Department of Comparative Biomedical Sciences, Royal Veterinary College, University of London, London, United Kingdom.
Department of Clinical Sciences, Faculty of Veterinary Medicine, Utrecht University, Utrecht, The Netherlands.
J Vet Intern Med. 2024 Jul-Aug;38(4):2180-2195. doi: 10.1111/jvim.17134. Epub 2024 Jul 1.
Plasma total magnesium concentration (tMg) is a prognostic indicator in cats with chronic kidney disease (CKD), shorter survival time being associated with hypomagnesemia. Whether this risk factor is modifiable with dietary magnesium supplementation remains unexplored.
Evaluate effects of a magnesium-enriched phosphate-restricted diet (PRD) on CKD-mineral bone disorder (CKD-MBD) variables.
Sixty euthyroid client-owned cats with azotemic CKD, with 27 and 33 allocated to magnesium-enriched PRD or control PRD, respectively.
Prospective double-blind, parallel-group randomized trial. Cats with CKD, stabilized on a PRD, without hypermagnesemia (tMg >2.43 mg/dL) or hypercalcemia (plasma ionized calcium concentration, (iCa) >6 mg/dL), were recruited. Both intention-to-treat and per-protocol (eating ≥50% of study diet) analyses were performed; effects of dietary magnesium supplementation on clinicopathological variables were evaluated using linear mixed effects models.
In the per-protocol analysis, tMg increased in cats consuming a magnesium-enriched PRD (β, 0.25 ± .07 mg/dL/month; P < .001). Five magnesium supplemented cats had tMg >2.92 mg/dL, but none experienced adverse effects. Rate of change in iCa differed between groups (P = .01), with decreasing and increasing trends observed in cats fed magnesium-enriched PRD and control PRD, respectively. Four control cats developed ionized hypercalcemia versus none in the magnesium supplemented group. Log-transformed plasma fibroblast growth factor-23 concentration (FGF23) increased significantly in controls (β, 0.14 ± .05 pg/mL/month; P = .01), but remained stable in the magnesium supplemented group (β, 0.05±.06 pg/mL/month; P =.37).
Magnesium-enriched PRD is a novel therapeutic strategy for managing feline CKD-MBD in cats, further stabilizing plasma FGF23 and preventing hypercalcemia.
血浆总镁浓度(tMg)是患有慢性肾脏病(CKD)的猫的预后指标,低镁血症与较短的生存时间相关。用膳食镁补充剂来改变这种风险因素是否可行仍未被探索。
评估富含镁的限制磷酸盐饮食(PRD)对 CKD-矿物质骨病(CKD-MBD)变量的影响。
60 只患有氮质血症性 CKD 的甲状腺功能正常的患宠猫,其中 27 只和 33 只分别被分配到富含镁的 PRD 或对照 PRD 中。
前瞻性双盲、平行组随机试验。招募患有 CKD、稳定在 PRD 上、无高镁血症(tMg>2.43mg/dL)或高钙血症(血浆离子钙浓度,(iCa)>6mg/dL)的猫。分别进行意向治疗和方案分析(食用≥50%研究饮食);使用线性混合效应模型评估膳食镁补充对临床病理变量的影响。
在方案分析中,食用富含镁的 PRD 的猫的 tMg 增加(β,0.25±0.07mg/dL/月;P<.001)。5 只接受镁补充的猫的 tMg 超过 2.92mg/dL,但没有出现不良反应。两组之间 iCa 的变化率不同(P=.01),分别观察到食用富含镁的 PRD 和对照 PRD 的猫的趋势分别为下降和增加。4 只对照猫出现离子性高钙血症,而补充镁的组中没有猫出现这种情况。对照组的血浆成纤维细胞生长因子 23 浓度(FGF23)的对数转换显著增加(β,0.14±0.05pg/mL/月;P=.01),但在补充镁的组中保持稳定(β,0.05±0.06pg/mL/月;P=.37)。
富含镁的 PRD 是一种治疗猫 CKD-MBD 的新策略,进一步稳定了血浆 FGF23 并防止了高钙血症。