A minimum of two years of undertreated primary hypothyroidism, as a result of drug-induced malabsorption of L-thyroxine, may have metabolic and cardiovascular consequences

被引:11
作者
Benvenga, Salvatore [1 ,2 ]
Pantano, Rachele [1 ]
Saraceno, Giovanna [3 ]
Lipari, Luigi [4 ]
Alibrando, Antonio [4 ]
Inferrera, Santi [4 ]
Pantano, Giuseppe [4 ]
Simone, Giuseppe [4 ]
Tama, Sebastiano [4 ]
Scoglio, Riccardo [4 ]
Ursino, Maria Giovanna [5 ]
Simone, Carmen [6 ]
Catalano, Antonino [1 ]
Alecci, Umberto [4 ]
机构
[1] Univ Messina, Dipartimento Med Clin & Sperimentale, Messina, Italy
[2] AOU Policlin G Martino, Programma Interdipartimentale Endocrinol Mol Clin, Messina, Italy
[3] Ist Auxol Italiano, Verbania, Italy
[4] Asp 5, Med Med Gen, Messina, Italy
[5] Soc Italiana Med Gen, Florence, Italy
[6] Univ Messina, Biol Nutr Endocrinol Infanzia Adolescenza & Donna, Messina, Italy
关键词
Subclinical hypothyroidism; Levothyroxine malabsorption; Diabetes mellitus; Dyslipidemia; Hypertension; Cardiovascular diseases; THYROID-STIMULATING HORMONE; BLOOD-PRESSURE; LEVOTHYROXINE REPLACEMENT; REFERENCE RANGE; RISK-FACTORS; TASK-FORCE; SERUM TSH; ASSOCIATION; THYROTROPIN; GUIDELINES;
D O I
10.1016/j.jcte.2019.100189
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: 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 (viz. 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. Method: 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 de novo onset of any of metabolic syndrome, impaired fasting glycemia (IFG), diabetes mellitus, dyslipidemia, hypertension, coronary heart disease (CHD), cerebrovascular disease (CVD). Result: 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] vs 1.27 +/- 1.34 [median 0.93], P = 2.2x10(-20)) and proportions of values > 4.12 mU/L (18.5% vs 4.7%, P = 1.2x10(-7)). Seventy-six patients (67%) had complications, whose rates of TSH > 4.12 mU/L were greater than in the 36 complication-free patients (22% vs 11%, P= 0.018). Conclusion: 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.
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页数:9
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