Abstract
Background and aims
Primary aldosteronism (PA) due to unilateral aldosterone-producing adenoma (APA) is preferentially treated by unilateral adrenalectomy (ADX), but little is known about the changes in lipid and glucose metabolism that may occur after ADX.
Methods
We studied 19 non-diabetic patients who did not use lipid-lowering drugs with PA due to APA before and 6 months after unilateral ADX. Fasting plasma lipids, lipoprotein subfractions, branched-chain amino acids (BCAA), and GlycA, a pro-inflammatory glycoprotein biomarker, were measured by nuclear magnetic resonance (NMR) spectroscopy. The Lipoprotein Insulin Resistance (LP-IR) score, which is based on six lipoprotein variables, was calculated.
Results
In all patients, hyperaldosteronism was resolved after ADX. Body mass index and fasting plasma glucose were unchanged, but HbA1c increased (p = 0.002). Plasma triglycerides, large triglyceride-rich lipoprotein (TRL) cholesterol, and large TRL particles were increased (p < 0.01), resulting in an increase in TRL size (p = 0.027). High-density lipoprotein size was decreased (p = 0.015). LP-IR scores (p = 0.001) and total BCAA (p = 0.017) were increased, but GlycA remained unaltered.
Conclusions
Based on increases in LP-IR scores and BCAA, which each have been shown to predict new onset type 2 diabetes mellitus independent of conventional risk factors in the general population, this preliminary study suggests that diabetes risk is not improved but may even be increased after ADX for APA despite remission of PA.
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Introduction
Primary aldosteronism (PA) is a well-recognized and rather frequent cause of secondary hypertension with deleterious effects on cardiometabolic health including high prevalence of Type 2 diabetes mellitus (T2D) [1,2,3,4,5]. Besides pro-inflammatory effects of aldosterone [6, 7], PA is likely to be associated with yet incompletely understood abnormalities in lipid and glucose metabolism [5, 8]. The majority of PA cases are due to either unilateral aldosterone-producing adenoma (APA) or bilateral adrenal hyperplasia (BAH) [9]. Laparoscopic adrenalectomy (ADX) is the preferred treatment modality for APA, and this procedure may result in relief of hyperaldosteronism in more than 90% of cases [9]. Clearly, this procedure offers the possibility to study abnormalities in lipid and glucose metabolism as part of routine follow-up of such patients.
Remarkably, three recent studies have suggested that the plasma lipoprotein profile may be worsened 1 year after unilateral ADX for PA [10,11,12]. In particular, an unexpected increase in plasma triglycerides (TG) was observed in all these studies [10,11,12]. In one of these studies, there was a small decrease in fasting plasma glucose (FPG), without a change in the classification of patients with impaired glucose tolerance or T2D mellitus [11]. Moreover, in a small group of APA patients, the first phase insulin response to intravenous glucose was diminished before treatment and increased after unilateral ADX [12]. On the other hand, we observed a small increase in glycated hemoglobin (HbA1c) after unilateral ADX [5], although insulin sensitivity, determined by the hyperinsulinemic-euglycemic clamp technique, did not significantly change after surgery [12].
During the past few years, nuclear magnetic resonance (NMR)-based techniques have been developed that allow for the high-throughput quantification of lipoprotein subfractions, glycosylated proteins, and metabolites such as branched-chain amino acids (BCAA) [13,14,15]. Using NMR, we observed lipoprotein abnormalities, including lower apolipoprotein B (apoB) and triglyceride-rich lipoprotein (TRL) concentrations in untreated PA patients together with higher levels of GlycA, a measure of inflammatory glycoproteins [7]. With this NMR method, the Lipoprotein Insulin Resistance (LP-IR) score has been developed, which is based on six NMR-based lipoprotein variables [15]. LP-IR scores are closely related to glucose disposal measured with the hyperinsulinemic-euglycemic clamp technique and are strongly correlated with homeostasis model assessment of insulin resistance (HOMA-IR) [15, 16]. Both the LP-IR and the plasma total BCAA concentration have been found to predict incident T2D in several population studies [16,17,18,19,20].
In the absence of data concerning effects of PA treatment on NMR-derived biomarkers, the present study was initiated to test the effects of unilateral ADX in APA patients on plasma lipoprotein subfractions, LP-IR, BCAA, and GlycA.
Materials and methods
Study population
The diagnostic work-up of the study participants was performed in accordance with the Endocrine Society Practice Guidelines [21]. Patients suspected for PA were screened using aldosterone-to-renin ratio (ARR; cut-off 12.0 ng/mU, sitting position). If elevated, antihypertensive medication was stopped for at least 1 week (e.g., angiotensin-converting enzyme inhibitors, beta blockers, calcium antagonists, and low-dose thiazides) and 4 weeks (e.g., mineralocorticoid antagonists) whenever possible, otherwise patients received drugs with minimal effect on the ARR, such as alpha-receptor (doxazosin) or calcium-channel blockers (verapamil). Thereafter all subjects were retested again. If ARR remained abnormal, confirmatory testing (e.g., sodium loading test, captopril challenge test) was performed. In case of confirmed diagnosis of PA, adrenal vein sampling was used for subtype differentiation between unilateral and bilateral disease. Abstaining from ACTH infusion, selectivity of the catheter was assumed if the cortisol concentration (using rapid intra-procedure cortisol measurement) within the adrenal vein was at least two times higher than that in the simultaneously drawn peripheral sample. The diagnosis of unilateral disease was made if the aldosterone-to-cortisol ratio (A/C-ratio) of one adrenal vein was at least four times higher than the A/C-ratio of the contralateral side [22, 23].
For the present analysis we selected 19 patients from the Munich center of the German Conn’s Registry–Else Kröner-Fresenius Hyperaldosteronism registry fulfilling the following criteria: (1) confirmed unilateral PA treated by ADX; (2) no evidence of postoperative adrenal insufficiency at 6-month follow-up according to ACTH stimulation testing; and (3) no evidence of T2D at baseline (defined as a FPG ≥ 126 mg/dl, a HbA1c value ≥6.5% (≥48 mmol/mol) or use of glucose lowering drugs) or other relevant metabolic disorders or treatment with lipid-lowering drugs. All patients were studied after an overnight fast and were re-evaluated 6 months after surgical treatment in a standardized fashion.
Blood samples were taken between 8:00 and 10:00 A.M. On each occasion, the evaluation included the collection of anthropometric data and clinical characteristics such as duration of hypertension and current medication. Blood pressure was obtained in the sitting position after at least 15 min of rest in our outpatient clinic. 24-h ambulatory blood pressure measurements were also performed before and after PA treatment. HOMA-IR was calculated as follows: (insulin fasting [μU/ml] × FPG [mg/dl])/405.
All patients gave written informed consent and the ethics committees of the University of Munich approved the protocol.
Laboratory methods
Laboratory work-up was performed immediately after the withdrawal of blood samples, in a fasting state in sitting position. Plasma aldosterone concentration and active renin concentration were measured using the Liaison chemiluminescence assay (Diasorin) and routine parameters using standard methods in our central laboratory [11]. Creatinine, glucose, and HbA1c were measured using routine methods [11]. Estimated glomerular filtration rate (eGFR) was calculated using the Modification of Diet in Renal Disease formula. Blood samples for NMR analysis were prepared by centrifugation at 1400 × g for 15 min, stored at −80 °C and sent frozen to LabCorp, Morrisville, NC, USA. NMR spectra were acquired on Vantera® Clinical Analyzers from ethylene diamine tetra acetic acid plasma samples at LabCorp as described in [16]. The NMR MetaboProfile analysis, which reports concentrations of lipids, apolipoproteins, lipoprotein particles and sizes, and BCAA, was performed using a recently developed deconvolution algorithm [15, 16]. Linear regression of the lipoprotein subclass signal areas against serum lipid and chemically measured apolipoprotein levels in a large study population provided the conversion factors to generate concentrations of total cholesterol (TC), TG, low-density lipoprotein cholesterol (LDL-C) and high-density lipoprotein cholesterol (HDL-C), apoB and apolipoprotein A-I. The inter-assay precision for these parameters ranges from 1.4 to 6.2%. The diameters for the lipoprotein classes reported by the LP4 algorithm are TRL particles (TRL-P) (24–240 nm) (subdivided into very large, large, medium, small and very small TRL-P), LDL particles (LDL-P) (19–23 nm) (subdivided into large, medium and small LDL-P), and HDL particles (HDL-P) (7.4–12.0 nm) (subdivided into large, medium and small HDL-P). Inter-assay precision for TRL-P, LDL-P, and HDL-P are 6.4%, 1.5%, and 2.4%, respectively. Mean TRL, LDL, and HDL particle sizes are weighted averages derived from the sum of the diameter of each subclass multiplied by its relative mass percentage. The LP-IR score was calculated using six NMR-measured lipoprotein variables: weighted average sizes of TRL, LDL, and HDL, combined with concentrations of large TRL-P, small LDL-P and large HDL-P [15]. LP-IR scores vary between 0 and 100; the higher the score the more insulin resistant the individual [15, 16]. Details for the quantification of the BCAA have been reported previously [19]. The inter-assay precisions are 3.1% for valine, 5.9% for leucine 14.1% for isoleucine, and 3.2% for total BCAA. The GlycA signal was quantified as described in [24, 25]. The GlycA NMR signal originates from highly mobile protons of N-acetylglucosamine residues located on the carbohydrate side-chains of circulating acute phase proteins (e.g., α1-acid glycoprotein, haptoglobin, α1-antitrypsin, α1-antichymotrypsin, and transferrin). The signals from these N-acetylglucosamine residues were used to calculate the concentrations of GlycA (µmol/L). The intra-assay and inter-assay precisions for GlycA are 1.9% and 2.6%, respectively.
Statistical analysis
Data analysis was performed using IBM SPSS software (version 25.0, SPSS Inc., USA). Results are given in median and 25th and 75th percentile if not mentioned otherwise. body mass index (BMI) was calculated as weight in kilograms divided by the square of the height in meters. Comparisons in variables before and after ADX were performed using Wilcoxon singed-rank test tests for paired observations. Spearman’s Rank Order test was used to determine the relationships between variables. Two-sided p values < 0.05 were considered to be statistically significant.
Results
Ten men and nine women participated (median age 46 years). All had at baseline high aldosterone levels and elevated blood pressure, as expected. Adrenal-venous sampling pointed to unilateral disease in all of them, with a right sided APA in ten and a left sided APA in nine patients. Imaging techniques confirmed the lateralization results in 10 of 19 cases. There was only one patient with contralateral mass as well as eight patients without any adrenal mass detected by imaging. Adrenal mass size was in median 10 mm and ranged from 2 to 22 mm.
Parameters of renal function as well as FPG and other parameters of glucose metabolism were within normal ranges (Table 1). With a median BMI of 25.6 kg/m2 patients were slightly overweight (Table 1). Six patients had a history of nicotine use whereas three of them were current smokers. Twelve patients consumed moderate amounts of alcohol while seven patients were abstainers.
Six months after unilateral ADX, aldosterone and renin levels were normalized (Table 1). Outpatient clinic systolic and diastolic blood pressure did not change significantly, but defined daily doses of antihypertensives as well as ambulatory 24-h systolic and diastolic blood pressure had reduced significantly. Expectedly, eGFR was reduced, consequent to reduced renal plasma flow after PA treatment (Table 1). BMI and FPG remained unaltered but HbA1c increased slightly after ADX. Postoperative plasma insulin levels were not available. Plasma TC and LDL-C were unchanged, whereas apoB levels tended to increase. Plasma TG increased, coinciding with an increase in TRL cholesterol. This increase in TG was attributable to an increase in large TRL-P and resulted in an increase in TRL size (Table 2). Although HDL-C and HDL-P did not change, small HDL-P increased, resulting in a decrease in HDL size (Table 2). Consequent to these changes in TRL and HDL subfractions, LP-IR scores increased (Table 2). This increase in LP-IR tended to be correlated with the increase in HbA1c (r = 0.352, p = 0.14) and was significantly correlated with the decrease in eGFR (r = −0.466, p = 0.044). In addition, we observed a positive correlation of LP-IR scores with HOMA-IR at baseline (r = 0.543, p = 0.016).
Of further note, plasma total BCAA increased after ADX, mainly due to increases in valine and isoleucine. This increase in total BCAA was not significantly related to the decrease in eGFR (r = 0.144, p = 0.556) or the increase in LP-IR scores (r = 0.322, p = 0.178). Plasma GlycA did not change after ADX (Table 2).
Discussion
In this preliminary study, we present for the first time results of NMR-measured lipoprotein subfractions and other targeted metabolomics biomarkers before and after unilateral ADX for APA. First, the current study shows that plasma TG are increased after ADX consequent to a rise in large TRLs. As a result, TRL size increased, and these changes were accompanied by a shift in HDL particle distribution with an increase in small HDL-P and a decrease in HDL particle size. Consequently, the LP-IR score, an NMR-based measure of insulin resistance, increased. Of further note, we observed a hitherto unreported rise in total plasma BCAA after ADX. Given that the LP-IR scores [16,17,18] and BCAA concentrations [20] have been shown to predict incident diabetes in population-based cohort studies, our present findings suggest that the risk of future diabetes development is not ameliorated and could even be worsened in PA patients without T2D initially despite remission of hyperaldosteronism after unilateral ADX.
The current results regarding the increase in plasma TG after ADX agree with and expand on previous publications showing an increase in TG after PA treatment [10,11,12]. In comparison, HDL-C tended to decrease, irrespective of the presence of dyslipidemia before surgery in a Japanese study [10]. We documented a drop in HDL-C 1 year after unilateral ADX in our earlier German study [11]. In the latter report, similar lipoprotein changes were observed in patients with BAH after mineralocorticoid receptor antagonist (MRA) treatment [11]. A recent study from the German Conn registry also reported a decrease in HDL-C after unilateral ADX [5]. In the present study, HDL-C and HDL-P remained unchanged but HDL size was decreased coinciding with an increase in large TRLs, which is conceivably attributable at least in part to effects of TRLs on HDL metabolism via the cholesteryl ester transfer process [26]. We did not observe significant increases in LDL-C and LDL-P after ADX, but the trends observed were comparable with those in the Japanese study which showed an increase in LDL-C after PA treatment [10]. The mechanisms responsible for plasma TRL increments after ADX for PA are not completely understood. In the previous reports, the development of dyslipidemia and changes in TG and HDL-C were found to be dependent on (changes) eGFR after treatment [10, 11]. In line, we observed that changes in LP-IR scores were correlated with changes in eGFR. However, the decline in eGFR after ADX as observed in the current study was modest, amounting to about 5%, which makes a contribution of a decline in kidney function on plasma lipoprotein alterations uncertain. Moreover, HDL-C is inversely rather than directly correlated with eGFR in subjects without chronic kidney disease [27], questioning whether such a limited decline in kidney function may explain a decrease in HDL-C after ADX. Of further relevance, co-secretion of cortisol in PA and relative adrenal insufficiency may affect glucose and lipid metabolism after ADX [5]. Notably, in all the cases included in the present series, adrenal function had recovered 6 months after ADX. Finally, it should be appreciated that the present study was carried out along with routine clinical treatment for PA due to APA. As a consequence, antihypertensive treatment was extensively reduced after surgery. Hence, we cannot exclude that cessation of certain drugs like MRA or doxazosin could have influenced lipid metabolism [28,29,30]. Yet, we found that MRA in case of bilateral disease elicits comparable changes in TG and HDL-C compared with ADX for APA [11].
The LP-IR signature reflects the multifaceted aspects of insulin resistance on lipoprotein metabolism [18]. The LP-IR index is robustly correlated with HOMA-IR [16], a finding which was reinforced in APA patients. Despite its strong relationship with HOMA-IR [16, 17], LP-IR scores predicted incident T2D even when taking account of HOMA-IR [16, 17]. Notably, LP-IR improves diabetes risk classification beyond the Framingham Offspring risk score [16, 17], and it has been proposed that LP-IR may reflect early insulin resistant dyslipidemia before development of hyperglycemia [18]. Hence, it could be proposed that the higher LP-IR scores after ADX represents an early marker of elevated diabetes risk before a rise in FPG becomes evident. Accumulating evidence supports the idea that BCAA are important in the pathogenesis of dysglycemia [31]. BCAA may disrupt the function of the mammalian target of rapamycin complex 1, which subsequently leads to insulin resistance and oxidative stress [32, 33]. In view of the recent findings demonstrating that plasma BCAA predicts new onset T2D [19] we surmise that higher total BCAA could translate into increased diabetes risk after ADX. Taken together, we postulate that two, at least in part, independent pathways are operating that could pose patients with biochemical remission of PA at increased risk for diabetes development after ADX.
Finally, we did not observe that GlycA decreased after ADX. This result suggests that low-grade systemic inflammation is unaffected by ADX, and is unexpected in view of the recent results showing higher GlycA levels in untreated PA patients compared with healthy subjects and subjects with (un)treated hypertension [7].
The current study was conducted in a limited number of patients, we consider the present findings preliminary. Moreover, we did not follow adrenal incidentaloma patients without evidence of hormonal hypersecretion as a control group to determine variations in NMR-derived biomarkers over time. However, our prospective observations in a rather homogeneous group of PA patients whose hyperaldosteronism was remitted biochemically after ADX can be seen as a strength of the present study. Nonetheless, it is evident that longitudinal studies with prolonged follow-up in larger patient groups are required to determine whether the long-term risk of new onset T2D is indeed elevated in this patient category.
In conclusion, based on an increase in both the LP-IR index and BCAA, our current findings suggest that diabetes risk is not improved but may even be increased after ADX for APA despite remission of PA in patients without T2D initially.
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Acknowledgements
Lipoprotein, LP-IR, GlycA, and BCAA analyses were performed at LabCorp, Morrisville, NC, USA, at no cost.
Funding
This work was supported by the Else Kröner-Fresenius Stiftung in support of the German Conns Registry-Else-Kröner Hyperaldosteronism Registry (2013_A182 and 2015_A171 to MR), the European Research Council (ERC) under the European Union’s Horizon 2020 research and innovation program (grant agreement No 694913 to MR), by the Deutsche Forschungsgemeinschaft (DFG) (within the CRC/Transregio 205/1 “The Adrenal: Central Relay in Health and Disease” to CA and MR).
Author contributions
Conception and design of study: CA, AMAB, MR, and RPFD. Data collection and analysis: CA, MR, and MAC. Interpretation of data: CA, AMAB, MAC, MR, and RPFD. Drafting the manuscript: CA, AMAB, and RPFD. All authors have revised and approved the submitted manuscript.
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Adolf, C., Berends, A.M.A., Connelly, M.A. et al. Lipoprotein insulin resistance score and branched-chain amino acids increase after adrenalectomy for unilateral aldosterone-producing adenoma: a preliminary study. Endocrine 68, 420–426 (2020). https://doi.org/10.1007/s12020-020-02235-2
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DOI: https://doi.org/10.1007/s12020-020-02235-2