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1.
Clin Endocrinol (Oxf) ; 101(3): 274-281, 2024 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-39012017

RESUMEN

OBJECTIVE: This study aimed to understand the effect of time to remission of acromegaly on survival in people living with acromegaly. DESIGN, PATIENTS AND MEASUREMENT: This cross-sectional study used data from the UK Acromegaly Register. We considered remission of acromegaly growth hormone controlled at ≤2 µg/L following the diagnosis of acromegaly. We used the accelerated failure time model to assess the effect of time to remission on survival in acromegaly. RESULTS: The study population comprises 3569 individuals with acromegaly, with a median age of diagnosis of 47.3 (36.5-57.8) years, 48% females and a majority white population (61%). The number of individuals with the first remission of acromegaly was 2472, and the median time to first remission was 1.92 (0.70-6.58) years. In this study, time to first remission in acromegaly was found to have a significant effect on survival (p < .001); for every 1-year increase in time to first remission, there was a median 1% reduction in survival in acromegaly. In an analysis adjusted for covariates, the survival rate was 52% higher (p < .001) in those who underwent surgery as compared to those who did not have surgery, 18% higher (p = .01) in those who received treatment with somatostatin analogues (SMA) as compared to those with dopamine agonists and 21% lower (p < .001) in those who received conventional radiotherapy as compared to those who did not receive radiotherapy. CONCLUSION: In conclusion, this population-based study conducted in patients with acromegaly revealed that faster remission time, surgical intervention and treatment with SMA are linked to improved survival outcomes.


Asunto(s)
Acromegalia , Sistema de Registros , Inducción de Remisión , Humanos , Acromegalia/mortalidad , Acromegalia/terapia , Femenino , Masculino , Persona de Mediana Edad , Adulto , Estudios Transversales , Reino Unido/epidemiología , Hormona de Crecimiento Humana/sangre , Factores de Tiempo
2.
Scand J Clin Lab Invest ; 76(3): 240-2, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-26924790

RESUMEN

Assay interference with heterophilic antibodies has been well described in literature. Rheumatoid factor is known to cause similar interference leading to falsely elevated hormone levels when measured by immunometric methods like enzyme-linked immunosorbent assay (ELISA) or multiplex immunoasays (MIA). We report a case of a 60-year-old male patient with a history of rheumatoid arthritis referred to our endocrine clinic for investigation of hypogonadism and was found to have high serum levels of LH, FSH, SHBG, Prolactin, HCG and TSH. We suspected assay interference and further tests were performed. We used Heteroblock tubes and PEG precipitation to eliminate the interference and the hormone levels post treatment were in the normal range. We believe the interference was caused by high serum levels of rheumatoid factor. Although he was treated with thyroxine for 3 years, we believe he may have been treated inappropriately as his Free T4 level was always normal despite high TSH due to assay interference. Our case illustrates the phenomenon of heterophilic antibody interference likely due to high levels of rheumatoid factor. It is essential for clinicians and endocrinologists in particular to be aware of this possibility when making treatment decisions in these groups of patients.


Asunto(s)
Anticuerpos Heterófilos/sangre , Hipogonadismo/diagnóstico , Factor Reumatoide/sangre , Artefactos , Reacciones Falso Negativas , Humanos , Hipogonadismo/sangre , Hipogonadismo/inmunología , Masculino , Persona de Mediana Edad
3.
BMJ Case Rep ; 12(7)2019 Jul 27.
Artículo en Inglés | MEDLINE | ID: mdl-31352397

RESUMEN

Muscular symptoms in hypothyroidism are common, including myalgia, fatigue and cramps; however, a significantly raised creatine kinase and muscle weakness are rare. Differential diagnosis of patients presenting with muscle weakness and a raised creatine kinase is wide, and hypothyroidism is rarely considered. We report this case of a 30-year-old female presenting with proximal muscle weakness as her primary symptom, hypothyroid symptoms of 3-month duration and a significantly raised creatine kinase. After ruling out other causes of a raised creatine kinase, thyroxine replacement was commenced, which led to complete resolution of her proximal weakness, myalgia and normalisation of creatine kinase level. This case illustrates severe proximal myopathy can be secondary to hypothyroidism, symptoms can resolve with thyroxine replacement and emphasises the importance of measuring thyroid function in patients with proximal weakness/myalgia and a significantly raised creatine kinase.


Asunto(s)
Enfermedad de Hashimoto/complicaciones , Debilidad Muscular/etiología , Tiroxina/uso terapéutico , Adulto , Creatina Quinasa/sangre , Femenino , Enfermedad de Hashimoto/sangre , Enfermedad de Hashimoto/fisiopatología , Terapia de Reemplazo de Hormonas , Humanos , Debilidad Muscular/sangre , Debilidad Muscular/tratamiento farmacológico , Debilidad Muscular/fisiopatología , Tiroxina/sangre , Resultado del Tratamiento
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