Skip to main content
. 2017 Feb 12;17(2):282–291. doi: 10.1177/1534735417692097

Table 2.

Changes in Inflammatory Biomarkers and QOL Scores.a

N= 20 Day 0 2 Weeks 4 Weeks P Value (Day 0 to 2 Weeks) P Value (Day 0 to 4 Weeks)
Baseline laboratory data (mean ± SEM) WBC (/µL) 6135 (±787) 6195 (±704) 1.00
Hb (g/dL) 11.2 (±0.4) 11.4 (±0.4) .98
Plt (×104/µL) 23.1 (±3.0) 24.9 (±3.9) .68
Neu (%) 58.2 (±3.2) 56.1 (±3.2) .79
Lym (%) 29.5 (±3.2) 31.0 (±2.4) .80
N/L 2.7 (±0.4) 2.3 (±0.4) .67
High-sensitivity CRP (ng/mL) 20 019 (±7408) 21 494 (±8626) 17 738 (±8337) .81 .90
Subsets of lymphocytes (%) (mean ± SEM) T cell (CD3+) 68.8 (±2.9) 64.7 (±3.2) .08
CD4+ T 41.4 (±2.4) 37.6 (±2.4) .10
CD8+ T 23.2 (±1.0) 24.5 (±1.7) .25
CD4 naïve T 32.5 (±3.0) 31.5 (±3.2) .37
CD4 memory T 67.5 (±3.0) 68.5 (±3.2) .37
Treg (CD4+CD25+) 5.6 (±0.7) 7.1 (±1.0) .24
CD8+CD28+ T 58.5 (±4.4) 51.5 (±3.8) .01b
B cell (CD20+) 11.3 (±2.2) 10.9 (±2.6) .47
NK cell 21.2 (±3.0) 25.1 (±2.9) .11
NK subset, CD56+CD16- 3.7 (±0.6) 4.2 (±0.8) .31
NK subset, CD56+CD16+ 15.9 (±2.5) 19.3 (±2.7) .10
NK subset, CD56-CD16+ 1.5 (±0.5) 1.5 (±0.3) .92
NK (CD56+CD16+) Perforin+Granzyme B+ 89.8 (±3.4) 89.8 (±2.6) .62
NK (CD56+CD16-) Perforin+Granzyme B+ 63.0 (±5.4) 59.0 (±5.1) .28
Cytokines (pg/mL), (mean ± SEM) IL-1β 358.2 (±62.7) 189.9 (±32.0) 273.4 (±75.2) .01b .16
IL-6 2198.6 (±564.3) 1522.8 (±367.0) 1624.1 (±301.3) .02b .23
TNF-α 4819.4 (±772.0) 3257.2 (±648.6) 3985.1 (±548.6) .03b .08
IFN-γ 2060.4 (±285.0) 1762.8 (±265.3) 2048.3 (±271.2) .19 .65
IL-2 396.5 (±123.8) 292.3 (±91.2) 421.4 (±136.4) .05 .65
IL-17 81.0 (±16.7) 92.7 (±21.3) 101 (±20.0) .51 .64
IL-23 138.4 (±19.5) 97.8 (±15.7) 100.9 (±18.0) .06 .24
QOL score (mean ± SEM)
Global health status/QoL 58.3 (±5.3) 53.5 (±6.8) 58.3 (±4.8) .25 .92
Functional scales (higher is better) Physical functioning 79.7 (±4.5) 76.8 (±5.4) 77.7 (±5.0) .44 .40
Role functioning 76.7 (±6.3) 76.5 (±6.4) 72.5 (±6.5) 1.00 .39
Emotional functioning 82.9 (±3.1) 78.5 (±4.5) 80.8 (±5.0) .63 .91
Cognitive functioning 83.3 (±4.5) 75.4 (±5.9) 80.0 (±5.2) .29 .62
Social functioning 86.7 (±4.3) 76.3 (±6.9) 81.7 (±5.5) .19 .27
Symptom scales (higher is worse) Fatigue 35.0 (±4.7) 38.6 (±6.3) 38.6 (±5.5) .93 .40
Nausea and vomiting 6.7 (±2.5) 4.4 (±2.8) 8.3 (±5.3) .50 1.00
Pain 24.2 (±6.1) 20.4 (±6.1) 21.7 (±6.2) .33 1.00
Dyspnea 20.0 (±6.1) 19.3 (±6.4) 18.3 (±6.2) 1.00 1.00
Insomnia 22.8 (±7.7) 19.3 (±5.9) 21.7 (±6.5) 1.00 .78
Appetite loss 25.0 (±6.3) 29.8 (±6.7) 23.3 (±6.0) .53 .77
Constipation 13.3 (±5.6) 12.3 (±5.8) 10.0 (±5.5) 1.00 .63
Diarrhea 23.3 (±7.3) 26.3 (±7.5) 21.7 (±5.0) .80 .81
Financial difficulties 35.0 (±7.0) 31.6 (±8.2) 20.0 (±5.6) .36 <.01b

Abbreviations: QOL, quality of life; SEM, standard error of the mean; WBC, white blood cells; Hb, hemoglobin; Plt, platelet; Neu: neutrophil; Lym, lymphocyte; CRP, C-reactive protein; CD, cluster of differentiation; NK, natural killer; IL, interleukin; TNF-α, tumor necrosis factor-α; IFN-γ, interferon-γ.

a

Blood samples from 20 patients were collected at day 0, indicating right before fucoidan ingestion, at 2 weeks, indicating ingestion of fucoidan for 2 weeks, and at 4 weeks, indicating ingestion of fucoidan for 4 weeks, and used for biochemical analyses. QOL scores were calculated using the European Organization for Research and Treatment of Cancer Quality-of-Life Questionnaire Core 30 (EORTC QLQ-C30) submitted by the participants.

b

P < .05.