Vasilatis Demitria M, Christopher Mary M
William R. Pritchard Veterinary Medical Teaching Hospital, School of Veterinary Medicine, University of California, Davis, Davis, CA, United States.
Department of Pathology, Microbiology and Immunology, School of Veterinary Medicine, University of California, Davis, Davis, CA, United States.
Front Vet Sci. 2023 Aug 17;10:1234233. doi: 10.3389/fvets.2023.1234233. eCollection 2023.
Domestic goats () are a food, fiber and companion animal. Abnormal erythrocyte shapes (poikilocytes) are considered normal in young goats, but their association with disease is not well described. Likewise, there is little information on the significance of poikilocytosis in adult goats.
The objective of this study was to investigate the prevalence, severity and type of poikilocytosis in young and adult goats and its association with age, sex, breed, laboratory results, and underlying disease.
We retrospectively examined clinical and laboratory data from 1254 goats presented at the University of California-Davis Veterinary Medical Teaching Hospital from 1997 to 2019. We analyzed 313 blood smears from goats with moderate or marked (MOD-MKD) poikilocytosis on initial blood smear evaluation. Number and type of poikilocytes per 1000 red blood cells (RBCs) were enumerated. Laboratory values and primary disease categories were compared with the severity and type of poikilocytosis.
Kids (<6 mos) and juveniles (>6 mos to <1 year) had a higher prevalence of MOD-MKD poikilocytosis (95/210, 45.2% kids; 27/59, 45.8% juveniles) than adult goats (≥1 year; 190/982, 19.3%) ( < 0.001). Kids had a higher percentage of elliptocytes, dacryocytes, and schistocytes and a lower percentage of polygonal and spiculated RBCs than juvenile and adult goats ( < 0.001). Of goats with MOD-MKD ( NONE-SLIGHT) poikilocytosis, kids had lower HGB and MCH, and higher RDW ( ≤ 0.02); juveniles and adult goats had lower HCT, MCV, MCH, and albumin concentration ( ≤ 0.01), and all age groups had lower total CO2 concentration and higher PLT counts ( < 0.03). Adult goats with MOD-MKD poikilocytosis also had higher BUN:Cr ratios ( = 0.005). Gastrointestinal parasitism, Johne's disease, diarrhea/enteritis, lice, hepatic disease and renal disease (but not urolithiasis) were significantly associated with MOD-MKD poikilocytosis ( < 0.001). Goats with hepatic and renal disease had a higher prevalence and percentage of spiculated cells ( = 0.001). Goats with Johne's disease had a higher prevalence of polygonal cells (93.3%) and dacryocytes (66.7%) than other diseases, and elliptocytes predominated in a higher proportion (36.0%) of adult goats with GI parasitism vs other diseases ( < 0.05).
These findings suggest that iron deficiency is an important pathophysiologic mechanism of poikilocytosis in juvenile and adult goats, and possibly in kids, whether due to iron-restricted erythropoiesis, chronic hemorrhage, functional iron deficiency, or a combination of these mechanisms. Further investigation into the detection and monitoring of iron deficiency and the value of poikilocytosis as a diagnostic marker of iron status in goats is warranted.
家山羊是一种食用、产毛及伴侣动物。异常红细胞形态(异形红细胞)在幼龄山羊中被认为是正常的,但它们与疾病的关联尚未得到充分描述。同样,关于成年山羊中异形红细胞增多症的意义也知之甚少。
本研究的目的是调查幼龄和成年山羊中异形红细胞增多症的患病率、严重程度和类型,以及它与年龄、性别、品种、实验室检查结果和潜在疾病的关联。
我们回顾性研究了1997年至2019年在加利福尼亚大学戴维斯分校兽医教学医院就诊的1254只山羊的临床和实验室数据。我们分析了313份首次血液涂片评估时存在中度或重度(MOD-MKD)异形红细胞增多症的山羊血液涂片。计算每1000个红细胞(RBC)中异形红细胞的数量和类型。将实验室检查值和主要疾病类别与异形红细胞增多症的严重程度和类型进行比较。
幼龄山羊(<6月龄)和幼年山羊(>6月龄至<1岁)中MOD-MKD异形红细胞增多症的患病率(95/210,45.2%幼龄山羊;27/59,45.8%幼年山羊)高于成年山羊(≥1岁;190/982,19.3%)(P<0.001)。与幼年和成年山羊相比,幼龄山羊的椭圆形红细胞、泪滴状红细胞和裂红细胞百分比更高,多边形和棘状红细胞百分比更低(P<0.001)。在患有MOD-MKD(无-轻度)异形红细胞增多症的山羊中,幼龄山羊的血红蛋白(HGB)和平均红细胞血红蛋白含量(MCH)更低,红细胞分布宽度(RDW)更高(P≤0.02);幼年和成年山羊的血细胞比容(HCT)、平均红细胞体积(MCV)、MCH和白蛋白浓度更低(P≤0.01),所有年龄组的总二氧化碳浓度更低,血小板计数更高(P<0.03)。患有MOD-MKD异形红细胞增多症的成年山羊的尿素氮与肌酐比值也更高(P=0.005)。胃肠道寄生虫病、副结核病、腹泻/肠炎、虱子、肝病和肾病(但不包括尿路结石)与MOD-MKD异形红细胞增多症显著相关(P<0.001)。患有肝病和肾病的山羊棘状细胞的患病率和百分比更高(P=0.001)。与其他疾病相比,患有副结核病的山羊多边形细胞(93.3%)和泪滴状红细胞(66.7%)的患病率更高,在患有胃肠道寄生虫病的成年山羊中,椭圆形红细胞占比更高(36.0%),而在其他疾病中占比相对较低(P<0.05)。
这些发现表明,缺铁是幼年和成年山羊异形红细胞增多症的重要病理生理机制,幼龄山羊可能也如此,无论其原因是铁限制的红细胞生成、慢性出血、功能性缺铁,还是这些机制的组合。有必要进一步研究山羊缺铁的检测和监测方法,以及异形红细胞增多症作为山羊铁状态诊断标志物的价值。