K. Raffelt et al., Systemic alterations in phospholipid concentrations of blood plasma in patients with thyroid carcinoma: an in-vitro P-31 high-resolution NMR study, NMR BIOMED, 13(1), 2000, pp. 8-13
In this study in-vitro P-31 high-resolution NMR spectroscopy of human blood
plasma was optimized to obtain absolute concentrations of the major plasma
phospholipids: phosphatidylethanolamine plus sphingomyelin /PE+ SM), 1- and
2-acyl-lysophosphatidylcholine (LPC1 and LPC2), phosphatidylinositol (PI)
and phosphatidylcholine (PC). Plasma spectra of 33 patients with thyroid ca
rcinoma were acquired at 121.49 MHz using a 300 MHz spectrometer. The patie
nts were rendered hypothyroid (TSH >30 mU/l) in preparation for a whole-bod
y scintigraphy. The whore-body scintigraphy showed tumour tissue or metasta
ses in 16 patients (group C). Owing to an inconclusive whole-body scintigra
phy, 17 patients were classified as being in remission (group B). After lev
othyroxine substitution 14 patients of group B were measured in euthyroidis
m too (group D). Besides these sub-groups, there was a control group made u
p of 23 healthy volunteers (group A). Group B showed significantly higher P
E + SM and PC concentrations than group C (0.59 +/- 0.02 mmol/l PE + SM in
B vs 0.48 +/- 0.02 mmol/l in C; 2.1 +/- 0.1 mmol/l PC in B vs 1.6 +/- 0.1 m
mol/l in C). In comparison with group D higher concentrations of the phosph
olipids PE + SM and PC as well as PI were found in group B (0.59 +/- 0.02 m
mol/l PE + SM in B vs 0.48 +/- 0.03 mmol/l in D; 0.074 +/- 0.005 mmol/l PI
in B vs 0.046 +/- 0.004 mmol/l in D; 2.1 +/- 0.1 mmol/l PC in B vs 1.6 +/-
0.1 mmol/l in D). The data indicate that under the condition of hypothyroid
ism only patients in remission (group B) show significantly increased phosp
holipid concentrations, whereas the values in patients with remaining tumou
r tissue (group C) do not differ from those of the reference groups A and D
. This finding is interpreted as an interference between the hormonal statu
s and the systemic effects of cancer. Copyright (C) 2000 John Wiley & Sons,
Ltd.