Genetics in endocrinology: impact of race and sex on genetic causes of aldosterone-producing adenomas
K Nanba, WE Rainey - European journal of endocrinology, 2021 - academic.oup.com
Primary aldosteronism (PA) is a common cause of secondary hypertension. Recent
technological advances in genetic analysis have provided a better understanding of the …
technological advances in genetic analysis have provided a better understanding of the …
Update on the genetics of primary aldosteronism and aldosterone-producing adenomas
Abstract Purpose of the Review Primary aldosteronism (PA) is the leading cause of
secondary hypertension, accounting for over 10% of patients with high blood pressure. It is …
secondary hypertension, accounting for over 10% of patients with high blood pressure. It is …
Prevalence of somatic mutations in aldosterone-producing adenomas in Japanese patients
K Nanba, Y Yamazaki, N Bick… - The Journal of …, 2020 - academic.oup.com
Context Results of previous studies demonstrated clear racial differences in the prevalence
of somatic mutations among patients with aldosterone-producing adenoma (APA). For …
of somatic mutations among patients with aldosterone-producing adenoma (APA). For …
[HTML][HTML] Aldosterone-potassium ratio predicts primary aldosteronism subtype
TH Puar, WJ Loh, DST Lim, LM Loh… - Journal of …, 2020 - journals.lww.com
Objective: Prediction models have been developed to predict either unilateral or bilateral
primary aldosteronism, and these have not been validated externally. We aimed to develop …
primary aldosteronism, and these have not been validated externally. We aimed to develop …
Biochemical, histopathological, and genetic characterization of posture-responsive and unresponsive APAs
Z Guo, K Nanba, A Udager… - The Journal of …, 2020 - academic.oup.com
Abstract Context and Objective Posture-responsive and posture-unresponsive aldosterone-
producing adenomas (APAs) account for approximately 40% and 60% of APAs, respectively …
producing adenomas (APAs) account for approximately 40% and 60% of APAs, respectively …
Update on genetics of primary aldosteronism
K Itcho, K Oki, H Ohno, M Yoneda - Biomedicines, 2021 - mdpi.com
Primary aldosteronism (PA) is the most common form of secondary hypertension, with a
prevalence of 5–10% among patients with hypertension. PA is mainly classified into two …
prevalence of 5–10% among patients with hypertension. PA is mainly classified into two …
[HTML][HTML] Primary aldosteronism diagnostics: KCNJ5 mutations and hybrid steroid synthesis in aldosterone-producing adenomas
Primary aldosteronism (PA) is characterized by autonomous aldosterone production by
renin-independent mechanisms and is most commonly sporadic. While 60–70% of sporadic …
renin-independent mechanisms and is most commonly sporadic. While 60–70% of sporadic …
Genetic dissection of primary aldosteronism in a patient with MEN1 and ipsilateral adrenocortical carcinoma and adenoma
S Parisien-La Salle, G Corbeil… - The Journal of …, 2023 - academic.oup.com
Background Adrenal tumors are found in up to 40% of patients with multiple endocrine
neoplasia type 1 (MEN1). However, adrenocortical carcinomas (ACC) and primary …
neoplasia type 1 (MEN1). However, adrenocortical carcinomas (ACC) and primary …
Recent development toward the next clinical practice of primary aldosteronism: A literature review
Y Tezuka, Y Yamazaki, Y Nakamura, H Sasano… - Biomedicines, 2021 - mdpi.com
For the last seven decades, primary aldosteronism (PA) has been gradually recognized as a
leading cause of secondary hypertension harboring increased risks of cardiovascular …
leading cause of secondary hypertension harboring increased risks of cardiovascular …
Non-neoplastic/hyperplastic primary aldosteronism–Its histopathology and genotype
Y Yamazaki, K Omata, Y Tezuka, X Gao… - Current Opinion in …, 2019 - Elsevier
Recent development of genetic analysis has revealed the molecular characteristics of
aldosterone-producing adrenocortical lesions, including gene mutations of KCNJ5, ATP1A1 …
aldosterone-producing adrenocortical lesions, including gene mutations of KCNJ5, ATP1A1 …