Raymond R Townsend, Abiy Agiro, Shan Luan, Kaylen Brzozowski, Erick Moyneur, Paule Tetreault-Langlois, Joanna Huang
{"title":"醛固酮失调后高血压和慢性肾病的风险。","authors":"Raymond R Townsend, Abiy Agiro, Shan Luan, Kaylen Brzozowski, Erick Moyneur, Paule Tetreault-Langlois, Joanna Huang","doi":"10.1093/ajh/hpaf183","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Excess aldosterone of > 15ng/dL, in the presence of low renin, is linked to hypertension (HTN) and chronic kidney disease (CKD). This study investigated the association of aldosterone dysregulation at lower plasma aldosterone levels (≥5ng/dL) with the risk of uncontrolled HTN and CKD prevalence.</p><p><strong>Methods: </strong>Patient plasma aldosterone measurements obtained during 2013-2023 were identified in the TriNetX Dataworks-USA Network of electronic medical records. Eligible patients (≥18 years) had a plasma renin activity measurement of ≤ 1ng/mL/h within 12 months prior, and a systolic blood pressure (SBP) measurement within 12 months following, the index aldosterone measurement. The primary outcome was uncontrolled HTN (SBP ≥130mmHg) prevalence. The secondary outcome was CKD prevalence (CKD diagnosis or eGFR measurement of < 60mL/min/1.73m2). The adjusted odds ratio (aOR) of uncontrolled HTN during a 12-month follow-up were calculated among plasma aldosterone groups (≥5 vs < 5ng/dL, ≥10 vs < 10ng/dL, and ≥15 vs < 15ng/dL).</p><p><strong>Results: </strong>Patients (N = 1,334) had mean age of 59 years and 55.9% were female. Patients with plasma aldosterone of ≥ 5ng/dL (N = 903) had a higher risk (aOR [95% CI]) of uncontrolled HTN (2.01 [1.38,2.92]; p < 0.001) versus <5ng/dL (N = 431). Similar findings were observed for plasma aldosterone levels of ≥ 10ng/dL and ≥15ng/dL. Patients with plasma aldosterone of ≥ 10ng/dL (N = 514) had a higher risk of CKD (1.49 [1.15,1.92]; p < 0.001) versus <10ng/dL (N = 820). Similar findings were observed for plasma aldosterone levels of ≥ 15ng/dL.</p><p><strong>Conclusions: </strong>Clinically relevant aldosterone dysregulation, in the presence of low renin, occurs at lower aldosterone levels than previously thought, and remains significantly associated with uncontrolled HTN and CKD prevalence.</p>","PeriodicalId":7578,"journal":{"name":"American Journal of Hypertension","volume":" ","pages":""},"PeriodicalIF":3.1000,"publicationDate":"2025-09-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Risk of Hypertension and Chronic Kidney Disease following Aldosterone Dysregulation.\",\"authors\":\"Raymond R Townsend, Abiy Agiro, Shan Luan, Kaylen Brzozowski, Erick Moyneur, Paule Tetreault-Langlois, Joanna Huang\",\"doi\":\"10.1093/ajh/hpaf183\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Excess aldosterone of > 15ng/dL, in the presence of low renin, is linked to hypertension (HTN) and chronic kidney disease (CKD). This study investigated the association of aldosterone dysregulation at lower plasma aldosterone levels (≥5ng/dL) with the risk of uncontrolled HTN and CKD prevalence.</p><p><strong>Methods: </strong>Patient plasma aldosterone measurements obtained during 2013-2023 were identified in the TriNetX Dataworks-USA Network of electronic medical records. Eligible patients (≥18 years) had a plasma renin activity measurement of ≤ 1ng/mL/h within 12 months prior, and a systolic blood pressure (SBP) measurement within 12 months following, the index aldosterone measurement. The primary outcome was uncontrolled HTN (SBP ≥130mmHg) prevalence. The secondary outcome was CKD prevalence (CKD diagnosis or eGFR measurement of < 60mL/min/1.73m2). The adjusted odds ratio (aOR) of uncontrolled HTN during a 12-month follow-up were calculated among plasma aldosterone groups (≥5 vs < 5ng/dL, ≥10 vs < 10ng/dL, and ≥15 vs < 15ng/dL).</p><p><strong>Results: </strong>Patients (N = 1,334) had mean age of 59 years and 55.9% were female. Patients with plasma aldosterone of ≥ 5ng/dL (N = 903) had a higher risk (aOR [95% CI]) of uncontrolled HTN (2.01 [1.38,2.92]; p < 0.001) versus <5ng/dL (N = 431). Similar findings were observed for plasma aldosterone levels of ≥ 10ng/dL and ≥15ng/dL. Patients with plasma aldosterone of ≥ 10ng/dL (N = 514) had a higher risk of CKD (1.49 [1.15,1.92]; p < 0.001) versus <10ng/dL (N = 820). Similar findings were observed for plasma aldosterone levels of ≥ 15ng/dL.</p><p><strong>Conclusions: </strong>Clinically relevant aldosterone dysregulation, in the presence of low renin, occurs at lower aldosterone levels than previously thought, and remains significantly associated with uncontrolled HTN and CKD prevalence.</p>\",\"PeriodicalId\":7578,\"journal\":{\"name\":\"American Journal of Hypertension\",\"volume\":\" \",\"pages\":\"\"},\"PeriodicalIF\":3.1000,\"publicationDate\":\"2025-09-10\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"American Journal of Hypertension\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1093/ajh/hpaf183\",\"RegionNum\":3,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q2\",\"JCRName\":\"PERIPHERAL VASCULAR DISEASE\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"American Journal of Hypertension","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1093/ajh/hpaf183","RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q2","JCRName":"PERIPHERAL VASCULAR DISEASE","Score":null,"Total":0}
Risk of Hypertension and Chronic Kidney Disease following Aldosterone Dysregulation.
Background: Excess aldosterone of > 15ng/dL, in the presence of low renin, is linked to hypertension (HTN) and chronic kidney disease (CKD). This study investigated the association of aldosterone dysregulation at lower plasma aldosterone levels (≥5ng/dL) with the risk of uncontrolled HTN and CKD prevalence.
Methods: Patient plasma aldosterone measurements obtained during 2013-2023 were identified in the TriNetX Dataworks-USA Network of electronic medical records. Eligible patients (≥18 years) had a plasma renin activity measurement of ≤ 1ng/mL/h within 12 months prior, and a systolic blood pressure (SBP) measurement within 12 months following, the index aldosterone measurement. The primary outcome was uncontrolled HTN (SBP ≥130mmHg) prevalence. The secondary outcome was CKD prevalence (CKD diagnosis or eGFR measurement of < 60mL/min/1.73m2). The adjusted odds ratio (aOR) of uncontrolled HTN during a 12-month follow-up were calculated among plasma aldosterone groups (≥5 vs < 5ng/dL, ≥10 vs < 10ng/dL, and ≥15 vs < 15ng/dL).
Results: Patients (N = 1,334) had mean age of 59 years and 55.9% were female. Patients with plasma aldosterone of ≥ 5ng/dL (N = 903) had a higher risk (aOR [95% CI]) of uncontrolled HTN (2.01 [1.38,2.92]; p < 0.001) versus <5ng/dL (N = 431). Similar findings were observed for plasma aldosterone levels of ≥ 10ng/dL and ≥15ng/dL. Patients with plasma aldosterone of ≥ 10ng/dL (N = 514) had a higher risk of CKD (1.49 [1.15,1.92]; p < 0.001) versus <10ng/dL (N = 820). Similar findings were observed for plasma aldosterone levels of ≥ 15ng/dL.
Conclusions: Clinically relevant aldosterone dysregulation, in the presence of low renin, occurs at lower aldosterone levels than previously thought, and remains significantly associated with uncontrolled HTN and CKD prevalence.
期刊介绍:
The American Journal of Hypertension is a monthly, peer-reviewed journal that provides a forum for scientific inquiry of the highest standards in the field of hypertension and related cardiovascular disease. The journal publishes high-quality original research and review articles on basic sciences, molecular biology, clinical and experimental hypertension, cardiology, epidemiology, pediatric hypertension, endocrinology, neurophysiology, and nephrology.