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Serum Betatrophin Levels and Its Influencing Factors in Patients With Hyperthyroidism

Conditions
Hyperthyroidism
Interventions
Drug: thionamide treatment for 3 months
Registration Number
NCT02812888
Lead Sponsor
Hu Hao
Brief Summary

Clustering of various metabolic parameters including abdominal obesity, hyperglycaemia, low high-density lipoprotein cholesterol, elevated triglycerides and hypertension have been used worldwide as metabolic syndrome to predict cardiometabolic risk. Thyroid dysfunction impacts on various levels of these components.

Recent evidence from HepG2 cells indicates that betatrophin, also known as TD26/RIFL/lipasin/ANGPTL8/C19orf80, a secreted protein that regulates glucose, lipid metabolism, and energy homeostasis, is induced by T3. However, the role of betatrophin in hyperthyroid patients is unknown.

The objective was to study serum betatrophin levels in hyperthyroid patients and the association of serum betatrophin levels with hyperthyroidism.

Detailed Description

Thyroid hormone (TH) is a critical hormone responsible for growth, development, and metabolism. It maintains basal metabolic rate (BMR), improves adaptive thermogenesis, and thus modulates body weight by fine-tuning energy expenditure and intake. Hyperthyroidism, a condition with excess TH, presents a status of negative energy balance that is characterized by weight loss, increased energy expenditure, and accelerated lipolysis and gluconeogenesis. The mechanism underlying hypermetabolic status in hyperthyroidism is complicated. In hyperthyroidism, excess TH promotes the metabolism rate primarily by binding to TH receptor α or β, and in turn by further influencing diverse metabolic pathways. Recent studies have revealed that TH signals were involved in cross talk with a range of other metabolic signaling pathways in different metabolic organs. In liver, TH interacts with peroxisome proliferator-activated receptor (PPAR) α, PPARγ, and liver X receptor α pathway; promotes fatty acid oxidation; decreases cholesterol; and enhances gluconeogenesis. The elements required for TH action are well documented, but understanding the interaction between TH and various pathways remains a challenge.

Betatrophin, also known as TD26/RIFL/lipasin/ANGPTL8/C19orf80, is a novel protein predominantly expressed in human liver. Increasing evidence has revealed associations between betatrophin expression, glycemia and serum lipid profiles, particularly in patients with obesity or diabetes. Stimulators of betatrophin, such as insulin, thyroid hormone, irisin, SIRT1 and caloric intake, are usually relevant to energy expenditure or thermogenesis. A previous report revealed that betatrophin mRNA is induced by the thyroid hormone in HepG2 cells. Subsequent studies confirmed that transcriptional regulation is dependent on the thyroid hormone receptor that binds to the betatrophin upstream element. Therefore, betatrophin is a novel gene dramatically activated by the thyroid hormone. However, there is no evidence to date showing that TH is capable of regulating betatrophin expression in human beings. The current study investigated the change of betatrophin levels in patients with hyperthyroidism before and after thionamide treatment and explored the association of serum betatrophin levels with hyperthyroidism.

Recruitment & Eligibility

Status
UNKNOWN
Sex
All
Target Recruitment
240
Inclusion Criteria
  • Clinical diagnosis of hyperthyroidism
  • Must be drug-naive before recruitment
Exclusion Criteria
  • diabetes
  • hypertension
  • cancer
  • pregnancy
  • lactation
  • subacute thyroiditis
  • postpartum thyroiditis
  • abnormal liver function
  • abnormal kidney function
  • infectious diseases

Study & Design

Study Type
OBSERVATIONAL
Study Design
Not specified
Arm && Interventions
GroupInterventionDescription
Hyperthyroid Patientsthionamide treatment for 3 monthsPatients with hyperthyroidism
Primary Outcome Measures
NameTimeMethod
Serum betatrophin levelsChange from baseline at 3 months
Secondary Outcome Measures
NameTimeMethod
blood lipid profileAt baseline and at the end of the third month
liver function indexAt baseline and at the end of the third month
hypersensitive c-reactive protein (hs-CRP)At baseline and at the end of the third month
Blood glucoseAt baseline and at the end of the third month
Serum insulin levelsAt baseline and at the end of the third month
Thyroid function indexAt baseline and at the end of the third month

Trial Locations

Locations (1)

The First People's Hospital of Xuzhou,

🇨🇳

Xuzhou, Jiangsu, China

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