Evidence map›Paper›PMID 31789380›Full record

ArticleThe Journal of clinical endocrinology and metabolism2020

Histological Characterization of Aldosterone-producing Adrenocortical Adenomas with Different Somatic Mutations.

Yoshikiyo Ono, Yuto Yamazaki, Kei Omata, Tobias Else, Scott A Tomlins, Yara Rhayem, Tracy Ann Williams, Martin Reincke, Tobias Carling, Silvia Monticone and 6 more

Open access · bronzeAbstract read
In one paragraph

Article in The Journal of clinical endocrinology and metabolism, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 27 papers.

0numbers the graph read from it
0cells of the map it votes in
27citing papers in PubMed
4.0field-weighted citation impact, top 5% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

27 citing papers in PubMed, 40 citations in OpenAlex.

  1. Trial
  2. Aldosterone-Producing Lesions HarboringHypertension (Dallas, Tex. : 1979) · 2026
    Article
  3. Article
  4. Primary aldosteronism.Nature reviews. Disease primers · 2026
    Review
  5. Review
  6. Article
  7. Article
  8. 18-Oxocortisol: A journey.The Journal of steroid biochemistry and molecular biology · 2023
    Article
  9. Article
  10. Clinical Translationality ofInternational journal of molecular sciences · 2022
    Review
  11. Genetics of Primary Aldosteronism.Hypertension (Dallas, Tex. : 1979) · 2022
    Review
  12. Review
  13. Review
  14. Review
  15. Review
  16. Article
  17. Review
  18. Article
  19. Review
  20. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

16 authors at 6 institutions in 5 countries.

Yoshikiyo OnoDivision of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Hospital, Sendai, Japan.
Yuto YamazakiDepartment of Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Kei OmataDivision of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Hospital, Sendai, Japan.
Tobias ElseDivision of Metabolism, Endocrine, and Diabetes, Department of Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.
Scott A TomlinsDepartment of Pathology, University of Michigan Medical School, Ann Arbor, Michigan.
Yara RhayemMedizinische Klinik und Poliklinik IV, Klinikum der Universität, Ludwig-Maximilians-Universität München, Munich, Germany.
Tracy Ann WilliamsMedizinische Klinik und Poliklinik IV, Klinikum der Universität, Ludwig-Maximilians-Universität München, Munich, Germany.
Martin ReinckeMedizinische Klinik und Poliklinik IV, Klinikum der Universität, Ludwig-Maximilians-Universität München, Munich, Germany.
Tobias CarlingYale Endocrine Neoplasia Laboratory, Yale School of Medicine, New Haven, Connecticut.
Silvia MonticoneDivision of Internal Medicine and Hypertension, Department of Medical Sciences, University of Torino, Torino, Italy.
Paolo MulateroDivision of Internal Medicine and Hypertension, Department of Medical Sciences, University of Torino, Torino, Italy.
Felix BeuschleinMedizinische Klinik und Poliklinik IV, Klinikum der Universität, Ludwig-Maximilians-Universität München, Munich, Germany.
Sadayoshi ItoDivision of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Hospital, Sendai, Japan.
Fumitoshi SatohDivision of Nephrology, Endocrinology, and Vascular Medicine, Tohoku University Hospital, Sendai, Japan.
William E RaineyDepartments of Molecular and Integrative Physiology & Internal Medicine, University of Michigan Medical School, Ann Arbor, Michigan.
Hironobu SasanoDepartment of Pathology, Tohoku University Graduate School of Medicine, Sendai, Japan.
Tohoku University · JPLMU Klinikum · DEUniversity of Michigan · USUniversity of Turin · ITTohoku University Hospital · JPYale University · US

Funding

Yale Clinical and Translational Science Award (U Component)UL1TR001863 · NCATS · YALE UNIVERSITY · PI John H. Krystal, LUCILA OHNO-MACHADO · 2016 to 2026
$102.9M
The Genetics of Primary AldosteronismR01HL130106 · NHLBI · UNIVERSITY OF MICHIGAN AT ANN ARBOR · PI ELSE, TOBIAS · 2016 to 2020
$1.9M
European Research Council 694913NCATS NIH HHS UL1 TR001863NHLBI NIH HHS R01 HL130106
6 · The paper itself

Abstract

contextAldosterone-producing adrenocortical adenomas (APAs) are mainly composed of clear (lipid rich) and compact (eosinophilic) tumor cells. The detailed association between these histological features and somatic mutations (KCNJ5, ATP1A1, ATP2B3, and CACNA1D) in APAs is unknown.

objectiveTo examine the association between histological features and individual genotypes in APAs.

methodsExamination of 39 APAs subjected to targeted next-generation sequencing (11 KCNJ5, 10 ATP1A1, 10 ATP2B3, and 8 CACNA1D) and quantitative morphological and immunohistochemical (CYP11B2 and CYP17A1) analyses using digital imaging software.

resultsKCNJ5- and ATP2B3-mutated APAs had clear cell dominant features (KCNJ5: clear 59.8% [54.4-64.6%] vs compact 40.2% (35.4-45.6%), P = .0022; ATP2B3: clear 54.3% [48.2-62.4 %] vs compact 45.7% (37.6-51.8 %), P = .0696). ATP1A1- and CACNA1D-mutated APAs presented with marked intratumoral heterogeneity. A significantly positive correlation of immunoreactivity was detected between CYP11B2 and CYP17A1 in tumor cells of KCNJ5-mutated APAs (P = .0112; ρ = 0.7237), in contrast, significantly inverse correlation was detected in ATP1A1-mutated APAs (P = .0025; ρ = -0.8667).

conclusionKCNJ5-mutated APAs, coexpressing CYP11B2 and CYP17A1, were more deviated in terms of zonation-specific differentiation of adrenocortical cells than ATP1A1- and ATP2B3-mutated APAs.

Indexed as

MutationAdrenal Cortex NeoplasmsAdrenocortical AdenomaAdultAldosteroneCalcium Channels, L-TypeFemaleGenotypeG Protein-Coupled Inwardly-Rectifying Potassium ChannelsHigh-Throughput Nucleotide SequencingHumansMaleMiddle AgedPhenotypePlasma Membrane Calcium-Transporting ATPasesSodium-Potassium-Exchanging ATPaseAldosteroneATP1A1 protein, humanATP2B3 protein, humanCACNA1D protein, humanCalcium Channels, L-TypeG Protein-Coupled Inwardly-Rectifying Potassium ChannelsKCNJ5 protein, humanPlasma Membrane Calcium-Transporting ATPasesSodium-Potassium-Exchanging ATPaseATP1A1ATP2B3CACNA1DCYP11B2KCNJ5primary aldosteronism

Identifiers

PMID31789380
PMCPMC7048684
OpenAlexW2993525891

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.