TY - JOUR
T1 - High prevalence of diabetes in patients with primary aldosteronism (PA) associated with subclinical hypercortisolism and prediabetes more prevalent in bilateral than unilateral PA
T2 - A large, multicenter cohort study in Japan
AU - behalf of the Japan Primary Aldosteronism Study Group
AU - Akehi, Yuko
AU - Yanase, Toshihiko
AU - Motonaga, Ryoko
AU - Umakoshi, Hironobu
AU - Tsuiki, Mika
AU - Takeda, Yoshiyu
AU - Yoneda, Takashi
AU - Kurihara, Isao
AU - Itoh, Hiroshi
AU - Katabami, Takuyuki
AU - Ichijo, Takamasa
AU - Wada, Norio
AU - Shibayama, Yui
AU - Yoshimoto, Takanobu
AU - Ashida, Kenji
AU - Ogawa, Yoshihiro
AU - Kawashima, Junji
AU - Sone, Masakatsu
AU - Inagaki, Nobuya
AU - Takahashi, Katsutoshi
AU - Fujita, Megumi
AU - Watanabe, Minemori
AU - Matsuda, Yuichi
AU - Kobayashi, Hiroki
AU - Shibata, Hirotaka
AU - Kamemura, Kohei
AU - Otsuki, Michio
AU - Fujii, Yuichi
AU - Yamamoto, Koichi
AU - Ogo, Atsushi
AU - Okamura, Shintaro
AU - Miyauchi, Shozo
AU - Fukuoka, Tomikazu
AU - Izawa, Shoichiro
AU - Hashimoto, Shigeatsu
AU - Yamada, Masanobu
AU - Yoshikawa, Yuichiro
AU - Kai, Tatsuya
AU - Suzuki, Tomoko
AU - Kawamura, Takashi
AU - Naruse, Mitsuhide
N1 - Funding Information:
Acknowledgments. The authors appreciate the technical assistance of Masashi Ishizu (Diabetes Therapeutics and Research Center, Institute of Advanced Medical Sciences, Tokushima University). The authors thank Dr. Trish Reynolds (Edanz Group; www.edanzediting.com/ac) for editing a draft of this manuscript. Funding. This research was supported by the Japan Agency for Medical Research and Development (grants JP17ek0109122 and JP18ek0109352). Duality of Interest. No potential conflicts of interest relevant to this article were reported. Author Contributions. Y.A. was the main statistical analyst in this study and is the first author of the manuscript. T.Ya. planned the analysis and was the main writer of the manuscript. R.M., H.U., M.T., Y.T., T.Yon., I.K., H.I., T.Kat., T.I., N.W., Y.S., T.Yos., K.A., Y.O., J.K., M.S., N.I., K.T., M.F., M.W., Y.M., H.K., H.S., K.K., M.O., Y.F., K.Y., A.O., S.O., S.M., T.F., S.I., S.H., M.Y., Y.Y., and T. Kai collaborated with each other to collect data in this multi-institutional study by JPAS and were responsible for critically reading the manuscript and discussion. T.S. and T.Kaw. contributed to JPAS as epidemiologic study specialists. M.N. organized and coordinated this JPAS study as the chief JPAS researcher. T.Ya. is the guarantor of this work and, as such, had full access to all the data in the study and takes responsibility for the integrity of the data and the accuracy of the data analysis. Prior Presentation. This study was presented in poster form at ENDO 2019, the Endocrine Society’s Annual Meeting, New Orleans, LA, 23–26 March 2019.
Publisher Copyright:
© 2019 by the American Diabetes Association.
PY - 2019/5/1
Y1 - 2019/5/1
N2 - OBJECTIVE To investigate the prevalence and causes of diabetes in patients with primary aldosteronism (PA) in a multi-institutional cohort study in Japan. RESEARCH DESIGN AND METHODS The prevalence of diabetes was determined in 2,210 patients with PA (diagnosed or glycated hemoglobin [HbA1c] ‡6.5% [‡48 mmol/mol]; NGSP) and compared with that of the Japanese general population according to age and sex. In 1,386 patients with PA and clear laterality (unilateral or bilateral), the effects of plasma aldosterone concentration (PAC), hypokalemia (<3.5 mEq/L), suspected subclinical hypercortisolism (SH; serum cortisol ‡1.8 mg/dL after 1-mg dexamethasone suppression test), and PA laterality on the prevalence of diabetes or prediabetes (5.7% £ HbA1c <6.5% [39 mmol/mol £ HbA1c <48 mmol/mol]) were examined. RESULTS Of the 2,210 patients with PA, 477 (21.6%) had diabetes. This prevalence is higher than that in the general population (12.1%) or in 10-year cohorts aged 30–69 years. Logistic regression or x2 test revealed a significant contribution of suspected SH to diabetes. Despite more active PA profiles (e.g., higher PAC and lower potassium concentrations) in unilateral than bilateral PA, BMI and HbA1c values were significantly higher in bilateral PA. PA laterality had no effect on the prevalence of diabetes; however, the prevalence of prediabetes was significantly higher in bilateral than unilateral PA. CONCLUSIONS Individuals with PA have a high prevalence of diabetes, which is associated mainly with SH. The prevalence of prediabetes is greater for bilateral than unilateral PA, suggesting a unique metabolic cause of bilateral PA.
AB - OBJECTIVE To investigate the prevalence and causes of diabetes in patients with primary aldosteronism (PA) in a multi-institutional cohort study in Japan. RESEARCH DESIGN AND METHODS The prevalence of diabetes was determined in 2,210 patients with PA (diagnosed or glycated hemoglobin [HbA1c] ‡6.5% [‡48 mmol/mol]; NGSP) and compared with that of the Japanese general population according to age and sex. In 1,386 patients with PA and clear laterality (unilateral or bilateral), the effects of plasma aldosterone concentration (PAC), hypokalemia (<3.5 mEq/L), suspected subclinical hypercortisolism (SH; serum cortisol ‡1.8 mg/dL after 1-mg dexamethasone suppression test), and PA laterality on the prevalence of diabetes or prediabetes (5.7% £ HbA1c <6.5% [39 mmol/mol £ HbA1c <48 mmol/mol]) were examined. RESULTS Of the 2,210 patients with PA, 477 (21.6%) had diabetes. This prevalence is higher than that in the general population (12.1%) or in 10-year cohorts aged 30–69 years. Logistic regression or x2 test revealed a significant contribution of suspected SH to diabetes. Despite more active PA profiles (e.g., higher PAC and lower potassium concentrations) in unilateral than bilateral PA, BMI and HbA1c values were significantly higher in bilateral PA. PA laterality had no effect on the prevalence of diabetes; however, the prevalence of prediabetes was significantly higher in bilateral than unilateral PA. CONCLUSIONS Individuals with PA have a high prevalence of diabetes, which is associated mainly with SH. The prevalence of prediabetes is greater for bilateral than unilateral PA, suggesting a unique metabolic cause of bilateral PA.
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U2 - 10.2337/dc18-1293
DO - 10.2337/dc18-1293
M3 - Article
C2 - 31010944
AN - SCOPUS:85065117204
SN - 1935-5548
VL - 42
SP - 938
EP - 945
JO - Diabetes Care
JF - Diabetes Care
IS - 5
ER -