Yun Hyejin, Koo Yoonhoi, Yun Taesik, Chae Yeon, Lee Dohee, Cha Sijin, Kim Jeeyune, Kim Hakhyun, Yang Mhan Pyo, Kang Byeong Teck
Laboratory of Veterinary Internal Medicine, College of Veterinary Medicine, Chungbuk National University, Cheongju, Chungbuk, South Korea.
College of Veterinary Medicine, Kyungpook National University, Daegu, South Korea.
Front Vet Sci. 2023 Aug 24;10:1200653. doi: 10.3389/fvets.2023.1200653. eCollection 2023.
Cardiovascular and renal diseases are known to affect each other in the cardiovascular renal axis disorder (CvRD). Although CvRD, which includes myxomatous mitral valve disease (MMVD) and chronic kidney disease (CKD), has been described in dogs, there are only a few reports on the progression of CKD in accordance with the severity of MMVD. The aim of this study was to evaluate whether the presence of MMVD is associated with the rate of progression of CKD in dogs. The time from the initial diagnosis to the worsening of the International Renal Interest Society (IRIS) stage and the time for the occurrence of hyperphosphatemia and isosthenuria were evaluated.
In this retrospective study, CKD progression was determined as an increase in the IRIS stage by at least one level and the development of hyperphosphatemia or isosthenuria. The CKD progression was compared in dogs with and without comorbid MMVD.
Dogs with CKD were divided into two groups: dogs with and without MMVD ( = 63, concurrent group; = 52, CKD group, respectively). The concurrent group was further divided into two subgroups based on the American College of Veterinary Internal Medicine guidelines (B1 group, = 24; B2 group, = 39). The time for progression of CKD from IRIS stage 1 to IRIS stage 2 was significantly shorter in the concurrent group than in the CKD group (log-rank test, < 0.001). MMVD was associated with an increased risk of progression from stage 1 to stage 2 (hazard ratio, 6.442; 95% confidence interval (CI), 2.354 to 18.850; < 0.001). The timing of the onset of hyperphosphatemia or isosthenuria in the concurrent group and the CKD group was not significantly different.
The results of this study suggest that MMVD could be a risk factor for the progression of CKD. Our findings may help predict the prognosis of dogs with both CKD and MMVD compared to CKD only.
已知心血管疾病和肾脏疾病在心血管-肾脏轴紊乱(CvRD)中相互影响。虽然犬类中已描述了包括黏液瘤性二尖瓣疾病(MMVD)和慢性肾脏病(CKD)在内的CvRD,但关于CKD根据MMVD严重程度进展的报道较少。本研究的目的是评估MMVD的存在是否与犬类CKD的进展速度相关。评估了从初始诊断到国际肾脏兴趣协会(IRIS)分期恶化的时间以及高磷血症和等渗尿发生的时间。
在这项回顾性研究中,CKD进展被确定为IRIS分期至少升高一级以及高磷血症或等渗尿的发生。比较了患有和未患有合并症MMVD的犬类的CKD进展情况。
患有CKD的犬被分为两组:患有和未患有MMVD的犬(分别为63只,合并组;52只,CKD组)。根据美国兽医内科学会指南,合并组进一步分为两个亚组(B1组,24只;B2组,39只)。合并组中CKD从IRIS 1期进展到IRIS 2期的时间明显短于CKD组(对数秩检验,P<0.001)。MMVD与从1期进展到2期的风险增加相关(风险比,6.442;95%置信区间(CI),2.354至18.850;P<0.001)。合并组和CKD组中高磷血症或等渗尿发作的时间没有显著差异。
本研究结果表明,MMVD可能是CKD进展的危险因素。我们的发现可能有助于预测同时患有CKD和MMVD的犬与仅患有CKD的犬相比的预后。