This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.
[Anonymous]. Physical status: the use and interpretation of anthropometry. Report of a WHO Expert Committee. World Health Organ Tech Rep Ser 1995; 854: 1–452[Anonymous]Physical status: the use and interpretation of anthropometry. Report of a WHO Expert CommitteeWorld Health Organ Tech Rep Ser19958541452Search in Google Scholar
[Anonymous]. Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults--The Evidence Report. National Institutes of Health. Obes Res 1998; 6 Suppl 2: 51S–209S[Anonymous]Clinical Guidelines on the Identification, Evaluation, and Treatment of Overweight and Obesity in Adults--The Evidence Report. National Institutes of HealthObes Res19986Suppl 251S209SSearch in Google Scholar
Snitker S. Use of body fatness cutoff points. Mayo Clin Proc 2010; 85: 1057; author reply 1057–1058SnitkerS.Use of body fatness cutoff pointsMayo Clin Proc2010851057author reply 1057–1058Search in Google Scholar
Collaboration NCDRF. Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128.9 million children, adolescents, and adults. Lancet 2017; 390: 2627–2642CollaborationNCDRF.Worldwide trends in body-mass index, underweight, overweight, and obesity from 1975 to 2016: a pooled analysis of 2416 population-based measurement studies in 128.9 million children, adolescents, and adultsLancet201739026272642Search in Google Scholar
Garvey WT, Mechanick JI, Brett EM et al. American Association of Clinical Endocrinologists and American College of Endocrinology Comprehensive Clinical Practice Guidelines for Medical Care of Patients with Obesity. Endocr Pract 2016; 22 Suppl 3: 1–203GarveyWTMechanickJIBrettEMAmerican Association of Clinical Endocrinologists and American College of Endocrinology Comprehensive Clinical Practice Guidelines for Medical Care of Patients with ObesityEndocr Pract201622Suppl 31203Search in Google Scholar
Wharton S, Lau DCW, Vallis M et al. Obesity in adults: a clinical practice guideline. CMAJ 2020; 192: E875–E891WhartonSLauDCWVallisMObesity in adults: a clinical practice guidelineCMAJ2020192E875E891Search in Google Scholar
Milewska EM, Szczepanek-Parulska E, Marciniak M et al. Selected organ and endocrine complications according to BMI and the metabolic category of obesity: A single Endocrine Center Study. Nutrients 2022; 14:MilewskaEMSzczepanek-ParulskaEMarciniakMSelected organ and endocrine complications according to BMI and the metabolic category of obesity: A single Endocrine Center StudyNutrients202214Search in Google Scholar
Alberti KG, Eckel RH, Grundy SM et al. Harmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of Obesity. Circulation 2009; 120: 1640–1645AlbertiKGEckelRHGrundySMHarmonizing the metabolic syndrome: a joint interim statement of the International Diabetes Federation Task Force on Epidemiology and Prevention; National Heart, Lung, and Blood Institute; American Heart Association; World Heart Federation; International Atherosclerosis Society; and International Association for the Study of ObesityCirculation200912016401645Search in Google Scholar
Lavie CJ, Laddu D, Arena R et al. Healthy Weight and Obesity Prevention: JACC Health Promotion Series. Journal of the American College of Cardiology 2018; 72: 1506–1531LavieCJLadduDArenaRHealthy Weight and Obesity Prevention: JACC Health Promotion SeriesJournal of the American College of Cardiology20187215061531Search in Google Scholar
Mongraw-Chaffin M, Foster MC, Anderson CAM et al. Metabolically Healthy Obesity, Transition to Metabolic Syndrome, and Cardiovascular Risk. Journal of the American College of Cardiology 2018; 71: 1857–1865Mongraw-ChaffinMFosterMCAndersonCAMMetabolically Healthy Obesity, Transition to Metabolic Syndrome, and Cardiovascular RiskJournal of the American College of Cardiology20187118571865Search in Google Scholar
Lin H, Zhang L, Zheng R et al. The prevalence, metabolic risk and effects of lifestyle intervention for metabolically healthy obesity: a systematic review and meta-analysis: A PRISMA-compliant article. Medicine (Baltimore) 2017; 96: e8838LinHZhangLZhengRThe prevalence, metabolic risk and effects of lifestyle intervention for metabolically healthy obesity: a systematic review and meta-analysis: A PRISMA-compliant articleMedicine (Baltimore)201796e883Search in Google Scholar
Kramer CK, Zinman B, Retnakaran R. Are metabolically healthy overweight and obesity benign conditions?: A systematic review and meta-analysis. Annals of internal medicine 2013; 159: 758–769KramerCKZinmanBRetnakaranR.Are metabolically healthy overweight and obesity benign conditions?: A systematic review and meta-analysisAnnals of internal medicine2013159758769Search in Google Scholar
Fontenelle LC, Feitosa MM, Severo JS et al. Thyroid Function in Human Obesity: Underlying Mechanisms. Hormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme 2016; 48: 787–794FontenelleLCFeitosaMMSeveroJSThyroid Function in Human Obesity: Underlying MechanismsHormone and metabolic research = Hormon- und Stoffwechselforschung = Hormones et metabolisme201648787794Search in Google Scholar
Song RH, Wang B, Yao QM et al. The Impact of Obesity on Thyroid Autoimmunity and Dysfunction: A Systematic Review and Meta-Analysis. Front Immunol 2019; 10: 2349SongRHWangBYaoQMThe Impact of Obesity on Thyroid Autoimmunity and Dysfunction: A Systematic Review and Meta-AnalysisFront Immunol2019102349Search in Google Scholar
Santini F, Marzullo P, Rotondi M et al. Mechanisms in endocrinology: the crosstalk between thyroid gland and adipose tissue: signal integration in health and disease. Eur J Endocrinol 2014; 171: R137–152SantiniFMarzulloPRotondiMMechanisms in endocrinology: the crosstalk between thyroid gland and adipose tissue: signal integration in health and diseaseEur J Endocrinol2014171R137152Search in Google Scholar
Marzullo P, Minocci A, Tagliaferri MA et al. Investigations of thyroid hormones and antibodies in obesity: leptin levels are associated with thyroid autoimmunity independent of bioanthropometric, hormonal, and weight-related determinants. J Clin Endocrinol Metab 2010; 95: 3965–3972MarzulloPMinocciATagliaferriMAInvestigations of thyroid hormones and antibodies in obesity: leptin levels are associated with thyroid autoimmunity independent of bioanthropometric, hormonal, and weight-related determinantsJ Clin Endocrinol Metab20109539653972Search in Google Scholar
Ayturk S, Gursoy A, Kut A et al. Metabolic syndrome and its components are associated with increased thyroid volume and nodule prevalence in a mild-to-moderate iodine-deficient area. Eur J Endocrinol 2009; 161: 599–605AyturkSGursoyAKutAMetabolic syndrome and its components are associated with increased thyroid volume and nodule prevalence in a mild-to-moderate iodine-deficient areaEur J Endocrinol2009161599605Search in Google Scholar
Siqueira RA, Noll M, Rodrigues APS et al. Factors Associated with the Occurrence of Thyroid Nodules in Severely Obese Patients: A Case-Control Study. Asian Pac J Cancer Prev 2019; 20: 693–697SiqueiraRANollMRodriguesAPSFactors Associated with the Occurrence of Thyroid Nodules in Severely Obese Patients: A Case-Control StudyAsian Pac J Cancer Prev201920693697Search in Google Scholar
Buscemi S, Massenti FM, Vasto S et al. Association of obesity and diabetes with thyroid nodules. Endocrine 2018; 60: 339–347BuscemiSMassentiFMVastoSAssociation of obesity and diabetes with thyroid nodulesEndocrine201860339347Search in Google Scholar
Harikrishna A, Ishak A, Ellinides A et al. The impact of obesity and insulin resistance on thyroid cancer: A systematic review. Maturitas 2019; 125: 45–49HarikrishnaAIshakAEllinidesAThe impact of obesity and insulin resistance on thyroid cancer: A systematic reviewMaturitas20191254549Search in Google Scholar
Schmid D, Ricci C, Behrens G et al. Adiposity and risk of thyroid cancer: a systematic review and meta-analysis. Obes Rev 2015; 16: 1042–1054SchmidDRicciCBehrensGAdiposity and risk of thyroid cancer: a systematic review and meta-analysisObes Rev20151610421054Search in Google Scholar
Lautenbach A, Wernecke M, Mann O et al. Thyroid-stimulating hormone levels in euthyroid patients 8 years following bariatric surgery. Int J Obes (Lond) 2022; 46: 825–830LautenbachAWerneckeMMannOThyroid-stimulating hormone levels in euthyroid patients 8 years following bariatric surgeryInt J Obes (Lond)202246825830Search in Google Scholar
van Hulsteijn LT, Pasquali R, Casanueva F et al. Prevalence of endocrine disorders in obese patients: systematic review and meta-analysis. Eur J Endocrinol 2020; 182: 11–21van HulsteijnLTPasqualiRCasanuevaFPrevalence of endocrine disorders in obese patients: systematic review and meta-analysisEur J Endocrinol20201821121Search in Google Scholar
Pasquali R, Casanueva F, Haluzik M et al. European Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesity. Eur J Endocrinol 2020; 182: G1–G32PasqualiRCasanuevaFHaluzikMEuropean Society of Endocrinology Clinical Practice Guideline: Endocrine work-up in obesityEur J Endocrinol2020182G1G32Search in Google Scholar
Szczepanek-Parulska E, Sokolowski J, Dmowska D et al. Lipid profile abnormalities associated with endocrine disorders. Endokrynol Pol 2022; DOI: 10.5603/EP.a2022.0059:Szczepanek-ParulskaESokolowskiJDmowskaDLipid profile abnormalities associated with endocrine disordersEndokrynol Pol202210.5603/EP.a2022.0059Open DOISearch in Google Scholar
Lopez M, Alvarez CV, Nogueiras R et al. Energy balance regulation by thyroid hormones at central level. Trends Mol Med 2013; 19: 418–427LopezMAlvarezCVNogueirasREnergy balance regulation by thyroid hormones at central levelTrends Mol Med201319418427Search in Google Scholar
Coppola A, Liu ZW, Andrews ZB et al. A central thermogenic-like mechanism in feeding regulation: an interplay between arcuate nucleus T3 and UCP2. Cell Metab 2007; 5: 21–33CoppolaALiuZWAndrewsZBA central thermogenic-like mechanism in feeding regulation: an interplay between arcuate nucleus T3 and UCP2Cell Metab200752133Search in Google Scholar
Weiner J, Kranz M, Kloting N et al. Thyroid hormone status defines brown adipose tissue activity and browning of white adipose tissues in mice. Sci Rep 2016; 6: 38124WeinerJKranzMKlotingNThyroid hormone status defines brown adipose tissue activity and browning of white adipose tissues in miceSci Rep2016638124Search in Google Scholar
Guzik TJ, Skiba DS, Touyz RM et al. The role of infiltrating immune cells in dysfunctional adipose tissue. Cardiovasc Res 2017; 113: 1009–1023GuzikTJSkibaDSTouyzRMThe role of infiltrating immune cells in dysfunctional adipose tissueCardiovasc Res201711310091023Search in Google Scholar
Maurizi G, Della Guardia L, Maurizi A et al. Adipocytes properties and crosstalk with immune system in obesity-related inflammation. J Cell Physiol 2018; 233: 88–97MauriziGDella GuardiaLMauriziAAdipocytes properties and crosstalk with immune system in obesity-related inflammationJ Cell Physiol20182338897Search in Google Scholar
Cao H. Adipocytokines in obesity and metabolic disease. J Endocrinol 2014; 220: T47–59CaoH.Adipocytokines in obesity and metabolic diseaseJ Endocrinol2014220T4759Search in Google Scholar
Haider DG, Schaller G, Kapiotis S et al. The release of the adipocytokine visfatin is regulated by glucose and insulin. Diabetologia 2006; 49: 1909–1914HaiderDGSchallerGKapiotisSThe release of the adipocytokine visfatin is regulated by glucose and insulinDiabetologia20064919091914Search in Google Scholar
Silswal N, Singh AK, Aruna B et al. Human resistin stimulates the pro-inflammatory cytokines TNF-alpha and IL-12 in macrophages by NF-kappaB-dependent pathway. Biochem Biophys Res Commun 2005; 334: 1092–1101SilswalNSinghAKArunaBHuman resistin stimulates the pro-inflammatory cytokines TNF-alpha and IL-12 in macrophages by NF-kappaB-dependent pathwayBiochem Biophys Res Commun200533410921101Search in Google Scholar
Longhi S, Radetti G. Thyroid function and obesity. J Clin Res Pediatr Endocrinol 2013; 5 Suppl 1: 40–44LonghiSRadettiG.Thyroid function and obesityJ Clin Res Pediatr Endocrinol20135Suppl 14044Search in Google Scholar
Pekary AE, Levin SR, Johnson DG et al. Tumor necrosis factor-alpha (TNF-alpha) and transforming growth factor-beta 1 (TGF-beta 1) inhibit the expression and activity of Na+/K(+)-ATPase in FRTL-5 rat thyroid cells. J Interferon Cytokine Res 1997; 17: 185–195PekaryAELevinSRJohnsonDGTumor necrosis factor-alpha (TNF-alpha) and transforming growth factor-beta 1 (TGF-beta 1) inhibit the expression and activity of Na+/K(+)-ATPase in FRTL-5 rat thyroid cellsJ Interferon Cytokine Res199717185195Search in Google Scholar
Kwakkel J, Surovtseva OV, de Vries EM et al. A novel role for the thyroid hormone-activating enzyme type 2 deiodinase in the inflammatory response of macrophages. Endocrinology 2014; 155: 2725–2734KwakkelJSurovtsevaOVde VriesEMA novel role for the thyroid hormone-activating enzyme type 2 deiodinase in the inflammatory response of macrophagesEndocrinology201415527252734Search in Google Scholar
Kissebah AH, Vydelingum N, Murray R, et al. Relation of body fat distribution to metabolic complications of obesity. J Clin Endocrinol Metab. 1982; 54: 254–260.KissebahAHVydelingumNMurrayRRelation of body fat distribution to metabolic complications of obesityJ Clin Endocrinol Metab.198254254260Search in Google Scholar
Chen YC, Jiao Y, Cui Y et al. Aberrant brain functional connectivity related to insulin resistance in type 2 diabetes: a resting-state fMRI study. Diabetes Care 2014; 37: 1689–1696ChenYCJiaoYCuiYAberrant brain functional connectivity related to insulin resistance in type 2 diabetes: a resting-state fMRI studyDiabetes Care20143716891696Search in Google Scholar
Zeyda M, Stulnig TM. Obesity, inflammation, and insulin resistance--a mini-review. Gerontology 2009; 55: 379–386ZeydaMStulnigTM.Obesity, inflammation, and insulin resistance--a mini-reviewGerontology200955379386Search in Google Scholar
Griffin ME, Marcucci MJ, Cline GW et al. Free fatty acid-induced insulin resistance is associated with activation of protein kinase C theta and alterations in the insulin signaling cascade. Diabetes 1999; 48: 1270–1274GriffinMEMarcucciMJClineGWFree fatty acid-induced insulin resistance is associated with activation of protein kinase C theta and alterations in the insulin signaling cascadeDiabetes19994812701274Search in Google Scholar
Matulewicz N, Karczewska-Kupczewska M. Insulin resistance and chronic inflammation. Postepy Hig Med Dosw (Online). 2016; 70: 1245–1258.MatulewiczNKarczewska-KupczewskaM.Insulin resistance and chronic inflammationPostepy Hig Med Dosw (Online).20167012451258Search in Google Scholar
Petersen MC, Shulman GI. Mechanisms of Insulin Action and Insulin Resistance. Physiol Rev. 2018; 98: 2133–2223PetersenMCShulmanGI.Mechanisms of Insulin Action and Insulin ResistancePhysiol Rev.20189821332223Search in Google Scholar
Jornayvaz FR, Samuel VT, Shulman GI. The role of muscle insulin resistance in the pathogenesis of atherogenic dyslipidemia and nonalcoholic fatty liver disease associated with the metabolic syndrome. Annu Rev Nutr. 2010; 30: 273–290.JornayvazFRSamuelVTShulmanGI.The role of muscle insulin resistance in the pathogenesis of atherogenic dyslipidemia and nonalcoholic fatty liver disease associated with the metabolic syndromeAnnu Rev Nutr.201030273290Search in Google Scholar
Sakurai Y, Kubota N, Yamauchi T, Kadowaki T. Role of insulin resistance in MAFLD. Int J Mol Sci. 2021; 22: 4156. Published 2021 Apr 16. doi:10.3390/ijms22084156SakuraiYKubotaNYamauchiTKadowakiT.Role of insulin resistance in MAFLDInt J Mol Sci.2021224156Published 2021 Apr 16.10.3390/ijms22084156Open DOISearch in Google Scholar
Michalaki MA, Vagenakis AG, Leonardou AS et al. Thyroid function in humans with morbid obesity. Thyroid 2006; 16: 73–78MichalakiMAVagenakisAGLeonardouASThyroid function in humans with morbid obesityThyroid2006167378Search in Google Scholar
Galofre JC, Pujante P, Abreu C et al. Relationship between thyroid-stimulating hormone and insulin in euthyroid obese men. Ann Nutr Metab 2008; 53: 188–194GalofreJCPujantePAbreuCRelationship between thyroid-stimulating hormone and insulin in euthyroid obese menAnn Nutr Metab200853188194Search in Google Scholar
Martinez-deMena R, Obregon MJ. Insulin increases the adrenergic stimulation of 5′ deiodinase activity and mRNA expression in rat brown adipocytes; role of MAPK and PI3K. J Mol Endocrinol 2005; 34: 139–151Martinez-deMenaRObregonMJ.Insulin increases the adrenergic stimulation of 5′ deiodinase activity and mRNA expression in rat brown adipocytes; role of MAPK and PI3KJ Mol Endocrinol200534139151Search in Google Scholar
Stepanek L, Horakova D, Stepanek L et al. Free triiodothyronine/free thyroxine (FT3/FT4) ratio is strongly associated with insulin resistance in euthyroid and hypothyroid adults: a cross-sectional study. Endokrynol Pol 2021; 72: 8–13StepanekLHorakovaDStepanekLFree triiodothyronine/free thyroxine (FT3/FT4) ratio is strongly associated with insulin resistance in euthyroid and hypothyroid adults: a cross-sectional studyEndokrynol Pol202172813Search in Google Scholar
Malaguarnera R, Vella V, Nicolosi ML et al. Insulin Resistance: Any Role in the Changing Epidemiology of Thyroid Cancer? Front Endocrinol (Lausanne) 2017; 8: 314MalaguarneraRVellaVNicolosiMLInsulin Resistance: Any Role in the Changing Epidemiology of Thyroid Cancer?Front Endocrinol (Lausanne)20178314Search in Google Scholar
Kimura T, Van Keymeulen A, Golstein J et al. Regulation of thyroid cell proliferation by TSH and other factors: a critical evaluation of in vitro models. Endocr Rev 2001; 22: 631–656KimuraTVan KeymeulenAGolsteinJRegulation of thyroid cell proliferation by TSH and other factors: a critical evaluation of in vitro modelsEndocr Rev200122631656Search in Google Scholar
Vella V, Pandini G, Sciacca L et al. A novel autocrine loop involving IGF-II and the insulin receptor isoform-A stimulates growth of thyroid cancer. J Clin Endocrinol Metab 2002; 87: 245–254VellaVPandiniGSciaccaLA novel autocrine loop involving IGF-II and the insulin receptor isoform-A stimulates growth of thyroid cancerJ Clin Endocrinol Metab200287245254Search in Google Scholar
Wang K, Yang Y, Wu Y et al. The association between insulin resistance and vascularization of thyroid nodules. J Clin Endocrinol Metab 2015; 100: 184–192WangKYangYWuYThe association between insulin resistance and vascularization of thyroid nodulesJ Clin Endocrinol Metab2015100184192Search in Google Scholar
Yu H, Li Q, Zhang M et al. Decreased leptin is associated with alterations in thyroid-stimulating hormone levels after Roux-en-Y gastric bypass surgery in obese euthyroid patients with Type 2 diabetes. Obes Facts 2019; 12: 272–280YuHLiQZhangMDecreased leptin is associated with alterations in thyroid-stimulating hormone levels after Roux-en-Y gastric bypass surgery in obese euthyroid patients with Type 2 diabetesObes Facts201912272280Search in Google Scholar
Betry C, Challan-Belval MA, Bernard A et al. Increased TSH in obesity: Evidence for a BMI-independent association with leptin. Diabetes Metab 2015; 41: 248–251BetryCChallan-BelvalMABernardAIncreased TSH in obesity: Evidence for a BMI-independent association with leptinDiabetes Metab201541248251Search in Google Scholar
Schaffler A, Binart N, Scholmerich J et al. Hypothesis paper Brain talks with fat--evidence for a hypothalamic-pituitary-adipose axis? Neuropeptides 2005; 39: 363–367SchafflerABinartNScholmerichJHypothesis paper Brain talks with fat--evidence for a hypothalamic-pituitary-adipose axis?Neuropeptides200539363367Search in Google Scholar
Karpuzoglu H, Ucal Y, Kumru P et al. Increased maternal leptin levels may be an indicator of subclinical hypothyroidism in a newborn. J Med Biochem 2022; 41: 156–161KarpuzogluHUcalYKumruPIncreased maternal leptin levels may be an indicator of subclinical hypothyroidism in a newbornJ Med Biochem202241156161Search in Google Scholar
Araujo RL, Andrade BM, Padron AS et al. High-fat diet increases thyrotropin and oxygen consumption without altering circulating 3,5,3′-triiodothyronine (T3) and thyroxine in rats: the role of iodothyronine deiodinases, reverse T3 production, and whole-body fat oxidation. Endocrinology 2010; 151: 3460–3469AraujoRLAndradeBMPadronASHigh-fat diet increases thyrotropin and oxygen consumption without altering circulating 3,5,3′-triiodothyronine (T3) and thyroxine in rats: the role of iodothyronine deiodinases, reverse T3 production, and whole-body fat oxidationEndocrinology201015134603469Search in Google Scholar
Araujo RL, Andrade BM, da Silva ML et al. Tissue-specific deiodinase regulation during food restriction and low replacement dose of leptin in rats. Am J Physiol Endocrinol Metab 2009; 296: E1157–1163AraujoRLAndradeBMda SilvaMLTissue-specific deiodinase regulation during food restriction and low replacement dose of leptin in ratsAm J Physiol Endocrinol Metab2009296E11571163Search in Google Scholar
Macek Jilkova Z, Pavelka S, Flachs P et al. Modulation of type I iodothyronine 5′-deiodinase activity in white adipose tissue by nutrition: possible involvement of leptin. Physiol Res 2010; 59: 561–569Macek JilkovaZPavelkaSFlachsPModulation of type I iodothyronine 5′-deiodinase activity in white adipose tissue by nutrition: possible involvement of leptinPhysiol Res201059561569Search in Google Scholar
Ghamari-Langroudi M, Vella KR, Srisai D et al. Regulation of thyrotropin-releasing hormone-expressing neurons in paraventricular nucleus of the hypothalamus by signals of adiposity. Mol Endocrinol 2010; 24: 2366–2381Ghamari-LangroudiMVellaKRSrisaiDRegulation of thyrotropin-releasing hormone-expressing neurons in paraventricular nucleus of the hypothalamus by signals of adiposityMol Endocrinol20102423662381Search in Google Scholar
Nannipieri M, Cecchetti F, Anselmino M et al. Expression of thyrotropin and thyroid hormone receptors in adipose tissue of patients with morbid obesity and/or type 2 diabetes: effects of weight loss. Int J Obes (Lond) 2009; 33: 1001–1006NannipieriMCecchettiFAnselminoMExpression of thyrotropin and thyroid hormone receptors in adipose tissue of patients with morbid obesity and/or type 2 diabetes: effects of weight lossInt J Obes (Lond)20093310011006Search in Google Scholar
Kurylowicz A, Jonas M, Lisik W et al. Obesity is associated with a decrease in expression but not with the hypermethylation of thermogenesis-related genes in adipose tissues. J Transl Med 2015; 13: 31KurylowiczAJonasMLisikWObesity is associated with a decrease in expression but not with the hypermethylation of thermogenesis-related genes in adipose tissuesJ Transl Med20151331Search in Google Scholar
Juiz-Valina P, Cordido M, Outeirino-Blanco E et al. Central resistance to thyroid hormones in morbidly obese subjects is reversed after bariatric surgery-induced weight loss. J Clin Med 2020; 9.Juiz-ValinaPCordidoMOuteirino-BlancoECentral resistance to thyroid hormones in morbidly obese subjects is reversed after bariatric surgery-induced weight lossJ Clin Med20209Search in Google Scholar
Tjorve E, Tjorve KM, Olsen JO et al. On commonness and rarity of thyroid hormone resistance: a discussion based on mechanisms of reduced sensitivity in peripheral tissues. Med Hypotheses 2007; 69: 913–921TjorveETjorveKMOlsenJOOn commonness and rarity of thyroid hormone resistance: a discussion based on mechanisms of reduced sensitivity in peripheral tissuesMed Hypotheses200769913921Search in Google Scholar
Laclaustra M, Moreno-Franco B, Lou-Bonafonte JM et al. Impaired sensitivity to thyroid hormones is associated with diabetes and metabolic syndrome. Diabetes Care 2019; 42: 303–310LaclaustraMMoreno-FrancoBLou-BonafonteJMImpaired sensitivity to thyroid hormones is associated with diabetes and metabolic syndromeDiabetes Care201942303310Search in Google Scholar
Moulin de Moraes CM, Mancini MC, de Melo ME et al. Prevalence of subclinical hypothyroidism in a morbidly obese population and improvement after weight loss induced by Roux-en-Y gastric bypass. Obes Surg 2005; 15: 1287–1291Moulin de MoraesCMManciniMCde MeloMEPrevalence of subclinical hypothyroidism in a morbidly obese population and improvement after weight loss induced by Roux-en-Y gastric bypassObes Surg20051512871291Search in Google Scholar
Moreira-Andrés MN, Del Cañizo-Gómez FJ, Black EG, Hoffenberg R. Long-term evaluation of thyroidal response to partial calorie restriction in obesity. Clin Endocrinol (Oxf). 1981;15: 621–626.Moreira-AndrésMNDel Cañizo-GómezFJBlackEGHoffenbergR.Long-term evaluation of thyroidal response to partial calorie restriction in obesityClin Endocrinol (Oxf).198115621626Search in Google Scholar
Kaptein EM, Beale E, Chan LS. Thyroid hormone therapy for obesity and nonthyroidal illnesses: a systematic review. J Clin Endocrinol Metab. 2009; 94: 3663–3675.KapteinEMBealeEChanLS.Thyroid hormone therapy for obesity and nonthyroidal illnesses: a systematic reviewJ Clin Endocrinol Metab.20099436633675Search in Google Scholar
Jonklaas J, Bianco AC, Bauer AJ, et al. Guidelines for the treatment of hypothyroidism: prepared by the american thyroid association task force on thyroid hormone replacement. Thyroid. 2014; 24: 1670–1751.JonklaasJBiancoACBauerAJGuidelines for the treatment of hypothyroidism: prepared by the american thyroid association task force on thyroid hormone replacementThyroid.20142416701751Search in Google Scholar
Villarroya F, Cereijo R, Villarroya J et al. Brown adipose tissue as a secretory organ. Nat Rev Endocrinol 2017; 13: 26–35VillarroyaFCereijoRVillarroyaJBrown adipose tissue as a secretory organNat Rev Endocrinol2017132635Search in Google Scholar
Bianco AC, Sheng XY, Silva JE. Triiodothyronine amplifies norepinephrine stimulation of uncoupling protein gene transcription by a mechanism not requiring protein synthesis. J Biol Chem 1988; 263: 18168–18175BiancoACShengXYSilvaJE.Triiodothyronine amplifies norepinephrine stimulation of uncoupling protein gene transcription by a mechanism not requiring protein synthesisJ Biol Chem19882631816818175Search in Google Scholar
Branco M, Ribeiro M, Negrao N et al. 3,5,3′-Triiodothyronine actively stimulates UCP in brown fat under minimal sympathetic activity. Am J Physiol 1999; 276: E179–187BrancoMRibeiroMNegraoN3,5,3′-Triiodothyronine actively stimulates UCP in brown fat under minimal sympathetic activityAm J Physiol1999276E179187Search in Google Scholar
Silva JE, Larsen PR. Potential of brown adipose tissue type II thyroxine 5′-deiodinase as a local and systemic source of triiodothyronine in rats. J Clin Invest 1985; 76: 2296–2305SilvaJELarsenPR.Potential of brown adipose tissue type II thyroxine 5′-deiodinase as a local and systemic source of triiodothyronine in ratsJ Clin Invest19857622962305Search in Google Scholar
Wang Q, Zhang M, Ning G et al. Brown adipose tissue in humans is activated by elevated plasma catecholamines levels and is inversely related to central obesity. PLoS One 2011; 6: e21006WangQZhangMNingGBrown adipose tissue in humans is activated by elevated plasma catecholamines levels and is inversely related to central obesityPLoS One20116e21006Search in Google Scholar
Reynisdottir S, Wahrenberg H, Carlstrom K et al. Catecholamine resistance in fat cells of women with upper-body obesity due to decreased expression of beta 2-adrenoceptors. Diabetologia 1994; 37: 428–435ReynisdottirSWahrenbergHCarlstromKCatecholamine resistance in fat cells of women with upper-body obesity due to decreased expression of beta 2-adrenoceptorsDiabetologia199437428435Search in Google Scholar
Chamberlain PD, Jennings KH, Paul F et al. The tissue distribution of the human beta3-adrenoceptor studied using a monoclonal antibody: direct evidence of the beta3-adrenoceptor in human adipose tissue, atrium and skeletal muscle. Int J Obes Relat Metab Disord 1999; 23: 1057–1065ChamberlainPDJenningsKHPaulFThe tissue distribution of the human beta3-adrenoceptor studied using a monoclonal antibody: direct evidence of the beta3-adrenoceptor in human adipose tissue, atrium and skeletal muscleInt J Obes Relat Metab Disord19992310571065Search in Google Scholar
Valentine JM, Ahmadian M, Keinan O et al. beta3-Adrenergic receptor downregulation leads to adipocyte catecholamine resistance in obesity. J Clin Invest 2022; 132:ValentineJMAhmadianMKeinanObeta3-Adrenergic receptor downregulation leads to adipocyte catecholamine resistance in obesityJ Clin Invest2022132Search in Google Scholar
Guo T, Marmol P, Moliner A et al. Adipocyte ALK7 links nutrient overload to catecholamine resistance in obesity. Elife 2014; 3: e03245GuoTMarmolPMolinerAAdipocyte ALK7 links nutrient overload to catecholamine resistance in obesityElife20143e03245Search in Google Scholar
Alcala M, Calderon-Dominguez M, Serra D et al. Mechanisms of Impaired Brown Adipose Tissue Recruitment in Obesity. Front Physiol 2019; 10: 94AlcalaMCalderon-DominguezMSerraDMechanisms of Impaired Brown Adipose Tissue Recruitment in ObesityFront Physiol20191094Search in Google Scholar
Villarroya F, Cereijo R, Villarroya J et al. Toward an Understanding of How Immune Cells Control Brown and Beige Adipobiology. Cell Metab 2018; 27: 954–961VillarroyaFCereijoRVillarroyaJToward an Understanding of How Immune Cells Control Brown and Beige AdipobiologyCell Metab201827954961Search in Google Scholar
Araujo RL, Carvalho DP. Bioenergetic impact of tissue-specific regulation of iodothyronine deiodinases during nutritional imbalance. J Bioenerg Biomembr 2011; 43: 59–65AraujoRLCarvalhoDP.Bioenergetic impact of tissue-specific regulation of iodothyronine deiodinases during nutritional imbalanceJ Bioenerg Biomembr2011435965Search in Google Scholar
de Heredia FP, Gómez-Martínez S, Marcos A. Obesity, inflammation and the immune system. Proc Nutr Soc. 2012; 71: 332–338.de HerediaFPGómez-MartínezSMarcosA.Obesity, inflammation and the immune systemProc Nutr Soc.201271332338Search in Google Scholar
Deng J, Neff LM, Rubert NC, et al. MRI characterization of brown adipose tissue under thermal challenges in normal weight, overweight, and obese young men. J Magn Reson Imaging. 2018; 47: 936–947. doi:10.1002/jmri.25836DengJNeffLMRubertNCMRI characterization of brown adipose tissue under thermal challenges in normal weight, overweight, and obese young menJ Magn Reson Imaging.20184793694710.1002/jmri.25836Open DOISearch in Google Scholar
Kang S, Bajnok L, Longo KA, et al. Effects of Wnt signaling on brown adipocyte differentiation and metabolism mediated by PGC-1alpha. Mol Cell Biol. 2005; 25: 1272–1282. doi:10.1128/MCB.25.4.1272-1282.2005KangSBajnokLLongoKAEffects of Wnt signaling on brown adipocyte differentiation and metabolism mediated by PGC-1alphaMol Cell Biol.2005251272128210.1128/MCB.25.4.1272-1282.2005Open DOISearch in Google Scholar
Villarroya F, Cereijo R, Gavaldà-Navarro A, Villarroya J, Giralt M. Inflammation of brown/beige adipose tissues in obesity and metabolic disease. J Intern Med. 2018; 284: 492–504.VillarroyaFCereijoRGavaldà-NavarroAVillarroyaJGiraltM.Inflammation of brown/beige adipose tissues in obesity and metabolic diseaseJ Intern Med.2018284492504Search in Google Scholar
Hollowell JG, Staehling NW, Flanders WD et al. Serum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III). J Clin Endocrinol Metab 2002; 87: 489–499HollowellJGStaehlingNWFlandersWDSerum TSH, T(4), and thyroid antibodies in the United States population (1988 to 1994): National Health and Nutrition Examination Survey (NHANES III)J Clin Endocrinol Metab200287489499Search in Google Scholar
Garmendia Madariaga A, Santos Palacios S, Guillen-Grima F et al. The incidence and prevalence of thyroid dysfunction in Europe: a meta-analysis. J Clin Endocrinol Metab 2014; 99: 923–931Garmendia MadariagaASantos PalaciosSGuillen-GrimaFThe incidence and prevalence of thyroid dysfunction in Europe: a meta-analysisJ Clin Endocrinol Metab201499923931Search in Google Scholar
Fierabracci P, Pinchera A, Martinelli S et al. Prevalence of endocrine diseases in morbidly obese patients scheduled for bariatric surgery: beyond diabetes. Obes Surg 2011; 21: 54–60FierabracciPPincheraAMartinelliSPrevalence of endocrine diseases in morbidly obese patients scheduled for bariatric surgery: beyond diabetesObes Surg2011215460Search in Google Scholar
Guo X, He Z, Shao S et al. Interaction effect of obesity and thyroid autoimmunity on the prevalence of hyperthyrotropinaemia. Endocrine 2020; 68: 573–583GuoXHeZShaoSInteraction effect of obesity and thyroid autoimmunity on the prevalence of hyperthyrotropinaemiaEndocrine202068573583Search in Google Scholar
Radetti G, Kleon W, Buzi F et al. Thyroid function and structure are affected in childhood obesity. J Clin Endocrinol Metab 2008; 93: 4749–4754RadettiGKleonWBuziFThyroid function and structure are affected in childhood obesityJ Clin Endocrinol Metab20089347494754Search in Google Scholar
Rotondi M, Cappelli C, Leporati P et al. A hypoechoic pattern of the thyroid at ultrasound does not indicate autoimmune thyroid diseases in patients with morbid obesity. Eur J Endocrinol 2010; 163: 105–109RotondiMCappelliCLeporatiPA hypoechoic pattern of the thyroid at ultrasound does not indicate autoimmune thyroid diseases in patients with morbid obesityEur J Endocrinol2010163105109Search in Google Scholar
Ittermann T, Markus MR, Schipf S et al. Metformin inhibits goitrogenous effects of type 2 diabetes. Eur J Endocrinol 2013; 169: 9–15IttermannTMarkusMRSchipfSMetformin inhibits goitrogenous effects of type 2 diabetesEur J Endocrinol2013169915Search in Google Scholar
Belfiore A, Malaguarnera R, Vella V, et al. Insulin receptor isoforms in physiology and disease: An updated view. Endocr Rev. 2017; 38: 379–431. doi:10.1210/er.2017-00073BelfioreAMalaguarneraRVellaVInsulin receptor isoforms in physiology and disease: An updated viewEndocr Rev.20173837943110.1210/er.2017-00073Open DOISearch in Google Scholar
Moruzzi N, Lazzeri-Barcelo F. Insulin Receptor Isoforms in Physiology and Metabolic Disease [Internet]. Evolving Concepts in Insulin Resistance. IntechOpen; 2022.MoruzziNLazzeri-BarceloF.Insulin Receptor Isoforms in Physiology and Metabolic Disease [Internet]Evolving Concepts in Insulin Resistance. IntechOpen2022Search in Google Scholar
Leibiger B, Leibiger IB, Moede T, et al. Selective insulin signaling through A and B insulin receptors regulates transcription of insulin and glucokinase genes in pancreatic beta cells. Mol Cell. 2001; 7: 559–570.LeibigerBLeibigerIBMoedeTSelective insulin signaling through A and B insulin receptors regulates transcription of insulin and glucokinase genes in pancreatic beta cellsMol Cell.20017559570Search in Google Scholar
Kaminska D, Hämäläinen M, Cederberg H, et al. Adipose tissue INSR splicing in humans associates with fasting insulin level and is regulated by weight loss. Diabetologia. 2014; 57: 347–351.KaminskaDHämäläinenMCederbergHAdipose tissue INSR splicing in humans associates with fasting insulin level and is regulated by weight lossDiabetologia.201457347351Search in Google Scholar
Rezzonico JN, Rezzonico M, Pusiol E et al. Increased prevalence of insulin resistance in patients with differentiated thyroid carcinoma. Metab Syndr Relat Disord 2009; 7: 375–380RezzonicoJNRezzonicoMPusiolEIncreased prevalence of insulin resistance in patients with differentiated thyroid carcinomaMetab Syndr Relat Disord20097375380Search in Google Scholar
Avgerinos KI, Spyrou N, Mantzoros CS et al. Obesity and cancer risk: Emerging biological mechanisms and perspectives. Metabolism 2019; 92: 121–135AvgerinosKISpyrouNMantzorosCSObesity and cancer risk: Emerging biological mechanisms and perspectivesMetabolism201992121135Search in Google Scholar
Lauby-Secretan B, Scoccianti C, Loomis D et al. Body fatness and cancer--Viewpoint of the IARC Working Group. N Engl J Med 2016; 375: 794–798Lauby-SecretanBScocciantiCLoomisDBody fatness and cancer--Viewpoint of the IARC Working GroupN Engl J Med2016375794798Search in Google Scholar
Wang Y, Lin H, Li Q et al. Association between different obesity phenotypes and hypothyroidism: a study based on a longitudinal health management cohort. Endocrine 2021; 72: 688–698WangYLinHLiQAssociation between different obesity phenotypes and hypothyroidism: a study based on a longitudinal health management cohortEndocrine202172688698Search in Google Scholar
Nie X, Ma X, Xu Y et al. Characteristics of Serum Thyroid Hormones in Different Metabolic Phenotypes of Obesity. Front Endocrinol (Lausanne) 2020; 11: 68NieXMaXXuYCharacteristics of Serum Thyroid Hormones in Different Metabolic Phenotypes of ObesityFront Endocrinol (Lausanne)20201168Search in Google Scholar
Kim JM, Kim BH, Lee H et al. The relationship between thyroid function and different obesity phenotypes in Korean euthyroid adults. Diabetes Metab J 2019; 43: 867–878KimJMKimBHLeeHThe relationship between thyroid function and different obesity phenotypes in Korean euthyroid adultsDiabetes Metab J201943867878Search in Google Scholar
Amouzegar A, Kazemian E, Abdi H et al. Association between thyroid function and development of different obesity phenotypes in euthyroid adults: A nine-year follow-up. Thyroid 2018; 28: 458–464AmouzegarAKazemianEAbdiHAssociation between thyroid function and development of different obesity phenotypes in euthyroid adults: A nine-year follow-upThyroid201828458464Search in Google Scholar
Shin JA, Mo EY, Kim ES et al. Association between lower normal free thyroxine concentrations and obesity phenotype in healthy euthyroid subjects. Int J Endocrinol 2014; 2014: 104318ShinJAMoEYKimESAssociation between lower normal free thyroxine concentrations and obesity phenotype in healthy euthyroid subjectsInt J Endocrinol20142014104318Search in Google Scholar
Amouzegar A, Kazemian E, Abdi H et al. Abdominal Obesity Phenotypes and Incidence of Thyroid Autoimmunity: A 9-Year Follow-up. Endocr Res 2020; 45: 202–209AmouzegarAKazemianEAbdiHAbdominal Obesity Phenotypes and Incidence of Thyroid Autoimmunity: A 9-Year Follow-upEndocr Res202045202209Search in Google Scholar
Yang H, Xia Q, Shen Y et al. Gender-specific impact of metabolic obesity phenotypes on the risk of Hashimoto's Thyroiditis: A retrospective data analysis using a health check-up database. J Inflamm Res 2022; 15: 827–837YangHXiaQShenYGender-specific impact of metabolic obesity phenotypes on the risk of Hashimoto's Thyroiditis: A retrospective data analysis using a health check-up databaseJ Inflamm Res202215827837Search in Google Scholar
Zhang C, Gao X, Han Y et al. Correlation Between Thyroid Nodules and Metabolic Syndrome: A Systematic Review and Meta-Analysis. Front Endocrinol (Lausanne) 2021; 12: 730279ZhangCGaoXHanYCorrelation Between Thyroid Nodules and Metabolic Syndrome: A Systematic Review and Meta-AnalysisFront Endocrinol (Lausanne)202112730279Search in Google Scholar
Zhang F, Li Y, Yu X et al. The Relationship and Gender Disparity Between Thyroid Nodules and Metabolic Syndrome Components Based on a Recent Nationwide Cross-Sectional Study and Meta-Analysis. Front Endocrinol (Lausanne) 2021; 12: 736972ZhangFLiYYuXThe Relationship and Gender Disparity Between Thyroid Nodules and Metabolic Syndrome Components Based on a Recent Nationwide Cross-Sectional Study and Meta-AnalysisFront Endocrinol (Lausanne)202112736972Search in Google Scholar
Guo W, Tan L, Chen W et al. Relationship between metabolic syndrome and thyroid nodules and thyroid volume in an adult population. Endocrine 2019; 65: 357–364GuoWTanLChenWRelationship between metabolic syndrome and thyroid nodules and thyroid volume in an adult populationEndocrine201965357364Search in Google Scholar
Xu L, Zeng F, Wang Y et al. Prevalence and associated metabolic factors for thyroid nodules: a cross-sectional study in Southwest of China with more than 120 thousand populations. BMC Endocr Disord 2021; 21: 175XuLZengFWangYPrevalence and associated metabolic factors for thyroid nodules: a cross-sectional study in Southwest of China with more than 120 thousand populationsBMC Endocr Disord202121175Search in Google Scholar
Song B, Zuo Z, Tan J et al. Association of thyroid nodules with adiposity: a community-based cross-sectional study in China. BMC Endocr Disord 2018; 18: 3SongBZuoZTanJAssociation of thyroid nodules with adiposity: a community-based cross-sectional study in ChinaBMC Endocr Disord2018183Search in Google Scholar
Su Y, Zhang YL, Zhao M et al. Association between thyroid nodules and volume and metabolic syndrome in an iodine-adequate area: A large community-based population study. Metab Syndr Relat Disord 2019; 17: 217–222SuYZhangYLZhaoMAssociation between thyroid nodules and volume and metabolic syndrome in an iodine-adequate area: A large community-based population studyMetab Syndr Relat Disord201917217222Search in Google Scholar
Son H, Lee H, Kang K et al. The risk of thyroid cancer and obesity: A nationwide population-based study using the Korea National Health Insurance Corporation cohort database. Surg Oncol 2018; 27: 166–171SonHLeeHKangKThe risk of thyroid cancer and obesity: A nationwide population-based study using the Korea National Health Insurance Corporation cohort databaseSurg Oncol201827166171Search in Google Scholar
Youssef MR, Reisner ASC, Attia AS et al. Obesity and the prevention of thyroid cancer: Impact of body mass index and weight change on developing thyroid cancer - Pooled results of 24 million cohorts. Oral Oncol 2021; 112: 105085YoussefMRReisnerASCAttiaASObesity and the prevention of thyroid cancer: Impact of body mass index and weight change on developing thyroid cancer - Pooled results of 24 million cohortsOral Oncol2021112105085Search in Google Scholar
He Q, Sun H, Li F et al. Obesity and risk of differentiated thyroid cancer: A large-scale case-control study. Clin Endocrinol (Oxf) 2019; 91: 869–878HeQSunHLiFObesity and risk of differentiated thyroid cancer: A large-scale case-control studyClin Endocrinol (Oxf)201991869878Search in Google Scholar
Kitahara CM, Pfeiffer RM, Sosa JA et al. Impact of Overweight and Obesity on US Papillary Thyroid Cancer Incidence Trends (1995–2015). J Natl Cancer Inst 2020; 112: 810–817KitaharaCMPfeifferRMSosaJAImpact of Overweight and Obesity on US Papillary Thyroid Cancer Incidence Trends (1995–2015)J Natl Cancer Inst2020112810817Search in Google Scholar
Fussey JM, Beaumont RN, Wood AR et al. Does obesity cause thyroid cancer? A Mendelian randomization study. J Clin Endocrinol Metab 2020; 105:FusseyJMBeaumontRNWoodARDoes obesity cause thyroid cancer? A Mendelian randomization studyJ Clin Endocrinol Metab2020105Search in Google Scholar
Rotondi M, Castagna MG, Cappelli C et al. Obesity does not modify the risk of differentiated thyroid cancer in a cytological series of thyroid nodules. Eur Thyroid J 2016; 5: 125–131RotondiMCastagnaMGCappelliCObesity does not modify the risk of differentiated thyroid cancer in a cytological series of thyroid nodulesEur Thyroid J20165125131Search in Google Scholar
Ahmadi S, Pappa T, Kang AS et al. Point of care measurement of Body Mass Index and thyroid nodule malignancy risk sssessment. Front Endocrinol (Lausanne) 2022; 13: 824226AhmadiSPappaTKangASPoint of care measurement of Body Mass Index and thyroid nodule malignancy risk sssessmentFront Endocrinol (Lausanne)202213824226Search in Google Scholar
Zheng X, Peng R, Xu H et al. The association between metabolic status and risk of cancer among patients with obesity: Metabolically Healthy Obesity vs. Metabolically Unhealthy Obesity. Front Nutr 2022; 9: 783660ZhengXPengRXuHThe association between metabolic status and risk of cancer among patients with obesity: Metabolically Healthy Obesity vs. Metabolically Unhealthy ObesityFront Nutr20229783660Search in Google Scholar
Lin CJ, Chang YC, Cheng TY et al. The association between metabolically healthy obesity and risk of cancer: A systematic review and meta-analysis of prospective cohort studies. Obes Rev 2020; 21: e13049LinCJChangYCChengTYThe association between metabolically healthy obesity and risk of cancer: A systematic review and meta-analysis of prospective cohort studiesObes Rev202021e13049Search in Google Scholar
Kwon H, Chang Y, Cho A et al. Metabolic obesity phenotypes and thyroid cancer risk: A cohort study. Thyroid 2019; 29: 349–358KwonHChangYChoAMetabolic obesity phenotypes and thyroid cancer risk: A cohort studyThyroid201929349358Search in Google Scholar
Nguyen DN, Kim JH, Kim MK. Association of metabolic health and central obesity with the risk of thyroid cancer: Data from the Korean Genome and Epidemiology Study. Cancer Epidemiol Biomarkers Prev 2022; 31: 543–553NguyenDNKimJHKimMK.Association of metabolic health and central obesity with the risk of thyroid cancer: Data from the Korean Genome and Epidemiology StudyCancer Epidemiol Biomarkers Prev202231543553Search in Google Scholar
Biondi B, Kahaly GJ, Robertson RP. Thyroid dysfunction and diabetes mellitus: Two closely associated disorders. Endocr Rev 2019; 40: 789–824BiondiBKahalyGJRobertsonRP.Thyroid dysfunction and diabetes mellitus: Two closely associated disordersEndocr Rev201940789824Search in Google Scholar
Sawicka-Gutaj N, Zybek-Kocik A, Kloska M et al. Effect of restoration of euthyroidism on visfatin concentrations and body composition in women. Endocr Connect 2021; 10: 462–470Sawicka-GutajNZybek-KocikAKloskaMEffect of restoration of euthyroidism on visfatin concentrations and body composition in womenEndocr Connect202110462470Search in Google Scholar
Stangierski A, Ruchala M, Krauze T et al. Treatment of severe thyroid function disorders and changes in body composition. Endokrynol Pol 2016; 67: 359–366StangierskiARuchalaMKrauzeTTreatment of severe thyroid function disorders and changes in body compositionEndokrynol Pol201667359366Search in Google Scholar
Jacobsen R, Lundsgaard C, Lorenzen J et al. Subnormal energy expenditure: a putative causal factor in the weight gain induced by treatment of hyperthyroidism. Diabetes Obes Metab 2006; 8: 220–227JacobsenRLundsgaardCLorenzenJSubnormal energy expenditure: a putative causal factor in the weight gain induced by treatment of hyperthyroidismDiabetes Obes Metab20068220227Search in Google Scholar
Roef GL, Rietzschel ER, Van Daele CM et al. Triiodothyronine and free thyroxine levels are differentially associated with metabolic profile and adiposity-related cardiovascular risk markers in euthyroid middle-aged subjects. Thyroid 2014; 24: 223–231RoefGLRietzschelERVan DaeleCMTriiodothyronine and free thyroxine levels are differentially associated with metabolic profile and adiposity-related cardiovascular risk markers in euthyroid middle-aged subjectsThyroid201424223231Search in Google Scholar
Teixeira P, Dos Santos PB, Pazos-Moura CC. The role of thyroid hormone in metabolism and metabolic syndrome. Ther Adv Endocrinol Metab 2020; 11: 2042018820917869TeixeiraPDos SantosPBPazos-MouraCC.The role of thyroid hormone in metabolism and metabolic syndromeTher Adv Endocrinol Metab202011204201882091786Search in Google Scholar
Bjergved L, Jorgensen T, Perrild H et al. Thyroid function and body weight: a community-based longitudinal study. PLoS One 2014; 9: e93515BjergvedLJorgensenTPerrildHThyroid function and body weight: a community-based longitudinal studyPLoS One20149e93515Search in Google Scholar
Soriguer F, Valdes S, Morcillo S et al. Thyroid hormone levels predict the change in body weight: a prospective study. Eur J Clin Invest 2011; 41: 1202–1209SoriguerFValdesSMorcilloSThyroid hormone levels predict the change in body weight: a prospective studyEur J Clin Invest20114112021209Search in Google Scholar
Olszanecka-Glinianowicz M, Chudek J, Szromek A et al. Changes of systemic microinflammation after weight loss and regain - a five-year follow up study. Endokrynol Pol 2012; 63: 432–438Olszanecka-GlinianowiczMChudekJSzromekAChanges of systemic microinflammation after weight loss and regain - a five-year follow up studyEndokrynol Pol201263432438Search in Google Scholar
Khan WF, Singla V, Aggarwal S et al. Outcome of bariatric surgery on hypothyroidism: experience from a tertiary care center in India. Surg Obes Relat Dis 2020; 16: 1297–1301KhanWFSinglaVAggarwalSOutcome of bariatric surgery on hypothyroidism: experience from a tertiary care center in IndiaSurg Obes Relat Dis20201612971301Search in Google Scholar
Ostrowska L, Gier D, Zysk B. The influence of reducing diets on changes in thyroid parameters in women suffering from obesity and Hashimoto's Disease. Nutrients 2021; 13:OstrowskaLGierDZyskB.The influence of reducing diets on changes in thyroid parameters in women suffering from obesity and Hashimoto's DiseaseNutrients202113Search in Google Scholar
Fruhbeck G, Busetto L, Dicker D et al. The ABCD of Obesity: An EASO Position Statement on a Diagnostic Term with Clinical and Scientific Implications. Obes Facts 2019; 12: 131–136FruhbeckGBusettoLDickerDThe ABCD of Obesity: An EASO Position Statement on a Diagnostic Term with Clinical and Scientific ImplicationsObes Facts201912131136Search in Google Scholar
Duntas LH, Biondi B. The interconnections between obesity, thyroid function, and autoimmunity: the multifold role of leptin. Thyroid 2013; 23: 646–653DuntasLHBiondiB.The interconnections between obesity, thyroid function, and autoimmunity: the multifold role of leptinThyroid201323646653Search in Google Scholar
Farghaly HS, Metwalley KA, Ahmed FA et al. Visfatin level in children and adolescents with autoimmune thyroiditis. Ther Adv Endocrinol Metab 2017; 8: 119–125FarghalyHSMetwalleyKAAhmedFAVisfatin level in children and adolescents with autoimmune thyroiditisTher Adv Endocrinol Metab20178119125Search in Google Scholar
Sawicka-Gutaj N, Zybek-Kocik A, Klimowicz A et al. Circulating visfatin in hypothyroidism is associated with free thyroid hormones and antithyroperoxidase antibodies. Int J Endocrinol 2016; 2016: 7402469Sawicka-GutajNZybek-KocikAKlimowiczACirculating visfatin in hypothyroidism is associated with free thyroid hormones and antithyroperoxidase antibodiesInt J Endocrinol201620167402469Search in Google Scholar
Belligoli A, Compagnin C, Sanna M et al. Characterization of subcutaneous and omental adipose tissue in patients with obesity and with different degrees of glucose impairment. Sci Rep 2019; 9: 11333BelligoliACompagninCSannaMCharacterization of subcutaneous and omental adipose tissue in patients with obesity and with different degrees of glucose impairmentSci Rep2019911333Search in Google Scholar