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1.
J Endocrinol Invest ; 42(2): 175-181, 2019 Feb.
Article in English | MEDLINE | ID: mdl-29777516

ABSTRACT

PURPOSE: Irisin is a newly identified myokine secreted by skeletal muscle and has significant effects on body metabolism. Thyroidal functional state has a profound influence on the metabolism of human body. Therefore, the aim of this study was to investigate the possible changes in serum irisin concentrations before and after treatment in hypothyroid subjects. METHODS: The study included 26 patients with overt hypothyroidism due to Hashimoto thyroiditis and 19 healthy subjects. Baseline serum thyroid function tests and presence of thyroid autoantibodies and levels of creatine kinase (CK) and irisin were measured in both groups. All measurements in the hypothyroid group were repeated after euthyroidism was achieved. RESULTS: Serum irisin levels were significantly lower in the hypothyroid groups than the control group (p < 0.001). Negative correlation between irisin and thyroid stimulating hormone and CK levels (r = - 0.623, p < 0.001 and r = - 0.389, p = 0.008, respectively) and a positive correlation between irisin and free thyroxine (fT4) levels (r = 0.570, p < 0.001) was found. Serum CK levels decreased significantly after treatment (p < 0.001). Serum irisin levels significantly increased (from 57.4 to 99.8 U/L, p < 0.001) when the hypothyroid patients were treated to achieve euthyroidism. CONCLUSIONS: To the best of our knowledge, this is the first study providing insight that low serum irisin levels significantly increased following treatment to euthyroid state in overt hypothyroid patients with Hashimoto thyroiditis. Larger scale studies are needed to confirm these results and to ensure irisin as a possible biomarker of Hashimoto's thyroiditis.


Subject(s)
Fibronectins/blood , Hashimoto Disease/blood , Thyroxine/therapeutic use , Adult , Creatine Kinase/blood , Female , Hashimoto Disease/drug therapy , Hormone Replacement Therapy , Humans , Male , Thyroid Function Tests , Thyrotropin/blood , Thyroxine/blood , Treatment Outcome
2.
Acta Gastroenterol Belg ; 80(1): 71-74, 2017.
Article in English | MEDLINE | ID: mdl-29364102

ABSTRACT

Hypertriglyceridemia is one of the rare causes of the acute pancreatitis. The prevalance of hypertriglyceridemia has increased recently due to the changing eating habits, sedentary lifestyle, alcohol consumption, obesity and concomitant diabetes mellitus. Therefore, the frequency of the acute pancreatitis due to hypertriglyceridemia may increase in coming years. Diagnosis of the acute pancreatitis by hypertriglyceridemia can be overlooked easily and may be very severe if untreated accurately on time. In addition to the standard management of pancreatitis, specific treatment for hypertriglyceridemia that is insulin, heparin and anti-hypertriglyceridemic drugs are used. Therapeutic plasmapheresis is the last treatment option and seems the most effective one in this subject through developing device and membrane technologies when we review the current literature. Not only triglycerides but also proinflammatory cytokines and adhesion molecules that play an active role in pathogenesis are removed by plasmapheresis. So, the effectiveness of treatment appears promising. However, the exact pathophysiology of hypertriglyceridemia-induced pancreatitis could not be fully understood and the majority of published experience comes from the case reports and the benefit of randomized clinical trials is not available. Therefore, there are no data about what are the exact indications and when we start therapeutic plasmapheresis in literature. This manuscript describes our hospital experience with treatment options and analyzes reports published recently about plasmapheresis as a treatment modality for hypertriglyceridemia induced acute pancreatitis.


Subject(s)
Hypertriglyceridemia/therapy , Pancreatitis/therapy , Plasmapheresis , Acute Disease , Adult , Female , Humans , Hypertriglyceridemia/complications , Male , Middle Aged , Pancreatitis/etiology
3.
J Endocrinol Invest ; 39(2): 185-9, 2016 Feb.
Article in English | MEDLINE | ID: mdl-26142741

ABSTRACT

PURPOSE: Chemokines play an important role in the pathogenesis of autoimmune thyroid diseases. Platelet factor 4 (PF4, CXCL4) released from activated platelets is a chemokine. However, its clinical importance in autoimmune thyroiditis remains unknown. This study is intended to determine circulating levels of PF4 levels in patients with autoimmune thyroiditis (AIT). METHODS: Circulating levels of PF4 were measured in 34 consecutive patients with newly diagnosed AIT and 18 euthyroid controls. Among AIT group, 16 patients were euthyroid and 18 had subclinic hypothyroidism. Controls and individuals with AIT were similar in terms of age. RESULTS: Serum levels of PF4 were comparable in patients with AIT and in controls. Among patients with AIT, PF4 was significantly lower in those with subclinical hypothyroidism than in euthyroid individuals (p = 0.001). In correlation analysis, PF4 was negatively correlated with TSH (r = -0.663, p = 0.000) and positively correlated with free T4 (r = 0.428, p = 0.012). There was not any significant correlation between PF4 and AbTPO, AbTg. CONCLUSION: The present study demonstrated for the first time that circulating PF4 levels are decreased in subclinically hypothyroid AIT. This result draws attention to the circulating PF4 levels in subclinically hypothyroid AIT and may shed light on further researches at this topic.


Subject(s)
Asymptomatic Diseases , Down-Regulation , Hashimoto Disease/blood , Platelet Factor 4/blood , Thyroiditis, Autoimmune/blood , Adolescent , Adult , Aged , Autoantibodies/analysis , Autoantigens , Biomarkers/blood , Female , Hashimoto Disease/immunology , Hashimoto Disease/physiopathology , Humans , Iodide Peroxidase/antagonists & inhibitors , Iron-Binding Proteins/antagonists & inhibitors , Middle Aged , Severity of Illness Index , Thyroiditis, Autoimmune/immunology , Thyroiditis, Autoimmune/physiopathology , Thyrotropin/blood , Thyroxine/blood , Young Adult
4.
Minerva Ginecol ; 66(6): 535-42, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25373013

ABSTRACT

AIM: The aim of this paper was to compare serum chemerin levels in nonobese and overweight/obese patients with polycystic ovary syndrome (PCOS) with lean controls. METHODS: Seventy women with newly diagnosed or untreated PCOS and 38 age-matched nonobese healthy controls were enrolled in the present study. Participants with PCOS were categorized as nonobese (Body Mass Index [BMI] <25 kg/m², N.=36) or overweight/obese (BMI 25-29.9 kg/m² and ≥30 kg/m², respectively, N.=34). Anthropometric, metabolic and hormonal patterns, and serum chemerin were measured. RESULTS: Serum chemerin tended to be higher in obese PCOS group than in nonobese PCOS women but did not reach statistical significance. Nonobese healthy controls had significantly lower chemerin levels than two PCOS groups (P<0.001). Fasting insulin (P<0.05) and homeostasis model assessment index (P<0.05) were significantly higher in obese women with PCOS than in other two groups. Also, these two parameters were higher in lean patients with PCOS than in healthy controls (P<0.05). In multiple linear regression analyses, chemerin was significantly associated with BMI (ß-coefficient =0.336, P<0.01), and triglyceride (ß-coefficient =0.298, P<0.05). CONCLUSION: Chemerin levels were significantly increased not only in obese PCOS women but also in nonobese PCOS women. The physiological significance of elevated serum chemerin in PCOS remains unclear.


Subject(s)
Chemokines/blood , Intercellular Signaling Peptides and Proteins/blood , Obesity/blood , Overweight/blood , Polycystic Ovary Syndrome/blood , Adult , Body Mass Index , Case-Control Studies , Female , Humans , Insulin/metabolism , Linear Models , Obesity/complications , Triglycerides/blood , Young Adult
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