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前瞻性评估替米沙坦抑制试验作为猫原发性醛固酮增多症的诊断工具。

Prospective evaluation of a telmisartan suppression test as a diagnostic tool for primary hyperaldosteronism in cats.

机构信息

Ecole Nationale Vétérinaire d'Alfort - CHUVA, Service de Médecine Interne, Maisons-Alfort, France.

Aquivet Clinique Veterinaire - Service de Médecine Interne, Eysines, France.

出版信息

J Vet Intern Med. 2023 Jul-Aug;37(4):1348-1357. doi: 10.1111/jvim.16741. Epub 2023 May 29.

DOI:10.1111/jvim.16741
PMID:37246725
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC10365049/
Abstract

BACKGROUND

In a previous study, telmisartan suppressed aldosterone secretion in healthy cats but not in cats with primary hyperaldosteronism (PHA).

HYPOTHESES

Telmisartan suppresses aldosterone secretion in middle-aged healthy cat and cats with diseases that may result in secondary hyperaldosteronism, but not in those with PHA.

ANIMALS

Thirty-eight cats: 5 with PHA; 16 with chronic kidney disease (CKD), subclassified as hypertensive (CKD-H) or non-hypertensive (CKD-NH); 9 with hyperthyroidism (HTH); 2 with idiopathic systemic arterial hypertension (ISH); and 6 healthy middle-aged cats.

METHODS

Prospective, cross-sectional study. Serum aldosterone concentration, potassium concentration, and systolic blood pressure were measured before and 1 and 1.5 hours after PO administration of 2 mg/kg of telmisartan. The aldosterone variation rate (AVR) was calculated for each cat.

RESULTS

No significant difference in the minimum AVR was observed among groups (median [quartile 1 (Q1); quartile 3 (Q3)]: 25 [0; 30]; 5 [-27; -75]; 10 [-6; -95]; 53 [19; 86]; 29 [5; 78]) for PHA, CKD, HTH, ISH, and healthy cats, respectively (P = .05). Basal serum aldosterone concentration (pmol/L) was significantly higher in PHA cats (median [Q1; Q3]: 2914 [2789; 4600]) than in CKD-H cats (median [Q1; Q3]: 239 [189; 577], corrected P value = .003) and CKD-NH cats (median [Q1; Q3]: 353 [136; 1371], corrected P value = .004).

CONCLUSIONS AND CLINICAL IMPORTANCE

The oral telmisartan suppression test using a single dose of 2 mg/kg telmisartan did not discriminate cats with PHA from healthy middle-aged cats or cats with diseases that may result in secondary hyperaldosteronism.

摘要

背景

在之前的一项研究中,替米沙坦抑制了健康猫的醛固酮分泌,但不能抑制原发性醛固酮增多症(PHA)猫的醛固酮分泌。

假设

替米沙坦抑制中年健康猫和可能导致继发性醛固酮增多症的疾病猫的醛固酮分泌,但不抑制 PHA 猫的醛固酮分泌。

动物

38 只猫:5 只为 PHA;16 只为慢性肾脏病(CKD),分为高血压(CKD-H)或非高血压(CKD-NH);9 只为甲状腺功能亢进(HTH);2 只为特发性系统性动脉高血压(ISH);6 只为健康中年猫。

方法

前瞻性、横断面研究。在 PO 给予 2mg/kg 的替米沙坦后 1 和 1.5 小时,测量血清醛固酮浓度、钾浓度和收缩压。计算每只猫的醛固酮变化率(AVR)。

结果

各组间最小 AVR 无显著差异(中位数[四分位数 1(Q1);四分位数 3(Q3)]:PHA 为 25[0;30];CKD 为-27[-75];HTH 为-10[-95];ISH 为 53[19;86];健康猫为 29[5;78])(P=0.05)。PHA 猫的基础血清醛固酮浓度(pmol/L)显著高于 CKD-H 猫(中位数[Q1;Q3]:2914[2789;4600])和 CKD-NH 猫(中位数[Q1;Q3]:353[136;1371])(校正 P 值分别为<0.001 和<0.001)。

结论和临床意义

单次口服 2mg/kg 替米沙坦的口服替米沙坦抑制试验未能将 PHA 猫与健康中年猫或可能导致继发性醛固酮增多症的疾病猫区分开来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/20fbcc680763/JVIM-37-1348-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/a4746e029f19/JVIM-37-1348-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/900911dff8c5/JVIM-37-1348-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/35eef97ab7ab/JVIM-37-1348-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/7de7b95088c4/JVIM-37-1348-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/20fbcc680763/JVIM-37-1348-g005.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/a4746e029f19/JVIM-37-1348-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/900911dff8c5/JVIM-37-1348-g004.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/35eef97ab7ab/JVIM-37-1348-g003.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/7de7b95088c4/JVIM-37-1348-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ffbd/10365049/20fbcc680763/JVIM-37-1348-g005.jpg

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