Single-Center Prospective Cohort Study on the Histopathology, Genotype, and Postsurgical Outcomes of Patients With Primary Aldosteronism

被引:45
作者
Meyer, Lucie S. [1 ]
Handgriff, Laura [1 ]
Lim, Jung Soo [3 ]
Udager, Aaron M. [4 ,5 ,6 ]
Kinker, Isabella-Sabrina [1 ]
Ladurner, Roland [7 ]
Wildgruber, Moritz [1 ,8 ]
Knoesel, Thomas [2 ]
Bidlingmaier, Martin
Rainey, William E. [3 ]
Reincke, Martin
Williams, Tracy Ann [1 ,9 ]
机构
[1] Ludwig Maximilians Univ Munchen, Klinikum Univ Munchen, Med Klin & Poliklin 4, D-80336 Munich, Germany
[2] Ludwig Maximilians Univ Munchen, Inst Pathol, D-80336 Munich, Germany
[3] Univ Michigan, Med Sch, Dept Mol & Integrat Physiol, Ann Arbor, MI 48109 USA
[4] Univ Michigan, Med Sch, Dept Pathol, Ann Arbor, MI 48109 USA
[5] Michigan Ctr Translat Pathol, Ann Arbor, MI USA
[6] Univ Michigan, Rogel Canc Ctr, Ann Arbor, MI 48109 USA
[7] Klinikum Univ Munchen, Klin Viszeral & Endokrine Chirurg, Munich, Germany
[8] Ludwig Maximilians Univ Munchen, Univ Hosp, Dept Radiol, Munich, Germany
[9] Univ Turin, Dept Med Sci, Div Internal Med & Hypertens, Turin, Italy
基金
欧洲研究理事会;
关键词
adenoma; adrenal glands aldosterone; genotype; hyperaldosteronism; hypertension; FUNCTIONAL HISTOPATHOLOGY; GENETIC CAUSES; MUTATIONS; ADRENALECTOMY; SUPPRESSION; PREVALENCE; DIAGNOSIS; CONSENSUS; BASAL;
D O I
10.1161/HYPERTENSIONAHA.121.17348
中图分类号
R6 [外科学];
学科分类号
1002 ; 100210 ;
摘要
Unilateral forms of primary aldosteronism are usually surgically treated to remove the source of aldosterone excess. After adrenalectomy, aldosteronism persists in some patients indicating abnormal aldosterone production from the unresected gland. Our objective was to investigate histopathology, genotype, and postsurgical outcomes in a 3-year prospective cohort of surgically treated patients for primary aldosteronism (from 2016 to 2018). The cohort comprised 60 consecutively operated patients categorized with classical or nonclassical histopathologic findings of unilateral primary aldosteronism. In the classical group were 45 solitary aldosterone-producing adenomas or dominant aldosterone-producing nodules; in the nonclassical group were 15 cases of multiple aldosterone-producing micronodules or nodules (12 cases) or aldosterone-producing diffuse hyperplasia (3 cases). The classical group displayed higher baseline plasma aldosterone concentrations (262 versus 155 pg/mL, P=0.008) and an increased aldosterone-to-renin ratio (81 versus 42, P=0.002). A high proportion of the classical group achieved complete biochemical success (97.6% versus 66.7% in the nonclassical group, P=0.002). The nonclassical versus classical group displayed an increased ratio of absolute aldosterone concentration in the contralateral adrenal vein to peripheral vein at adrenal venous sampling (3.8 versus 2.0, P=0.004). Variants in aldosterone-driver genes were identified in 85% of 41 aldosterone-producing adenomas and were excluded in the remaining 15% by CYP11B2 guided next-generation sequencing. There were no differences in clinical or biochemical outcomes in patients with a solitary aldosterone-producing adenoma categorized by KCNJ5 mutation status. In conclusion, adrenals with a nonclassical histopathology of unilateral primary aldosteronism are associated with a higher incidence of postsurgical disease persistence and increased aldosterone production from the unresected adrenal.
引用
收藏
页码:738 / 746
页数:9
相关论文
共 38 条
[1]   Outcome after surgery for primary hyperaldosteronism may depend on KCNJ5 tumor mutation status: a population-based study from Western Norway [J].
Arnesen, Thomas ;
Glomnes, Nina ;
Stromsoy, Siri ;
Knappskog, Stian ;
Heie, Anette ;
Akslen, Lars A. ;
Grytaas, Marianne ;
Varhaug, Jan Erik ;
Gimm, Oliver ;
Brauckhoff, Michael .
LANGENBECKS ARCHIVES OF SURGERY, 2013, 398 (06) :869-874
[2]   Adrenal Cortex Remodeling and Functional Zona Glomerulosa Hyperplasia in Primary Aldosteronism [J].
Boulkroun, Sheerazed ;
Samson-Couterie, Benoit ;
Dzib, Jose-Felipe Golib ;
Lefebvre, Herve ;
Louiset, Estelle ;
Amar, Laurence ;
Plouin, Pierre-Francois ;
Lalli, Enzo ;
Jeunemaitre, Xavier ;
Benecke, Arndt ;
Meatchi, Tchao ;
Zennaro, Maria-Christina .
HYPERTENSION, 2010, 56 (05) :885-U326
[3]   Genetic, Cellular, and Molecular Heterogeneity in Adrenals With Aldosterone-Producing Adenoma [J].
De Sousa, Kelly ;
Boulkroun, Sheerazed ;
Baron, Stephanie ;
Nanba, Kazutaka ;
Wack, Maxime ;
Rainey, William E. ;
Rocha, Angelique ;
Giscos-Douriez, Isabelle ;
Meatchi, Tchao ;
Amar, Laurence ;
Travers, Simon ;
Fernandes-Rosa, Fabio L. ;
Zennaro, Maria-Christina .
HYPERTENSION, 2020, 75 (04) :1034-1044
[4]   Basal contralateral aldosterone suppression is rare in lateralized primary aldosteronism [J].
Desrochers, Marie-Josee ;
St-Jean, Matthieu ;
El Ghorayeb, Nada ;
Bourdeau, Isabelle ;
So, Benny ;
Therasse, Eric ;
Kline, Gregory ;
Lacroix, Andre .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2020, 183 (04) :399-409
[5]   Basal and Post-ACTH Aldosterone and Its Ratios Are Useful During Adrenal Vein Sampling in Primary Aldosteronism [J].
El Ghorayeb, Nada ;
Mazzuco, Tania L. ;
Bourdeau, Isabelle ;
Mailhot, Jean-Philippe ;
Zhu, Ping Shi ;
Therasse, Eric ;
Lacroix, Andre .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2016, 101 (04) :1826-1835
[6]   Different Somatic Mutations in Multinodular Adrenals With Aldosterone-Producing Adenoma [J].
Fernandes-Rosa, Fabio Luiz ;
Giscos-Douriez, Isabelle ;
Amar, Laurence ;
Gomez-Sanchez, Celso E. ;
Meatchi, Tchao ;
Boulkroun, Sheerazed ;
Zennaro, Maria-Christina .
HYPERTENSION, 2015, 66 (05) :1014-1022
[7]   The Management of Primary Aldosteronism: Case Detection, Diagnosis, and Treatment: An Endocrine Society Clinical Practice Guideline [J].
Funder, John W. ;
Carey, Robert M. ;
Mantero, Franco ;
Murad, M. Hassan ;
Reincke, Martin ;
Shibata, Hirotaka ;
Stowasser, Michael ;
Young, William F., Jr. .
JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM, 2016, 101 (05) :1889-1916
[8]   Development of monoclonal antibodies against human CYP11B1 and CYP11B2 [J].
Gomez-Sanchez, Celso E. ;
Qi, Xin ;
Velarde-Miranda, Carolina ;
Plonczynski, Maria W. ;
Parker, C. Richard ;
Rainey, William ;
Satoh, Fumitoshi ;
Maekawa, Takashi ;
Nakamura, Yasuhiro ;
Sasano, Hironobu ;
Gomez-Sanchez, Elise P. .
MOLECULAR AND CELLULAR ENDOCRINOLOGY, 2014, 383 (1-2) :111-117
[9]   Primary aldosteronism: key characteristics at diagnosis: a trend toward milder forms [J].
Heinrich, Daniel A. ;
Adolf, Christian ;
Rump, Lars C. ;
Quack, Ivo ;
Quinkler, Marcus ;
Hahner, Stefanie ;
Januszewicz, Andrzej ;
Seufert, Jochen ;
Willenberg, Holger S. ;
Nirschl, Nina ;
Sturm, Lisa ;
Beuschlein, Felix ;
Reincke, Martin .
EUROPEAN JOURNAL OF ENDOCRINOLOGY, 2018, 178 (06) :605-611
[10]   Mutations in KCNJ5 determines presentation and likelihood of cure in primary hyperaldosteronism [J].
Ip, Julian C. Y. ;
Pang, Tony C. Y. ;
Pon, Cindy K. ;
Zhao, Jing Ting ;
Sywak, Mark S. ;
Gill, Anthony J. ;
Soon, Patsy S. ;
Sidhu, Stan B. .
ANZ JOURNAL OF SURGERY, 2015, 85 (04) :279-283