 (1.43 to 2.26) 2.52 (1.95 to 3.24) <0.001
 3750

Continuous results are reported as odds ratios per 1-SD increase in ln-transformed FGF23. N, number; ln, natural log; FGF23, fibroblast growth factor 23; 95% CI, 95% confidence interval.

a

Adjusts for age, sex, race, and ethnicity.

b

Adjusts for factors in model 1 as well as cardiovascular disease, systolic BP, diabetes, smoking, and C-reactive protein.

c

Adjusts for factors in model 2 as well as eGFR and urinary albumin-to-creatinine ratio.

d

Full multivariable model: adjusts for factors in model 3 as well as calcium, phosphate, and parathyroid hormone.