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. 2021 Jan 12;8(2):1130–1138. doi: 10.1002/ehf2.13153

Table 3.

Biomarker differences over a 12 month period between patients with heart failure with preserved ejection fraction without and with diabetes

Biomarker % change (95% CI) a Trend
n Non‐DM DM P b Adj c P
eGFR (mL/min/1.73 m2) 225 −14% (−17, −10) −14% (−18, −10) 0.38 0.34
UPCR (mg/mmol) 187 −2% (−14, +10) −6%, (−20, +11) 0.20 0.10
Urinary protein level (mg/dL) 187 −4% (−19, +12) −2% (−20, +20) 0.20 0.24
hs‐CRP (mg/L) 183 +1% (−5, +3) −11% (−27, +7) 0.74 0.54
Uric acid (mg/dL) 188 −1% (−5, +3) +0% (−5, +6) 0.12 0.23
NT‐proBNP (pg/mL) 189 −2% (−12, +10) −5% (−21, +13) 0.90 0.48
hs‐TnT (ng/mL) 189 −1% (−14, +13) +11% (−3, +27) 0.06 0.016
sST2 (ng/mL) 188 −1% (−7, +5) −4% (−9, +2) 0.54 0.60
Aldosterone (ng/L) 200 +17% (+9, +26) +23% (+14, +33) 0.58 0.76
PICP (ng/mL) 164 +6% (−5, +18) +5% (−6, +18) 0.22 0.10
CITP (ng/mL) 78 −25% (−45, +2) −19% (−38, +6) 0.77 0.89
PIIINP (ng/mL) 168 +8% (−1, +18) +10% (+1, +20) 0.11 0.15
MMP‐2 (ng/mL) 203 −0% (−4, +4) −3% (−7, +1) 0.59 0.72
MMP‐9 (ng/mL) 203 −6% (−13, +3) −1% (−11, +10) 0.23 0.35
TIMP‐1 (ng/mL) 203 −1% (−4, +2) −2% (−5, +2) 0.67 0.59
Gal‐3 (ng/mL) 189 +6% (+3, +10) +9% (+4, +14) 0.27 0.52

CI, confidence interval; CITP, collagen type I; DM, diabetes mellitus; eGFR, estimated glomerular filtration rate; Gal‐3, galectin‐3; hs‐CRP, high‐sensitivity C‐reactive protein; hs‐TnT, high‐sensitivity troponin T; MMP‐2, matrix metalloproteinase 2; MMP‐9, matrix metalloproteinase 9; NT‐proBNP, N‐terminal pro‐B‐type natriuretic peptide; PICP, pro‐collagen type I carboxy‐terminal peptide; PIIINP, pro‐collagen type III amino‐terminal peptide; sST2, soluble ST2; TIMP‐1, tissue inhibitor of metalloproteinase 1; UPCR, urinary protein to creatinine ratio.

a

Change in geometric means estimated via linear regression after log transformation.

b

Adjusted for baseline value of biomarker only.

c

Additionally adjusted for age, gender, strata, and treatment group (spironolactone vs. placebo per Treatment of Preserved Cardiac Function Heart Failure with an Aldosterone Antagonist randomization).