Medical treatment of Cushing's disease with concurrent diabetes mellitus

被引:6
作者
Mehlich, Anna [1 ]
Bolanowski, Marek [2 ]
Mehlich, Dawid [3 ,4 ,5 ]
Witek, Przemyslaw [1 ]
机构
[1] Med Univ Warsaw, Dept Internal Med Endocrinol & Diabet, Warsaw, Poland
[2] Wroclaw Med Univ, Chair & Dept Endocrinol Diabet Isotope Treatment, Wroclaw, Poland
[3] Machines IMol Polish Acad Sci, Int Inst Mol Mech, Lab Mol OncoSignalling, Warsaw, Poland
[4] Univ Warsaw, Med Univ Warsaw, Doctoral Sch Med, Warsaw, Poland
[5] Med Univ Warsaw, Lab Expt Med, Warsaw, Poland
来源
FRONTIERS IN ENDOCRINOLOGY | 2023年 / 14卷
关键词
Cushing's disease; diabetes mellitus; insulin resistance; medical therapies; metabolic comorbidities; glucose metabolism; INDUCED INSULIN-RESISTANCE; PANCREATIC BETA-CELLS; LONG-TERM TREATMENT; GLUCOCORTICOID-RECEPTOR; 11-BETA-HYDROXYLASE INHIBITOR; COMBINATION THERAPY; PASIREOTIDE SOM230; SKELETAL-MUSCLE; WEIGHT-GAIN; PHASE-III;
D O I
10.3389/fendo.2023.1174119
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Cushing's disease (CD) is a severe endocrine disorder characterized by chronic hypercortisolaemia secondary to an overproduction of adrenocorticotropic hormone (ACTH) by a pituitary adenoma. Cortisol excess impairs normal glucose homeostasis through many pathophysiological mechanisms. The varying degrees of glucose intolerance, including impaired fasting glucose, impaired glucose tolerance, and Diabetes Mellitus (DM) are commonly observed in patients with CD and contribute to significant morbidity and mortality. Although definitive surgical treatment of ACTH-secreting tumors remains the most effective therapy to control both cortisol levels and glucose metabolism, nearly one-third of patients present with persistent or recurrent disease and require additional treatments. In recent years, several medical therapies demonstrated prominent clinical efficacy in the management of patients with CD for whom surgery was non-curative or for those who are ineligible to undergo surgical treatment. Cortisol-lowering medications may have different effects on glucose metabolism, partially independent of their role in normalizing hypercortisolaemia. The expanding therapeutic landscape offers new opportunities for the tailored therapy of patients with CD who present with glucose intolerance or DM, however, additional clinical studies are needed to determine the optimal management strategies. In this article, we discuss the pathophysiology of impaired glucose metabolism caused by cortisol excess and review the clinical efficacy of medical therapies of CD, with particular emphasis on their effects on glucose homeostasis.
引用
收藏
页数:12
相关论文
共 138 条
  • [51] Dexamethasone induces posttranslational degradation of GLUT2 and inhibition of insulin secretion in isolated pancreatic beta cells - Comparison with the effects of fatty acids
    Gremlich, S
    Roduit, R
    Thorens, B
    [J]. JOURNAL OF BIOLOGICAL CHEMISTRY, 1997, 272 (06) : 3216 - 3222
  • [52] EFFECTS OF DEXAMETHASONE ON GLUCOSE-INDUCED INSULIN AND PROINSULIN RELEASE IN LOW AND HIGH INSULIN RESPONDERS
    GRILL, V
    PIGON, J
    HARTLING, SG
    BINDER, C
    EFENDIC, S
    [J]. METABOLISM-CLINICAL AND EXPERIMENTAL, 1990, 39 (03): : 251 - 258
  • [53] GSK-3β mediates dexamethasone-induced pancreatic β cell apoptosis
    Guo, Bin
    Zhang, Wenjian
    Xu, Shiqing
    Lou, Jinning
    Wang, Shuxia
    Men, Xiuli
    [J]. LIFE SCIENCES, 2016, 144 : 1 - 7
  • [54] Cardio-metabolic consequences of glucocorticoid replacement: relevance of ultradian signalling
    Henley, David E.
    Lightman, Stafford L.
    [J]. CLINICAL ENDOCRINOLOGY, 2014, 80 (05) : 621 - 628
  • [55] Hyperglycemia Associated With Pasireotide: Results From a Mechanistic Study in Healthy Volunteers
    Henry, Robert R.
    Ciaraldi, Theodore P.
    Armstrong, Debra
    Burke, Paivi
    Ligueros-Saylan, Monica
    Mudaliar, Sunder
    [J]. JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2013, 98 (08) : 3446 - 3453
  • [56] Long-term results after microsurgery for Cushing disease:: experience with 426 primary operations over 35 years
    Hofmann, Bernd Markus
    Hlavac, Michal
    Martinez, Ramon
    Buchfelder, Michael
    Mueller, Otto Albrecht
    Fahlbusch, Rudolf
    [J]. JOURNAL OF NEUROSURGERY, 2008, 108 (01) : 9 - 18
  • [57] Glucocorticoid induced insulin resistance impairs basal but not glucose entrained high-frequency insulin pulsatility in humans
    Hollingdal, M
    Juhl, CB
    Dall, R
    Sturis, J
    Veldhuis, JD
    Schmitz, O
    Porksen, N
    [J]. DIABETOLOGIA, 2002, 45 (01) : 49 - 55
  • [58] Identification of the Clinical Candidate (R)-(1-(4-Fluoropheny1)-6-((1methyl-1H-pyrazol-4-yl)sulfonyl)-4,4a,5,6,7,8-hexahydro-1H-pyrazolo[3,4-g]isoquinolin-4a-yl)(4-(trifluoromethyl)pyridin-2-yl)methanone (CORT125134): A Selective Glucocorticoid Receptor (GR) Antagonist
    Hunt, Hazel J.
    Belanoff, Joseph K.
    Walters, Iain
    Gourdet, Benoit
    Thomas, Jennifer
    Barton, Naomi
    Unitt, John
    Phillips, Timothy
    Swift, Denise
    Eaton, Emily
    [J]. JOURNAL OF MEDICINAL CHEMISTRY, 2017, 60 (08) : 3405 - 3421
  • [59] METYRAPONE IN LONG-TERM MANAGEMENT OF CUSHINGS-DISEASE
    JEFFCOATE, WJ
    REES, LH
    TOMLIN, S
    JONES, AE
    EDWARDS, CRW
    BESSER, GM
    [J]. BRITISH MEDICAL JOURNAL, 1977, 2 (6081) : 215 - 217
  • [60] INHIBITION OF GLUCOCORTICOSTEROID ACTION IN CULTURED L-929 MOUSE FIBROBLASTS BY RU486, A NEW ANTI-GLUCOCORTICOSTEROID OF HIGH-AFFINITY FOR THE GLUCOCORTICOSTEROID RECEPTOR
    JUNGTESTAS, I
    BAULIEU, EE
    [J]. EXPERIMENTAL CELL RESEARCH, 1983, 147 (01) : 177 - 182