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1 M significantly increased serum ferritin and transferrin saturation.
2 els, and serum iron correlated strongly with transferrin saturation.
3 -off value was used to define elevated serum transferrin saturation.
4 higher ferritin/transferrin levels and lower transferrin saturation.
5 re correlated positively with maternal serum transferrin saturation.
6 eived iron depletion therapy; all had normal transferrin saturation.
7 epcidin, accompanied by a major reduction in transferrin saturation.
8 rum ferritin and normal to slightly elevated transferrin saturation.
9 ations were proportional to the increment in transferrin saturation.
10 ygous for TFR2 mutations, all with increased transferrin saturation.
11 245X) mutant mice also demonstrated elevated transferrin saturations.
12 1.83 (95% CI: 1.21, 2.76; P < 0.01); HR for transferrin saturation: 1.68 (95% CI: 1.18, 2.38; P < 0.
13 : 2.45 (95% CI:1.12, 5.34; P < 0.05); HR for transferrin saturation: 1.90 (95% CI:1.02, 3.56; P < 0.0
14 ntrol (ferritin=628+/-367 ng/ml [mean+/-SD]; transferrin saturation=30%+/-12%; P<0.001 for both).
15 eters (ferritin=899+/-488 ng/ml [mean+/-SD]; transferrin saturation=39%+/-17%) versus subjects on act
16 pared with HFE+/+ littermates, with elevated transferrin saturations (68.4% vs. 49.8%) and elevated l
17 high-sensitivity C-reactive peptide), higher transferrin saturation (a marker of iron stores), and th
18 tivation of the Smad1/5/8 signaling pathway, transferrin saturation activates the downstream Smad1/5/
21 ipants with HFE mutations, the average serum transferrin saturation and ferritin levels were slightly
23 normal ALT levels (P < 0.05) included higher transferrin saturation and iron and selenium concentrati
26 erythropoiesis, and significantly decreased transferrin saturation and lung iron stores after 2 week
27 /fl);Cre(+) mice exhibited approximately 90% transferrin saturation and massive liver iron overload,
28 C326Y, which can be associated with greater transferrin saturation and more prominent iron depositio
30 he latter category of FPN mutation have high transferrin saturation and tend to deposit iron througho
31 roots of the proportion with the lowest mean transferrin saturation and the proportion with the highe
32 rom all three strains demonstrated increased transferrin saturations and liver iron concentrations co
34 associated with increases in iron transport (transferrin saturation) and stores (serum ferritin) amon
35 um iron, total iron binding capacity (TIBC), transferrin saturation, and ferritin in a Hispanic/Latin
38 study-wise type 1 error for serum ferritin, transferrin saturation, and intravenous iron and erythro
39 haracterized by high serum ferritin, reduced transferrin saturation, and macrophage iron loading.
40 er operator curve analysis of CHr, ferritin, transferrin saturation, and MCV demonstrates that CHr ha
41 es of iron status (including serum ferritin, transferrin saturation, and non-transferrin-bound iron)
42 rtal distribution and increased plasma iron, transferrin saturation, and non-transferrin-bound iron,
43 atory tests, including complete blood count, transferrin saturation, and other chemistries; serum fer
44 ical data, including hemoglobin, serum iron, transferrin saturation, and serum ferritin concentration
45 t group had significantly higher hemoglobin, transferrin saturation, and serum ferritin values and a
47 >/=2 of 3 tests (erythrocyte protoporphyrin, transferrin saturation, and serum ferritin) and a low he
48 sed indicators, such as serum ferritin (SF), transferrin saturation, and soluble transferrin receptor
49 uration subpopulation and support the use of transferrin saturation as an inexpensive screening test
50 testinal (59)Fe uptake, lower serum iron and transferrin saturation, but no change in liver non-heme
51 yed the decrease in hepcidin until after the transferrin saturation, but not the ferritin concentrati
53 low iron levels (cutoff 10.5 mumol/mL), low transferrin saturation (cutoff 55%), and high serum tran
54 Statistical mixture modeling was applied to transferrin saturation data for African Americans and Ca
56 arrow iron depletion in patients with normal transferrin saturations, elevated serum ferritins, eleva
58 no significant difference between groups in transferrin saturation, erythrocyte zinc protoporphyrin
60 creases in serum iron levels, percentages of transferrin saturation, ferritin levels, elevations in h
61 3 +/- 5.6 mumol/L (P < 0.0001) and increased transferrin saturation from 35.7 +/- 16.3% to 45.4 +/- 1
62 ID) diet for 24 hours, the rapid decrease of transferrin saturation from 71% to 24% (control vs ID di
63 versus 37.5% of compound heterozygotes with transferrin saturation > 50%; p = 0.003), serum ferritin
64 on, serum ferritin levels of 300-2000 ng/mL, transferrin saturation >/= 45%, and no known history of
65 300 mug/L in men and >200 mug/L in women and transferrin saturation >45% in women and 50% in men.
66 tely 11% to 22% of those with elevated serum transferrin saturation had concurrently elevated serum f
67 a whole, these subpopulations of increasing transferrin saturations had progressively increasing mea
68 hromatosis screening program that uses serum transferrin saturation has been proposed, but few data e
69 ther with serum ferritin, serum transferrin, transferrin saturation, hemoglobin, and alanine aminotra
70 symptomatic Australians to estimate the mean transferrin saturation in hemochromatosis heterozygotes
71 aims of this study were to estimate the mean transferrin saturation in hemochromatosis heterozygotes
74 with Kupffer-cell iron deposition and normal transferrin saturation in vivo, whereas patients with th
75 that was seen at both high and low levels of transferrin saturation in white women should be confirme
77 addition, only after the older transfusion, transferrin saturation increased progressively over 4 ho
78 groups initially had 30% declines in plasma transferrin saturation, increases in plasma ferritin con
79 icantly, but it had no discernible effect on transferrin saturation, iron-deficient erythropoiesis, h
80 To test the hypothesis that relatively high transferrin saturation is associated with increased stro
82 aditional population screening measuring the transferrin saturation is unlikely to be cost-effective
84 males showed differences across genotypes in transferrin saturation levels (100% of homozygotes versu
86 ablished primary hematopoietic cultures with transferrin saturation levels that restricted erythropoi
87 Consistent with this, iron, ferritin, and transferrin saturation levels were reduced and red cell
91 o 30 ml/min, 46% of women and 19% of men had transferrin saturation <20%, and 47% of women and 44% of
93 itin <or= 450 pmol/L or <or= 675 pmol/L with transferrin saturation <or= 19%) receiving subcutaneousl
94 rin receptor >or=8.4 or >10.0 microg/mL, and transferrin saturation <or=13.2% or <10.0%, respectively
95 ron measures, including serum ferritin (SF), transferrin saturation, mean cell volume, and hemoglobin
96 icant difference in baseline serum ferritin, transferrin saturation, mean cell volume, mean cell hemo
97 a for iron overload using serum ferritin and transferrin saturation measurements and HFE genotyping.
98 ciated positively with increasing deciles of transferrin saturation (odds ratio [OR] per decile, 1.10
101 When erythropoietin resistance is present, transferrin saturation of < 27% or serum ferritin < 300
102 .2% of the truncated sample had a lower mean transferrin saturation of 24.1%, whereas 11.8% had an in
107 hemochromatosis; and 23 patients had a serum transferrin saturation of 55% or more with no identifiab
108 opulation with a mean +/- standard deviation transferrin saturation of 63.4% +/- 5.7% (postulated hom
113 a high-iron diet revealed no differences in transferrin saturation or tissue iron stores between WT
114 =2 of 3 abnormal concentrations in ferritin, transferrin saturation, or erythrocyte protoporphyrin (t
115 ion in hematocrit value, reticulocyte count, transferrin saturation, or ferritin level in the experim
116 h levels of free erythrocyte protoporphyrin, transferrin saturation, or hemoglobin (percent change =
120 increases in AUC for serum iron (P < 0.01), transferrin saturation (P < 0.001), and nontransferrin-b
121 oots of the proportions with the lowest mean transferrin saturation (P = .925) and the highest (q = 0
122 tate significantly reduced tHcy (P = 0.017), transferrin saturation (P = 0.027), and ferritin (P = 0.
124 or length gain or in hemoglobin, hematocrit, transferrin saturation, plasma zinc, or erythrocyte ribo
125 who ingested 65 mg of iron, the increase in transferrin saturation preceded by hours the increase in
126 , older age, higher urea reduction ratio and transferrin saturation, prescription of intravenous iron
129 Cut-off values used to define elevated serum transferrin saturation ranged from greater than 45% to g
131 s more severe in the restrictive group (peak transferrin saturation: restrictive group 83.9+/-13.0%,
132 tion studies for serum iron, serum ferritin, transferrin saturation (SAT) and total iron binding capa
137 um ferritin, total iron-binding capacity and transferrin saturation), serum hepcidin and genome-wide
138 y was defined as > or =2 abnormal values for transferrin saturation, serum ferritin, and erythrocyte
140 nces in hematocrit, mean corpuscular volume, transferrin saturation, serum ferritin, and serum iron.
142 emochromatosis heterozygotes form a distinct transferrin saturation subpopulation and support the use
143 of this new study was to determine if these transferrin saturation subpopulations have different lev
144 consistent with the concept that population transferrin saturation subpopulations reflect different
145 ritin concentrations were determined for the transferrin saturation subpopulations that were identifi
146 1) to encourage laboratories to provide the transferrin saturation test as part of routine laborator
147 f 45% or more on initial testing had a serum transferrin saturation test done under fasting condition
148 eening for hemochromatosis done by using the transferrin saturation test has been advocated by expert
149 screening for hemochromatosis done by using transferrin saturation testing can be recommended, labor
150 parameters of iron metabolism, particularly transferrin saturation, that reflect serum iron availabi
151 e in hematocrit, hemoglobin, serum iron, and transferrin saturation, the appearance of microcytic ani
152 serum ferritin, total-iron-binding capacity, transferrin saturation, the ratio of enzymatic to immuno
154 d evaluation of iron status (ferritin level, transferrin saturation, transferrin receptor level, reti
155 hereditary hemochromatosis (HHC) by means of transferrin saturation (TS) levels has been advocated an
156 t possible to assess the association between transferrin saturation (TS) subpopulations and HFE mutat
157 globin, mean corpuscular volume (MCV), serum transferrin saturation (TS), serum ferritin, and white b
158 end maintaining ferritin > or =100 ng/ml and transferrin saturation (TSAT) > or =20% to ensure adequa
162 dose, intravenous (IV) iron dose, ferritin, transferrin saturation (TSAT) concentration, parathyroid
163 Subjects on FC had increased ferritin and transferrin saturation (TSAT) levels compared with subje
166 ents who are responsive to erythropoietin, a transferrin saturation value < 18% or serum ferritin lev
167 atosis be defined by repeated elevated serum transferrin saturation values(with or without DNA test r
175 ated with overexpression of hepcidin and low transferrin saturation was found to be associated with b
177 matocrit was measured weekly for four weeks, transferrin saturation was measured, and coexisting illn
178 a standard diet, by 10 weeks of age, fasting transferrin saturation was significantly elevated compar
180 of septic ICU subjects, low iron levels and transferrin saturation went along with a nonlethal outco
181 ancer), higher serum iron concentrations and transferrin saturation were associated with increased ri
182 ncreasing weight, urea reduction ration, and transferrin saturation were associated with lower EPO do
183 ochromatosis homozygotes, two populations of transferrin saturation were identified in asymptomatic A
184 t for diurnal variation, 3 subpopulations of transferrin saturation were identified in each racial gr
186 results indicated a close correlation of low transferrin saturation with decreased hepcidin mRNA.
187 served a significant U-shaped association of transferrin saturation with risk of incident stroke (> 4
188 total-iron-binding capacity and increase in transferrin saturation (%) with resistive training are l
190 demonstrated strain-dependent differences in transferrin saturation, with the highest values in AKR m
191 ansferrin receptor (sTfR) concentrations and transferrin saturation without affecting hemoglobin conc
192 of greater than 60% to define elevated serum transferrin saturation would identify an estimated 1.4 t
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