Scinovex
article Open Access

Hematological and biochemical analysis of benign prostatic hyperplasia treatment in dogs: Finasteride vs. Castration

International Journal of Advanced Biochemistry Research · 2026 · Vol. 10(6) · pp. 806–808
Selim AkramKalyani RayDipanjan ChakrabortyAjeet Kumar JhaAmit Kumar NathKeshav Kumar

Abstract

Canine prostatic disorders, which are mainly benign prostatic hyperplasia (BPH), significantly impact old male dogs. This study investigated hematological and biochemical changes in 24 intact male dogs with BPH and compared the effects of finasteride (Group I, n = 12) and castration (Group II, n = 12) over a period of 45 days. Before and after treatment, Hematological parameters (hemoglobin, PCV, TEC, TLC, DLC), biochemical markers (BUN, creatinine, ALP, SGPT, SGOT), and the serum biomarker DHT were evaluated. In the pre-treatment group, dogs showed reduced hemoglobin and PCV levels, with elevated BUN, creatinine, and ALP levels, which indicates renal and hepatic stress. Neutrophilia was noticed in BPH cases. After treatment, these parameters showed significantly normal (p≤0.05) in both groups, with castration demonstrating slightly greater improvement in biochemical markers.

Full Text

Tables and figures are in the full-text PDF.

Introduction

Benign prostatic hyperplasia (BPH) is common in uncastrated male dogs. BPH affects more than 80% of dogs older than 5 years (Johnston et al., 2000) [9] . Urinary and digestive complications resulting from prostate enlargement and compression of adjacent structures (Alonge et al., 2018) [2] are the primary symptoms. Hematological, biochemical, and serum biomarker analyses, including dihydrotestosterone (DHT), are necessary for evaluating systemic health, detecting internal complications, and monitoring treatment efficacy. When the blood biochemical parameters, such as blood urea nitrogen (BUN), creatinine, and alkaline phosphatase (ALP) are elevated, it indicates renal or hepatic stress, while hematological changes, such as reduction in hemoglobin or neutrophilia, may indicate chronic blood loss or infection (Das et al., 2017) [5] . This study evaluates hematological and biochemical changes in dogs with BPH and compares outcomes of medical (finasteride, Group I) and surgical (castration, Group II) interventions.

Materials and Methods

Study Population: Twenty-four intact male dogs, above 5 years of age and exhibiting clinical signs of prostatic disorders (e.g., hematuria, dysuria, tenesmus), were selected at the Department of Veterinary Gynaecology and Obstetrics, West Bengal University of Animal and Fishery Sciences, from March 2023 to December 2023. After taking the owners' concerns into account, the affected dogs were divided into two groups. Group I and Group II, with 12 dogs in each. Group I received finasteride (0.5 mg/kg/day, orally) for 45 days, and Group II underwent open castration under general anesthesia (Fossum, 2018) [6] .

Diagnostic and analytical procedures: For Hematological Analysis, blood samples were collected in EDTA tubes on day 0 (before treatment) and day 45 (after treatment). Hemoglobin (g/dL), PCV (%), TEC (x10 6 /µL), TLC (x10 3 /µL), and DLC (neutrophils, lymphocytes, monocytes, eosinophils, and basophils) were measured and summarized in Table 1. For Biochemical Analysis, serum samples collected before treatment (day 0) and after treatment (day 45) were analyzed for BUN (mg/dL), creatinine (mg/dL), ALP (IU/L), SGPT (IU/L), and SGOT (IU/L). Results are presented in Table 2. Serum DHT levels were measured using a 96-well ELISA kit. For Data Analysis, parameter data were compiled, and standard statistical methods described by Snedecor and Cochran (1967) [13] were used to evaluate the results.

Results

Hematological Findings: Hemoglobin levels were low in both groups of dogs before treatment. Group I had 11.8 grams per deciliter (g/dL), and Group II had 11.6 g/dL, both below the normal range of 12-18 g/dL. The packed cell volume (PCV) was also low. PCV for Group I was 35.2%, and for Group II was 34.8%, while the normal range is 37-55%. This was due to blood in their urine. The total erythrocyte count (TEC) was slightly low, with Group I at 5.1 million cells per microliter and Group II at 5.0 x10 6 /µL (normal is 5.5-8.5 x10 6 /µL). The total leucocyte count (TLC) was normal in both groups, with Group I at 10.2 x10 3 /µL and Group II at 10.4 x10 3 /µL (normal is 6-17 x10 3 /µL). However, in dogs with BPH, the neutrophil count was elevated: 75.6% in Group I and 76.1% in Group II (normal, 60-70%). After treatment, hemoglobin levels improved to 14.2 g/dL in Group I and 14.5 g/dL in Group II, both within the normal range. The PCV also normalized, at 41.3% in Group I and 42.1% in Group II. Neutrophil counts decreased to 65.4% in Group I and 64.8% in Group II among dogs with prostatitis. No significant differences were observed between the two groups after treatment.

Biochemical Findings

Before treatment, levels of BUN (blood urea nitrogen), creatinine, and alkaline phosphatase (ALP) were higher than normal. In Group I, BUN was 32.4±4.5 mg/dL, creatinine was 1.8±0.3 mg/dL, and ALP was 180±25 IU/L. In Group II, BUN was 33.1±4.7 mg/dL, creatinine was 1.9±0.4 mg/dL, and ALP was 185±27 IU/L (Table 2). This suggests kidney and liver stress, as these results were statistically significant (p≤0.05). Levels of serum glutamic-pyruvic transaminase (SGPT) and serum glutamic-oxaloacetic transaminase (SGOT) were normal and within limits in both groups.

After treatment, BUN levels decreased to 18.2±2.

Discussion

Before treatment, reductions in hemoglobin and PCV were observed in 25% of dogs, mainly due to hematuria from prostatic enlargement (Das et al., 2017) [5] . Corrada et al.

(2004) [4] and Barsanti (2008) [3] reported similar findings; they also reported neutrophilia in BPH cases, indicating an inflammatory response and infection (Akram et al., 2025) [1] Normalization of these parameters after treatment reflects resolution of hematuria and infection, which may be due to reduced prostate size and elimination of androgen-driven hyperplasia in dogs, achieved through finasteride treatment and castration (Sirinarumitr et al., 2001) [12] . Before treatment, elevated BUN and creatinine levels suggest renal stress from urethral obstruction; the same finding was reported by Mahendran et al. (2013) [10] . Both finasteride and castration effectively managed canine prostatic disorders and normalized hematological, biochemical, and DHT levels. The significant reduction in DHT in both groups supports the role of androgens in BPH, as noted by Gloyna et al. (1970) [7] and Isaacs & Coffey (1981) [8] . Castration may more effectively reduce DHT and prostatic size by completely removing testicular androgens, whereas finasteride inhibits DHT production through 5α-reductase inhibition. The normalization of biochemical parameters indicates improvement of renal and hepatic stress. The improved results of castration are similar to findings by Corrada et al. (2004) [4] and Barsanti (2008) [3] . Finasteride is a better option for dogs at risk of anesthesia, as supported by Menon et al. (2011) [11] . Hematological and biochemical tests are necessary for diagnosing and monitoring canine prostatic diseases. Dogs with BPH exhibited decreased hemoglobin and PCV, along with increased BUN, creatinine, and ALP, indicating systemic problems. Normalization in Post-treatment dogs confirm the effectiveness of both finasteride and castration. Castration showed slightly better laboratory results. Both treatments are effective, while with castration showed greater reductions in prostatic size and DHT levels. Finasteride serves as a good non-surgical alternative for high-risk patients. Continuous assessment of blood, biochemical, and biomarker parameters is necessary to evaluate treatment success and ensure the overall health of the patient.

Acknowledgement

AcknowledgementThe Authors have no conflict of interest in this study. The authors are highly thankful to the Head, VCC, Belgachia complex, WBUAFS. Part of this research was funded through a research grant from the Department of Animal Reproduction, Gynecology and Obstetrics, WBUAFS.

References

  1. Akram S, Chakraborty D, Mandal S, Ray K. Antibiotic sensitivity profiling in canine prostatic disorders: A clinical investigation from Kolkata, West Bengal. Int J Vet Sci Anim Husb. 2025;10(4):335-337.
  2. Alonge S, Melandri M, Aiudi G, Lacalandra GM. Advances in prostatic diagnostics in dogs: The role of canine prostatic specific esterase in the early diagnosis of prostatic disorders. Top Companion Anim Med. 2018;33(4):105-108.
  3. Barsanti J. Canine prostatic disease. In: Proc Int SCIVAC Congr. 2008. p. 37-38.
  4. Corrada Y, Arias D, Rodríguez R, Spaini E, Fava F, Gobello C. Effect of tamoxifen citrate on reproductive parameters of male dogs. Theriogenology. 2004;61(78):1327-1341.
  5. Das MR, Patra RC, Das RK, Rath PK, Mishra BP. Hemato-biochemical alterations and urinalysis in dogs suffering from benign prostatic hyperplasia. Vet World. 2017;10(3):331-335.
  6. Fossum TW. Small animal surgery. 5th ed. St. Louis (MO): Mosby; 2018.
  7. Gloyna RE, Siiteri PK, Wilson JD. Dihydrotestosterone in prostatic hypertrophy: II. The formation and content of dihydrotestosterone in the hypertrophic canine prostate and the effect of dihydrotestosterone on prostate growth in the dog. J Clin Invest. 1970;49(9):1746-1753.
  8. Isaacs JT, Coffey DS. Changes in dihydrotestosterone metabolism associated with the development of canine benign prostatic hyperplasia. Endocrinology. 1981;108(2):445-453.
  9. Johnston SD, Kamolpatana K, Root-Kustritz MV, Johnston GR. Prostatic disorders in the dog. Anim Reprod Sci. 2000;60-61:405-415.
  10. Mahendran K, Priyanka KS, Dey S, Mondal DB. Acute bacterial prostatitis in dogs. Indian Vet J. 2013;90(3):90-91.
  11. Menon K, Devaraj M, Krishnaswamy A, Honnappa TG. Prevalence and influence of age and breed on prostatic diseases in dogs. Indian J Anim Reprod. 2011;32(1):5960.
  12. Sirinarumitr K, Johnston SD, Kustritz MV, Johnston GR, Sarkar DK, Memon MA. Effects of finasteride on the size of the prostate gland and semen quality in dogs with benign prostatic hypertrophy. J Am Vet Med Assoc. 2001;218(8):1275-1280.
  13. Snedecor GW, Cochran WG. Statistical methods. 6th ed. Ames (IA): Iowa State University Press; 1967.
Veterinary Medicine and SurgeryUrinary Bladder and Prostate ResearchUrologic and reproductive health conditionsbenign prostatic hyperplasiafinasteridecastrationhepatic stressneutrophiliahematological parametersdogs
Citations
0
FWCI
0.00
field-weighted impact
References
0
Percentile
46%
vs. same field & year
Citation Network

How this paper connects to the literature. Drag to explore, click any node to open that paper.