Table 1.

Comparison of Clinical Characteristics and Parameters at Baseline in Patients With Primary Aldosteronism Who Underwent CCT or SIT

Captopril Challenge TestSaline Infusion Test
Positive (n = 1912)Negative (n = 344)P valuePositive (n = 953)Negative (n = 231)P value
Age, y52 (44–62)51 (43–60)0.5250 (43–60)58 (50–66)< 0.01
Female, n (%)1056 (55.2)164 (47.7)0.01453 (47.5)168 (72.7)< 0.01
Body mass index24.2 (21.8–27.0)25.2 (23.0–28.0)< 0.0124.6 (22.2–27.7)23.5 (21.4–25.6)< 0.01
Systolic BP, mmHg140 (129–152)140 (130–151)0.85140 (129–150)140 (128–149)0.39
Diastolic BP, mmHg87 (78–96)87 (80–97)0.2488 (79–96)83 (74–91)< 0.01
Serum potassium, mEq/L3.8 (3.4–4.1)3.9 (3.6–4.1)< 0.013.7 (3.4–4.0)4.0 (3.8–4.2)< 0.01
Hypokalemia, n (%)790 (41.3)83 (24.1)< 0.01429 (45.0)23 (10.0)< 0.01
Oral potassium supplements, n (%)425 (22.2)27 (7.8)< 0.01235 (24.7)4 (1.7)< 0.01
eGFR78.4 (67.1–91.0)78.8 (68.5–91.3)0.6678.3 (67.2–91.2)77.3 (69.2–89.7)0.94
PAC, ng/dL18.2 (12.9–28.6)17.0 (12.7–23.4)0.0120.1 (14.5–29.2)12.9 (10.1–17.2)< 0.01
PRA, ng/mL/h0.3 (0.2–0.4)0.5 (0.4–0.7)< 0.010.3 (0.2–0.5)0.3 (0.2–0.4)< 0.05
ARR63.2 (39.3–123.8)32.1 (25.1–44.6)< 0.0161.0 (36.8–118.0)43.8 (31.5–69.7)< 0.01
Adrenal nodule(s) on CT, n (%)726 (38.0)72 (20.9)< 0.01323 (33.9)53 (22.9)< 0.01
Unilateral PA, n (%)517 (27.0)21 (6.1)< 0,01250 (26.2)6 (2.6)< 0.01
CCT pos/neg, n SIT pos/neg, n FUT pos/neg, n1,912/0 754/203 1,076/1100/344 181/26 230/ 57-754/181 953/0 468/118203/26 0/231 147/13-
Captopril Challenge TestSaline Infusion Test
Positive (n = 1912)Negative (n = 344)P valuePositive (n = 953)Negative (n = 231)P value
Age, y52 (44–62)51 (43–60)0.5250 (43–60)58 (50–66)< 0.01
Female, n (%)1056 (55.2)164 (47.7)0.01453 (47.5)168 (72.7)< 0.01
Body mass index24.2 (21.8–27.0)25.2 (23.0–28.0)< 0.0124.6 (22.2–27.7)23.5 (21.4–25.6)< 0.01
Systolic BP, mmHg140 (129–152)140 (130–151)0.85140 (129–150)140 (128–149)0.39
Diastolic BP, mmHg87 (78–96)87 (80–97)0.2488 (79–96)83 (74–91)< 0.01
Serum potassium, mEq/L3.8 (3.4–4.1)3.9 (3.6–4.1)< 0.013.7 (3.4–4.0)4.0 (3.8–4.2)< 0.01
Hypokalemia, n (%)790 (41.3)83 (24.1)< 0.01429 (45.0)23 (10.0)< 0.01
Oral potassium supplements, n (%)425 (22.2)27 (7.8)< 0.01235 (24.7)4 (1.7)< 0.01
eGFR78.4 (67.1–91.0)78.8 (68.5–91.3)0.6678.3 (67.2–91.2)77.3 (69.2–89.7)0.94
PAC, ng/dL18.2 (12.9–28.6)17.0 (12.7–23.4)0.0120.1 (14.5–29.2)12.9 (10.1–17.2)< 0.01
PRA, ng/mL/h0.3 (0.2–0.4)0.5 (0.4–0.7)< 0.010.3 (0.2–0.5)0.3 (0.2–0.4)< 0.05
ARR63.2 (39.3–123.8)32.1 (25.1–44.6)< 0.0161.0 (36.8–118.0)43.8 (31.5–69.7)< 0.01
Adrenal nodule(s) on CT, n (%)726 (38.0)72 (20.9)< 0.01323 (33.9)53 (22.9)< 0.01
Unilateral PA, n (%)517 (27.0)21 (6.1)< 0,01250 (26.2)6 (2.6)< 0.01
CCT pos/neg, n SIT pos/neg, n FUT pos/neg, n1,912/0 754/203 1,076/1100/344 181/26 230/ 57-754/181 953/0 468/118203/26 0/231 147/13-

Abbreviations: BP, blood pressure; CCT, captopril challenge test; CT, computed tomography; eGFR, estimated glomerular filtration rate; FUT, furosemide upright test; neg, negative; PA, primary aldosteronism; pos, positive; SIT, saline infusion test.

Table 1.

Comparison of Clinical Characteristics and Parameters at Baseline in Patients With Primary Aldosteronism Who Underwent CCT or SIT

Captopril Challenge TestSaline Infusion Test
Positive (n = 1912)Negative (n = 344)P valuePositive (n = 953)Negative (n = 231)P value
Age, y52 (44–62)51 (43–60)0.5250 (43–60)58 (50–66)< 0.01
Female, n (%)1056 (55.2)164 (47.7)0.01453 (47.5)168 (72.7)< 0.01
Body mass index24.2 (21.8–27.0)25.2 (23.0–28.0)< 0.0124.6 (22.2–27.7)23.5 (21.4–25.6)< 0.01
Systolic BP, mmHg140 (129–152)140 (130–151)0.85140 (129–150)140 (128–149)0.39
Diastolic BP, mmHg87 (78–96)87 (80–97)0.2488 (79–96)83 (74–91)< 0.01
Serum potassium, mEq/L3.8 (3.4–4.1)3.9 (3.6–4.1)< 0.013.7 (3.4–4.0)4.0 (3.8–4.2)< 0.01
Hypokalemia, n (%)790 (41.3)83 (24.1)< 0.01429 (45.0)23 (10.0)< 0.01
Oral potassium supplements, n (%)425 (22.2)27 (7.8)< 0.01235 (24.7)4 (1.7)< 0.01
eGFR78.4 (67.1–91.0)78.8 (68.5–91.3)0.6678.3 (67.2–91.2)77.3 (69.2–89.7)0.94
PAC, ng/dL18.2 (12.9–28.6)17.0 (12.7–23.4)0.0120.1 (14.5–29.2)12.9 (10.1–17.2)< 0.01
PRA, ng/mL/h0.3 (0.2–0.4)0.5 (0.4–0.7)< 0.010.3 (0.2–0.5)0.3 (0.2–0.4)< 0.05
ARR63.2 (39.3–123.8)32.1 (25.1–44.6)< 0.0161.0 (36.8–118.0)43.8 (31.5–69.7)< 0.01
Adrenal nodule(s) on CT, n (%)726 (38.0)72 (20.9)< 0.01323 (33.9)53 (22.9)< 0.01
Unilateral PA, n (%)517 (27.0)21 (6.1)< 0,01250 (26.2)6 (2.6)< 0.01
CCT pos/neg, n SIT pos/neg, n FUT pos/neg, n1,912/0 754/203 1,076/1100/344 181/26 230/ 57-754/181 953/0 468/118203/26 0/231 147/13-
Captopril Challenge TestSaline Infusion Test
Positive (n = 1912)Negative (n = 344)P valuePositive (n = 953)Negative (n = 231)P value
Age, y52 (44–62)51 (43–60)0.5250 (43–60)58 (50–66)< 0.01
Female, n (%)1056 (55.2)164 (47.7)0.01453 (47.5)168 (72.7)< 0.01
Body mass index24.2 (21.8–27.0)25.2 (23.0–28.0)< 0.0124.6 (22.2–27.7)23.5 (21.4–25.6)< 0.01
Systolic BP, mmHg140 (129–152)140 (130–151)0.85140 (129–150)140 (128–149)0.39
Diastolic BP, mmHg87 (78–96)87 (80–97)0.2488 (79–96)83 (74–91)< 0.01
Serum potassium, mEq/L3.8 (3.4–4.1)3.9 (3.6–4.1)< 0.013.7 (3.4–4.0)4.0 (3.8–4.2)< 0.01
Hypokalemia, n (%)790 (41.3)83 (24.1)< 0.01429 (45.0)23 (10.0)< 0.01
Oral potassium supplements, n (%)425 (22.2)27 (7.8)< 0.01235 (24.7)4 (1.7)< 0.01
eGFR78.4 (67.1–91.0)78.8 (68.5–91.3)0.6678.3 (67.2–91.2)77.3 (69.2–89.7)0.94
PAC, ng/dL18.2 (12.9–28.6)17.0 (12.7–23.4)0.0120.1 (14.5–29.2)12.9 (10.1–17.2)< 0.01
PRA, ng/mL/h0.3 (0.2–0.4)0.5 (0.4–0.7)< 0.010.3 (0.2–0.5)0.3 (0.2–0.4)< 0.05
ARR63.2 (39.3–123.8)32.1 (25.1–44.6)< 0.0161.0 (36.8–118.0)43.8 (31.5–69.7)< 0.01
Adrenal nodule(s) on CT, n (%)726 (38.0)72 (20.9)< 0.01323 (33.9)53 (22.9)< 0.01
Unilateral PA, n (%)517 (27.0)21 (6.1)< 0,01250 (26.2)6 (2.6)< 0.01
CCT pos/neg, n SIT pos/neg, n FUT pos/neg, n1,912/0 754/203 1,076/1100/344 181/26 230/ 57-754/181 953/0 468/118203/26 0/231 147/13-

Abbreviations: BP, blood pressure; CCT, captopril challenge test; CT, computed tomography; eGFR, estimated glomerular filtration rate; FUT, furosemide upright test; neg, negative; PA, primary aldosteronism; pos, positive; SIT, saline infusion test.

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