| Literature DB >> 34059026 |
Fang Sun1, Yangning Hong1, Hexuan Zhang1, Xiaoli Liu1, Zhigang Zhao1, Hongbo He1, Zhencheng Yan1, Zhiming Zhu2.
Abstract
BACKGROUND: Primary aldosteronism (PA) is highly prevalent in hypertensive population. Adrenal vein sampling (AVS) is the only procedure to assess adrenal aldosterone hypersecretion in PA. PA patients without aldosterone-producing adenomas (APA) frequently have unilateral aldosterone hypersecretion (UAH). These patients could bear inappropriate adrenalectomy without AVS. This study aims to identify which clinical characteristics should be recommended to perform AVS in these PA patients.Entities:
Keywords: Adrenal vein sampling; Primary aldosteronism; Unilateral aldosterone hypersecretion
Mesh:
Substances:
Year: 2021 PMID: 34059026 PMCID: PMC8167985 DOI: 10.1186/s12902-021-00770-1
Source DB: PubMed Journal: BMC Endocr Disord ISSN: 1472-6823 Impact factor: 2.763
Fig. 1Patient selection and distribution. Adrenal vein catheterization was considered successful when selectivity index (SI) was ≥2 without cosyntropin administration. Unilateral PA was diagnosed if lateralized index (LI) was ≥2. Abbreviation:PA, primary aldosteronism; AVS, Adrenal vein sampling
Baseline characteristics of included patients
| Variable | Lateralized | Non-lateralized | |
|---|---|---|---|
| Lateralization index | 12.1 ± 28.0 | 1.5 ± 0.4 | < 0.001 |
| Mean Age | 49.2 ± 10.3 | 50.0 ± 10.0 | 0.88 |
| Sex, M/F(n%) | 44 (48.9%)/46 (52.2%) | 22 (43.1%)/29 (56.9%) | 0.51 |
| BMI (Kg/m2) | 25.9 ± 2.7 | 25.2 ± 3.7 | 0.07 |
| Systolic BP (mmHg) | 145 ± 19 | 144 ± 21 | 0.32 |
| Diastolic BP (mmHg) | 91 ± 13 | 90 ± 15 | 0.24 |
| Serum potassium (mmol/L) | 3.6 ± 0.5 | 3.7 ± 0.5 | 0.98 |
| Serum sodium (mmol/L) | 137.1 ± 21.1 | 140.1 ± 2.1 | 0.07 |
| Urinary potassium (mmol/d) | 40.1 ± 15.9 | 37.8 ± 14.5 | 0.64 |
| Urinary sodium (mmol/d) | 181.5 ± 108.8 | 168.8 ± 97.8 | 0.75 |
| Recumbent PAC (ng/dL) | 11.9 [8.9–18.1] | 11.1 [8.4–16.5] | 0.70 |
| Recumbent DRC (mU/L) | 1.6 [0.9–5.0] | 2.9 [1.3–5.6] | 0.07 |
| Recumbent ARR (ng/dL)/(mU/L) | 4.8 [1.9–8.9] | 3.1 [1.7–5.9] | 0.19 |
| Post-CCT/SIT ARR (ng/dL)/(mU/L) | 2.9 [1.05–6.90] | 2.2 [1.0–4.0] | 0.24 |
| ACR (mg/mmol) | 118.7.1 ± 428.2 | 44.2 ± 76.5 | 0.09 |
| Serum creatine (umol/L) | 68.7 ± 23.5 | 70.4 ± 48.5 | 0.24 |
| eGFR (ml/min/1.73 m2) | 131.7 ± 41.0 | 137.0 ± 33.2 | 0.21 |
| Hypertensive heart disease, n(%) | 6 (8.8%) | 2 (5.1%) | 0.32 |
| Ischemic heart disease, n(%) | 31 (44.9%) | 13 (33.3%) | 0.71 |
| Hypertensive Nephropathy,n(%) | 26 (42.6%) | 10 (27.8%) | 0.31 |
| Peripheral vascular disease, n(%) | 11 (16.7%) | 2 (5.1%) | 0.19 |
| Cerebrovascular disease, n(%) | 27 (50.0%) | 18 (51.4%) | 0.13 |
| Metabolic syndrome, n(%) | 6 (8.8%) | 2 (5.1%) | 1.0 |
Continuous variables are expressed as the mean ± SD or the medians [interquartile range] unless noted otherwise
Abbreviations: LI Lateralization index, BMI body mass index, CCT captopril challenge test, SIT saline infusion test, ARR ratio of aldosterone/renin, PAC plasma aldosterone concentration, DRC direct renin concentration, ACR urinary albumin/creatinine ratio
Multivariable logistic regression analyzed for five variable
| Variable | B | SE | Wald | OR | 95%CI | |
|---|---|---|---|---|---|---|
| ARR after CCT/SIT | 0.01 | 0.005 | 4.071 | 0.044 | 1.010 | 1.000 to 1.021 |
| Age | N/A | N/A | N/A | 0.829 | N/A | N/A |
| Serum potassium | N/A | N/A | N/A | 0.722 | N/A | N/A / |
| eGFR | N/A | N/A | N/A | 0.898 | N/A | N/A |
| PAC | N/A | N/A | N/A | 0.528 | N/A | N/A |
P value < 0.05 is considered statistically significant. Stepwise method with all relative parameters as independent variables including age, serum potassium, eGFR, PAC, and ARR after confirmatory test. Boldface indicates the factor with significant association (p < 0.05)
Abbreviations: B regression coefficient, SE standard error, OR Odds ratio, CI confidence interval, CCT captopril challenge test, SIT saline infusion test, PAC Plasma aldosterone concentration, ARR aldosterone to renin ratio, eGFR estimated glomerular filtration rate, N/A not applicable
Sensitivity and specificity of various parameters
| Diagnostic criteria | N | Sensitivity | Specificity |
|---|---|---|---|
| PAC > 171 ng/dL | 32/141 | 26.7%(17.8–37.4) | 84.3%(71.2–92.2) |
| Serum potassium< 3.5 mmol/L | 54/141 | 36.7%(26.8–47.5) | 58.8%(44.2–72.4) |
| Post-CCT/SIT ARR > 10(ng/dL)/(mU/L) | 15/108 | 22.1%(12.9–33.8) | 100%(93.2–100.0) |
| Hypertension; Serum potassium< 3.5 mmol/L;Post-CCT/SIT ARR > 10(ng/dL)/(mU/L) | 9/108 | 13.0%(6.1–23.3) | 100%(91.0–100.0) |
Serum potassium< 3.5 mmol/L or Post-CCT/SIT ARR > 10(ng/dL)/(mU/L) | 51/108 | 49.3%(37.0–61.6) | 56.4%(39.6–72.2) |
The data are expressed as n(%) unless noted otherwise;
Abbreviations: CCT captopril challenge test, SIT saline infusion test, ARR ratio of aldosterone/renin, PAC plasma aldosterone concentration