Benvenga Salvatore, Pantano Rachele, Saraceno Giovanna, Lipari Luigi, Alibrando Antonio, Inferrera Santi, Pantano Giuseppe, Simone Giuseppe, Tamà Sebastiano, Scoglio Riccardo, Ursino Maria Giovanna, Simone Carmen, Catalano Antonino, Alecci Umberto
Dipartimento di Medicina Clinica e Sperimentale, Università di Messina, Messina, Italy.
Programma Interdipartimentale di Endocrinologia Molecolare Clinica e Salute Endocrina della Donna, AOU Policlinico G. Martino, Messina, Italy.
J Clin Transl Endocrinol. 2019 Apr 10;16:100189. doi: 10.1016/j.jcte.2019.100189. eCollection 2019 Jun.
Cross-sectional studies have reported that TSH above or close to the upper normal limit correlates with unfavorable metabolic and cardiovascular outcomes. Certain medications impair intestinal absorption of levothyroxine (L-T4), resulting in undertreated hypothyroidism (. failure of serum TSH to reach target levels, if hypothyroidism is primary).Further to evaluating the magnitude of sub-optimally treated primary hypothyroidism as a result of co-ingestion of those medications, we wished to ascertain whether the above complications would occur during a low number of years under polypharmacy.
In this retrospective study in collaboration with 8 family physicians, we enrolled adults with primary hypothyroidism under L-T4 therapy that, for 2 years minimum, was not associated with those medications (non-exposure, baseline) and that, for another 2 years minimum, it was (exposure). Outcomes were serum levels and proportions of serum TSH levels >4.12 mU/L, and proportions of complications. Complications were aggravation of pre-existing or onset of any of metabolic syndrome, impaired fasting glycemia (IFG), diabetes mellitus, dyslipidemia, hypertension, coronary heart disease (CHD), cerebrovascular disease (CVD).
A total of 114 patients were enrolled. Duration of exposure to the interfering medication was 32.1 ± 6.9 months (median 31; range 24-55). Compared with non-exposure, the exposure period resulted in greater TSH levels (2.81 ± 3.62 [median 1.79] 1.27 ± 1.34 [median 0.93], P = 2.2 × 10) and proportions of values >4.12 mU/L (18.5% 4.7%, P = 1.2 × 10). Seventy-six patients (67%) had complications, whose rates of TSH >4.12 mU/L were greater than in the 36 complication-free patients (22% 11%, P = 0.018).
During a median period of 31 months, there are relevant consequences for L-T4 treated adult hypothyroid patients resulting from hyperthyrotropinemia caused by medications impairing L-T4 absorption. This should be taken into account by future guidelines on hypothyroidism management.
横断面研究报告称,促甲状腺激素(TSH)高于或接近正常上限与不良代谢和心血管结局相关。某些药物会损害左甲状腺素(L-T4)的肠道吸收,导致甲状腺功能减退治疗不足(如果是原发性甲状腺功能减退,则血清TSH未能达到目标水平)。除了评估因同时服用这些药物导致的原发性甲状腺功能减退治疗不充分的程度外,我们还希望确定在联合用药的短短几年内是否会出现上述并发症。
在这项与8名家庭医生合作开展的回顾性研究中,我们纳入了接受L-T4治疗的成年原发性甲状腺功能减退患者,这些患者至少2年未服用上述药物(非暴露组,基线),且至少另外2年服用了这些药物(暴露组)。观察指标为血清水平、血清TSH水平>4.12 mU/L的比例以及并发症的比例。并发症包括既往存在的代谢综合征加重或出现任何一种以下情况:空腹血糖受损(IFG)、糖尿病、血脂异常、高血压、冠心病(CHD)、脑血管疾病(CVD)。
共纳入114例患者。暴露于干扰药物的时间为32.1±6.9个月(中位数31个月;范围24 - 55个月)。与非暴露组相比,暴露期导致TSH水平更高(2.81±3.62[中位数1.79]对1.27±1.34[中位数0.93],P = 2.2×10)以及TSH>4.12 mU/L值的比例更高(18.5%对4.7%,P = 1.2×10)。76例患者(67%)出现并发症,其TSH>4.12 mU/L的比例高于36例无并发症患者(22%对11%,P = 0.018)。
在中位数为31个月的时间里,因药物损害L-T4吸收导致促甲状腺激素血症,给接受L-T4治疗的成年甲状腺功能减退患者带来了相关后果。这一点应被未来甲状腺功能减退管理指南所考虑。