# Cracking the Code: A Case Report on Low-Renin Hypertension

**Authors:** Fawwad A Ansari, Bilal Hamid, Inemesit Akpan, Ghida Akhdar, Muhammad Umer Riaz Gondal

PMC · DOI: 10.7759/cureus.65335 · 2024-07-25

## TL;DR

This case report describes a patient with low-renin hypertension who successfully responded to spironolactone treatment.

## Contribution

The paper highlights LRH as an under-recognized cause of uncontrolled hypertension and suggests effective treatment strategies.

## Key findings

- A 57-year-old female with resistant hypertension had low renin levels and normal aldosterone.
- The patient's blood pressure normalized after treatment with spironolactone.
- LRH patients may respond well to diuretics, mineralocorticoid receptor blockers, and ENaC blockers.

## Abstract

Low-renin hypertension (LRH) is characterized by hypertension accompanied by low serum renin levels. LRH is a spectrum, including low-renin essential hypertension (LREH), primary hyperaldosteronism, and several acquired or familial secondary forms. Here, we present a case of LRH. A 57-year-old female with resistant hypertension on multiple antihypertensive medications presented for blood pressure management. Workup for secondary causes of hypertension revealed low renin levels with normal aldosterone. The patient was initiated on spironolactone and responded quickly with normal blood pressure on a follow-up visit. LRH is an under-recognized etiology for uncontrolled hypertension. It can be secondary to several different causes. Although treatment of LREH is essentially the same as regular patients, these patients tend to respond well to sodium-volume-depleting diuretics, mineralocorticoid receptor blockers, and epithelial sodium channels (ENaC) blockers.

## Linked entities

- **Chemicals:** spironolactone (PubChem CID 5833)
- **Diseases:** primary hyperaldosteronism (MONDO:0001422)

## Full-text entities

- **Genes:** NR3C2 (nuclear receptor subfamily 3 group C member 2) [NCBI Gene 4306] {aka MCR, MLR, MR, NR3C2VIT}, REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}
- **Diseases:** primary hyperaldosteronism (MESH:D006929), LREH (MESH:D000075222), LRH (MESH:D006973)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

1 figure with captions in the complete paper: https://tomesphere.com/paper/PMC11344372/full.md

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Source: https://tomesphere.com/paper/PMC11344372