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Issue number 34.2 Other Scientific

How I use… C-reactive protein in daily practice

Published 31/01/2025

Written by José Cerón and Asta Tvarijonaviciute

Also available in Français , Deutsch , Italiano and Español

Not sure about how to use C-reactive protein assays? This paper offers seven key pointers to successfully incorporating it into everyday clinical practice.

A dog showing nasal discharge.

Key points

C-reactive protein (CRP) can be used routinely in first opinion practice in many situations, assuming the available assay is adequately validated.


CRP can be used not only to detect an inflammatory response, but also to aid in diagnosis of the underlying cause.


In inflammatory conditions, CRP is particularly useful for monitoring of treatment and predicting disease occurrence.


CRP values should be interpreted in the context of the entire clinical picture and available information, and alongside other acute phase proteins if possible.


Introduction

C-reactive protein (CRP) is an acute phase protein (APP), a term that describes proteins whose concentration changes in response to inflammation or immune system stimulation, regardless of the cause. CRP is generated quickly, with significant increases observed just a few hours after the inflammatory stimulus (e.g., 4 hours after a surgical intervention), and peak concentrations are reached at approximately 24 hours. This reaction is part of the innate immune response, which means that it is rapid and non-specific, and it can be triggered by any process that damages the animal 1. After more than 20 years of using and providing external services for CRP measurement at our laboratory, we have found that practitioners who regularly use CRP consider it to be one of the most important biomarkers of inflammation. Included as a part of their routine analytical profiles, CRP assay is employed for periodic check-ups, diagnostics, treatment monitoring, and predicting the outcome of inflammatory disease. This seven-point review will provide updated information and practical examples on how CRP can be employed in clinical practice, and will follow the initial consensus established some years ago about the use of CRP in companion animals 1.

Always use a validated assay 

Any method used to assess CRP in practice must be validated to ensure the results can be trusted. Various manufacturers currently offer certified in-house (“benchtop”) canine-specific tests, and the larger clinical pathology laboratories also provide assays. Although certain human assays may not be suitable for dogs, others can be effective and provide a cost-efficient means of measuring CRP 2. However, it is always to be recommended that standardization of the assay (using purified protein or pools of acute phase serum) and control samples should be of canine origin. 

Serum, EDTA or heparinized plasma can be employed for CRP measurements, and because the protein is fairly stable, samples can be refrigerated for several days or frozen for long-term preservation. It is important to know the effect of hemolysis, lipemia and bilirubinemia on the CRP values obtained, as the effects can vary depending on the method used. In our laboratory, the reference range for CRP in healthy dogs is below 12 mg/L, and whilst this value can vary between laboratories, it is usually not higher than 20 mg/L. There are no evident changes in reference ranges due to age or gender, although in pregnant bitches CRP increases at 21 days after fertilization, coinciding with embryonic implantation.

Other APPs can be used alongside CRP 

The possibility of using CRP along with other APPs will be considered later, but the different APPs will be described here. APPs that increase concentration after an inflammatory stimulus are known as POSITIVE APPs, while others that decrease after such a stimulus are called NEGATIVE APPs (Figure 1).

Positive APPs are further classified into two groups, namely major and moderate: Major APPs in dogs are CRP and serum amyloid A (SAA). While these proteins are present in low level in healthy animals, their concentration can increase by 10-100 times when stimulated. Moderate APPs are haptoglobin (Hp), ferritin and fibrinogen. Their concentrations increase 2-10-fold following stimulation. Major APPs exhibit a rapid increase in concentration followed by a steep decline, usually within hours, while moderate APPs take longer to both increase from and return to normal levels.

Albumin and paraoxonase-1 (PON-1) are examples of negative APPs. During inflammation, the albumin serum concentration decreases. This may be because albumin is the most abundant protein in serum, and its decrease can promote the synthesis of other proteins related to inflammation. PON-1 has an antioxidant function, and its decrease in inflammatory processes is possibly due to the associated oxidative stress that consumes this protein.

Schematic representation of the behavior of different groups of acute phase proteins after inflammatory stimulus.

Figure 1. A schematic representation of how the different groups of Acute Phase Proteins (APPs) behave after an inflammatory (red arrow) stimulus and its resolution (green arrow). 

CRP for infection and inflammation 

The main reason to use a CRP assay is to confirm or rule out an inflammatory or infectious process. Whilst the most widely used tool for detecting inflammation is the evaluation of white blood cells (WBCs), ideally CRP should be measured and interpreted at the same time. Moreover, CRP has several advantages over WBCs in detecting and evaluating the severity of inflammation, especially as it has better sensitivity. For example, higher sensitivity of CRP has been reported in cases of babesiosis (Figure 2) 3 or various surgical procedures 4, and this is particularly important where there is decreased bone marrow activity. In addition, CRP is highly stable, allowing for long-term storage of samples, which is not possible with WBCs.

Red blood cells with Babesia canis parasites inside.

Figure 2. Babesia canis parasites inside canine red blood cells. Babesiosis is a disease in which CRP can increase before the onset of clinical signs; it also causes a divergence in acute phase proteins, with an elevation in the CRP value and a decrease in Hp levels.
© Shutterstock

Whilst elevated CRP levels are very useful in detecting inflammation in the dog, it is important to note that a CRP within the reference range is also a significant clinical finding, as it suggests the absence of an acute inflammatory or infectious process. In addition to detect or rule out inflammation, CRP can also provide additional information for the clinician, as shown in Table 1.

 

Table 1. What information can CRP provide beyond detecting inflammation?

Additional information Examples
Evaluate the severity of the inflammation or inflammatory disease. This is because increases in CRP are usually related to the magnitude of the inflammation.
  • In dogs infected with Ehrlichia canis, those with myelosuppression have higher CRP values compared to those with the uncomplicated disease 5.
  • In surgery, CRP has higher concentrations where there is more severe tissue injury 4.
An increase in CRP in conditions where it is usually within the reference range may indicate the presence of complications or a severe form of the disease.
  • In benign or non-metastatic mammary tumors, CRP levels are usually within the reference range, whilst CRP levels tend to increase in cases with histologic evidence of malignancy, metastasis or local inflammation (Figure 5) 6. Similarly, in lymphomas, higher CRP values are associated with advanced stages and dissemination 7.
  • In cases of localized forms of canine demodicosis, CRP levels are within the reference range, whilst they increase in generalized cases; this can help determine whether a case is localized or generalized 8.
  • In dogs with IBD, CRP levels are usually within the reference range or show a mild increase 9,10. Therefore, significant increases would indicate a complication of this disease.
José Cerón

Major Acute Phase Proteins (APPs) exhibit a rapid increase in concentration followed by a steep decline, usually within hours, while moderate APPs take longer to both increase from, and return to, normal levels.

José Cerón

CRP may aid identification of a possible etiology 

Although CRP cannot identify the cause of inflammation, due to its non-specific nature, its magnitude of increase can help to narrow down the list of possible causes and guide the diagnostic process (Table 2; Figure 3). This can lead to various practical applications, as outlined in Table 3. In addition, it is important to note that there are situations where CRP may significantly aid in differentiating between the causes of a problem, such as:

  • Nasal disease: slight increases in CRP values have been observed in cases of aspergillosis, non-specific rhinitis, or neoplasia 17. However, if there is a marked elevation in CRP levels in a dog with signs of nasal disease (Figure 4), it may indicate an underlying inflammatory problem that is of clinical significance.
  • Gastrointestinal (GI) disease: some conditions that cause chronic GI signs in dogs, such as inflammatory bowel disease (IBD), parasitic infections, dietary and antibiotic responsive diarrhea, GI neoplasia or presumed motility disorders may not show marked increases in CRP 9. Also, intestinal malabsorption caused by exocrine pancreatic insufficiency, wheat-sensitive enteropathy or anaerobic bacterial overgrowth has been reported not to produce increases in CRP in dogs 18. Therefore, if there is a noticeable increase in CRP associated with any of these conditions, it can indicate the presence of a complicating systemic inflammatory condition.

 

Table 2. Clinical interpretation of the magnitude of serum CRP increase in dogs (from 11).

 CRP (mg/L)  Comment
 0-12 Normal (the reference range can vary depending on the laboratory)
 12-20

Slight increase of uncertain diagnostic value:

  • very mild inflammation
  • uncomplicated gastrointestinal disease 
  • uncomplicated nasal disease 
 20-39

Increased levels:

  • mild inflammation
  • uncomplicated viral disease 
 40-100

Significantly increased levels:

  • moderate inflammation
  • generalized demodicosis
  • possible metastasis (in cases of tumors such as mammary neoplasia or lymphoma)
 > 100

Severe inflammation:

  • systemic inflammatory response syndrome/septicemia (SIRS)
  • immune-mediated disorder (steroid-responsive meningitis-arteritis, immune-mediated hemolytic anemia, immune-mediated polyarthritis)

 

Table 3. Potential usefulness of CRP in narrowing the list of causes and guiding diagnosis.

Application and explanation  Examples 
Suspicion of sepsis or immune-mediated disorder: Increases in CRP > 100 mg/L are usually associated with either SIRS, which in the case of a positive bacterial culture could indicate sepsis, or an immune-mediated disorder.
  • In dogs with clinical signs of respiratory disease, bacterial pneumonia was identified with 100% specificity when CRP levels exceeded 100 mg/L. Other respiratory diseases/syndromes had significantly lower CRP values, such as bacterial tracheobronchitis (23 mg/L), chronic bronchitis (13 mg/L), eosinophilic bronchopneumonitis (5 mg/L), canine idiopathic pulmonary fibrosis (17 mg/L) and cardiogenic pulmonary edema (19 mg/L) 12.
  • In dogs with parvovirus infection, a CRP level around or higher than 100 mg/L may indicate a septicemia complication associated with a compromised intestinal barrier 13. This is because the two components involved in parvovirus infection (i.e., GI disease and a viral infection) usually produce only mild (< 40 mg/L) changes in CRP 9.
 
Suspicion of an infectious-inflammatory cause: Where clinical signs could be caused by either inflammatory or non-inflammatory factors, a CRP level above the reference range indicates a possible infectious-inflammatory cause.
  • In cases of lameness, CRP can aid in distinguishing between immune-mediated polyarthritis, which typically results in significant increases, and other conditions, such as osteoarthritis or intervertebral disc disease, which do not affect CRP levels 14.
  • In dogs presenting with neurological signs, a significant rise in serum CRP may aid in the diagnosis of steroid-responsive meningitis-arteritis, as opposed to other potential diagnoses such as other causes of meningoencephalitis, intervertebral disc disease, degenerative lumbosacral stenosis, central nervous system neoplasia or idiopathic epilepsy, which do not typically result in major increases in serum CRP levels 15.
  • In pyometra, CRP levels can help to distinguish it from cystic endometrial hyperplasia/mucometra (CEH). One study 16 found CRP concentrations of 200 mg/L in pyometra cases compared to 53 mg/L in CEH cases. This is because CEH is not caused by bacterial infection, but rather results from accumulation of mucus material in the uterus.

 

This point only refers to CRP measurement as a stand-alone test, but additional examples of how CRP can be used in combination with other APPs to identify the cause of certain conditions are discussed below.

CRP concentration may aid identification of a possible etiology.

Figure 3. The magnitude of the increase in CRP levels is related to the severity of the immune system response.

A dog showing nasal discharge.

Figure 4. Detecting marked elevation in CRP levels in a dog with signs of nasal disease can indicate an underlying inflammatory problem. 
© Shutterstock

CRP helps monitor response to treatment 

CRP values returning to normal levels in an infectious-inflammatory disease indicates that a dog is responding to treatment and implies a good prognosis. This has been demonstrated in numerous inflammatory diseases, such as acute pancreatitis, where CRP can be a useful tool for monitoring clinical progression and response to treatment 19. CRP has been shown to better reflect the evolution of inflammation after treatment compared to WBCs in conditions such as immune-mediated polyarthritis, indicating periods of relapse and remission of the disease 20. Examples of interpretation are:

  • Positive response → decrease in CRP: If the dog’s initial CRP levels are high, a return to the reference range along with clinical improvement indicates that treatment can be stopped. In this way, antibiotic treatments can be greatly optimized. For instance, in a study involving dogs with bacterial pneumonia, the duration of antibiotic administration was significantly reduced when normalization of serum CRP was used to guide the treatment 21. In this study, antibiotics were discontinued 5-7 days after serum CRP returned to normal, as opposed to the conventional approach of treating for 1-2 weeks beyond the resolution of alveolar density on thoracic radiographs. This reduction in treatment duration did not increase the number of relapses.
  • Negative response → little or no decrease in CRP: The absence of a decrease in CRP after treatment would indicate that either the diagnosis or the treatment was inadequate, and should necessitate a thorough evaluation of the patient. This could be considered a “red-light” alert. For example, CRP levels after surgery are typically low by the time sutures are removed 4. Therefore, an increase in CRP during the postoperative period may indicate the presence of complications, such as incision site infection that can appear after surgical treatment for pyometra.

 

CRP can predict the presence of an inflammatory-infectious disease

CRP’s high sensitivity and fast stimulation of response allow detection of subclinical inflammation, with changes in APPs occurring before clinical signs develop. Therefore, this protein is highly suitable for routine health checks, where an increase in APPs in an apparently healthy animal can indicate the presence of a subclinical disease or predict the development of active disease in the near future. For example, in a study on dogs infected with Babesia gibsoni, high concentrations of CRP were documented despite the absence of obvious clinical signs or parasitemia 22. Similarly, high CRP values are reported in asymptomatic dogs infected with Leishmania infantum – and it can be assumed that these animals may develop clinical signs at a later stage 23.

Mammary tumors in a bitch.

Figure 5. Mammary tumors cannot be identified as benign or malignant simply on clinical examination; however, CRP levels are usually within the reference range for benign or non-metastatic mammary tumors, whilst they tend to increase where there is metastasis, local inflammation or histologic evidence of malignancy. 
© Shutterstock

The future: APPs profiles

Divergences between major and moderate APPs can provide useful clinical information, so if possible, it is recommended to use a laboratory profile that includes at least one major and one moderate APP. The term “divergence” describes a situation where APPs of the two groups do not change as expected in the presence of an inflammatory stimulus. Some relevant examples are:

  • ↑ Hp & ↔ CRP (increased Hp concentration with CRP values remaining in the reference range). Given that CRP usually shows a greater increase than Hp in an inflammatory situation, detecting this profile in a dog with no history of glucocorticoid treatment could indicate increased production of endogenous steroids. Glucocorticoids stimulate increases in haptoglobin and decreases in CRP 24, making this profile a potential indicator of canine hyperadrenocorticism. If a dog diagnosed with hyperadrenocorticism shows an increase in CRP, it indicates the presence of a severe inflammatory stimulus that can overcome the inhibitory effect of the endogenous corticosteroids. This may suggest the need to investigate potential inflammatory complications such as severe sepsis, urinary infection, deep pyoderma, severe mastitis or immune-mediated hemolytic anemia 24.
  • ↔ Hp & ↑ CRP (steady or decreased levels of Hp accompanied by an increase in CRP levels). This profile may indicate hemolysis or internal hemorrhage leading to hemolysis. This is because Hp binds to hemoglobin released from damaged erythrocytes to facilitate its degradation and prevent the oxidative stress caused by hemoglobin; therefore, Hp can be consumed after hemolysis. As an example, in dogs naturally infected with B. canis, the concentration of CRP increased (mean value of 170 mg/L), while the concentration of Hp remained within the reference range (mean value of 2.7 g/L). The haptoglobin values could reflect the mixed effects of inflammation, which is associated with moderate increases, and hemolysis, which reduces the haptoglobin concentration 3.
  • ↑ CRP & ↔ Ferritin (increased CRP and normal levels of ferritin). In canine pyometra there is a significant increase in serum CRP, indicating a severe inflammatory condition. However, serum ferritin, despite being a moderate positive APP, does not show a significant increase. This divergence in the dynamics of these APPs could be a useful tool for suspecting cases of this disease 25.
Asta Tvarijonaviciute

Whilst the most widely used tool for detecting inflammation is the evaluation of white blood cells, ideally CRP should be measured and interpreted at the same time.

Asta Tvarijonaviciute

Conclusion

CRP is a valuable diagnostic tool in routine canine practice and is an excellent assay to incorporate when testing both in disease situations and in routine health screens. It is expected that the information present in this paper will assist practitioners already using CRP to maximize its benefits, and encourage those unfamiliar with CRP to consider its applications. This review will provide updated information and practical examples on how CRP can be employed in clinical practice, and will follow the initial consensus based on a seven point plan established some years ago about the use of CRP in companion animals 1

 

Conflict of interest statement; Neither author has a financial or personal relationship with other people or organizations that could inappropriately influence or bias the content of the paper.

 

Acknowledgement

The authors would like to dedicate this work to Dr. Marco Caldin, one of the pioneers and main contributors to the application of CRP in canine practice; his vision, knowledge and legacy is a continuous source of inspiration to us and other many researchers in this field. The authors would also like to thank Silvia Martinez-Subiela for her advice and help in the preparation of this manuscript.


References

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  23. Cerón JJ, Pardo-Marin L, Caldin M, et al. Use of acute phase proteins for the clinical assessment and management of canine leishmaniosis: general recommendations. BMC Vet. Res. 2018;14(1):196. Available from: https://pubmed.ncbi.nlm.nih.gov/29925385/

  24. Caldin M, Tasca S, Carli E, et al. Serum acute phase protein concentrations in dogs with hyperadrenocorticism with and without concurrent inflammatory conditions. Vet. Clin. Pathol. 2009;38(1):63-68. Available from: https://pubmed.ncbi.nlm.nih.gov/19228354/

  25. Cerón JJ, Pardo-Marin L, Wdowiak A, et al. Divergences between serum C-reactive protein and ferritin concentrations in canine pyometra. BMC Vet. Res. 2023;19(1):1-6. Available from: https://bmcvetres.biomedcentral.com/articles/10.1186/s12917-023-03630-3

José Cerón

José Cerón

Dr. Cerón is a full professor at Murcia University Veterinary School and Diplomate of the European College of Veterinary Clinical Pathology Read more

Asta Tvarijonaviciute

Asta Tvarijonaviciute

Dr. Tvarijonaviciute is currently a lecturer in the Small Animal Internal Medicine Service at Murcia University Veterinary Teaching Hospital Read more

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