Paltrinieri S, Sironi G, Giori L, Faverzani S, Longeri M
Department of Veterinary Sciences and Public Health, University of Milan, Milan, Italy.
J Vet Intern Med. 2015 Mar-Apr;29(2):505-12. doi: 10.1111/jvim.12561. Epub 2015 Mar 16.
Diagnosis of familial amyloidosis (FA) in Abyssinian cats usually is made on postmortem examination.
HYPOTHESIS/OBJECTIVES: Sequential analysis of serum SAA (sSAA), urinary SAA (uSAA), urinary protein:creatinine (UPC) ratio, or sodium-dodecylsulfate agarose gel electrophoresis (SDS-AGE) may facilitate early identification of cats with FA.
Twenty-three Abyssinian cats belonging to cattery A or B (low and high prevalence of FA, respectively).
Prospective longitudinal study using 109 blood and 100 urine samples collected over 4-year period every 4 months, if possible, or more frequently in case of illness. Cats that died during study were necropsied. Health status of live cats was checked 5 years after enrollment. Serum amyloid A (sSAA) and urinary SAA (uSAA) were measured using ELISA kit. The UPC ratio and SDS-AGE also was performed.
Familial amyloidosis was not identified in cattery A, whereas 7/14 cats from cattery B had FA. Serum amyloid A concentrations were not significantly different between cats in catteries A and B or between cats with or without FA, despite frequent peaks in cats from cattery B. Conversely, uSAA was significantly higher in cattery B, especially in the terminal phases of FA. Proteinuria occasionally was found in cats from both catteries, especially in those with FA. Urine protein electrophoresis identified mixed proteinuria only in cats with FA.
Serum amyloid A and UPC ratio are not helpful for early identification of Abyssinian cats with FA. Conversely, increases in uSAA with or without mixed proteinuria may be found before onset of clinical signs in cats with FA.
阿比西尼亚猫家族性淀粉样变性(FA)的诊断通常在死后检查时做出。
假设/目的:对血清淀粉样蛋白A(sSAA)、尿淀粉样蛋白A(uSAA)、尿蛋白:肌酐(UPC)比值或十二烷基硫酸钠琼脂糖凝胶电泳(SDS-AGE)进行序贯分析,可能有助于早期识别患有FA的猫。
属于猫舍A或B的23只阿比西尼亚猫(分别为FA低患病率和高患病率)。
前瞻性纵向研究,在4年期间尽可能每4个月收集109份血液样本和100份尿液样本,如有疾病则更频繁收集。研究期间死亡的猫进行尸检。入组5年后检查存活猫的健康状况。使用ELISA试剂盒测量血清淀粉样蛋白A(sSAA)和尿淀粉样蛋白A(uSAA)。同时进行UPC比值和SDS-AGE检测。
在猫舍A中未发现家族性淀粉样变性,而猫舍B的14只猫中有7只患有FA。猫舍A和B的猫之间,以及患有或未患有FA的猫之间,血清淀粉样蛋白A浓度无显著差异,尽管猫舍B的猫中经常出现峰值。相反,猫舍B中uSAA明显更高,尤其是在FA的终末期。两个猫舍的猫偶尔都会出现蛋白尿,尤其是患有FA的猫。尿蛋白电泳仅在患有FA的猫中发现混合性蛋白尿。
血清淀粉样蛋白A和UPC比值无助于早期识别患有FA的阿比西尼亚猫。相反,在患有FA的猫出现临床症状之前,可能会发现uSAA升高,伴有或不伴有混合性蛋白尿。