Andersen Mette Nygaard, Olsen Anne-Marie Schjerning, Madsen Jesper Clausager, Faber Jens, Torp-Pedersen Christian, Gislason Gunnar Hilmar, Selmer Christian
Department of Cardiology, Gentofte University Hospital, Hellerup, Denmark.
Elective Laboratory of the Capital Region, Copenhagen, Denmark.
PLoS One. 2015 Jun 12;10(6):e0129793. doi: 10.1371/journal.pone.0129793. eCollection 2015.
Subclinical hypothyroidism is associated with a number of cardiovascular risk factors, yet only limited data exist on long-term outcome of levothyroxine treatment of this condition with respect to hard end-points. The aim of this retrospective cohort study was to determine effects of levothyroxine treatment on myocardial infarction (MI), cardiovascular death and all-cause mortality, in patients with subclinical hypothyroidism.
Primary care patients aged 18 years and older that underwent thyroid function tests between 2000 and 2009 were enrolled. Participants were identified by individual-level linkage of nationwide registers. Patients with subclinical hypothyroidism at baseline were included in the study. Exclusion criteria included a history of thyroid disease, related medication or medication affecting thyroid function. The total cohort comprised 628,953 patients of which 12,212 (1.9%) had subclinical hypothyroidism (mean age 55.2 [SD ± 18.8] years; 79.8% female). Within the first six months 2,483 (20.3%) patients claimed a prescription for levothyroxine. During a median follow-up of 5.0 (IQR: 5.2) years, 358 MI's and 1,566 (12.8%) deaths were observed. Out of these, 766 of the deaths were cardiovascular related. No beneficial effects were found in levothyroxine treated patients on MI (IRR 1.08 [95% CI: 0.81 to 1.44]), cardiovascular death (IRR 1.02 [95% CI: 0.83 to 1.25]) or all-cause mortality (IRR 1.03 [95% CI: 0.90 to 1.19]), except in patients under the age of 65 years (IRR 0.63 [95% CI: 0.40 to 0.99]).
Levothyroxine substitution in subclinical hypothyroid patients does not indicate an association with lower mortality or decreased risk of MI.
亚临床甲状腺功能减退与多种心血管危险因素相关,但关于左甲状腺素治疗该疾病的长期硬终点结局的数据有限。这项回顾性队列研究的目的是确定左甲状腺素治疗对亚临床甲状腺功能减退患者心肌梗死(MI)、心血管死亡和全因死亡率的影响。
纳入2000年至2009年间接受甲状腺功能测试的18岁及以上的初级保健患者。通过全国登记册的个人层面链接识别参与者。基线时患有亚临床甲状腺功能减退的患者被纳入研究。排除标准包括甲状腺疾病史、相关药物治疗或影响甲状腺功能的药物。总队列包括628,953名患者,其中12,212名(1.9%)患有亚临床甲状腺功能减退(平均年龄55.2[标准差±18.8]岁;79.8%为女性)。在头六个月内,2483名(20.3%)患者开具了左甲状腺素处方。在中位随访5.0(四分位间距:5.2)年期间,观察到358例心肌梗死和1566例(12.8%)死亡。其中,766例死亡与心血管相关。在左甲状腺素治疗的患者中,未发现对心肌梗死(发病率比值比1.08[95%置信区间:0.81至1.44])、心血管死亡(发病率比值比1.02[95%置信区间:0.83至1.25])或全因死亡率(发病率比值比1.03[95%置信区间:0.90至1.19])有有益影响,但65岁以下患者除外(发病率比值比0.63[95%置信区间:0.40至0.99])。
亚临床甲状腺功能减退患者使用左甲状腺素替代治疗并未显示出与较低死亡率或降低心肌梗死风险相关。