Diagnostic accuracy of adrenal imaging for subtype diagnosis in primary aldosteronism: systematic review and meta-analysis

Yaqiong Zhou, Dan Wang, Licheng Jiang, Fei Ran, Sichao Chen, Peng Zhou, Peijian Wang, Yaqiong Zhou, Dan Wang, Licheng Jiang, Fei Ran, Sichao Chen, Peng Zhou, Peijian Wang

Abstract

Objectives: Accurate subtype classification in primary aldosteronism (PA) is critical in assessing the optimal treatment options. This study aimed to evaluate the diagnostic accuracy of adrenal imaging for unilateral PA classification.

Methods: Systematic searches of PubMed, EMBASE and the Cochrane databases were performed from 1 January 2000 to 1 February 2020, for all studies that used CT or MRI in determining unilateral PA and validated the results against invasive adrenal vein sampling (AVS). Summary diagnostic accuracies were assessed using a bivariate random-effects model. Subgroup analyses, meta-regression and sensitivity analysis were performed to explore the possible sources of heterogeneity.

Result: A total of 25 studies, involving a total of 4669 subjects, were identified. The overall analysis revealed a pooled sensitivity of 68% (95% CI: 61% to 74%) and specificity of 57% (95% CI 50% to 65%) for CT/MRI in identifying unilateral PA. Sensitivity was higher in the contrast-enhanced (CT) group versus the traditional CT group (77% (95% CI 66% to 85%) vs 58% (95% CI 50% to 66%). Subgroup analysis stratified by screening test for PA showed that the sensitivity of the aldosterone-to-renin ratio (ARR) group was higher than that of the non-ARR group (78% (95% CI 69% to 84%) vs 66% (95% CI 58% to 72%)). The diagnostic accuracy of PA patients aged ≤40 years was reported in four studies, and the overall sensitivity was 71%, with 79% specificity. Meta-regression revealed a significant impact of sample size on sensitivity and of age and study quality on specificity.

Conclusion: CT/MRI is not a reliable alternative to invasive AVS without excellent sensitivity or specificity for correctly identifying unilateral PA. Even in young patients (≤40 years), 21% of patients would have undergone unnecessary adrenalectomy based on imaging results alone.

Keywords: cardiology; endocrine tumours; hypertension.

Conflict of interest statement

Competing interests: None declared.

© Author(s) (or their employer(s)) 2020. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ.

Figures

Figure 1
Figure 1
Flow diagram of the review process. AVS, adrenal vein sampling.
Figure 2
Figure 2
Assessment of methodological quality of included studies using the QUADAS-2 Criteria. Stacked bars represent the proportion of studies with a high (red), or unclear (yellow) or low (green) risk of bias and applicability concerns. QUADAS-2, Quality Assessment of Diagnostic Accuracy Studies-2 criteria.
Figure 3
Figure 3
Forest plots of sensitivity and specificity of adrenal imaging compared with AVS. Horizontal lines are the 95% CIs. AVS, adrenal vein sampling.
Figure 4
Figure 4
Hierarchical SROC plot showing average sensitivity and specificity estimate of the study results with 95% confidence region. The 95% prediction region represents the confidence region for a forecast of the true sensitivity (SENS) and specificity (SPEC) in a future study. AUC, area under the curve; SROC, summary receiver operating characteristic.

References

    1. Monticone S, Burrello J, Tizzani D, et al. . Prevalence and Clinical Manifestations of Primary Aldosteronism Encountered in Primary Care Practice. J Am Coll Cardiol 2017;69:1811–20. 10.1016/j.jacc.2017.01.052
    1. Catena C, Colussi G, Nadalini E, et al. . Cardiovascular outcomes in patients with primary aldosteronism after treatment. Arch Intern Med 2008;168:80–5. 10.1001/archinternmed.2007.33
    1. Pillai PR, Griffith M, Schwarcz MD, et al. . Primary aldosteronism: cardiovascular risk, diagnosis, and management. Cardiol Rev 2020;28:84–91. 10.1097/CRD.0000000000000281
    1. Hundemer GL, Curhan GC, Yozamp N, et al. . Cardiometabolic outcomes and mortality in medically treated primary aldosteronism: a retrospective cohort study. Lancet Diabetes Endocrinol 2018;6:51–9. 10.1016/S2213-8587(17)30367-4
    1. Funder JW. Primary aldosteronism: where are we now? Where to from here? Horm Metab Res 2020;52:459–66. 10.1055/a-1120-8623
    1. Williams TA, Reincke M. Management of endocrine disease: diagnosis and management of primary aldosteronism: the endocrine Society guideline 2016 revisited. Eur J Endocrinol 2018;179:R19–29. 10.1530/EJE-17-0990
    1. Byrd JB, Turcu AF, Auchus RJ. Primary aldosteronism: practical approach to diagnosis and management. Circulation 2018;138:823–35. 10.1161/CIRCULATIONAHA.118.033597
    1. Funder JW, Carey RM, Mantero F, et al. . The management of primary aldosteronism: case detection, diagnosis, and treatment: an endocrine Society clinical practice guideline. J Clin Endocrinol Metab 2016;101:1889–916. 10.1210/jc.2015-4061
    1. Ruco A, Dossa F, Tinmouth J, et al. . Social media and mobile health technology for cancer screening: a systematic review and meta-analysis protocol. BMJ Open 2020;10:e035411. 10.1136/bmjopen-2019-035411
    1. Kempers MJE, Lenders JWM, van Outheusden L, et al. . Systematic review: diagnostic procedures to differentiate unilateral from bilateral adrenal abnormality in primary aldosteronism. Ann Intern Med 2009;151:329–37. 10.7326/0003-4819-151-5-200909010-00007
    1. Liberati A, Altman DG, Tetzlaff J, et al. . The PRISMA statement for reporting systematic reviews and meta-analyses of studies that evaluate health care interventions: explanation and elaboration. Ann Intern Med 2009;151:W65–94. 10.7326/0003-4819-151-4-200908180-00136
    1. Whiting PF, Rutjes AWS, Westwood ME, et al. . QUADAS-2: a revised tool for the quality assessment of diagnostic accuracy studies. Ann Intern Med 2011;155:529–36. 10.7326/0003-4819-155-8-201110180-00009
    1. Devillé WL, Buntinx F, Bouter LM, et al. . Conducting systematic reviews of diagnostic studies: didactic guidelines. BMC Med Res Methodol 2002;2:9. 10.1186/1471-2288-2-9
    1. Reitsma JB, Glas AS, Rutjes AWS, et al. . Bivariate analysis of sensitivity and specificity produces informative summary measures in diagnostic reviews. J Clin Epidemiol 2005;58:982–90. 10.1016/j.jclinepi.2005.02.022
    1. Chu H, Guo H, Zhou Y. Bivariate random effects meta-analysis of diagnostic studies using generalized linear mixed models. Med Decis Making 2010;30:499–508. 10.1177/0272989X09353452
    1. Lijmer JG, Bossuyt PMM, Heisterkamp SH. Exploring sources of heterogeneity in systematic reviews of diagnostic tests. Stat Med 2002;21:1525–37. 10.1002/sim.1185
    1. Asmar M, Wachtel H, Yan Y, et al. . Reversing the established order: should adrenal venous sampling precede cross-sectional imaging in the evaluation of primary aldosteronism? J Surg Oncol 2015;112:144–8. 10.1002/jso.23963
    1. Pedersen M, Karlsen MA, Ankjærgaard KL, et al. . Primary hyperaldosteronism diagnosed with adrenal vein sampling. Characteristics and follow-up after adrenalectomy in a Danish study. Scand J Clin Lab Invest 2016;76:45–50. 10.3109/00365513.2015.1092047
    1. Campbell RA, Young DS, Shaver CN, et al. . Influence of adrenal venous sampling on management in patients with primary aldosteronism independent of lateralization on cross-sectional imaging. J Am Coll Surg 2019;229:116–24. 10.1016/j.jamcollsurg.2019.03.012
    1. Sam D, Kline GA, So B, et al. . Discordance between imaging and adrenal vein sampling in primary aldosteronism irrespective of interpretation criteria. J Clin Endocrinol Metab 2019;104:1900–6. 10.1210/jc.2018-02089
    1. Nandra G, Duxbury O, Patel P, et al. . Technical and interpretive pitfalls in adrenal imaging. Radiographics 2020;40:1041–60. 10.1148/rg.2020190080
    1. Deeks JJ, Macaskill P, Irwig L. The performance of tests of publication bias and other sample size effects in systematic reviews of diagnostic test accuracy was assessed. J Clin Epidemiol 2005;58:882–93. 10.1016/j.jclinepi.2005.01.016
    1. Magill SB, Raff H, Shaker JL, et al. . Comparison of adrenal vein sampling and computed tomography in the differentiation of primary aldosteronism. J Clin Endocrinol Metab 2001;86:1066–71. 10.1210/jc.86.3.1066
    1. Young WF, Stanson AW, Thompson GB, et al. . Role for adrenal venous sampling in primary aldosteronism. Surgery 2004;136:1227–35. 10.1016/j.surg.2004.06.051
    1. Nwariaku FE, Miller BS, Auchus R, et al. . Primary hyperaldosteronism: effect of adrenal vein sampling on surgical outcome. Arch Surg 2006;141:497–502. 10.1001/archsurg.141.5.497
    1. Minami I, Yoshimoto T, Hirono Y, et al. . Diagnostic accuracy of adrenal venous sampling in comparison with other parameters in primary aldosteronism. Endocr J 2008;55:839–46. 10.1507/endocrj.K07E-164
    1. Mulatero P, Bertello C, Rossato D, et al. . Roles of clinical criteria, computed tomography scan, and adrenal vein sampling in differential diagnosis of primary aldosteronism subtypes. J Clin Endocrinol Metab 2008;93:1366–71. 10.1210/jc.2007-2055
    1. Mathur A, Kemp CD, Dutta U, et al. . Consequences of adrenal venous sampling in primary hyperaldosteronism and predictors of unilateral adrenal disease. J Am Coll Surg 2010;211:384–90. 10.1016/j.jamcollsurg.2010.05.006
    1. Sarlon-Bartoli G, Michel N, Taieb D, et al. . Adrenal venous sampling is crucial before an adrenalectomy whatever the adrenal-nodule size on computed tomography. J Hypertens 2011;29:1196–202. 10.1097/HJH.0b013e32834666af
    1. Küpers EM, Amar L, Raynaud A, et al. . A clinical prediction score to diagnose unilateral primary aldosteronism. J Clin Endocrinol Metab 2012;97:3530–7. 10.1210/jc.2012-1917
    1. Oh EM, Lee KE, Yoon K, et al. . Value of adrenal venous sampling for lesion localization in primary aldosteronism. World J Surg 2012;36:2522–7. 10.1007/s00268-012-1695-9
    1. Lau JHG, Sze WCC, Reznek RH, et al. . A prospective evaluation of postural stimulation testing, computed tomography and adrenal vein sampling in the differential diagnosis of primary aldosteronism. Clin Endocrinol 2012;76:182–8. 10.1111/j.1365-2265.2011.04202.x
    1. Salem V, Hopkins TG, El-Gayar H, et al. . Adrenal venous sampling as a diagnostic procedure for primary hyperaldosteronism: experience from a tertiary referral centre. Hormones 2012;11:151–9. 10.14310/horm.2002.1342
    1. Burton TJ, Mackenzie IS, Balan K, et al. . Evaluation of the sensitivity and specificity of (11)C-metomidate positron emission tomography (PET)-CT for lateralizing aldosterone secretion by Conn's adenomas. J Clin Endocrinol Metab 2012;97:100–9. 10.1210/jc.2011-1537
    1. Riester A, Fischer E, Degenhart C, et al. . Age below 40 or a recently proposed clinical prediction score cannot bypass adrenal venous sampling in primary aldosteronism. J Clin Endocrinol Metab 2014;99:E1035–9. 10.1210/jc.2013-3789
    1. Sze WCC, Soh LM, Lau JH, et al. . Diagnosing unilateral primary aldosteronism - comparison of a clinical prediction score, computed tomography and adrenal venous sampling. Clin Endocrinol 2014;81:25–30. 10.1111/cen.12374
    1. Kocjan T, Janez A, Stankovic M, et al. . A new clinical prediction criterion accurately determines a subset of patients with bilateral primary aldosteronism before adrenal venous sampling. Endocr Pract 2016;22:587–94. 10.4158/EP15982.OR
    1. Zhu L, Zhang Y, Zhang H, et al. . Comparison between adrenal venous sampling and computed tomography in the diagnosis of primary aldosteronism and in the guidance of adrenalectomy. Medicine 2016;95:e4986. 10.1097/MD.0000000000004986
    1. Kamemura K, Wada N, Ichijo T, et al. . Significance of adrenal computed tomography in predicting laterality and indicating adrenal vein sampling in primary aldosteronism. J Hum Hypertens 2017;31:195–9. 10.1038/jhh.2016.61
    1. Nanba AT, Nanba K, Byrd JB, et al. . Discordance between imaging and immunohistochemistry in unilateral primary aldosteronism. Clin Endocrinol 2017;87:665–72. 10.1111/cen.13442
    1. Umakoshi H, Tsuiki M, Takeda Y, et al. . Significance of computed tomography and serum potassium in predicting subtype diagnosis of primary aldosteronism. J Clin Endocrinol Metab 2018;103:900–8. 10.1210/jc.2017-01774
    1. Aono D, Kometani M, Karashima S, et al. . Primary aldosteronism subtype discordance between computed tomography and adrenal venous sampling. Hypertens Res 2019;42:1942–50. 10.1038/s41440-019-0310-y
    1. Li S, Ren Y, Zhu Y, et al. . The potential clinical application of a lower bilateral adrenal limb width ratio (L/RW) in patients with bilateral primary hyperaldosteronism. Endocr Pract 2019;25:830–5. 10.4158/EP-2019-0009
    1. Laurent I, Astère M, Zheng F, et al. . Adrenal venous sampling with or without adrenocorticotropic hormone stimulation: a meta-analysis. J Clin Endocrinol Metab 2019;104:1060–8. 10.1210/jc.2018-01324
    1. Zeiger MA, Thompson GB, Duh Q-Y, et al. . The American association of clinical endocrinologists and American association of endocrine surgeons medical guidelines for the management of adrenal incidentalomas. Endocr Pract 2009;15(Suppl 1):1–20. 10.4158/EP.15.S1.1
    1. Taguchi R, Yamada M, Nakajima Y, et al. . Expression and mutations of KCNJ5 mRNA in Japanese patients with aldosterone-producing adenomas. J Clin Endocrinol Metab 2012;97:1311–9. 10.1210/jc.2011-2885
    1. Wang B, Li X, Zhang X, et al. . Prevalence and characterization of somatic mutations in Chinese aldosterone-producing adenoma patients. Medicine 2015;94:e708. 10.1097/MD.0000000000000708
    1. Satoh F, Morimoto R, Ono Y, et al. . Measurement of peripheral plasma 18-oxocortisol can discriminate unilateral adenoma from bilateral diseases in patients with primary aldosteronism. Hypertension 2015;65:1096–102. 10.1161/HYPERTENSIONAHA.114.04453

Source: PubMed

3
Subskrybuj