Which thyroid-stimulating hormone level should be sought in hypothyroid patients under L-thyroxine replacement therapy?

• Published in: International journal of clinical practice (Esher) Vol. 60; no. 6; p. 655
• Main Authors: Gursoy, A, Ozduman Cin, M, Kamel, N, Gullu, S
• Format: Journal Article
• Language: English
• Published: England 01-06-2006
• Subjects: C-Reactive Protein - metabolism; Cardiovascular Diseases - chemically induced; Cohort Studies; Cross-Sectional Studies; Fibrin Fibrinogen Degradation Products - metabolism; Fibrinogen; Homocysteine - blood; Humans; Hypothyroidism - drug therapy; Middle Aged; Risk Factors; Thyrotropin - blood; Thyroxine - therapeutic use
• ISSN: 1368-5031
• DOI: 10.1111/j.1368-5031.2006.00822.x

We sought to determine whether relationships exist between level of thyroid-stimulating hormone (TSH) suppression and cardiovascular risk parameters such as plasma homocysteine, C-reactive protein (CRP), fibrinogen, D-dimer and serum cholesterol in patients taking L-thyroxine-replacement therapy (LT4-RT). Four hundred and two hypothyroid patients under LT4-RT were cross-sectionally evaluated. Patients were grouped according to their achieved TSH (mIU/l) levels under LT4-RT on an arbitrary manner. Those patients having a TSH value 0.4-2 were defined as group 1 (n = 154), a TSH level of 2 to less than 5.5 were defined as group 2 (n = 176) and a TSH level of 5.5 to less than 20 with a normal free T3 and free T4 level were defined as group 3 (n = 72). The three groups of patients were also compared with overt hypothyroid patients (n = 71) and healthy controls (n = 97). Homocysteine levels (micromol/l) were significantly different between the three groups (10.4 +/- 4 for group 1, 11.3 +/- 3.7 for group 2 and 13.5 +/- 4.7 for group 3; p < 0.01 for all groups). Significant differences in CRP (mg /l) levels were present between the three groups (2.6 +/- 2.6 for group 1, 3.3 +/- 2.9 for group 2 and 4.8 +/- 4.1 for group 3; p < 0.01 for all groups). Univariate analysis showed that both homocysteine and CRP levels significantly correlated with free T4 and TSH level (p < 0.01 for both groups). No statistically significant differences were noticed in respect to fibrinogen and d-dimer levels between three groups. In examining the effect of LT4-RT on lipid parameters, a tendency towards beneficial effects without achieving statistical significance was observed. Practically speaking, a target TSH level of less than 2 might be advisable to lower CRP levels and homocysteine levels, and possibly lipid parameters.