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<article xmlns:mml="http://www.w3.org/1998/Math/MathML" xmlns:xlink="http://www.w3.org/1999/xlink" xmlns:xsi="http://www.w3.org/2001/XMLSchema-instance" xmlns:ali="http://www.niso.org/schemas/ali/1.0/" article-type="review-article" dtd-version="1.2" xml:lang="en"><front><journal-meta><journal-id journal-id-type="publisher-id">Kazan medical journal</journal-id><journal-title-group><journal-title xml:lang="en">Kazan medical journal</journal-title><trans-title-group xml:lang="ru"><trans-title>Казанский медицинский журнал</trans-title></trans-title-group></journal-title-group><issn publication-format="print">0368-4814</issn><issn publication-format="electronic">2587-9359</issn><publisher><publisher-name xml:lang="en">Eco-Vector</publisher-name></publisher></journal-meta><article-meta><article-id pub-id-type="publisher-id">11539</article-id><article-id pub-id-type="doi">10.17816/KMJ2019-277</article-id><article-categories><subj-group subj-group-type="toc-heading" xml:lang="en"><subject>Reviews</subject></subj-group><subj-group subj-group-type="toc-heading" xml:lang="ru"><subject>Обзоры</subject></subj-group><subj-group subj-group-type="article-type"><subject>Review Article</subject></subj-group></article-categories><title-group><article-title xml:lang="en">Adrenal incidentaloma: management of patients with functionally autonomous cortisol synthesis</article-title><trans-title-group xml:lang="ru"><trans-title>Инциденталома надпочечников: ведение пациентов с функционально автономным синтезом кортизола</trans-title></trans-title-group></title-group><contrib-group><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Chzhen</surname><given-names>T R</given-names></name><name xml:lang="ru"><surname>Чжен</surname><given-names>Татьяна Романовна</given-names></name></name-alternatives><email>doctortr@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Kiseleva</surname><given-names>T P</given-names></name><name xml:lang="ru"><surname>Киселёва</surname><given-names>Татьяна Петровна</given-names></name></name-alternatives><email>doctortr@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib><contrib contrib-type="author"><name-alternatives><name xml:lang="en"><surname>Torosyan</surname><given-names>M R</given-names></name><name xml:lang="ru"><surname>Торосян</surname><given-names>Маргарита Рафаеловна</given-names></name></name-alternatives><email>doctortr@mail.ru</email><xref ref-type="aff" rid="aff1"/></contrib></contrib-group><aff-alternatives id="aff1"><aff><institution xml:lang="en">Ural State Medical University</institution></aff><aff><institution xml:lang="ru">Уральский государственный медицинский университет</institution></aff></aff-alternatives><pub-date date-type="pub" iso-8601-date="2019-03-29" publication-format="electronic"><day>29</day><month>03</month><year>2019</year></pub-date><volume>100</volume><issue>2</issue><issue-title xml:lang="en">VOL 100, NO2 (2019)</issue-title><issue-title xml:lang="ru">ТОМ 100, №2 (2019)</issue-title><fpage>277</fpage><lpage>287</lpage><history><date date-type="received" iso-8601-date="2019-03-29"><day>29</day><month>03</month><year>2019</year></date></history><permissions><copyright-statement xml:lang="en">Copyright ©; 2019, Chzhen T.R., Kiseleva T.P., Torosyan M.R.</copyright-statement><copyright-statement xml:lang="ru">Copyright ©; 2019, Чжен Т.Р., Киселёва Т.П., Торосян М.Р.</copyright-statement><copyright-year>2019</copyright-year><copyright-holder xml:lang="en">Chzhen T.R., Kiseleva T.P., Torosyan M.R.</copyright-holder><copyright-holder xml:lang="ru">Чжен Т.Р., Киселёва Т.П., Торосян М.Р.</copyright-holder><ali:free_to_read xmlns:ali="http://www.niso.org/schemas/ali/1.0/"/><license><ali:license_ref xmlns:ali="http://www.niso.org/schemas/ali/1.0/">http://creativecommons.org/licenses/by-nc-sa/4.0</ali:license_ref></license></permissions><self-uri xlink:href="https://kazanmedjournal.ru/kazanmedj/article/view/11539">https://kazanmedjournal.ru/kazanmedj/article/view/11539</self-uri><abstract xml:lang="en"><p>Over recent decades due to improved visualization (ultrasound, computer tomography and magnetic resonance imaging) prevalence of adrenal incidentaloma has increased. The term «adrenal incidentaloma» is generic and includes a group of tumors of various morphology and over 1 cm in diameter accidentally discovered during radiologic investigation. The found tumor can be hormonally inactive or actively releasing different hormones, malignant or benign, and originating from different adrenal zones or having non-specific organ origin. Based on the frequency of revealing and clinical significance the most noteworthy is functionally autonomous cortisol synthesis. It means changes of hypothalamic pituitary adrenal axis without classic clinically prominent signs of cortisol excess such as proximal myopathy, stretch marks, body fat redistribution and other metabolic changes related to cortisol. Currently a large number of recommendations on the management and tactics of treatment of adrenal incidentaloma can be found in the literature. Based on the analysis of these guidelines the conclusions were made about the diagnostic errors and incorrect approaches to the choice of treatment of such patients. Recently a lot of studies have been directed to the early detection of carbohydrate and lipid metabolism disorders, relation with obesity and type 2 diabetes mellitus, arterial hypertension and osteoporosis for preserved quality of life of such patients. Influence of hypercorticism is considered to worsen the course of these conditions but at the moment no effect of adrenalectomy on mortality and life duration was confirmed.</p></abstract><trans-abstract xml:lang="ru"><p>В последние десятилетия в связи с усовершенствованием методов визуализации (ультразвуковое исследование, компьютерная и магнитно-резонансная томография) увеличилась распространённость инциденталом надпочечника. Термин «инциденталома надпочечника» является собирательным, включающим разнообразную по морфологии группу опухолей более 1 см в диаметре, случайно выявленных при радиологическом исследовании. Обнаруженное образование может оказаться как гормонально неактивным, так и активно синтезирующим различные гормоны, как злокачественным, так и доброкачественным, а также исходить из различных зон надпочечника или иметь неспецифичную органную принадлежность. По частоте выявления и клинической значимости наибольшего внимания клиницистов заслуживает функционально автономный синтез кортизола. Он подразумевает изменения оси гипоталамус-гипофиз-надпочечники без классических клинически явных признаков избытка кортизола, таких как проксимальная миопатия, полосы растяжения, перераспределение жировой ткани и другие метаболические изменения, связанные с кортизолом. В настоящее время в литературе существует большое количество рекомендаций по ведению и тактике лечения инциденталом надпочечника. На основании анализа этих рекомендаций были сделаны выводы в отношении диагностических ошибок и неправильных подходов к выбору лечения таких пациентов. В последнее время много исследований направлено на раннее выявление нарушений углеводного и липидного обмена, связи с ожирением и сахарным диабетом 2-го типа, артериальной гипертензии и остеопороза для сохранения качества жизни таких пациентов. Считают, что влияние гиперкортицизма усугубляет течение этих состояний, однако на данный момент не доказано влияние адреналэктомии на смертность и продолжительность жизни этих пациентов.</p></trans-abstract><kwd-group xml:lang="en"><kwd>adrenal incidentaloma</kwd><kwd>functionally autonomous cortisol secretion</kwd><kwd>Cushing’s syndrome</kwd><kwd>hypercortisolism</kwd></kwd-group><kwd-group xml:lang="ru"><kwd>инциденталома надпочечников</kwd><kwd>функционально автономный синтез кортизола</kwd><kwd>синдром Кушинга</kwd><kwd>гиперкортицизм</kwd></kwd-group><funding-group/></article-meta></front><body></body><back><ref-list><ref id="B1"><label>1.</label><citation-alternatives><mixed-citation xml:lang="en">Nieman L.K., Biller B.M., Findling J.W. et al. Treatment of Cushing's syndrome: An Endocrine Society Cli­nical Practice Guideline. J. Clin. Endocrinol. Metab. 2015; 100 (8): 2807–2831. DOI: 10.1210/jc.2015-1818.</mixed-citation><mixed-citation xml:lang="ru">Nieman L.K., Biller B.M., Findling J.W. et al. Treatment of Cushing's syndrome: An Endocrine Society Clinical Practice Guideline. J. Clin. Endocrinol. Metab. 2015; 100 (8): 2807-2831. DOI: 10.1210/jc.2015-1818.</mixed-citation></citation-alternatives></ref><ref id="B2"><label>2.</label><citation-alternatives><mixed-citation xml:lang="en">Beltsevich D.G., Melnichenko G.A., Kuznetsov N.S. et al. Russian Association of Endocrino­logists clinical practice guideline for adrenal incidentalomas differential diagnosis. Endokrinnaya khirurgiya. 2016; 10 (4): 31–42. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">Бельцевич Д.Г., Мельниченко Г.А., Кузнецов Н.С. и др. Клинические рекомендации Российской ассоциации эндокринологов по дифференциальной диагностике инциденталом надпочечников. Эндокрин. хир. 2016; 10 (4): 31-42. DOI: 10.14341/serg2016431-42.</mixed-citation></citation-alternatives></ref><ref id="B3"><label>3.</label><citation-alternatives><mixed-citation xml:lang="en">Kuznetsov N.S., Tikhonova O.V. Subclinical Cushing's syndrome due to unilateral or bilateral adrenal incidentalomas. Problems of diagnostic and indication to surgical treatment. Review of literature. Endokrinnaya khirurgiya. 2015; 9 (1): 22–34. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">Кузнецов Н.С., Тихонова О.В. Субклинический синдром Кушинга, обусловленный одно- и двусторонними образованиями надпочечников. Проблемы диагностики и показаний к хирургическому лечению. Обзор литературы. Эндокрин. хир. 2015; 9 (1): 22-34. DOI: 10.14341/serg2015122-34.</mixed-citation></citation-alternatives></ref><ref id="B4"><label>4.</label><citation-alternatives><mixed-citation xml:lang="en">Di Dalmazi G., Pasquali R., Beuschlein F. et al. Subclinical hypercortisolism: a state, a syndrome, or a disease? Eur. J. Endocrinol. 2015; 173 (4): 61–71. DOI: 10.1530/</mixed-citation><mixed-citation xml:lang="ru">Di Dalmazi G., Pasquali R., Beuschlein F. et al. Subclinical hypercortisolism: a state, a syndrome, or a disease? Eur. J. Endocrinol. 2015; 173 (4): 61-71. DOI: 10.1530/ EJE-15-0272.</mixed-citation></citation-alternatives></ref><ref id="B5"><label>5.</label><citation-alternatives><mixed-citation xml:lang="en">EJE-15-0272.</mixed-citation><mixed-citation xml:lang="ru">Berruti A., Baudin E., Gelderblom H. et al. Adrenal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2012; 23 (7): 131-138. DOI: 10.1093/annonc/mds231.</mixed-citation></citation-alternatives></ref><ref id="B6"><label>6.</label><citation-alternatives><mixed-citation xml:lang="en">Berruti A., Baudin E., Gelderblom H. et al. Adrenal cancer: ESMO Clinical Practice Guidelines for diagnosis, treatment and follow-up. Ann. Oncol. 2012; 23 (7): 131–138. DOI: 10.1093/annonc/mds231.</mixed-citation><mixed-citation xml:lang="ru">Fassnacht M., Arlt W., Bancos I. et al. Management of adrenal incidentalomas: European Society of Endocrinology Clinical Practice Guideline in collaboration with the European Network for the Study of Adrenal Tumors. Eur. J. Endocrinol. 2016; 175 (2): 1-34. DOI: 10.1530/eje-16-0467.</mixed-citation></citation-alternatives></ref><ref id="B7"><label>7.</label><citation-alternatives><mixed-citation xml:lang="en">Fassnacht M., Arlt W., Bancos I. et al. Management of adrenal incidentalomas: European Society of Endocrinology Clinical Practice Guideline in collaboration with the European Network for the Study of Adrenal Tumors. Eur. J. Endocrinol. 2016; 175 (2): 1–34. DOI: 10.1530/eje-16-0467.</mixed-citation><mixed-citation xml:lang="ru">Lacroix A., Feelders R.A., Stratakis C.E. et al. Cushing’s syndrome. Lancet. 2015; 386 (9996): 913-927. DOI: 10.1016/S0140-6736(14)61375-1.</mixed-citation></citation-alternatives></ref><ref id="B8"><label>8.</label><citation-alternatives><mixed-citation xml:lang="en">Lacroix A., Feelders R.A., Stratakis C.E. et al. Cu­shing’s syndrome. Lancet. 2015; 386 (9996): 913–927. DOI: 10.1016/S0140-6736(14)61375-1.</mixed-citation><mixed-citation xml:lang="ru">Lacroix A., Ndiaye N., Tremblay J. et al. Ectopic and abnormal hormone receptors in adrenal Cushing’s syndrome. Endocrine Rev. 2001; 22 (1): 75-110. DOI: 10.1210/edrv.22.1.0420.</mixed-citation></citation-alternatives></ref><ref id="B9"><label>9.</label><citation-alternatives><mixed-citation xml:lang="en">Lacroix A., Ndiaye N., Tremblay J. et al. Ectopic and abnormal hormone receptors in adrenal Cushing’s syndrome. Endocrine Rev. 2001; 22 (1): 75–110. DOI: 10.1210/edrv.22.1.0420.</mixed-citation><mixed-citation xml:lang="ru">Cao Y., He M., Gao Z. et al. Activating hotspot L205R mutation in PRKACA and adrenal Cushing’s syndrome. Science. 2014; 344 (6186): 913-917. DOI: 10.1126/science.1249480.</mixed-citation></citation-alternatives></ref><ref id="B10"><label>10.</label><citation-alternatives><mixed-citation xml:lang="en">Cao Y., He M., Gao Z. et al. Activating hotspot L205R mutation in PRKACA and adrenal Cushing’s syndrome. Science. 2014; 344 (6186): 913–917. DOI: 10.1126/science.1249480.</mixed-citation><mixed-citation xml:lang="ru">Goh G., Scholl U.I., Healy J.M. et al. Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors. Nature Genet. 2014; 46 (6): 613-617. DOI: 10.1038/ng.2956.</mixed-citation></citation-alternatives></ref><ref id="B11"><label>11.</label><citation-alternatives><mixed-citation xml:lang="en">Goh G., Scholl U.I., Healy J.M. et al. Recurrent activating mutation in PRKACA in cortisol-producing adrenal tumors. Nature Genet. 2014; 46 (6): 613–617. DOI: 10.1038/ng.2956.</mixed-citation><mixed-citation xml:lang="ru">Light K., Jenkins P.J., Weber A. et al. Are activating mutations of the adrenocorticotropin receptor involved in adrenal cortical neoplasia? Life Sci. 1995; 56 (18): 1523-1527. DOI: 10.1016/0024-3205(95)00114-L.</mixed-citation></citation-alternatives></ref><ref id="B12"><label>12.</label><citation-alternatives><mixed-citation xml:lang="en">Light K., Jenkins P.J., Weber A. et al. Are activa­ting mutations of the adrenocorticotropin receptor involved in adrenal cortical neoplasia? Life Sci. 1995; 56 (18): 1523–1527. DOI: 10.1016/0024-3205(95)00114-L.</mixed-citation><mixed-citation xml:lang="ru">Swords F.M., Noon L.A., King P.J., Clark A.J. Constitutive activation of the human ACTH receptor resulting from a synergistic interaction between two naturally occurring missense mutations in the MC2R gene. Mol. Cell. Endocrinol. 2004; 213 (2): 149-154. DOI: 10.1016/j.mce.2003.10.052.</mixed-citation></citation-alternatives></ref><ref id="B13"><label>13.</label><citation-alternatives><mixed-citation xml:lang="en">Swords F.M., Noon L.A., King P.J., Clark A.J. Constitutive activation of the human ACTH receptor resul­ting from a synergistic interaction between two naturally occurring missense mutations in the MC2R gene. Mol. Cell. Endocrinol. 2004; 213 (2): 149–154. DOI: 10.1016/j.mce.2003.10.052.</mixed-citation><mixed-citation xml:lang="ru">Alencar G.A., Lerario A.M., Nishi M.Y. et al. ARMC5 mutations are a frequent cause of primary macronodular adrenal hyperplasia. J. Clin. Endocrinol. Metabol. 2014; 99 (8): 1501-1509. DOI: 10.1210/jc.2013-4237.</mixed-citation></citation-alternatives></ref><ref id="B14"><label>14.</label><citation-alternatives><mixed-citation xml:lang="en">Alencar G.A., Lerario A.M., Nishi M.Y. et al. ARMC5 mutations are a frequent cause of primary macronodular adrenal hyperplasia. J. Clin. Endocrinol. Metabol. 2014; 99 (8): 1501–1509. DOI: 10.1210/jc.2013-4237.</mixed-citation><mixed-citation xml:lang="ru">Assie G., Libe R., Espiard S. et al. ARMC5 mutations in macronodular adrenal hyperplasia with Cushing’s syndrome. New Engl. J. Med. 2013; 369: 2105-2114. DOI: 10.1056/NEJMoa1304603.</mixed-citation></citation-alternatives></ref><ref id="B15"><label>15.</label><citation-alternatives><mixed-citation xml:lang="en">Assie G., Libe R., Espiard S. et al. ARMC5 mutations in macronodular adrenal hyperplasia with Cushing’s syndrome. New Engl. J. Med. 2013; 369: 2105–2114. DOI: 10.1056/NEJMoa1304603.</mixed-citation><mixed-citation xml:lang="ru">Elbelt U., Trovato A., Kloth M. et al. Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma. J. Clin. Endocrinol. Metabol. 2015; 100 (1): 119-128. DOI: 10.1210/jc.2014-2648.</mixed-citation></citation-alternatives></ref><ref id="B16"><label>16.</label><citation-alternatives><mixed-citation xml:lang="en">Elbelt U., Trovato A., Kloth M. et al. Molecular and clinical evidence for an ARMC5 tumor syndrome: concurrent inactivating germline and somatic mutations are associated with both primary macronodular adrenal hyperplasia and meningioma. J. Clin. Endocrinol. Metabol. 2015; 100 (1): 119–128. DOI: 10.1210/jc.2014-2648.</mixed-citation><mixed-citation xml:lang="ru">Schorr I., Ney R.L. Abnormal hormone responses of an adrenocortical cancer adenyl cyclase. J. Clin. Invest. 1971; 50 (6): 1295-1300. DOI: 10.1172/JCI106608.</mixed-citation></citation-alternatives></ref><ref id="B17"><label>17.</label><citation-alternatives><mixed-citation xml:lang="en">Schorr I., Ney R.L. Abnormal hormone responses of an adrenocortical cancer adenyl cyclase. J. Clin. Invest. 1971; 50 (6): 1295–1300. DOI: 10.1172/JCI106608.</mixed-citation><mixed-citation xml:lang="ru">Hamet P., Larochelle P., Franks D.J. et al. Cushing syndrome with food-dependent periodic hormonogenesis. Clin. Invest. Med. 1987; 10 (6): 530-533. PMID: 2831001.</mixed-citation></citation-alternatives></ref><ref id="B18"><label>18.</label><citation-alternatives><mixed-citation xml:lang="en">Hamet P., Larochelle P., Franks D.J. et al. Cushing syndrome with food-dependent periodic hormonogenesis. Clin. Invest. Med. 1987; 10 (6): 530–533. PMID: 2831001.</mixed-citation><mixed-citation xml:lang="ru">Lacroix A., Bolte E., Tremblay J. et al. Gastric inhibitory polypeptide dependent cortisol hypersecretion - a new cause of Cushing’s syndrome. New Engl. J. Med. 1992; 327: 974-980. DOI: 10.1056/NEJM199210013271402.</mixed-citation></citation-alternatives></ref><ref id="B19"><label>19.</label><citation-alternatives><mixed-citation xml:lang="en">Lacroix A., Bolte E., Tremblay J. et al. Gastric inhibitory polypeptide dependent cortisol hypersecretion — a new cause of Cushing’s syndrome. New Engl. J. Med. 1992; 327: 974–980. DOI: 10.1056/NEJM199210013271402.</mixed-citation><mixed-citation xml:lang="ru">Reznik Y., Allali-Zerah V., Chayvialle J.A. et al. Food-dependent Cushing’s syndrome mediated by aberrant adrenal sensitivity to gastric inhibitory polypeptide. New Engl. J. Med. 1992; 327 (14): 981-986. DOI: 10.1056/NEJM199210013271403.</mixed-citation></citation-alternatives></ref><ref id="B20"><label>20.</label><citation-alternatives><mixed-citation xml:lang="en">Reznik Y., Allali-Zerah V., Chayvialle J.A. et al. Food-dependent Cushing’s syndrome mediated by aberrant adrenal sensitivity to gastric inhibitory polypeptide. New Engl. J. Med. 1992; 327 (14): 981–986. DOI: 10.1056/NEJM199210013271403.</mixed-citation><mixed-citation xml:lang="ru">Lacroix A., Baldacchino V., Bourdeau I. et al. Cushing’s syndrome variants secondary to aberrant hormone receptors. Trends Endocrinol. Metabol. 2004; 15 (8): 375-382. DOI: 10.1016/S1043-2760(04)00188-2.</mixed-citation></citation-alternatives></ref><ref id="B21"><label>21.</label><citation-alternatives><mixed-citation xml:lang="en">Lacroix A., Baldacchino V., Bourdeau I. et al. Cu­shing’s syndrome variants secondary to aberrant hormone receptors. Trends Endocrinol. Metabol. 2004; 15 (8): ­375–382. DOI: 10.1016/S1043-2760(04)00188-2.</mixed-citation><mixed-citation xml:lang="ru">Lacroix A., Bourdeau I., Lampron A. et al. Aberrant G-protein coupled receptor expression in relation to adrenocortical overfunction. Clin. Endocrinol. 2010; 73 (1): 1-15. DOI: 10.1111/j.1365-2265.2009.03689.x.</mixed-citation></citation-alternatives></ref><ref id="B22"><label>22.</label><citation-alternatives><mixed-citation xml:lang="en">Lacroix A., Bourdeau I., Lampron A. et al. Aberrant G-protein coupled receptor expression in relation to adrenocortical overfunction. Clin. Endocrinol. 2010; 73 (1): 1–15. DOI: 10.1111/j.1365-2265.2009.03689.x.</mixed-citation><mixed-citation xml:lang="ru">Mermejo L.M., Mazzuco T.L., Grunenwald S. et al. ACTH-independent macronodular adrenal hyperplasia. Endocrinol. Metabol. 2011; 26 (1): 1-11. DOI: 10.3803/EnM.2011.26.1.1.</mixed-citation></citation-alternatives></ref><ref id="B23"><label>23.</label><citation-alternatives><mixed-citation xml:lang="en">Mermejo L.M., Mazzuco T.L., Grunenwald S. et al. ACTH-independent macronodular adrenal hyperplasia. Endocrinol. Metabol. 2011; 26 (1): 1–11. DOI: 10.3803/EnM.2011.26.1.1.</mixed-citation><mixed-citation xml:lang="ru">Mircescu H., Jilwan J., N’Diaye N. et al. Are ectopic or abnormal membrane hormone receptors frequently present in adrenal Cushing’s syndrome? J. Clin. Endocrinol. Metabol. 2000; 85 (10): 3531-3536. DOI: 10.1210/jcem.85.10.6865.</mixed-citation></citation-alternatives></ref><ref id="B24"><label>24.</label><citation-alternatives><mixed-citation xml:lang="en">Mircescu H., Jilwan J., N’Diaye N. et al. Are ectopic or abnormal membrane hormone receptors frequently present in adrenal Cushing’s syndrome? J. Clin. Endocrinol. Metabol. 2000; 85 (10): 3531–3536. DOI: 10.1210/jcem.85.10.6865.</mixed-citation><mixed-citation xml:lang="ru">Reznik Y., Lefebvre H., Rohmer V. et al. Aberrant adrenal sensitivity to multiple ligands in unilateral incidentaloma with subclinical autonomous cortisol hypersecretion: a prospective clinical study. Clin. Endocrinol. 2004; 61 (3): 311-319. DOI: 10.1111/j.1365-2265.2004.02048.x.</mixed-citation></citation-alternatives></ref><ref id="B25"><label>25.</label><citation-alternatives><mixed-citation xml:lang="en">Reznik Y., Lefebvre H., Rohmer V. et al. Aberrant adrenal sensitivity to multiple ligands in unilateral incidentaloma with subclinical autonomous cortisol hypersecretion: a prospective clinical study. Clin. Endocrinol. 2004; 61 (3): 311–319. DOI: 10.1111/j.1365-2265.2004.02048.x.</mixed-citation><mixed-citation xml:lang="ru">Libe R., Coste J., Guignat L. et al. Aberrant cortisol regulations in bilateral macronodular adrenal hyperplasia: a frequent finding in a prospective study of 32 patients with overt or subclinical Cushing’s syndrome. Eur. J. Endocrinol. 2010; 163 (1): 129-138. DOI: 10.1530/EJE-10-0195.</mixed-citation></citation-alternatives></ref><ref id="B26"><label>26.</label><citation-alternatives><mixed-citation xml:lang="en">Libe R., Coste J., Guignat L. et al. Aberrant cortisol regulations in bilateral macronodular adrenal hyperplasia: a frequent finding in a prospective study of 32 patients with overt or subclinical Cushing’s syndrome. Eur. J. Endocrinol. 2010; 163 (1): 129–138. DOI: 10.1530/EJE-10-0195.</mixed-citation><mixed-citation xml:lang="ru">Hofland J., Hofland L.J., van Koetsveld P.M. et al. ACTH-independent macronodularadrenocortical hyperplasia reveals prevalent aberrant in vivo and in vitro responses to hormonal stimuli and coupling of argininevasopressin type 1a receptor to 11b-hydroxylase. Orphanet J. Rare Dis. 2013; 8: 142. DOI: 10.1186/1750-1172-8-142.</mixed-citation></citation-alternatives></ref><ref id="B27"><label>27.</label><citation-alternatives><mixed-citation xml:lang="en">Hofland J., Hofland L.J., van Koetsveld P.M. et al. ACTH-independent macronodularadrenocortical hyperplasia reveals prevalent aberrant in vivo and in vitro respon­ses to hormonal stimuli and coupling of argininevasopressin type 1a receptor to 11b-hydroxylase. Orphanet J. Rare Dis. 2013; 8: 142. DOI: 10.1186/1750-1172-8-142.</mixed-citation><mixed-citation xml:lang="ru">Hsiao H.P., Kirschner L.S., Bourdeau I. et al. Clinical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropinin dependent macronodular adrenal hyperplasia compared with other adrenocortical tumors. J. Clin. Endocrinol. Metab. 2009; 94 (8): 2930-2937. DOI: 10.1210/jc.2009-0516.</mixed-citation></citation-alternatives></ref><ref id="B28"><label>28.</label><citation-alternatives><mixed-citation xml:lang="en">Hsiao H.P., Kirschner L.S., Bourdeau I. et al. Cli­nical and genetic heterogeneity, overlap with other tumor syndromes, and atypical glucocorticoid hormone secretion in adrenocorticotropinin dependent macronodular adrenal hyperplasia compared with other adrenocortical tumors. J. Clin. Endocrinol. Metab. 2009; 94 (8): 2930–2937. DOI: 10.1210/jc.2009-0516.</mixed-citation><mixed-citation xml:lang="ru">Joubert M., Louiset E., Rego J.L. et al. Aberrant adrenal sensitivity to vasopressin in adrenal tumours associated with subclinical or overt autonomous hypercortisolism: is this explained by an overexpression of vasopressin receptors? Clin. Endocrinol. 2008; 68 (5): 692-699. DOI: 10.1111/j.1365-2265.2007.03106.x.</mixed-citation></citation-alternatives></ref><ref id="B29"><label>29.</label><citation-alternatives><mixed-citation xml:lang="en">Joubert M., Louiset E., Rego J.L. et al. Aberrant adrenal sensitivity to vasopressin in adrenal tumours ­associated with subclinical or overt autonomous hypercortisolism: is this explained by an overexpression of vasopressin receptors? Clin. Endocrinol. 2008; 68 (5): 692–699. DOI: 10.1111/j.1365-2265.2007.03106.x.</mixed-citation><mixed-citation xml:lang="ru">Albiger N.M., Occhi G., Mariniello B. et al. Food-dependent Cushing’s syndrome: from molecular characterization to therapeutical results. Eur. J. Endocrinol. 2007; 157 (6): 771-778. DOI: 10.1530/EJE-07-0253.</mixed-citation></citation-alternatives></ref><ref id="B30"><label>30.</label><citation-alternatives><mixed-citation xml:lang="en">Albiger N.M., Occhi G., Mariniello B. et al. Food-dependent Cushing’s syndrome: from molecular cha­racterization to therapeutical results. Eur. J. Endocrinol. 2007; 157 (6): 771–778. DOI: 10.1530/EJE-07-0253.</mixed-citation><mixed-citation xml:lang="ru">Bertherat J., Contesse V., Louiset E. et al. In vivo and in vitro screening for illegitimate receptors in adrenocorticotropin-independent macronodular adrenal hyperplasia causing Cushing’s syndrome: identification of two cases of gonadotropin/gastric inhibitory polypeptide-dependent hypercortisolism. J. Clin. Endocrinol. Metab. 2005; 90 (3): 1302-1310. DOI: 10.1210/jc.2004-1256.</mixed-citation></citation-alternatives></ref><ref id="B31"><label>31.</label><citation-alternatives><mixed-citation xml:lang="en">Bertherat J., Contesse V., Louiset E. et al. In vivo and in vitro screening for illegitimate receptors in adrenocorticotropin-independent macronodular adrenal hyperplasia causing Cushing’s syndrome: identification of two cases of gonadotropin/gastric inhibitory polypeptide-dependent hypercortisolism. J. Clin. Endocrinol. Metab. 2005; 90 (3): 1302–1310. DOI: 10.1210/jc.2004-1256.</mixed-citation><mixed-citation xml:lang="ru">Lampron A., Bourdeau I., Hamet P. et al. Whole genome expression profiling of glucose-dependent insulinotropic peptide (GIP) - and adrenocorticotropin-dependent adrenal hyperplasias reveals novel targets for the study of GIP-dependent Cushing’s syndrome. J. Clin. Endocrinol. Metab. 2006; 91 (9): 3611-3618. DOI: 10.1210/jc.2006-0221.</mixed-citation></citation-alternatives></ref><ref id="B32"><label>32.</label><citation-alternatives><mixed-citation xml:lang="en">Lampron A., Bourdeau I., Hamet P. et al. Whole genome expression profiling of glucose-dependent insulinotropic peptide (GIP) — and adrenocorticotropin-dependent adrenal hyperplasias reveals novel targets for the study of GIP-dependent Cushing’s syndrome. J. Clin. Endocrinol. Metab. 2006; 91 (9): 3611–3618. DOI: 10.1210/jc.2006-0221.</mixed-citation><mixed-citation xml:lang="ru">N’Diaye N., Hamet P., Tremblay J. et al. Asynchronous development of bilateral nodular adrenal hyperplasia in gastric inhibitory polypeptide-dependent Cushing’s syndrome. J. Clin. Endocrinol. Metab. 1999; 84 (8): 2616-2622. DOI: 10.1210/jcem.84.8.5930.</mixed-citation></citation-alternatives></ref><ref id="B33"><label>33.</label><citation-alternatives><mixed-citation xml:lang="en">N’Diaye N., Hamet P., Tremblay J. et al. Asynchronous development of bilateral nodular adrenal hyperplasia in gastric inhibitory polypeptide-dependent Cu­shing’s syndrome. J. Clin. Endocrinol. Metab. 1999; 84 (8): 2616–2622. DOI: 10.1210/jcem.84.8.5930.</mixed-citation><mixed-citation xml:lang="ru">Chabre O., Liakos P., Vivier J. et al. Gastric inhibitory polypeptide (GIP) stimulates cortisol secretion, cAMP production and DNA synthesis in an adrenal adenoma responsible for food-dependent Cushing’s syndrome. Endocrine Res. 1998; 24 (3-4): 851-856. DOI: 10.3109/07435809809032696.</mixed-citation></citation-alternatives></ref><ref id="B34"><label>34.</label><citation-alternatives><mixed-citation xml:lang="en">Chabre O., Liakos P., Vivier J. et al. Gastric inhibitory polypeptide (GIP) stimulates cortisol secretion, cAMP production and DNA synthesis in an adrenal ade­noma responsible for food-dependent Cushing’s syndrome. Endocrine Res. 1998; 24 (3–4): 851–856. DOI: 10.3109/07435809809032696.</mixed-citation><mixed-citation xml:lang="ru">Swords F.M., Aylwin S., Perry L. et al. The aberrant expression of the gastric inhibitory polypeptide (GIP) receptor in adrenal hyperplasia: does chronic adrenocorticotropin exposure stimulate up-regulation of GIP receptors in Cushing’s disease? J. Clin. Endocrinol. Metab. 2005; 90 (5): 3009-3016. DOI: 10.1210/jc.2004-0946.</mixed-citation></citation-alternatives></ref><ref id="B35"><label>35.</label><citation-alternatives><mixed-citation xml:lang="en">Swords F.M., Aylwin S., Perry L. et al. The aberrant expression of the gastric inhibitory polypeptide (GIP) receptor in adrenal hyperplasia: does chronic adrenocorticotropin exposure stimulate up-regulation of GIP receptors in Cushing’s disease? J. Clin. Endocrinol. Metab. 2005; 90 (5): 3009–3016. DOI: 10.1210/jc.2004-0946.</mixed-citation><mixed-citation xml:lang="ru">Antonini S.R., Baldacchino V., Tremblay J. et al. Expression of ACTH receptor pathway genes in glucose-dependent insulinotrophic peptide (GIP)-dependent Cushing’s syndrome. Clin. Endocrinol. 2006; 64 (1): 29-36. DOI: 10.1111/j.1365-2265.2005.02411.x.</mixed-citation></citation-alternatives></ref><ref id="B36"><label>36.</label><citation-alternatives><mixed-citation xml:lang="en">Antonini S.R., Baldacchino V., Tremblay J. et al. Expression of ACTH receptor pathway genes in glucose-dependent insulinotrophic peptide (GIP)-dependent Cushing’s syndrome. Clin. Endocrinol. 2006; 64 (1): 29–36. DOI: 10.1111/j.1365-2265.2005.02411.x.</mixed-citation><mixed-citation xml:lang="ru">Mazzuco T.L., Chabre O., Sturm N. et al. Ectopic expression of the gastric inhibitory polypeptide receptor gene is a sufficient genetic event to induce benign adrenocortical tumor in a xenotransplantation model. Endocrinology. 2006; 147 (2): 782-790. DOI: 10.1210/en.2005-0921.</mixed-citation></citation-alternatives></ref><ref id="B37"><label>37.</label><citation-alternatives><mixed-citation xml:lang="en">Mazzuco T.L., Chabre O., Sturm N. et al. Ectopic expression of the gastric inhibitory polypeptide receptor gene is a sufficient genetic event to induce benign adrenocortical tumor in a xenotransplantation model. Endocrino­logy. 2006; 147 (2): 782–790. DOI: 10.1210/en.2005-0921.</mixed-citation><mixed-citation xml:lang="ru">Chui M.H., Ozbey N.C., Ezzat S. et al. Case report: adrenal LH/hCG receptor overexpression and gene amplification causing pregnancy-induced Cushing’s syndrome. Endocrin. Pathol. 2009; 20 (4): 256-261. DOI: 10.1007/s12022-009-9090-2.</mixed-citation></citation-alternatives></ref><ref id="B38"><label>38.</label><citation-alternatives><mixed-citation xml:lang="en">Chui M.H., Ozbey N.C., Ezzat S. et al. Case report: adrenal LH/hCG receptor overexpression and gene amplification causing pregnancy-induced Cushing’s syndrome. Endocrin. Pathol. 2009; 20 (4): 256–261. DOI: 10.1007/s12022-009-9090-2.</mixed-citation><mixed-citation xml:lang="ru">Blake M.A., Cronin C.G., Boland G.W. Adrenal imaging. AJR Am. J. Roentgenol. 2010; 194 (6): 1450-1460. DOI: 10.2214/AJR.10.4547.</mixed-citation></citation-alternatives></ref><ref id="B39"><label>39.</label><citation-alternatives><mixed-citation xml:lang="en">Blake M.A., Cronin C.G., Boland G.W. Adrenal ima­ging. AJR Am. J. Roentgenol. 2010; 194 (6): 1450–1460. DOI: 10.2214/AJR.10.4547.</mixed-citation><mixed-citation xml:lang="ru">Olsen H., Nordenström E., Bergenfelz A. et al. Subclinical hypercortisolism and CT appearance in adrenal incidentalomas: a multicenter study from Southern Sweden. Endocrine. 2012; 42 (1): 164-173. DOI: 10.1007/s12020-012-9622-2.</mixed-citation></citation-alternatives></ref><ref id="B40"><label>40.</label><citation-alternatives><mixed-citation xml:lang="en">Olsen H., Nordenström E., Bergenfelz A. et al. Subclinical hypercortisolism and CT appearance in adrenal incidentalomas: a multicenter study from Southern Sweden. Endocrine. 2012; 42 (1): 164–173. DOI: 10.1007/s12020-012-9622-2.</mixed-citation><mixed-citation xml:lang="ru">Kohara K. Sarcopenic obesity in aging population: current status and future directions for research. Endocrine. 2014; 45 (1): 15-25. DOI: 10.1007/s12020-013-9992-0.</mixed-citation></citation-alternatives></ref><ref id="B41"><label>41.</label><citation-alternatives><mixed-citation xml:lang="en">Kohara K. Sarcopenic obesity in aging population: current status and future directions for research. Endocrine. 2014; 45 (1): 15–25. DOI: 10.1007/s12020-013-9992-0.</mixed-citation><mixed-citation xml:lang="ru">Schneider H.J., Dimopoulou C., Stalla G.K. et al. Discriminatory value of signs and symptoms in Cushing’s syndrome revisited: what has changed in 30 years? Clin. Endocrinol. 2013; 78 (1): 153-154. DOI: 10.1111/j.1365-2265.2012.04488.x.</mixed-citation></citation-alternatives></ref><ref id="B42"><label>42.</label><citation-alternatives><mixed-citation xml:lang="en">Schneider H.J., Dimopoulou C., Stalla G.K. et al. Discriminatory value of signs and symptoms in Cu­shing’s syndrome revisited: what has changed in 30 years? Clin. ­Endocrinol. 2013; 78 (1): 153–154. DOI: 10.1111/j.1365-2265.2012.04488.x.</mixed-citation><mixed-citation xml:lang="ru">NIH state-of-the-science statement on management of the clinically inapparent adrenal mass («incidentaloma»). NIH Consensus and State-of-the-Science Statements. 2002; 19 (2): 1-25. PMID: 14768652.</mixed-citation></citation-alternatives></ref><ref id="B43"><label>43.</label><citation-alternatives><mixed-citation xml:lang="en">NIH state-of-the-science statement on management of the clinically inapparent adrenal mass («incidentaloma»). NIH Consensus and State-of-the-Science Statements. 2002; 19 (2): 1–25. PMID: 14768652.</mixed-citation><mixed-citation xml:lang="ru">Nieman L.K., Biller B.M., Findling J.W. et al. The diagnosis of Cushing’s syndrome: an Endocrine Society Clinical Practice Guideline. J. Clin. Endocrinol. Metab. 2008; 93 (5): 1526-1540. DOI: 10.1210/jc.2008-0125.</mixed-citation></citation-alternatives></ref><ref id="B44"><label>44.</label><citation-alternatives><mixed-citation xml:lang="en">Nieman L.K., Biller B.M., Findling J.W. et al. The diagnosis of Cushing’s syndrome: an Endocrine Society Clinical Practice Guideline. J. Clin. Endocrinol. Metab. 2008; 93 (5): 1526–1540. DOI: 10.1210/jc.2008-0125.</mixed-citation><mixed-citation xml:lang="ru">Tabarin A., Bardet S., Bertherat J. et al. French Society of Endocrinology Consensus. Exploration and management of adrenal incidentalomas. French Society of Endocrinology Consensus. Annales d’Endocrinologie. 2008; 69 (6): 487-500. DOI: 10.1016/j.ando.2008.09.003.</mixed-citation></citation-alternatives></ref><ref id="B45"><label>45.</label><citation-alternatives><mixed-citation xml:lang="en">Tabarin A., Bardet S., Bertherat J. et al. French Society of Endocrinology Consensus. Exploration and ma­nagement of adrenal incidentalomas. French Society of Endocrinology Consensus. Annales d’Endocrinologie. 2008; 69 (6): 487–500. DOI: 10.1016/j.ando.2008.09.003.</mixed-citation><mixed-citation xml:lang="ru">Zeiger M.A., Thompson G.B., Duh Q.Y. et al. American Association of Clinical Endocrinologists; American Association of Endocrine Surgeons. The American Association of Clinical Endocrinologists and American Association of Endocrine Surgeons medical guidelines for the management of adrenal incidentalomas. Endocrin. Pract. 2009; 15 (1): 1-20. DOI: 10.4158/EP.15.S1.1.</mixed-citation></citation-alternatives></ref><ref id="B46"><label>46.</label><citation-alternatives><mixed-citation xml:lang="en">Zeiger M.A., Thompson G.B., Duh Q.Y. et al. Ame­rican Association of Clinical Endocrinologists; American Association of Endocrine Surgeons. The American Association of Clinical Endocrinologists and American Association of Endocrine Surgeons medical guidelines for the ma­nagement of adrenal incidentalomas. Endocrin. Pract. 2009; 15 (1): 1–20. DOI: 10.4158/EP.15.S1.1.</mixed-citation><mixed-citation xml:lang="ru">Terzolo M., Stigliano A., Chiodini I. et al. Italian Association of Clinical Endocrinologists. AME position statement on adrenal incidentaloma. Eur. J. Endocrinol. 2011; 164 (6): 851-870. DOI: 10.1530/EJE-10-1147.</mixed-citation></citation-alternatives></ref><ref id="B47"><label>47.</label><citation-alternatives><mixed-citation xml:lang="en">Terzolo M., Stigliano A., Chiodini I. et al. Italian Association of Clinical Endocrinologists. AME position statement on adrenal incidentaloma. Eur. J. Endocrinol. 2011; 164 (6): 851–870. DOI: 10.1530/EJE-10-1147.</mixed-citation><mixed-citation xml:lang="ru">Shen J., Sun M., Zhou B., Yan J. Nonconformity in the clinical practice guidelines for subclinical Cushing’s syndrome: which guidelines are trustworthy? Eur. J. Endocrinol. 2014; 171 (4): 421-431. DOI: 10.1530/EJE-14-0345.</mixed-citation></citation-alternatives></ref><ref id="B48"><label>48.</label><citation-alternatives><mixed-citation xml:lang="en">Shen J., Sun M., Zhou B., Yan J. Nonconformity in the clinical practice guidelines for subclinical Cushing’s syndrome: which guidelines are trustworthy? Eur. J. Endocrinol. 2014; 171 (4): 421–431. DOI: 10.1530/EJE-14-0345.</mixed-citation><mixed-citation xml:lang="ru">Chiodini I. Clinical review: diagnosis and treatment of subclinical hypercortisolism. J. Clin. Endocrinol. Metab. 2011; 96 (5): 1223-1236. DOI: 10.1210/jc.2010-2722.</mixed-citation></citation-alternatives></ref><ref id="B49"><label>49.</label><citation-alternatives><mixed-citation xml:lang="en">Chiodini I. Clinical review: diagnosis and treatment of subclinical hypercortisolism. J. Clin. Endocrinol. Metab. 2011; 96 (5): 1223–1236. DOI: 10.1210/jc.2010-2722.</mixed-citation><mixed-citation xml:lang="ru">Кузнецов Н.С., Бельцевич Д.Г., Ванушко В.Э. и др. Дифференциальная диагностика инциденталом надпочечников. Эндокрин. хир. 2011; (1): 5-16. DOI: 10.14341/2306-3513-2011-1-5-16.</mixed-citation></citation-alternatives></ref><ref id="B50"><label>50.</label><citation-alternatives><mixed-citation xml:lang="en">Kuznetsov N.S., Beltsevich D.G., Vanushko V.E. et al. Differential diagnosis of adrenal incidentalomas. Endokrinnaya khirurgiya. 2011; (1): 5–16. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">Молашенко Н.В., Платонова Н.М., Бельцевич Д.Г и др. Дифференциальная диагностика инциденталом надпочечников. Ожирение и метаболизм. 2016; 13 (4): 39-44. DOI: 10.14341/OMET2016439-44.</mixed-citation></citation-alternatives></ref><ref id="B51"><label>51.</label><citation-alternatives><mixed-citation xml:lang="en">Molashenko N.V., Platonova N.M., Beltsevich D.G. et al. Diagnosis and differential diagnosis of adrenal incidentalomas. Ozhirenie i metabolizm. 2016; 13 (4): 39–44. (In Russ.)</mixed-citation><mixed-citation xml:lang="ru">De Leo M., Pivonello R., Auriemma R.S. et al. Cardiovascular disease in Cushing’s syndrome: heart versus vasculature. Neuroendocrinology. 2010; 92 (1): 50-54. DOI: 10.1159/000318566.</mixed-citation></citation-alternatives></ref><ref id="B52"><label>52.</label><citation-alternatives><mixed-citation xml:lang="en">De Leo M., Pivonello R., Auriemma R.S. et al. Cardiovascular disease in Cushing’s syndrome: heart versus vasculature. Neuroendocrinology. 2010; 92 (1): 50–54. DOI: 10.1159/000318566.</mixed-citation><mixed-citation xml:lang="ru">Anagnostis P., Athyros V.G., Tziomalos K. et al. Clinical review: the pathogenetic role of cortisol in the metabolic syndrome: a hypothesis. J. Clin. Endocrinol. Metabol. 2009; 94 (8): 2692-2701. DOI: 10.1210/jc.2009-0370.</mixed-citation></citation-alternatives></ref><ref id="B53"><label>53.</label><citation-alternatives><mixed-citation xml:lang="en">Anagnostis P., Athyros V.G., Tziomalos K. et al. Clinical review: the pathogenetic role of cortisol in the me­tabolic syndrome: a hypothesis. J. Clin. Endocrinol. Metabol. 2009; 94 (8): 2692–2701. DOI: 10.1210/jc.2009-0370.</mixed-citation><mixed-citation xml:lang="ru">Iacobone M., Citton M., Scarpa M. et al. Systematic review of surgical treatment of subclinical Cushing’s syndrome. Brit. J. Surg. 2015; 102 (4): 318-330. DOI: 10.1002/bjs.9742.</mixed-citation></citation-alternatives></ref><ref id="B54"><label>54.</label><citation-alternatives><mixed-citation xml:lang="en">Iacobone M., Citton M., Scarpa M. et al. Systematic review of surgical treatment of subclinical Cushing’s syndrome. Brit. J. Surg. 2015; 102 (4): 318–330. DOI: 10.1002/bjs.9742.</mixed-citation><mixed-citation xml:lang="ru">Ivović M., Marina L.V., Vujović S. et al. Nondiabetic patients with either subclinical Cushing’s or nonfunctional adrenal incidentalomas have lower insulin sensitivity than healthy controls: clinical implications. Metabolism. 2013; 62 (6): 786-792. DOI: 10.1016/j.metabol.2012.12.006.</mixed-citation></citation-alternatives></ref><ref id="B55"><label>55.</label><citation-alternatives><mixed-citation xml:lang="en">Ivović M., Marina L.V., Vujović S. et al. Nondiabe­tic patients with either subclinical Cushing’s or nonfunctional adrenal incidentalomas have lower insulin sensitivity than healthy controls: clinical implications. Metabolism. 2013; 62 (6): 786–792. DOI: 10.1016/j.metabol.2012.12.006.</mixed-citation><mixed-citation xml:lang="ru">Androulakis I.I., Kaltsas G.A., Kollias G.E. et al. Patients with apparently nonfunctioning adrenal incidentalomas may be at increased cardiovascular risk due to excessive cortisol secretion. J. Clin. Endocrinol. Metabol. 2014; 99 (8): 2754-2762. DOI: 10.1210/jc.2013-4064.</mixed-citation></citation-alternatives></ref><ref id="B56"><label>56.</label><citation-alternatives><mixed-citation xml:lang="en">Androulakis I.I., Kaltsas G.A., Kollias G.E. et al. Patients with apparently nonfunctioning adrenal incidentalomas may be at increased cardiovascular risk due to ­excessive cortisol secretion. J. Clin. Endocrinol. Metabol. 2014; 99 (8): 2754–2762. DOI: 10.1210/jc.2013-4064.</mixed-citation><mixed-citation xml:lang="ru">Debono M., Prema A., Hughes T.J. et al. Visceral fat accumulation and postdexamethasone serum cortisol levels in patients with adrenal incidentaloma. J. Clin. Endocrinol. Metabol. 2013; 98 (6): 2383-2391. DOI: 10.1210/jc.2012-4276.</mixed-citation></citation-alternatives></ref><ref id="B57"><label>57.</label><citation-alternatives><mixed-citation xml:lang="en">Debono M., Prema A., Hughes T.J. et al. Visceral fat accumulation and postdexamethasone serum cortisol levels in patients with adrenal incidentaloma. J. Clin. Endocrinol. Metabol. 2013; 98 (6): 2383–2391. DOI: 10.1210/jc.2012-4276.</mixed-citation><mixed-citation xml:lang="ru">Papanastasiou L., Pappa T., Samara C. et al. Nonalcoholic fatty liver disease in subjects with adrenal incidentaloma. Eur. J. Clin. Invest. 2012; 42 (11): 1165-1172. DOI: 10.1111/j.1365-2362.2012.02707.x.</mixed-citation></citation-alternatives></ref><ref id="B58"><label>58.</label><citation-alternatives><mixed-citation xml:lang="en">Papanastasiou L., Pappa T., Samara C. et al. Nonalcoholic fatty liver disease in subjects with adrenal incidentaloma. Eur. J. Clin. Invest. 2012; 42 (11): 1165–1172. DOI: 10.1111/j.1365-2362.2012.02707.x.</mixed-citation><mixed-citation xml:lang="ru">Tо́th M., Grossman A. Glucocorticoid-induced osteoporosis: lessons from Cushing’s syndrome. Clin. Endocrinol. 2013; 79 (1): 1-11. DOI: 10.1111/cen.12189.</mixed-citation></citation-alternatives></ref><ref id="B59"><label>59.</label><citation-alternatives><mixed-citation xml:lang="en">Tо́th M., Grossman A. Glucocorticoid-induced osteo­porosis: lessons from Cushing’s syndrome. Clin. Endocrinol. 2013; 79 (1): 1–11. DOI: 10.1111/cen.12189.</mixed-citation><mixed-citation xml:lang="ru">Tauchmanova` L., Pivonello R., De Martino M.C. et al. Effects of sex steroids on bone in women with subclinical or overt endogenous hypercortisolism. Eur. J. Endocrinol. 2007; 157 (3): 359-366. DOI: 10.1530/EJE-07-0137.</mixed-citation></citation-alternatives></ref><ref id="B60"><label>60.</label><citation-alternatives><mixed-citation xml:lang="en">Tauchmanova` L., Pivonello R., De Martino M.C. et al. Effects of sex steroids on bone in women with subclinical or overt endogenous hypercortisolism. Eur. J. Endocrinol. 2007; 157 (3): 359–366. DOI: 10.1530/EJE-07-0137.</mixed-citation><mixed-citation xml:lang="ru">Chiodini I., Morelli V., Masserini B. et al. Bone mineral density, prevalence of vertebral fractures, and bone quality in patients with adrenal incidentalomas with and without subclinical hypercortisolism: an Italian multicenter study. J. Clin. Endocrin. Metabol. 2009; 94 (9): 3207-3214. DOI: 10.1210/jc.2009-0468.</mixed-citation></citation-alternatives></ref><ref id="B61"><label>61.</label><citation-alternatives><mixed-citation xml:lang="en">Chiodini I., Morelli V., Masserini B. et al. Bone mineral density, prevalence of vertebral fractures, and bone quality in patients with adrenal incidentalomas with and without subclinical hypercortisolism: an Italian multicenter study. J. Clin. Endocrin. Metabol. 2009; 94 (9): 3207–3214. DOI: 10.1210/jc.2009-0468.</mixed-citation><mixed-citation xml:lang="ru">Morelli V., Eller-Vainicher C., Salcuni A.S. et al. Risk of new vertebral fractures in patients with adrenal incidentaloma with and without subclinical hypercortisolism: a multicenter longitudinal study. J. Bone Miner. Res. 2011; 26 (8): 1816-1821. DOI: 10.1002/jbmr.398.</mixed-citation></citation-alternatives></ref><ref id="B62"><label>62.</label><citation-alternatives><mixed-citation xml:lang="en">Morelli V., Eller-Vainicher C., Salcuni A.S. et al. Risk of new vertebral fractures in patients with adrenal incidentaloma with and without subclinical hypercortisolism: a multicenter longitudinal study. J. Bone Miner. Res. 2011; 26 (8): 1816–1821. DOI: 10.1002/jbmr.398.</mixed-citation><mixed-citation xml:lang="ru">Miller W.L., Auchus R.J. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. Endocrine Rev. 2011; 32 (1): 81-151. DOI: 10.1210/er.2010-0013.</mixed-citation></citation-alternatives></ref><ref id="B63"><label>63.</label><citation-alternatives><mixed-citation xml:lang="en">Miller W.L., Auchus R.J. The molecular biology, biochemistry, and physiology of human steroidogenesis and its disorders. Endocrine Rev. 2011; 32 (1): 81–151. DOI: 10.1210/er.2010-0013.</mixed-citation><mixed-citation xml:lang="ru">Baulieu E.E., Thomas G., Legrain S. et al. Dehydroepiandrosterone (DHEA) DHEA sulfate, and aging: contribution of the DHEA ge Study to a sociobiomedical issue. PNAS. 2000; 97 (8): 4279-4284. DOI: 10.1073/pnas.97.8.4279.</mixed-citation></citation-alternatives></ref><ref id="B64"><label>64.</label><citation-alternatives><mixed-citation xml:lang="en">Baulieu E.E., Thomas G., Legrain S. et al. Dehydro­epiandrosterone (DHEA) DHEA sulfate, and aging: contribution of the DHEA ge Study to a sociobiomedical issue. PNAS. 2000; 97 (8): 4279–4284. DOI: 10.1073/pnas.97.8.4279.</mixed-citation><mixed-citation xml:lang="ru">Nair K.S., Rizza R.A., O’Brien P. et al. DHEA in elderly women and DHEA or testosterone in elderly men. New Engl. J. Med. 2006; 355 (16): 1647-1659. DOI: 10.1056/NEJMoa054629.</mixed-citation></citation-alternatives></ref><ref id="B65"><label>65.</label><citation-alternatives><mixed-citation xml:lang="en">Nair K.S., Rizza R.A., O’Brien P. et al. DHEA in elderly women and DHEA or testosterone in elderly men. New Engl. J. Med. 2006; 355 (16): 1647–1659. DOI: 10.1056/NEJMoa054629.</mixed-citation><mixed-citation xml:lang="ru">Tauchmanova` L., Rossi R., Biondi B. et al. Patients with subclinical Cushing’s syndrome due to adrenal adenoma have increased cardiovascular risk. J. Clin. Endocrinol. Metabol. 2002; 87 (11): 4872-4878. DOI: 10.1210/jc.2001-011766.</mixed-citation></citation-alternatives></ref><ref id="B66"><label>66.</label><citation-alternatives><mixed-citation xml:lang="en">Tauchmanova` L., Rossi R., Biondi B. et al. Patients with subclinical Cushing’s syndrome due to adrenal adenoma have increased cardiovascular risk. J. Clin. Endocrinol. Metabol. 2002; 87 (11): 4872–4878. DOI: 10.1210/jc.2001-011766.</mixed-citation><mixed-citation xml:lang="ru">Di Dalmazi G., Vicennati V., Rinaldi E. et al. Progressively increased patterns of subclinical cortisol hypersecretion in adrenal incidentalomas differently predict major metabolic and cardiovascular outcomes: a large cross-sectional study. Eur. J. Endocrinol. 2012; 166 (4): 669-677. DOI: 10.1530/EJE-11-1039.</mixed-citation></citation-alternatives></ref><ref id="B67"><label>67.</label><citation-alternatives><mixed-citation xml:lang="en">Di Dalmazi G., Vicennati V., Rinaldi E. et al. Progressively increased patterns of subclinical cortisol hypersecretion in adrenal incidentalomas differently predict major metabolic and cardiovascular outcomes: a large cross-sectional study. Eur. J. Endocrinol. 2012; 166 (4): 669–677. DOI: 10.1530/EJE-11-1039.</mixed-citation><mixed-citation xml:lang="ru">Di Dalmazi G., Vicennati V., Garelli S. et al. Cardiovascular events and mortality in patients with adrenal incidentalomas that are either non-secreting or associated with intermediate phenotype or subclinical Cushing’s syndrome: a 15-year retrospective study. Lancet. Diabetes Endocrinol. 2014; 2 (5): 396-405. DOI: 10.1016/S2213-8587(13)70211-0.</mixed-citation></citation-alternatives></ref><ref id="B68"><label>68.</label><citation-alternatives><mixed-citation xml:lang="en">Di Dalmazi G., Vicennati V., Garelli S. et al. Cardiovascular events and mortality in patients with adrenal incidentalomas that are either non-secreting or associated with intermediate phenotype or subclinical Cushing’s syndrome: a 15-year retrospective study. Lancet. Diabetes Endocrinol. 2014; 2 (5): 396–405. DOI: 10.1016/S2213-8587(13)70211-0.</mixed-citation><mixed-citation xml:lang="ru">Morelli V, Reimondo G., Giordano R. et al. Long-term follow-up in adrenal incidentalomas: an Italian multicenter study. J. Clin. Endocrinol. Metabol. 2014; 99 (3): 827-834. DOI: 10.1210/jc.2013-3527.</mixed-citation></citation-alternatives></ref><ref id="B69"><label>69.</label><citation-alternatives><mixed-citation xml:lang="en">Morelli V, Reimondo G., Giordano R. et al. Long-term follow-up in adrenal incidentalomas: an Italian multicenter study. J. Clin. Endocrinol. Metabol. 2014; 99 (3): 827–834. DOI: 10.1210/jc.2013-3527.</mixed-citation><mixed-citation xml:lang="ru">Debono M., Bradburn M., Bull M. et al. Cortisol as a marker for increased mortality in patients with incidental adrenocortical adenomas. J. Clin. Endocrinol. Metabol. 2014; 99 (12): 4462-4470. DOI: 10.1210/jc.2014-3007.</mixed-citation></citation-alternatives></ref><ref id="B70"><label>70.</label><citation-alternatives><mixed-citation xml:lang="en">Debono M., Bradburn M., Bull M. et al. Cortisol as a marker for increased mortality in patients with incidental adrenocortical adenomas. J. Clin. Endocrinol. Metabol. 2014; 99 (12): 4462–4470. DOI: 10.1210/jc.2014-3007.</mixed-citation><mixed-citation xml:lang="ru">Barry M.K., van Heerden J.A., Farely D.R. et al. Can adrenal incidentalomas be safely observed? World J. Surg. 1998; 22 (6): 599-604. DOI: 10.1007/s002689900441.</mixed-citation></citation-alternatives></ref><ref id="B71"><label>71.</label><citation-alternatives><mixed-citation xml:lang="en">Barry M.K., van Heerden J.A., Farely D.R. et al. Can adrenal incidentalomas be safely observed? World J. Surg. 1998; 22 (6): 599–604. DOI: 10.1007/s002689900441.</mixed-citation><mixed-citation xml:lang="ru">Sirе́n J., Tervahartiala P., Sivula A. et al. Natural course of adrenal incidentalomas: seven-year follow-up study. World J. Surg. 2000; 24 (5): 579-582. DOI: 10.1007/s002689910095.</mixed-citation></citation-alternatives></ref><ref id="B72"><label>72.</label><mixed-citation>Sirе́n J., Tervahartiala P., Sivula A. et al. Natural course of adrenal incidentalomas: seven-year follow-up study. World J. Surg. 2000; 24 (5): 579–582. DOI: 10.1007/s002689910095.</mixed-citation></ref></ref-list></back></article>
