Table 5.
Analyte (matrix)4, unit | Fasting (<3 vs. ≥8 h) |
Inflammation (yes vs. no)5 |
Renal function (CKD stage 3–5 vs. normal)6 |
Pregnancy (yes vs. no) |
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---|---|---|---|---|---|---|---|---|
SLR7 | MLR8 | SLR | MLR | SLR | MLR | SLR | MLR9 | |
Water-soluble vitamins and related metabolites | ||||||||
FOL (S), % | 10.4* | 9.5* | −4.2* | −4.5* | 36.5* | 6.8* | 31.4* | 17.9* |
FOL (RBC), % | 5.3* | 4.9* | 5.1* | 5.5* | 28.3* | 8.5* | 36.8* | 26.2* |
PLP (S), % | 10.7* | 9.3* | −33.9* | −28.5* | 0.4 | 2.9 | −0.7 | −12.6 |
4PA (S), % | 29.6* | 28.2* | −5.1 | −3.9 | 151.6* | 66.3* | 47.2* | 33.8* |
B-12 (S), % | 3.1 | 3.8 | −1.0 | −1.7 | 8.0* | 5.3* | −17.1* | −21.5* |
tHcy (P), % | −2.4 | −2.5* | −1.6 | −1.5 | 53.8* | 32.3* | −36.7* | −29.6* |
MMA (P), % | 21.4* | 21.0* | −0.3 | −1.1 | 72.4* | 42.3* | −11.8 | −4.2 |
VIC (S), μmol/L | 3.9* | 3.4* | −7.5* | −8.2* | 6.1* | −1.3 | 10.1* | 3.8* |
Fat-soluble vitamins and (micro)nutrients | ||||||||
VIA (S), % | −0.1 | −0.9 | −9.2* | −8.2* | 27.0* | 20.2* | −23.0* | −21.5* |
VIE (S), % | 3.6* | 3.7* | 0.7 | 0.1 | 22.5* | −0.7 | 17.1* | 22.2* |
CAR (S), % | 5.4* | 3.8 | −19.0* | −18.3* | −6.6* | −5.4 | 9.9 | 11.9* |
XAN (S), % | 2.8 | 2.9 | −19.2* | −20.6* | 3.3 | −3.9 | 34.1* | 32.3* |
25OHD (S), nmol/L | 0.2 | −0.5 | −5.8* | −3.9* | −1.6 | −0.7 | 9.7* | 6.6* |
SFA (P), % | N/A10 | N/A | 10.7* | 9.5* | 4.6* | −4.8* | 22.6* | 28.0* |
MUFA (P), % | N/A | N/A | 11.3* | 10.9* | 14.4* | 0.9 | 22.9* | 29.0* |
PUFA (P), % | N/A | N/A | 4.0* | 2.9* | −0.8 | −7.5* | 14.7* | 18.6* |
tFA (P), % | N/A | N/A | 7.3* | 6.1* | 4.0* | −4.2 | 19.0* | 22.9* |
Trace elements | ||||||||
FER (S), % | 1.0 | 1.8 | 24.0* | 24.6* | 9.1 | 5.9 | −33.8* | −33.1* |
sTfR (S), % | −3.4 | −2.7 | 4.4* | 2.5 | 14.0 | 10.8 | −1.9 | −3.0 |
BI (S), mg/kg | 0.1 | 0.1 | 0.6* | 0.7* | −0.2 | −0.2 | −1.4* | −1.4* |
uI (U), % | 8.3 | 26.4* | 7.5* | 1.6 | 46.2* | 7.1 | 19.7 | 8.1 |
Phytoestrogens | ||||||||
GEN (U), % | −13.0 | 4.3 | −1.4 | −4.4 | 24.0 | 2.5 | −7.0 | 2.5 |
DAZ (U), % | −6.8 | 11.4 | −5.8 | −9.1 | 16.2 | −4.9 | −10.7 | 5.1 |
EQU (U), % | −21.3* | −5.8 | 0.5 | −2.4 | −9.0 | −17.2 | 7.8 | 18.1 |
DMA (U), % | −23.1 | −15.4 | −31.4* | −35.5* | 43.8 | 11.8 | −26.2 | −9.7 |
ETD (U), % | −28.2* | −14.1 | −16.9 | −20.8* | −0.9 | −18.3 | 36.5 | 44.0 |
ETL (U), % | −17.3 | −5.7 | −35.7* | −37.9* | 28.5 | −1.5 | 4.0 | 8.9 |
Acrylamide hemoglobin adducts | ||||||||
HbAA (B), % | 6.9 | 4.4 | −4.0 | −4.8* | −23.1* | −5.7 | −28.6* | −10.4* |
HbGA (B), % | −0.9 | 1.9 | 6.9* | 5.8* | −24.8* | −8.3* | −8.9 | 6.3 |
Change represents percent change in geometric mean for all biomarkers except for vitamin C, vitamin D, and body iron where change in arithmetic mean represents concentration units.
25OHD, 25-hydroxyvitamin D; 4PA, 4-pyridoxic acid; B-12, total cobalamin; BI, body iron; CAR, carotenes; DAZ, daidzein; DMA, O-desmethylangolensin; EQU, equol; ETD, enterodiol; ETL, enterolactone; FER, ferritin; FOL, folate; GEN, genistein; HbAA, acrylamide hemoglobin adduct; HbGA, glycidamide hemoglobin adduct; MMA, methylmalonic acid; PLP, pyridoxal-5′-phosphate; sTfR, soluble transferrin receptor; tFA, total fatty acids; tHcy, total homocysteine; uI, urine iodine; VIA, retinol; VIC, ascorbic acid; VIE, alpha-tocopherol; XAN, xanthophylls.
MMA, SFA, MUFA, PUFA, tFA, HbAA and HbGA data only available for NHANES 2003–2004; PLP, 4PA, VIA, VIE, CAR, and XAN data only available for NHANES 2005–2006.
S, serum; P, plasma; U, urine; B, whole blood.
C-reactive protein (CRP, mg/L) was used to assess inflammation status (<5, no inflammation; ≥5, inflammation).
Estimated glomerular filtration rate (eGFR) was used to assess renal function; normal was defined as eGFR ≥60 mL/(min·1.73 m2) and absence of albuminuria; stage 1 or 2 chronic kidney disease (CKD) was defined as eGFR ≥60 mL/(min·1.73 m2) and presence of albuminuria; stage 3–5 CKD was defined as eGFR <60 mL/(min·1.73 m2).
Simple linear regression (model 1).
Multiple linear regression model controlled for age, sex, race-ethnicity, smoking, supplement use, fasting, inflammation, and renal function (and urine creatinine for urine biomarkers) (model 2).
Multiple linear regression model for women 20–49 y controlled for pregnancy in addition to the above mentioned variables (model 2).
N/A as all subjects were fasting for ≥8 h.
Change is significantly different from 0; P <0.05.