Skip to main content
Journal of the Endocrine Society logoLink to Journal of the Endocrine Society
. 2019 Aug 22;3(11):2012–2022. doi: 10.1210/js.2019-00295

Predictors of Clinical Success After Surgery for Primary Aldosteronism in the Japanese Nationwide Cohort

Mitsuha Morisaki 1, Isao Kurihara 1,, Hiroshi Itoh 1, Mitsuhide Naruse 2,3, Yoshiyu Takeda 4, Takuyuki Katabami 5, Takamasa Ichijo 6, Norio Wada 7, Takanobu Yoshimoto 8, Yoshihiro Ogawa 9, Masakatsu Sone 10, Mika Tsuiki 2, Hirotaka Shibata 11, Junji Kawashima 12, Megumi Fujita 13, Minemori Watanabe 14, Yuichi Matsuda 15, Hiroki Kobayashi 16, Tomoko Suzuki 17; JPAS Study Group
PMCID: PMC6795022  PMID: 31637342

Abstract

Context

Aldosterone-producing adenomas are a curable subtype of primary aldosteronism (PA); however, hypertension persists in some patients after adrenalectomy.

Objective

To identify factors associated with, and develop prediction models for, blood pressure (BP) normalization or improvement after adrenalectomy.

Design

Retrospective analysis of patients treated between 2006 and 2018, with a 6-month follow-up.

Setting

A nationwide, 29-center Japanese registry encompassing 15 university hospitals and 14 city hospitals.

Patients

We categorized 574 participants in the Japan Primary Aldosteronism Study, who were diagnosed with PA and underwent adrenalectomy, as BP normalized or improved, on the basis of their presentations at 6 months postsurgery.

Main Outcome Measure

The rate of complete, partial, and absent clinical success. Predictive factors related to BP outcomes after PA surgery were also evaluated.

Results

Complete clinical success was achieved in 32.6% and partial clinical success was achieved in 53.0% of the patients at 6 months postsurgery. The following five variables were independent predictors for BP normalization: ≤7 years of hypertension, body mass index ≤25 kg/m2, no more than one antihypertensive medication, absence of medical history of diabetes, and female sex. The area under the receiver operator characteristic curve was 0.797 in the BP normalization model.

Conclusion

We established models that predicted postoperative BP normalization in patients with PA. These should be useful for shared decision-making regarding adrenalectomy for PA.

Keywords: primary aldosteronism, surgery, hypertension, predictive model, cure, improvement


Primary aldosteronism (PA) afflicts 6% to 15% of all hypertensive patients [15] and is the most common cause of secondary hypertension. Owing to this PA epidemic, we recently established the Japan Primary Aldosteronism Study (JPAS), which includes a nationwide, multicenter PA registry as a research tool [613], and is dedicated to improving the clinical management of patients with PA.

Aldosterone-producing adenomas (APAs) and bilateral (idiopathic) adrenal hyperplasia are the major subtypes of PA. APAs can be cured by unilateral adrenalectomy [14, 15]; nevertheless, approximately half of patients with APA experience persistent hypertension after surgery [16, 17]. In a recent meta-analysis [18], the overall rate of hypertension resolution after PA surgery was 52%, although the rates varied from 24% to 86%. The Primary Aldosteronism Surgical Outcome (PASO) study [19] also found that 37% of subjects achieved resolution of their hypertension and an additional 47% had improved blood pressure (BP) based on consensus definitions of clinical outcomes among participating countries. The rate of hypertension resolution after PA surgery is not sufficiently high; therefore, it is critical for clinicians and patients to be aware of markers that predict more favorable clinical outcomes.

Previous studies have proposed several models for predicting the resolution of hypertension after PA surgery. Zarnegar et al. [20] devised the Aldosteronoma Resolution Score, which is a scoring system encompassing four predictive factors: fewer antihypertensive medications (no more than two), lower body mass index (BMI; ≤25 kg/m2), fewer years of hypertension (no more than 6 years), and female sex. This model was established on the basis of analyzing a database of patients with PA in the United States and subsequently proved useful for Japanese patients with PA as well [21, 22]. Moreover, Utsumi et al. [23] proposed a novel nomogram comprising four independent predictors: duration of hypertension, number of antihypertensive drug classes, age, and sex. This scoring model was established on the basis of data from a single-center study of Japanese patients with PA.

In our study, we first aimed to develop a prediction model for postoperative hypertension resolution by using nationwide cohort data of Japanese patients with PA. Importantly, although several prediction models for the postoperative cure of hypertension have been reported, these sometimes mislead patients into foregoing surgery if the BP is not predicted to be resolved. However, even if the hypertension resolution prediction score is low, most patients who undergo surgery may still benefit from an improvement in their hypertension, even if normalization is not achieved. Therefore, we also aimed to identify predictive factors for absence of hypertension improvement after surgery for PA.

1. Methods

A. Study Design and Patients

This investigation was conducted as a part of the JPAS. A nationwide, 29-center PA registry was established in Japan that encompassed 15 university hospitals and 14 city hospitals. The JPAS included patients >20 years of age who were diagnosed with PA between January 2006 and October 2018 and who underwent adrenal vein sampling (AVS). Patients who were diagnosed with PA after adrenalectomy were also enrolled even if they did not undergo AVS. The number of patients with PA who skipped AVS was only 10 (1.7%) of the total number of patients in this study.

Patients eligible for the current study were those who were diagnosed with unilateral PA, underwent adrenalectomy, and were followed at 6 months postsurgery. The baseline clinical characteristics, biochemical findings, results of confirmatory testing, AVS results, surgical findings, postoperative outcomes, and related follow-up data were electronically collected using the WEB registry system. System construction, data security, and maintenance of the registered data were outsourced to EPS Corporation (Tokyo, Japan). The study protocol was approved by the ethics committee of each participating center.

B. Diagnosis of PA

All patients were diagnosed with PA according to the guidelines of the Japan Endocrine Society [24] and the Japan Society of Hypertension [25]. PA was diagnosed on the basis of a ratio of plasma aldosterone concentration (PAC; measured in picograms per milliliter) to plasma renin activity (PRA; measured in nanograms per milliliter per hour) of >200, or on a PAC-to-active renin concentration (measured in picograms per milliliter) ratio of >40, and at least one positive result from a confirmatory test such as the captopril challenge, saline infusion, furosemide upright, or oral salt-loading test. Antihypertensive medications were usually changed to calcium channel blockers or α-adrenergic blockers, as appropriate, until the final diagnosis was made. Hypokalemia was considered present if the serum potassium level was ≤3.5 mEq/L or when a patient was taking a potassium supplement. Oral potassium was administered if hypokalemia was present.

The diagnosis of the PA subtype was determined based on AVS results with ACTH (cosyntropin) stimulation, the procedures for which were previously described [26]. Adrenal vein cannulation was considered successful if the selectivity index was >5 [27]; the selectivity index was defined as the ratio of cortisol concentration in the adrenal vein to that in the inferior vena cava. Unilateral hyperaldosteronism on AVS was defined as a lateralized ratio (LR) >4 [27]. The LR was calculated by dividing the aldosterone-to-cortisol ratio on the dominant side by that on the opposite side. AVS data after ACTH stimulation were used for analysis in the current study.

C. Definition of Clinical Outcomes

After adrenalectomy, patients were categorized as having achieved complete clinical success if their systolic BP (SBP) was <140 mm Hg and diastolic BP (DBP) was <90 mm Hg with no antihypertensive medications at 6 months postsurgery. Patients were categorized as having achieved partial clinical success if the number or dose, which was evaluated by Defined Daily Dose, of antihypertensive medications was reduced after surgery, or if their SBP decreased by ≥20 mm Hg or their DBP decreased by ≥10 mm Hg at 6 months postsurgery with no change in the number of antihypertensive medications. The rest of clinical outcome was categorized as absent clinical success. These BP outcomes were defined according to the previously described worldwide consensus used in the PASO study [19].

D. Data Collection

We collected the following data: age, sex, family history of hypertension, history of diabetes mellitus and dyslipidemia, smoking habits, drinking habits, SBP, DBP, cardiothoracic ratio, echocardiography of the left ventricular hypertrophy (Cornell product), duration of hypertension, number of antihypertensive medications, BMI, and proteinuria. Furthermore, blood test results were collected that included levels of Na+, K+, CL, serum creatinine, uric acid, triglycerides, and high- and low-density lipoprotein cholesterol; estimated glomerular filtration rate (eGFR); HbA1c, based on the National Glycohemoglobin Standardization Program; PAC; PRA; aldosterone-to-renin ratio; LR after ACTH stimulation on AVS; and contralateral ratio after ACTH stimulation on AVS. PAC was measured by commercial RIA kits (SPAC-S Aldosterone kit; Fuji Rebio, Tokyo, Japan) in all centers. PRA was measured by commercial RIA kits (FR RIA kit, Fuji Rebio; PRA RIA kit, Yamasa, Choshi, Japan) or enzyme immunoassay (PRA EIA kit, Yamasa). Plasma active renin concentration was measured by immunoradiometric assay (Renin IRMA-FR; Fuji Rebio). The active renin concentration value was used for analysis by converting to PRA. The eGFR was measured using an abbreviated equation, as follows:

eGFR(mL×min1×1.73m2)=186×(creatinine)1.094×(age)0.287×(0.742 for women)

E. Statistical Analyses

We retrospectively surveyed the clinical variables associated with postoperative resolution and improvement of hypertension. SPSS software, version 25 (IBM, Armonk, NY) was used for each analysis. One-way ANOVA with post hoc Tukey analysis was used for quantitative normally distributed variables. Kruskal-Wallis or Mann-Whitney-U test was used for quantitative nonnormally distributed variables, and the χ2 test or Fisher exact test was used for categorical variables.

Next, we subjected variables that were linked to postoperative BP normalization on univariate analysis to multivariate logistic regression analysis. Variables independently associated with resolution of hypertension (P < 0.05) were then ranked according to the magnitudes of their ORs. Only factors that were easily accessible at clinical presentation were chosen to create a highly versatile model. Next, we assigned these predictors appropriate scores on the basis of the β values and ORs, and generated receiver operating characteristic (ROC) curves to assess the accuracy of the model. The univariate analysis results are described as median (range) or mean ± SD, as appropriate. Statistical significance was defined at the level of P < 0.05.

2. Results

Among a total of 919 patients who underwent adrenalectomy for unilateral PA, 574 patients were eligible for this study. BP was postoperatively normalized in 187 patients (32.6%) and improved in 304 patients (53.0%; Table 1) at 6 months postsurgery.

Table 1.

Univariate Analyses of Candidate Predictor Variables in the JPAS Database

Clinical Success Pairwise Comparison P Value
Variablea Total Cohort Complete Partial Absent Overall P Value C vs P C vs A P vs A
Clinical outcome, no. (%) 574 (100) 187 (32.6) 304 (53.0) 83 (14.5) NA NA NA NA
Sex, female/male 291/283 130/57 121/183 40/43 <0.001 <0.001 0.001 0.169
Family history of hypertension, Y/N (n = 523) 334/189 105/69 188/88 41/32 0.144 NA NA NA
Diabetes mellitus, Y/N 86/488 9/178 65/239 12/71 <0.001 <0.001 0.006 0.161
Dyslipidemia, Y/N 145/429 24/163 97/207 24/59 <0.001 <0.001 0.001 0.602
Current or past drinking, Y/N (n = 530) 293/237 79/95 174/108 40/34 0.010 0.003 0.260 0.248
Current or past smoking, Y/N (n = 535) 202/333 48/130 128/155 26/48 0.001 <0.001 0.082 0.131
Potassium supplementation, Y/N (n = 572) 333/239 113/74 179/123 41/42 0.205 NA NA NA
Age, mean ± SD, y (n = 573) 51.4 ± 11.7 46.3 ± 11.3 53.7 ± 11.2 54.6 ± 11.1 <0.001 <0.001 <0.001 0.513
Duration of hypertension, median (IQR), y (n = 536) 8.0 (3.0–15.0) 4.0 (1.0–8.0) 10.0 (6.0–19.3) 8.5 (4.0–15.3) <0.001 <0.001 <0.001 0.073
Preoperative no. of antihypertensive medications, median (IQR) 1.42 (0–5) 1.01 (0–2) 1.80 (0–5) 0.96 (0–3) <0.001 <0.001 0.456 <0.001
BMI, mean ± SD, kg/m2 (n = 573) 24.1 ± 4.1 22.6 ± 3.3 24.9 ± 4.4 24.8 ± 3.9 <0.001 <0.001 <0.001 0.803
SBP, mean ± SD, mm Hg (n = 568) 142.5 ± 19.1 136.7 ± 17.9 146.3 ± 19.6 141.4 ± 17.0 <0.001 <0.001 0.044 0.040
DBP, mean ± SD, mm Hg (n = 568) 87.8 ± 12.6 86.8 ± 11.5 88.7 ± 13.0 86.7 ± 13.4 0.216 NA NA NA
CTR, mean ± SD, % (n = 519) 48.1 ± 4.9 46.4 ± 4.9 49.0 ± 4.6 48.3 ± 5.2 <0.001 <0.001 0.007 0.199
LVH, mean ± SD, Cornell product (n = 302) 2056.7 ± 844.2 1912.2 ± 829.8 2133.8 ± 854.8 2089.8 ± 815.2 0.121 NA NA NA
Proteinuria (1–5),b median (IQR) (n = 529) 1.67 (1–5) 1.40 (1–5) 1.84 (1–5) 1.62 (1–5) <0.001 <0.001 0.054 0.211
Creatinine, mean ± SD, mg/dL (n = 569) 0.78 ± 0.42 0.66 ± 0.17 0.86 ± 0.53 0.77 ± 0.20 <0.001 <0.001 <0.001 0.119
eGFR, mean ± SD, mL/min/1.73m2 (n = 569) 79.5 ± 23.5 88.8 ± 23.2 74.8 ± 23.4 76.1 ± 18.0 <0.001 <0.001 <0.001 0.576
Uric acid, mean ± SD, mg/dL (n = 529) 5.33 ± 1.60 4.75 ± 1.70 5.56 ± 1.49 5.71 ± 1.42 <0.001 <0.001 <0.001 0.441
Na+, mean ± SD, mEq/L (n = 571) 142.8 ± 2.2 142.4 ± 2.2 143.0 ± 2.3 143.3 ± 2.1 0.003 0.004 0.003 0.337
K+, mean ± SD, mEq/L (n = 431) 2.84 ± 0.45 2.86 ± 0.45 2.81 ± 0.45 2.92 ± 0.41 0.173 NA NA NA
Cl+, mean ± SD, mEq/L (n = 569) 103.9 ± 7.9 103.9 ± 7.9 104.0 ± 6.6 103.7 ± 11.4 0.954 NA NA NA
HbA1c (NGSP), mean ± SD, % (n = 468) 5.54 ± 0.77 5.34 ± 0.65 5.65 ± 0.81 5.52 ± 0.74 0.001 <0.001 0.084 0.222
TG, mean ± SD, mg/dL (n = 512) 113.2 ± 68.7 89.1 ± 48.7 122.1 ± 70.5 132.4 ± 84.2 <0.001 <0.001 <0.001 0.287
HDL, mean ± SD, mg/dL (n = 511) 57.5 ± 16.7 62.4 ± 17.2 55.3 ± 16.6 54.5 ± 13.3 <0.001 <0.001 <0.001 0.651
LDL, mg/dL (n = 516) 112.1 ± 28.0 110.7 ± 24.4 110.3 ± 28.6 121.9 ± 31.4 0.005 0.877 0.007 0.003
PAC, median (IQR), pg/mL (n = 571) 310.0 (196.0–464.5) 310.0 (201.5–452.3) 325.0 (201.0–493.0) 250.0 (159.0–399.0) 0.025 0.584 0.024 0.008
PRA, median (IQR), ng/mL/h (n = 565) 0.2 (0.1–0.4) 0.2 (0.1–0.4) 0.2 (0.1–0.4) 0.2 (0.2–0.4) 0.732 NA NA NA
ARR, median (IQR), PRA pg/mL per ng/mL/h (n = 565) 1140.0 (600.0–2330.0) 1323.3 (650.8–2313.8) 1117.5 (565.1–2499.4) 760.0 (475.7–2193.3) 0.084 NA NA NA
LR, median (IQR) (n = 455) 13.3 (4.4–32.3) 18.7 (6.7–39.1) 12.7 (4.4–29.0) 5.8 (2.2–31.1) 0.003 0.036 0.001 0.038
CR, median (IQR) (n = 465) 0.5 (0.3–0.9) 0.4 (0.3–0.7) 0.5 (0.3–0.9) 0.7 (0.3–1.5) 0.001 0.014 0.001 0.035
LR after ACTH, median (IQR) (n = 522) 10.6 (4.7–24.2) 11.4 (4.5–29.6) 11.7 (5.0–24.3) 6.1 (3.5–13.2) 0.003 0.569 0.003 0.001
CR after ACTH, median (IQR) (n = 525) 0.4 (0.2–0.7) 0.3 (0.2–0.7) 0.3 (0.2–0.7) 0.5 (0.3–1.2) 0.005 0.999 0.004 0.002

Abbreviations: ARR, aldosterone to renin ratio; CR, contralateral ratio; CTR, cardiothoracic ratio; HDL, high-density lipoprotein cholesterol; IQR, interquartile range; LDL, low-density lipoprotein cholesterol; LVH, left ventricular hypertrophy; NA, not applicable; NGSP, National Glycohemoglobin Standardization Program; TG, triglycerides.

a

Where the number of patients on which the data were calculated was less than the total cohort, the number is indicated in parentheses.

b

Proteinuria: 1: negative; 2: ±; 3, +; 4, ++;, 5, +++.

We considered the correction of hypokalemia and normalization of aldosterone-to-renin ratio as postoperative biochemical cure, on the basis of the recent international PASO consensus [19]. Complete biochemical cure was achieved in 88.2% of the patients at the 6-month time point. Normokalemia was achieved in 99.1% of the patients, and ARR normalization was achieved in 89.0%.

Table 1 lists the results of preoperative variables that were candidates for being associated with postoperative resolution and improvement of hypertension. The following variables were significantly different among three groups of postoperative clinical outcomes and were potentially linked to BP normalization: sex, medical history of diabetes and dyslipidemia, drinking, smoking, age, duration of hypertension, the number of antihypertensive medications, BMI, preoperative SBP under antihypertensive medications, cardiothoracic ratio on chest radiography, proteinuria, creatinine, eGFR, uric acid, serum sodium levels, HbA1c (National Glycohemoglobin Standardization Program), triglyceride levels, high-density lipoprotein cholesterol level, and lateralized ratio and contralateral ratio of AVS without ACTH administration. On the contrary, the following variables were potentially associated with absent clinical success: the number of antihypertensive medications, preoperative SBP under antihypertensive medications, low-density lipoprotein cholesterol level, preoperative PAC, and lateralized ratio and contralateral ratio of AVS with and without ACTH administration.

The variables that were associated with postoperative BP outcomes were subjected to multivariate logistic regression analysis. Continuous variables were dichotomized and optimum cutoffs for dichotomization were selected by analyzing the ROC curve for each variable. The following five variables were found to be independent predictors of hypertension resolution: duration of hypertension ≤7 years, BMI ≤25 kg/m2, no more than one antihypertensive medication, absence of diabetes mellitus, and female sex (Table 2). We assigned these variables graded scores on the basis of their β values and developed prediction models for postoperative outcomes (Table 3), and we subsequently generated ROC curves for these models with calculated areas under the curve to assess the accuracy of their predictive scores. The area under the curve value was 0.797 (95% CI, 0.759 to 0.836) in the hypertension resolution model (Fig. 1). The ratio of patients with BP normalization was none of 12 patients (0%) in the group with a hypertension resolution score of 0, and 64 of 90 patients (71.1%) in the group with a hypertension resolution score of 6. The proportion of patients who achieved hypertension resolution increased as the score increased [Fig. 2(A) and 2(B)].

Table 2.

Results of Multivariate Logistic Regression Analysis of the Major Predictors of BP Normalization

Major Predictor of BP Normalization β OR P Value 95% CI
Years of hypertension ≤7 1.507 4.513 <0.001 2.924 to 6.966
Absence of diabetes mellitus 1.041 2.832 0.013 1.249 to 6.421
≤1 Antihypertensive medication 1.027 2.793 <0.001 1.706 to 4.574
Female sex 0.781 2.184 <0.001 1.407 to 3.389
BMI ≤25 kg/m2 0.768 2.156 0.002 1.327 to 3.502

Table 3.

Prediction Model: BP Normalization

Points
Major Predictor of BP Normalization Present Absent
Years of hypertension ≤7 2 0
Absence of diabetes mellitus 1 0
≤1 Antihypertensive medication 1 0
Female sex 1 0
BMI ≤ 25 kg/m2 1 0

Figure 1.

Figure 1.

The ROC curve of the variables correlated with BP normalization (duration of hypertension ≤7 y, BMI ≤ 25 kg/m2, no more than one antihypertensive medication, absence of diabetes mellitus, and female sex). The values of the area under the curve is 0.797 (95% CI, 0.759 to 0.836).

Figure 2.

Figure 2.

Performance of the normalization scores as indicated by the (A) number of patients and (B) ratio of patients. The populations of patients with normalization are represented for each score; the proportions of patients experiencing normalization increased with greater predictive scores.

3. Discussion

Although unilateral PA can be cured by adrenalectomy, BP outcomes, including hypertension resolution and hypertension improvement, are sometimes dissociated from the biochemical outcomes of PA surgery. In our JPAS cohort, 32.6% of the patients achieved hypertension resolution and 53.0% achieved improvement; the rate of complete clinical success was lower than that of biochemical cure after surgery. The dissociation of biochemical and clinical outcomes sometimes discourages patients from opting for surgical treatment of PA; therefore, a prediction model for postoperative BP outcomes is clinically valuable, and several such models have been developed and reported.

Zarneger et al. [20] established the Aldosteronoma Resolution Score to predict the resolution of hypertension after adrenalectomy, and Utsumi et al. [23] developed a nomogram for the same reason. Both models consider a short hypertension duration, fewer antihypertensive medications, and female sex as important predictors for favorable outcomes. Notably, our own predictive model is most similar to that of Zarneger et al. model, because it also found that the duration of hypertension, BMI, number of antihypertensive medications, and female sex are the prevailing predictive factors related to curing hypertension after adrenalectomy for PA. On the other hand, we found that the absence of diabetes mellitus is a predictive factor related to BP normalization. Additional studies should be performed to determine whether diabetes mellitus is a factor that is specific to Japanese/Asian people or has wider applicability.

In the meantime, fewer studies have investigated the factors that predict the absence of BP improvement after adrenalectomy. Williams et al. [19] reported that male sex, preoperative SBP and DBP, and the number of antihypertensive medications were determinants of absent clinical success. Some predictors are also similar to ours as related to absent clinical success. The reproducibility of these data across multiple studies strongly supports their reliability.

Previous studies have found that the presence of essential hypertension affects the persistence of such hypertension after adrenalectomy [20, 28]. Metabolic abnormalities such as high BMI [29] and the presence of diabetes [3032] are strongly associated with progression of essential hypertension; as such, our findings that low BMI and the absence of diabetes are significant predictors of hypertension resolution are consistent with these notions. Female sex has proven to be relevant to hypertension resolution and improvement, although the underlying mechanism for this association remains unclear. Previous studies in vivo, including human clinical studies, showed that female sex hormones have a protective effect on salt-sensitive BP [33] as well as on cardiac [34, 35] and renal disease [36] outcomes. Other in vitro studies revealed that estrogens are potentially vasoprotective, because they suppress renin-angiotensin-aldosterone system activity [37, 38].

Our study has some limitations. This is a long-term retrospective cohort study, which could increase the risk of bias. The Japanese PA guideline was issued in 2009 and has not been revised until now; therefore, most of the study period was covered under the same guideline. Because advanced medical institutions tend to accept patients with intractable conditions, the rates of hypertension resolution and improvement might be underestimated in this study. Moreover, most participants in our study were Japanese, and our models were not validated for populations of other races. In addition, subtle difference of PA guideline between in Japan and in the United States might potentially affect the results of this study. Hence, the quality of our model should be additionally validated in future studies.

In contrast, our prediction models had a number of advantages. They were developed on the basis of a larger patient database than in past studies of this kind. Moreover, our prediction models are practical because they are based on easily obtained clinical variables. As such, they have the potential to help patients diagnosed with unilateral PA with their decision-making regarding surgical intervention and pursuing their optimal treatment options.

Acknowledgments

We thank the following JPAS investigators for collecting the clinical data: Shozo Miyauchi (Department of Internal Medicine, Uwajima City Hospital, Uwajima, Japan), Kohei Kamemura (Department of Cardiology, Akashi Medical Center, Akashi, Japan), Tomikazu Fukuoka (Department of Internal Medicine, Matsuyama Red Cross Hospital, Matsuyama, Japan), Koichi Yamamoto (Department of Geriatric and General Medicine, Osaka University Graduate School of Medicine, Osaka, Japan), Michio Otsuki (Department of Metabolic Medicine, Osaka University Graduate School of Medicine, Osaka, Japan), Yuichi Fujii (Department of Cardiology, JR Hiroshima Hospital, Hiroshima, Japan), Atsushi Ogo (Clinical Research Institute, National Hospital Organization Kyusyu Medical Center, Fukuoka, Japan), Shintaro Okamura (Department of Endocrinology, Tenriyorozu Hospital, Tenri, Nara, Japan), Toshihiko Yanase (Department of Endocrinology and Diabetes Mellitus, Faculty of Medicine, Fukuoka University, Fukuoka, Japan), Shoichiro Izawa (Department of Endocrinology and Metabolism, Tottori University Hospital, Tottori, Japan), Chiba Yoshiro (Endovascular Treatment Group, Mito Saiseikai General Hospital, Mito, Japan), Yuichiro Yoshikawa (Department of Endocrinology and Diabetes Mellitus, Misato Kenwa Hospital, Misato, Japan), Shigeatsu Hashimoto (Division of Nephrology, Hypertension, Endocrinology, and Diabetology/ Metabolism, Fukushima Medical University Hospital, Fukushima, Japan), Masanobu Yamada (Department of Medicine and Molecular Science, Gunma University Graduate School of Medicine, Maebashi, Japan), Tatsuya Kai (Department of Cardiology, Saiseikai Tondabayashi Hospital, Tondabayashi, Japan), and Ryuichi Sakamoto (Department of Diabetes and Endocrinology, Saiseikai Fukuoka General Hospital, Fukuoka, Japan).

Financial Support: This study was conducted as a part of the JPAS and JRAS by a Research Grant from the Japan Agency for Medical Research and Development(AMED) under Grant Number JP17ek0109122 and JP19ek0109352, and the National Center for Global Health and Medicine, Japan (27-1402, 30-1008). This work was partly supported by a grant from the Ministry of Health, Labour and Welfare, Japan (Nanbyo-Ippan-046).

Additional Information

Disclosure Summary: The authors have nothing to disclose.

Glossary

Abbreviations:

APA

aldosterone-producing adenoma

AVS

adrenal vein sampling

BMI

body mass index

BP

blood pressure

DBP

diastolic blood pressure

eGFR

estimated glomerular filtration rate

JPAS

Japan Primary Aldosteronism Study

LR

lateralized ratio

PA

primary aldosteronism

PAC

plasma aldosterone concentration

PASO

Primary Aldosteronism Surgical Outcome

ROC

receiver operating characteristic

SBP

systolic blood pressure

References and Notes

  • 1. Rossi GP, Bernini G, Caliumi C, Desideri G, Fabris B, Ferri C, Ganzaroli C, Giacchetti G, Letizia C, Maccario M, Mallamaci F, Mannelli M, Mattarello MJ, Moretti A, Palumbo G, Parenti G, Porteri E, Semplicini A, Rizzoni D, Rossi E, Boscaro M, Pessina AC, Mantero F; PAPY Study Investigators. A prospective study of the prevalence of primary aldosteronism in 1,125 hypertensive patients. J Am Coll Cardiol. 2006;48(11):2293–2300. [DOI] [PubMed] [Google Scholar]
  • 2. Young WF. Primary aldosteronism: renaissance of a syndrome. Clin Endocrinol (Oxf). 2007;66(5):607–618. [DOI] [PubMed] [Google Scholar]
  • 3. Käyser SC, Dekkers T, Groenewoud HJ, van der Wilt GJ, Carel Bakx J, van der Wel MC, Hermus AR, Lenders JW, Deinum J. Study heterogeneity and estimation of prevalence of primary aldosteronism: a systematic review and meta-regression analysis. J Clin Endocrinol Metab. 2016;101(7):2826–2835. [DOI] [PubMed] [Google Scholar]
  • 4. Fogari R, Preti P, Zoppi A, Rinaldi A, Fogari E, Mugellini A. Prevalence of primary aldosteronism among unselected hypertensive patients: a prospective study based on the use of an aldosterone/renin ratio above 25 as a screening test. Hypertens Res. 2007;30(2):111–117. [DOI] [PubMed] [Google Scholar]
  • 5. Douma S, Petidis K, Doumas M, Papaefthimiou P, Triantafyllou A, Kartali N, Papadopoulos N, Vogiatzis K, Zamboulis C. Prevalence of primary hyperaldosteronism in resistant hypertension: a retrospective observational study. Lancet. 2008;371(9628):1921–1926. [DOI] [PubMed] [Google Scholar]
  • 6. Shibayama Y, Wada N, Naruse M, Kurihara I, Ito H, Yoneda T, Takeda Y, Umakoshi H, Tsuiki M, Ichijo T, Fukuda H, Katabami T, Yoshimoto T, Ogawa Y, Kawashima J, Ohno Y, Sone M, Fujita M, Takahashi K, Shibata H, Kamemura K, Fujii Y, Yamamoto K, Suzuki T. The occurrence of apparent bilateral aldosterone suppression in adrenal vein sampling for primary aldosteronism. J Endocr Soc. 2018;2(5):398–407. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 7. Umakoshi H, Tsuiki M, Takeda Y, Kurihara I, Itoh H, Katabami T, Ichijo T, Wada N, Yoshimoto T, Ogawa Y, Kawashima J, Sone M, Inagaki N, Takahashi K, Watanabe M, Matsuda Y, Kobayashi H, Shibata H, Kamemura K, Otsuki M, Fujii Y, Yamamto K, Ogo A, Yanase T, Suzuki T, Naruse M; JPAS Study Group. Significance of computed tomography and serum potassium in predicting subtype diagnosis of primary aldosteronism. J Clin Endocrinol Metab. 2018;103(3):900–908. [DOI] [PubMed] [Google Scholar]
  • 8. Umakoshi H, Ogasawara T, Takeda Y, Kurihara I, Itoh H, Katabami T, Ichijo T, Wada N, Shibayama Y, Yoshimoto T, Ogawa Y, Kawashima J, Sone M, Inagaki N, Takahashi K, Watanabe M, Matsuda Y, Kobayashi H, Shibata H, Kamemura K, Otsuki M, Fujii Y, Yamamto K, Ogo A, Yanase T, Okamura S, Miyauchi S, Suzuki T, Tsuiki M, Naruse M. Accuracy of adrenal computed tomography in predicting the unilateral subtype in young patients with hypokalaemia and elevation of aldosterone in primary aldosteronism. Clin Endocrinol (Oxf). 2018;88(5):645–651. [DOI] [PubMed] [Google Scholar]
  • 9. Ohno Y, Sone M, Inagaki N, Yamasaki T, Ogawa O, Takeda Y, Kurihara I, Itoh H, Umakoshi H, Tsuiki M, Ichijo T, Katabami T, Tanaka Y, Wada N, Shibayama Y, Yoshimoto T, Ogawa Y, Kawashima J, Takahashi K, Fujita M, Watanabe M, Matsuda Y, Kobayashi H, Shibata H, Kamemura K, Otsuki M, Fujii Y, Yamamoto K, Ogo A, Okamura S, Miyauchi S, Fukuoka T, Izawa S, Yoneda T, Hashimoto S, Yanase T, Suzuki T, Kawamura T, Tabara Y, Matsuda F, Naruse M; Nagahama Study; JPAS Study Group. Prevalence of cardiovascular disease and its risk factors in primary aldosteronism: a multicenter study in Japan. Hypertension. 2018;71(3):530–537. [DOI] [PubMed] [Google Scholar]
  • 10. Kobayashi H, Abe M, Soma M, Takeda Y, Kurihara I, Itoh H, Umakoshi H, Tsuiki M, Katabami T, Ichijo T, Wada N, Yoshimoto T, Ogawa Y, Kawashima J, Sone M, Inagaki N, Takahashi K, Watanabe M, Matsuda Y, Shibata H, Kamemura K, Yanase T, Otsuki M, Fujii Y, Yamamoto K, Ogo A, Nanba K, Tanabe A, Suzuki T, Naruse M; JPAS Study Group. Development and validation of subtype prediction scores for the workup of primary aldosteronism. J Hypertens. 2018;36(11):2269–2276. [DOI] [PubMed] [Google Scholar]
  • 11. Ohno Y, Sone M, Inagaki N, Yamasaki T, Ogawa O, Takeda Y, Kurihara I, Umakoshi H, Ichijo T, Katabami T, Wada N, Ogawa Y, Yoshimoto T, Kawashima J, Watanabe M, Matsuda Y, Kobayashi H, Shibata H, Miyauchi S, Kamemura K, Fukuoka T, Yamamoto K, Otsuki M, Suzuki T, Naruse M; JPAS Study Group. Obesity as a key factor underlying idiopathic hyperaldosteronism. J Clin Endocrinol Metab. 2018;103(12):4456–4464. [DOI] [PubMed] [Google Scholar]
  • 12. Takeda M, Yamamoto K, Akasaka H, Rakugi H, Naruse M, Takeda Y, Kurihara I, Itoh H, Umakoshi H, Tsuiki M, Ichijo T, Katabami T, Wada N, Shibayama Y, Yoshimoto T, Ogawa Y, Kawashima J, Sone M, Inagaki N, Takahashi K, Fujita M, Watanabe M, Matsuda Y, Kobayashi H, Shibata H, Kamemura K, Otsuki M, Fujii Y, Ogo A, Okamura S, Miyauchi S, Yanase T, Suzuki T, Kawamura T; JPAS Study Group. Clinical characteristics and postoperative outcomes of primary aldosteronism in the elderly. J Clin Endocrinol Metab. 2018;103(10):3620–3629. [DOI] [PubMed] [Google Scholar]
  • 13. Umakoshi H, Tsuiki M, Yokomoto-Umakoshi M, Takeda Y, Takashi Y, Kurihara I, Itoh H, Katabami T, Ichijo T, Wada N, Shibayama Y, Yoshimoto T, Ashida K, Ogawa Y, Kawashima J, Sone M, Inagaki N, Takahashi K, Watanabe M, Matsuda Y, Kobayashi H, Shibata H, Kamemura K, Otsuki M, Fujii Y, Yamamto K, Ogo A, Okamura S, Miyauchi S, Fukuoka T, Izawa S, Yanase T, Hashimoto S, Yamada M, Yoshikawa Y, Kai T, Suzuki T, Kawamura T, Naruse M. Correlation between lateralization index of adrenal venous sampling and standardized outcome in primary aldosteronism. J Endocr Soc. 2018;2(8):893–902. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 14. Lin YC, Lee HY, Juang GD, Yeh CH, Cheng YH, Chuo KY, Chen HE, Tsai TF, Hwang TI. Technical modification of retroperitoneal laparoscopic adrenalectomy for primary hyperaldosteronism and clinical outcomes. Asian J Surg. 2013;36(1):20–25. [DOI] [PubMed] [Google Scholar]
  • 15. Waldmann J, Maurer L, Holler J, Kann PH, Ramaswamy A, Bartsch DK, Langer P. Outcome of surgery for primary hyperaldosteronism. World J Surg. 2011;35(11):2422–2427. [DOI] [PubMed] [Google Scholar]
  • 16. Steichen O, Zinzindohoué F, Plouin PF, Amar L. Outcomes of adrenalectomy in patients with unilateral primary aldosteronism: a review. Horm Metab Res. 2012;44(3):221–227. [DOI] [PubMed] [Google Scholar]
  • 17. Rossi GP, Bolognesi M, Rizzoni D, Seccia TM, Piva A, Porteri E, Tiberio GA, Giulini SM, Agabiti-Rosei E, Pessina AC. Vascular remodeling and duration of hypertension predict outcome of adrenalectomy in primary aldosteronism patients. Hypertension. 2008;51(5):1366–1371. [DOI] [PubMed] [Google Scholar]
  • 18. Benham JL, Eldoma M, Khokhar B, Roberts DJ, Rabi DM, Kline GA. Proportion of patients with hypertension resolution following adrenalectomy for primary aldosteronism: a systematic review and meta-analysis. J Clin Hypertens (Greenwich). 2016;18(12):1205–1212. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Williams TA, Lenders JWM, Mulatero P, Burrello J, Rottenkolber M, Adolf C, Satoh F, Amar L, Quinkler M, Deinum J, Beuschlein F, Kitamoto KK, Pham U, Morimoto R, Umakoshi H, Prejbisz A, Kocjan T, Naruse M, Stowasser M, Nishikawa T, Young WF Jr, Gomez-Sanchez CE, Funder JW, Reincke M; Primary Aldosteronism Surgery Outcome (PASO) investigators. Outcomes after adrenalectomy for unilateral primary aldosteronism: an international consensus on outcome measures and analysis of remission rates in an international cohort. Lancet Diabetes Endocrinol. 2017;5(9):689–699. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 20. Zarnegar R, Young WF Jr, Lee J, Sweet MP, Kebebew E, Farley DR, Thompson GB, Grant CS, Clark OH, Duh QY. The aldosteronoma resolution score: predicting complete resolution of hypertension after adrenalectomy for aldosteronoma. Ann Surg. 2008;247(3):511–518. [DOI] [PubMed] [Google Scholar]
  • 21. Utsumi T, Kawamura K, Imamoto T, Kamiya N, Komiya A, Suzuki S, Nagano H, Tanaka T, Nihei N, Naya Y, Suzuki H, Tatsuno I, Ichikawa T. High predictive accuracy of Aldosteronoma Resolution Score in Japanese patients with aldosterone-producing adenoma. Surgery. 2012;151(3):437–443. [DOI] [PubMed] [Google Scholar]
  • 22. Namekawa T, Utsumi T, Tanaka T, Kaga M, Nagano H, Kono T, Kawamura K, Kamiya N, Imamoto T, Suzuki H, Ichikawa T. Hypertension cure following laparoscopic adrenalectomy for hyperaldosteronism is not universal: trends over two decades. World J Surg. 2017;41(4):986–990. [DOI] [PubMed] [Google Scholar]
  • 23. Utsumi T, Kamiya N, Endo T, Yano M, Kamijima S, Kawamura K, Imamoto T, Naya Y, Ichikawa T, Suzuki H. Development of a novel nomogram to predict hypertension cure after laparoscopic adrenalectomy in patients with primary aldosteronism. World J Surg. 2014;38(10):2640–2644. [DOI] [PubMed] [Google Scholar]
  • 24. Nishikawa T, Omura M, Satoh F, Shibata H, Takahashi K, Tamura N, Tanabe A; Task Force Committee on Primary Aldosteronism, The Japan Endocrine Society. Guidelines for the diagnosis and treatment of primary aldosteronism--the Japan Endocrine Society 2009. Endocr J. 2011;58(9):711–721. [DOI] [PubMed] [Google Scholar]
  • 25. Shimamoto K, Ando K, Fujita T, Hasebe N, Higaki J, Horiuchi M, Imai Y, Imaizumi T, Ishimitsu T, Ito M, Ito S, Itoh H, Iwao H, Kai H, Kario K, Kashihara N, Kawano Y, Kim-Mitsuyama S, Kimura G, Kohara K, Komuro I, Kumagai H, Matsuura H, Miura K, Morishita R, Naruse M, Node K, Ohya Y, Rakugi H, Saito I, Saitoh S, Shimada K, Shimosawa T, Suzuki H, Tamura K, Tanahashi N, Tsuchihashi T, Uchiyama M, Ueda S, Umemura S; Japanese Society of Hypertension Committee for Guidelines for the Management of Hypertension. The Japanese Society of Hypertension Guidelines for the Management of Hypertension (JSH 2014). Hypertens Res. 2014;37(4):253–390. [DOI] [PubMed] [Google Scholar]
  • 26. Umakoshi H, Wada N, Ichijo T, Kamemura K, Matsuda Y, Fuji Y, Kai T, Fukuoka T, Sakamoto R, Ogo A, Suzuki T, Tsuiki M, Naruse M; WAVES-J Study Group. Optimum position of left adrenal vein sampling for subtype diagnosis in primary aldosteronism. Clin Endocrinol (Oxf). 2015;83(6):768–773. [DOI] [PubMed] [Google Scholar]
  • 27. Young WF, Stanson AW, Thompson GB, Grant CS, Farley DR, van Heerden JA. Role for adrenal venous sampling in primary aldosteronism. Surgery. 2004;136(6):1227–1235. [DOI] [PubMed] [Google Scholar]
  • 28. Giacchetti G, Ronconi V, Rilli S, Guerrieri M, Turchi F, Boscaro M. Small tumor size as favorable prognostic factor after adrenalectomy in Conn’s adenoma. Eur J Endocrinol. 2009;160(4):639–646. [DOI] [PubMed] [Google Scholar]
  • 29. Willett WC, Dietz WH, Colditz GA. Guidelines for healthy weight. N Engl J Med. 1999;341(6):427–434. [DOI] [PubMed] [Google Scholar]
  • 30. Epstein M, Sowers JR. Diabetes mellitus and hypertension. Hypertension. 1992;19(5):403–418. [DOI] [PubMed] [Google Scholar]
  • 31. Nosadini R, Sambataro M, Thomaseth K, Pacini G, Cipollina MR, Brocco E, Solini A, Carraro A, Velussi M, Frigato F, Crepaldi G. Role of hyperglycemia and insulin resistance in determining sodium retention in non-insulin-dependent diabetes. Kidney Int. 1993;44(1):139–146. [DOI] [PubMed] [Google Scholar]
  • 32. Cruickshank K, Riste L, Anderson SG, Wright JS, Dunn G, Gosling RG. Aortic pulse-wave velocity and its relationship to mortality in diabetes and glucose intolerance: an integrated index of vascular function? Circulation. 2002;106(16):2085–2090. [DOI] [PubMed] [Google Scholar]
  • 33. Manosroi W, Tan JW, Rariy CM, Sun B, Goodarzi MO, Saxena AR, Williams JS, Pojoga LH, Lasky-Su J, Cui J, Guo X, Taylor KD, Chen YI, Xiang AH, Hsueh WA, Raffel LJ, Buchanan TA, Rotter JI, Williams GH, Seely EW. The association of estrogen receptor-β gene variation with salt-sensitive blood pressure. J Clin Endocrinol Metab. 2017;102(11):4124–4135. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 34. Mihailidou AS, Ashton AW. Cardiac effects of aldosterone: does gender matter? Steroids. 2014;91:32–37. [DOI] [PubMed] [Google Scholar]
  • 35. dos Santos RL, da Silva FB, Ribeiro RF Jr, Stefanon I. Sex hormones in the cardiovascular system. Horm Mol Biol Clin Investig. 2014;18(2):89–103. [DOI] [PubMed] [Google Scholar]
  • 36. Komukai K, Mochizuki S, Yoshimura M. Gender and the renin-angiotensin-aldosterone system. Fundam Clin Pharmacol. 2010;24(6):687–698. [DOI] [PubMed] [Google Scholar]
  • 37. Barrett Mueller K, Lu Q, Mohammad NN, Luu V, McCurley A, Williams GH, Adler GK, Karas RH, Jaffe IZ. Estrogen receptor inhibits mineralocorticoid receptor transcriptional regulatory function. Endocrinology. 2014;155(11):4461–4472. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Nickenig G, Bäumer AT, Grohè C, Kahlert S, Strehlow K, Rosenkranz S, Stäblein A, Beckers F, Smits JF, Daemen MJ, Vetter H, Böhm M. Estrogen modulates AT1 receptor gene expression in vitro and in vivo. Circulation. 1998;97(22):2197–2201. [DOI] [PubMed] [Google Scholar]

Articles from Journal of the Endocrine Society are provided here courtesy of The Endocrine Society

RESOURCES