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ACTA ENDOCRINOLOGICA (BUC)
The International Journal of Romanian Society of Endocrinology / Registered in 1938in Web of Science Master Journal List
Acta Endocrinologica(Bucharest) is live in PubMed Central
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Endocrine Care
Szanto Z, Kun IZ, Borda A, Jung J
Thyroid cancer in two representative medical centers in Mures County between 1984-2007Acta Endo (Buc) 2009 5(2): 199-211 doi: 10.4183/aeb.2009.199
AbstractAim: to evaluate the epidemiology of thyroid cancer (including their different forms)\r\nin two representative medical centers of Mure? County during 1984-2007 under the impact of\r\npossible regional risk factors: ionized radiation from Chernobyl, mild/ moderate iodine\r\ndeficiency (before 2003) and universal iodization of alimentary salt (from 2004).\r\nMethods: In our retrospective study we analysed the data of 288 patients diagnosed\r\nwith thyroid cancer in Endocrinology Clinic and Institute of Pathology T?rgu Mure? in this\r\nperiod. During 1984-1991 the incidence of thyroid cancer did not change practically, it began\r\nto increase progressively from 1992. This first significant elevation between 1992-1999 was\r\nassigned mainly to the newly appeared papillary thyroid carcinomas. Between 2000-2007 a\r\nsecond ascending wave in thyroid cancer incidence was recorded, with a progressively\r\nincreasing tendency.\r\nResults: The incidence was significantly higher compared to 1992-1999 (p<0.0001,\r\nRR=2.05, 95% CI=1.59 - 2.64). This second increase may be assigned, besides the radiation\r\nexposure, to the extension of diagnostic methods (thyroid ultrasonography from 1998 and\r\nfine-needle aspiration cytology from 2000). While before 1991 there were not found thyroid\r\ncancers in children in our county, during 1991-2006 there were registered 10 cases (most in\r\nthe first period): 7 papillary, 2 follicular and one papillary form associated with insular\r\ncarcinoma.\r\nConclusion: the universal iodine prophylaxis (applied from 2004) might influence the\r\ntype of thyroid cancers, increasing the papillary/follicular carcinoma ratio. -
General Endocrinology
Mena F, Navarro N, Castilla A
Autocrine Regulation of Prolactin Secretion by Prolactin Variants Released from Lactating Rat AdenohypophysisActa Endo (Buc) 2012 8(2): 199-214 doi: 10.4183/aeb.2012.199
AbstractBackground. Previous work has shown that the in vitro released prolactin (PRL) from the anterior pituitary (AP) of\r\nlactating rats, contains PRL variants i.e., from 7-14 to 70-97 kDa that when incubated with AP lactotrophs of male rats, and of rats in other conditions, they promoted the selective stimulation and/or inhibition of the in vitro release of PRL variants from APs of male rats and of rats in other conditions.\r\nMethods. In the present experiments, we sought to determine whether PRL variants, released in vitro from lactotrophs of\r\nlactating rats, non-suckled (NS) for 6h or suckled (S) for 15 min after NS, were electroeluted from SDS-PAGE, and then\r\nwere divided into 6 fractions, would influence the in vitro release of PRL variants from lactotrophs of NS and S rat APs.\r\nResults. The results obtained showed that, under non-reducing conditions, the fractions contained PRL variants of 7-23 to 97 kDa, and between 1 and more than 20 ng/μl of PRL protein. Thus similar amounts of total PRL (about 60 ng/μl), were released from each AP region of NS and S rats, except for the higher amount of PRL (80 ng/μl) released from the central AP region of NS rats. The effects of PRL variants\r\nreleased from lactotrophs of NS and S rat APs i.e., of stimulatory and/or inhibitory type were exerted upon the release of PRL variants, and of total PRL.\r\nConclusions. These results indicate that in addition to hypothalamic influence, the release of PRL variants from the\r\nlactating rat AP is regulated also by autocrine influences exerted upon the gland by the previously released PRL variants. -
General Endocrinology
Sagun G, Mesci B, Oguz A
Does Lipoprotein-Associated Phospholipase A2 Level Correlate with Insulin Resistance States in Metabolic Syndrome, an Early Atherosclerotic Phase?Acta Endo (Buc) 2011 7(2): 199-208 doi: 10.4183/aeb.2011.199
AbstractBackground. Lipoprotein-associated phospholipase A2 is a novel inflammation marker that generates pro-inflammatory\r\nmolecules from oxidized LDL.\r\nAim. We aimed to investigate its role in individuals with insulin resistance and metabolic syndrome which is representative of early stages of atherosclerosis.\r\nMethods. We evaluated 114 subjects with metabolic syndrome in a cross-sectional pattern. Waist circumference was measured. Fasting plasma glucose, total cholesterol,\r\ntriglycerides, high-density lipoprotein cholesterol (HDL-C), LDL-cholesterol (LDLC), fasting insulin were measured by standard assays. Oral glucose tolerance test was applied\r\nto patients with fasting blood glucose < 126 mg/dL. Patients were classified to tertiles according to their insulin resistance states. Lp-PLA2 mass levels were measured.\r\nResults. There was a correlation between hypertension and HOMA tertiles; HDL-C, hypertriglyceridemia, hyperglycemia\r\nwere not correlated with HOMA tertiles (p = 0.024, p=0.66, p=0.66, p = 0.18, respectively). We cannot find any association between HOMA tertiles and Lp-PLA2 levels. Triglyceride was negatively correlated with Lp-PLA2.\r\nConclusion. Lp-PLA2 is not correlated with insulin resistance in subjects with metabolic syndrome. -
Endocrine Care
Rahemi Karizaki S, Alamdaran SA, Bonakdaran S, Morovatdar N, Jafarain AH, Hadadzade A, Hadad AS
New Proposed Formula of TI-RADS Classification Based on Ultrasound FindingsActa Endo (Buc) 2020 16(2): 199-207 doi: 10.4183/aeb.2020.199
AbstractIntroduction. The present study aimed to introduce a new formula for classification of nodules in TI-RADS and describe ultrasonography features of benign and malignant thyroid nodules. Methods. This study was conducted on thyroid mass in 1033 patients. The incidence of malignancy for thyroid nodules was determined by selecting malignancy coefficients. Then the patients were first classified using conventional TI-RADS classification criteria and once again according to a new proposed formula. Results. Among ultrasonography features of thyroid nodules, the irregular shape (46.7%), unclear margin (47.3%), extension to the capsule (irregular and infiltrative margin) (85%), the marked hypo-echoic nodules (63.8%), micro-calcification (49%), and to have vertical axis (74.0%) were associated with high incidence of malignancy. Conclusion. According to the proposed new formula for TI-RADS, there are four coefficients of 7, 3, 1 and 0 for incidence of malignancy of each one of ultrasound findings that help to standardization and unifying of TIRADS classification. The incidence of malignancy in TIRADS classification according to the new proposed formula was achieved as follows: group 2: 0.0%, group 3: 0.7%, groups 4a, 4b, 4c: 16.7%, 43.4%, 68.5%, and group 5: 95.2%, respectively. -
Endocrine Care
Batman A, Altuntas Y
Risk of Hypercalcemia in Elderly Patients with Hypervitaminosis D and IntoxicationActa Endo (Buc) 2021 17(2): 200-206 doi: 10.4183/aeb.2021.200
AbstractObjective. We aimed to determine the risk of hypercalcemia in a geriatric population with very high dose levels of 25-hydroxy-vitamin D (25(OH)D). Patients and Method. This study was designed as a retrospective, cross-sectional two-center study for examining the elderly patients with very high 25(OH)D levels (>88ng/mL) between January 2014 and December 2019. After recruitment, subgroup analyses of the patients were performed based on their calcium and vitamin D levels. Results. A total of 81.101 elderly patients, who had been evaluated for their vitamin D levels, were screened. Of the 458 (0.6%) elderly patients with 25(OH)D>88 ng/ mL according to our criteria, 217 patients with complete data were accepted into our study. The median 25(OH)D level was 103.7ng/mL (min-max:88.2-275.9). Most of the elderly patients (86.6%) with very high 25(OH)D levels were normocalcemic. When patients with hypercalcemia were compared with normocalcemic group, no difference was observed in the levels of 25(OH)D, intact parathormone (iPTH), phosphorus, alkaline phosphatase (ALP), and their age. However, the PTH suppression rate was significantly higher in hypercalcemic group (p=0.005). Conclusion. The elderly patients with very high 25(OH)D levels would appear to be mostly normocalcemic whereas life-threatening hypercalcemia would also occur. Treatment and follow-up planning should be done according to the clinical guideline recommendations. -
Endocrine Care
Bolu F, Bolu S
Congenital Hypothyroidism Screening Results in the Turkish Province of Adiyaman in 2015-2020Acta Endo (Buc) 2024 20(2): 201-206 doi: 10.4183/aeb.2024.201
AbstractContext. Congenital hypothyroidism (CH) is one of the most common preventable causes of intellectual disability, and can be diagnosed in the early period through neonatal screening programs. Objective. The purpose of this study was to determine the prevalence of CH and recall rates in the province of Adıyaman. Design. This retrospective study evaluated the data of newborn screening program in Adıyaman province between January 2015 and December 2020. Subjects and Methods. The thyroid-stimulating hormone (TSH) cut-off value in the screening program is 5.5 mIU/L and TSH values lower than 5.5 mIU/L are regarded as normal. Babies with TSH levels exceeding 5.5 mIU/L were defined as ‘recalled’. TSH measurements and clinical diagnoses of the recalled babies were evaluated. Results. TSH was <5.5 mIU/L in 62270 (90.08%) of the newborns, 5.5-20 mIU/L in 6114 (8.84%), and >20 mIU/L in 742 (1.07%). Venous T4-TSH values were normal in 673 of the 742 babies with TSH levels exceeding 20 mIU/L, while 63 babies were diagnosed with CH. Heel blood results were normal in 5880 of the 6114 babies with TSH levels of 5.5-20 mIU/L and for whom repeat heel blood was requested. TSH levels in repeat heel blood were >5.5 mIU/L in 184 babies and 93 of them were diagnosed with hypothyroidism. The recall rate among babies undergoing heel blood TSH measurement in the province of Adıyaman was 9.9%. 156 babies were started on thyroid replacement therapy with diagnoses of CH. The incidence of babies diagnosed with hypothyroidism was 1/443. Conclusion. According to the CH screening results, the recall rate and incidence of CH in the province of Adıyaman were higher than the global general figures. Both the low TSH threshold value employed in neonatal hypothyroidism screening and the province falling within the iodine deficiency region may account for this. -
Endocrine Care
Gunen Yilmaz S, Bayrak S
Determination of Mandibular Bone Changes in Patients with Primary Hypothyroidism Treated with Levothyroxine SodiumActa Endo (Buc) 2023 19(2): 201-207 doi: 10.4183/aeb.2023.201
AbstractBackground. This study aimed to assess fractal dimension (FD) and the radiomorphometric indexes on the digital panoramic radiography (DPR) of patient with primary hypothyroidism receiving levothyroxine sodium replacement therapy. Methods. A total of 115 subjects were included in this cross sectional retrospective study. According to the results of the thyroid function tests, the subjects were divided into two groups as primary hypothyroidism (levothyroxine sodium replacement therapy given), (n = 57) and the healthy control group (n = 58). The fractal dimension (FD), panoramic mandibular index (PMI), mandibular cortical width (MCW), gonial index (GI) and mandibular cortical index (MCI) values of all patients were calculated on DPRs. The statistical analysis of all data was performed with SPSS version 22. Results. The distributions of age and gender in the primary hypothroidism group were similar to control group (p = 0.19 and p = 0.62, respectively). The two groups did not differ statistically significantly in terms of FD, PMI, MCW, GI, and MCI. Conclusion. We determined that mandibular cortical and trabecular bone structure did not significantly differ between healthy individuals and patients receiving drug replacement theraphy due to hypothyroidism, but our results should be further supported with the investigation of clinical parameters. -
Endocrine Care
Stojanovic SS, Arsenijevic NA, Djukic A, Djukic S, Zivancevic Simonovic S, Jovanovic M, Pejnovic N, Nikolic V, Zivanovic S, Stefanovic M, Petrovic D
Adiponectin as a Potential Biomarker of Low Bone Mineral Density in Postmenopausal Women with Metabolic SyndromeActa Endo (Buc) 2018 14(2): 201-207 doi: 10.4183/aeb.2018.201
AbstractContext. Adiponectin is an abundant adipokine, which has antiinflammatory, anti-atherosclerotic and vasoprotective actions, and potential antiresorptive effects on bone metabolism. It seems to be directly involved in the improvement and control of energy homeostasis, protecting bone health and predicting osteoporotic fracture risk. Objective. To examine the relationship between adiponectin level and bone mineral density (BMD) in postmenopausal women with metabolic syndrome (MetS) and low BMD, and to estimate the prognostic significance of adiponectin in osteoporosis. Design. Clinical-laboratory cross-sectional study including 120 middle-aged and elder women (average 69.18±7.56 years). Subjects and Methods. The anthropometric parameters were measured for all examinees. Lumbar spine and hip BMD, as well as body fat percentage, were measured using a Hologic DEXA scanner. In all subjects serum adiponectin concentration was measured by ELISA method. Results. The level of adiponectin was significantly positively correlated with BMD-total, BMD of the lumbar spine and BMD of the femoral neck (r=0.618, r=0.521, r=0.567; p<0.01). Levels of adiponectin and BMD are significantly lower in post-menopausal women with MetS and osteoporosis compared to patients with osteopenia (856.87±453.43 vs. 1287.32±405.21 pg/mL, p<0.01; BMD, p<0.05), and the highest values in healthy examinees. A cutoff value of adiponectin level for osteoporosis/osteopenia was 1076.22/1392.74 pg/mL. Conclusions. Post-menopausal women with MetS have significantly lower adiponectin level and low BMD compared to healthy examinees. Adiponectin may be an early, significant and independent predictor of developing osteoporosis in women with MetS, especially in postmenopausal period. -
Case Report
Balmes E, Burcea A, Belgun M, Alexandrescu D, Badiu C
Marine-Lenhart syndrome. Case report and literature reviewActa Endo (Buc) 2007 3(2): 201-208 doi: 10.4183/aeb.2007.201
AbstractGraves’ disease and toxic nodular goiter both cause thyrotoxicosis by different pathophysiological mechanisms. Rare cases associates both etiologies are undertaken by the diagnosis of Marine-Lenhart syndrome. A woman aged 38, with Graves’ unilateral ophthalmopathy and a solitary, echo-dense thyroid nodule, developed thyrotoxicosis within the following 3 months. The diagnosis was certified by suppressed TSH (0.002 mIU/L), high fT4 (5.6 ng/mL) associated with elevated TRAb (3.5 IU/L), moderately elevated TPOAb (63.1 IU/mL) and ATGl (248 IU/mL). The thyroid radioiodine scan revealed a solitary hot nodule in the left lobe with an elevated radioiodine uptake. Methyl prednisolone was started by oral and pulse therapy, with stabilization of ophthalmopathy within 5 months. After four months with antithyroid drug therapy followed by radioiodine (25 mCi 131I), the thyroid scan revealed diffuse radioiodine uptake. Nine months after radioiodine therapy, the patient was in clinical and biochemical hypothyroidism and substitutive therapy was instituted. A broad literature review suggested that in such rare cases, underlying autoimmune mechanisms might be involved in the development of thyroid nodules with variable function and proliferation activity. -
Endocrine Care
Fica SV, Albu A, Vadareanu F, Barbu C, Bunghez R, Nitu L, Marinescu D
Endocrine disorders in ?-thalassemia major: cross-sectional dataActa Endo (Buc) 2005 1(2): 201-212 doi: 10.4183/aeb.2005.201
Abstract ReferencesChronic transfusion regimen and chelating therapy has dramatically improved the life expectancy of thalassemic patients. The aim of this study was to assess the prevalence of endocrine disturbances in patients with beta-thalassemia major. Subjects were 64 patients with a mean age of 19.45 ? 6.82 years found in haematological care at the National Institute of Transfusional Haematology. All the patients were evaluated clinically and biologically. LH, FSH, estradiol, testosterone, TSH, free T4, insulin were measured by chemiluminescence; mean ferritin value was used to assess iron overload. Fifty one patients (79.68%) -27 male and 24 female in our group were at pubertal or adult age. Eleven boys (40.74%) had delayed puberty, 10 (37%) arrested puberty and 4 (14.8%) had reached complete sexual maturation. In the female group, 6 (25%) had delayed puberty, 4 (16.66%) arrested puberty and 14 (58.32%) reached full sexual development. Half of both the male and female patients with complete sexual maturation had hypogonadotropic hypogonadism at the evaluation moment. Moreover, 34 (53.12%) of our patients had pathological short stature, 11 (17.18%) primary hypothyroidism, 5 (7.8%) hypoparathyroidism, 3 (4.68%) diabetes mellitus and 6 (9.37%) insulin resistance. We found a significantly higher mean ferritin value in patients with endocrine disturbances of any type compared to subjects without endocrinopathies. In conclusion, our data showed that hypogonadism and short stature were the most frequently found endocrine disturbances. Early form of hypogonadism had a major clinical impact on sexual development and final height. These results suggest that early endocrine evaluation and treatment are necessary in order to improve the quality of life of these patients.1. Olivieri NF, Brittenham GM. Iron-Chelating Therapy and the Treatment of Thalassemia. Blood 1997; 89:739-761.2. Italian Working Group on Endocrine Complication in Non-endocrine Diseases. Multicenter study on prevalence of endocrine complications in thalassaemia major. Clinical Endocrinology 1995; 42:581-586.3. Guidelines for the Clinical Management of Thalassaemia:Thalassaemia International Federation, 2002. (Accessed July 16, 2005, at site <http://www.thalassaemia.org.cy/books/book1/ch1-ch2.doc).4. Talmaci R, Traeger-Synodinos J, Kanavakis E, Coriu D, Colita D, Gavrila L. Scanning of β-globin gene for identification of β-thalassemia mutation in Romanian population. J Cell Mol 2004; 2:232-240. [CrossRef]5. Kuczmarski RJ, Ogden CL, Grummer-Strawn LM. CDC Growth charts: United States. Advance Data from Vital and Health Statistics of the Centers for Disease Control and Prevention/National Center for Health Statistics 2000; No 314.6. Fica S, Barbu C, Vladareanu F, Rotaru R, Albu A. The effects of chronic transfusional regimens on sexual development among homozygous beta thalassemic parients. Abstracts of the 12th International Congress of Endocrinology. Lisbon 2004.7. Shalitin S et al. Serum ferritin level as a predictor of impaired growth and puberty in thalassemia major patients. Eur J Haematol 2005;74:93-100. [CrossRef]8. Shamshirsaz AA et al. Metabolic and endocrinologic complications in beta-thalassemia major: a multicenter study in Tehran. BMC Endocrine Disorders 2003; 3:4. [CrossRef]9. Prototonotariou A, Katopodi A, Zervas A, Livadas S, Konstantellou E, Tolis G. Homozygous β-thalassemia and the gonad. Abstracts of the 3rd International Conference on Recent Developments on the Diagnosis and Therapy of Endocrine and Metabolic Proble10. Bergeron C, Kovacs K. Pituitary siderosis: A histologic, immunocytologic, and ultrastructural study. Am J Pathol 1978; 9:295-309.11. Bronspeigel-Weintrob N, Olivieri NF, Tyler BJ, Andrews D, Freedman MH, Holland FJ. Effect of age at the start of iron chelation therapy on gonadal function in β-thalassemia major. N Engl J Med 1990; 323:713-719. [CrossRef]12. Sklar CA, Lew LQ, Yoon DJ, David R. Adrenal function in thalassemia major following long term treatment with multiple transfusions and chelation therapy. Evidence for dissociation of cortisol and adrenal androgen secretion. Am J Dis Child 1990; 141:327-13. Maurer HS, Lloyd-Still JD, Ingrisano C, Gonzalez-Crussi F, Honig CR. A prospective evaluation of iron chelation therapy in children with severe beta-thalassaemia: A six-year study. Am J Dis Child 1988; 142:287-292.14. Borgna-Pignatti et al. Growth and sexual maturation in thalassemia major. J Pediatr 1985;106:150-155. [CrossRef]15. Chatterjee R, Katz M, Cox TF, Porter JB. Prospective study of the hypothalamic-pituitary axis in thalassaemic patients who developed secondary amenorrhea. Clin Endocrinol 1993; 39:287-290. [CrossRef]16. De Sanctis V, Wonke B. Growth and endocrine complications in thalassaemia. Roma: Mediprint 1998;17-1917. Piga A, Luzzatto L, Capalbo P, Gambotto S, Tricta F, Gabutti V. High-dose deferoxamine as a cause of growth failure in thalassaemic patients. Eur J Haematol 1988; 40:380-381. [CrossRef]18. DeVirgilis S et al. Deferoxamine-induced growth retardation in patients with thalassemia major. J Pediatr 1988; 113:661-669. [CrossRef]19. Olivieri NF et al. Growth failure and bony changes induced by deferoxamine. Am J Ped Hematol Oncol 1992; 14:48-56. [CrossRef]20. Arcasoy A et al. Effects of zinc supplementation on linear growth in beta thalassemia (a new approach). Am J Hematol 1987; 24:127-136. [CrossRef]21. Leek JC, Vogler JB, Gershwin ME, Golub MS, Hurley LS, Hendrickx AG. Studies of marginal zinc deprivation in rhesus monkeys. Fetal and infant skeletal effects. Am J Clin Nutr 1984; 40:1203-1212.22. Nishi Y, Hatano S, Aihara K, Fujie A, Kihara M. Transient partial growth hormone deficiency due to zinc deficiency. J Am Coll Nutr 1989; 8:93-97.23. Bozzola M et al. Effect of human chorionic gonadotropin on growth velocity and biological growth parameters in adolescents with thalassaemia major. Eur J Pediatr 1989;148:300-303. [CrossRef]24. Soliman A. Growth hormone (GH) response to provocation, circulating insuline-like growth factor-1 (IGF-1) and IGF-binding protein-3 concentrations, IGF-1 generation tests and clinical response to GH therapy in children with beta-thalassemia. Abstracts o25. Caruso-Nicoletti M et al. Management of puberty for optimal auxological results in betathalassaemia major. J Pediatr Endocrinol Metab 2001;14:939-944.26. Aleem A, Al-Momen A, Al-Harakati MS, Hassan A, Al-Fawaz I. Hypocalcemia due to hypoparathyroidism in β-thalassemia major patients. Ann Saudi Med. 2000; 20:364-366.27. De Sanctis V, Zurlo MG, Senesi E, Boffa C, Cavallo L, Di Gregorio F. Insulin dependent diabetes in thalassaemia. Arch Dis Child 1988; 63:58-62. [CrossRef]28. Dmochowski K, Finegood DT, Francombe WH, Tyler B, Zinman B. Factors determining glucose tolerance in patients with thalassemia major. J Clin Endocrinol Metab 1993; 77:478-483. [CrossRef]29. Cavallo-Perin P, Pacini B, Cerutti F, Bessone A, Condo C, Sacchetti L, Piga A, Pagano G. Insulin resistance and hyperinsulinemia in homozygous beta-thalassemia. Metabolism 1995; 44:281-286.30. Brittenham GM, Griffith PM, Nienhuis AW, McLaren CE, Young NS, Tucker EE, Allen CJ, Farrell DE, Harris JW. Efficacy of deferoxamine in preventing complications of iron overload in patients with thalassemia major. N Engl J Med 1994; 331:567-573. [CrossRef]31. Olivieri NF et al. Survival of medically treated patients with homozygous thalassemia. N Engl J Med 1994; 331:574-578. [CrossRef]