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. 2021 May 25;32(4):326–e90. doi: 10.1111/vde.12970

The usefulness of a hydrolysed fish and rice starch elimination diet for the diagnosis of adverse food reactions in cats: an open clinical trial

Chiara Noli 1,, Giorgia Beltrando 2
PMCID: PMC8361712  PMID: 34033172

Abstract

Background

Diagnosis of adverse food reaction (AFR) is based on an eight week elimination diet (ED) and is confirmed by relapse upon re‐challenge with the previously fed diet. Hydrolysed EDs are commonly used for this purpose.

Objective

To evaluate the commercially available hydrolysed fish protein and rice starch ED Farmina UltraHypo (FUH) for the diagnosis of feline AFR.

Animals

Thirty‐two nonseasonally pruritic cats.

Methods and materials

Pruritus was assessed with a new dual Visual Analog Scale, lesions with the Scoring Feline Allergic Dermatitis scale and Quality of Life with a validated questionnaire on days 0 and 56. Short‐acting corticosteroids or oclacitinib were permitted during the first six weeks. Cats showing 50% pruritus and/or lesional improvement were separately challenged with their prior diet, fish and rice. Cats not responding to the study diet were fed another hydrolysed diet for two months.

Results

Twenty‐five cats completed the ED: four dropped out due to vomiting and/or diarrhoea, one owing to low palatability and two were lost to follow‐up. In 17 cats, pruritus improved by >50% and these underwent dietary challenges. Of these, nine reacted to their prior diet and/or fish and/or rice and were diagnosed with AFR, while eight did not relapse (and a diagnosis of AFR was considered to be doubtful). Of the eight cats in which pruritus did not improve, four underwent a second ED with no improvement.

Conclusion and clinical importance

FUH may be a useful ED for the diagnosis of feline AFR, even in cats reacting to fish or rice.

Short abstract

Background – Diagnosis of adverse food reaction (AFR) is based on an eight week elimination diet (ED) and is confirmed by relapse upon re‐challenge with the previously fed diet. Hydrolysed EDs are commonly used for this purpose. Objective – To evaluate the commercially available hydrolysed fish protein and rice starch ED Farmina UltraHypo (FUH) for the diagnosis of feline AFR. Conclusion and clinical importance – FUH may be a useful ED for the diagnosis of feline AFR, even in cats reacting to fish or rice.

Introduction

Adverse food reaction (AFR) is defined as any unexpected reaction to food due to immunological and nonimmunological mechanisms, and thus encompasses both food allergy and food intolerance.1 Prevalence of feline AFR is estimated to be approximately 5% of all skin diseases, and ≤21% of all feline pruritic skin conditions.2

The most common dermatological signs of feline AFR are nonseasonal pruritus, leading to self‐induced alopecia and excoriations, miliary dermatitis and eosinophilic lesions, affecting the face/head, the ears, the ventrum and the feet.3 Cats with AFR also may show gastrointestinal signs – mainly vomiting and diarrhoea, while salivating and flatulence are less frequently reported.4 The diagnosis of feline AFR relies on the administration of an elimination diet (ED) for at least eight weeks, as in vitro testing is reported to be unreliable for this purpose.5, 6 An improvement of the skin and/or gastrointestinal condition followed by relapse of clinical signs after re‐feeding the usual diet, followed by renewed improvement when feeding the ED, is required to confirm AFR. For this purpose, the selection of a proper ED, containing ingredients unknown to the cat and/or that do not elicit an adverse response, is a key factor for the diagnosis of AFR. Limited antigen diets are not always reliable, as a consequence of frequent label discrepancies and potential cross‐reactions, albeit not yet determined in cats.7, 8, 9

Hydrolysed EDs are currently considered a valuable tool for the diagnosis of AFR, able to overcome the above‐mentioned drawbacks of limited antigen diets. However, only a few investigations on undeclared protein content in these diets have been conducted.10 Hydrolysis is an enzymatic proteolytic process that cleaves large proteins into small peptides, thereby reducing the allergenicity of food components. Extensive protein hydrolysation (<10 kD) is important to prevent allergen recognition.11 Proteins present in vegetables also can be recognised by the immune system, and starch rather than flour preferably should be contained in these foods.12 Interestingly, one small in vitro study suggests that even hydrolysed diets could elicit an adverse response in cats comparable to that of their basal diet containing the same intact proteins.13

Two studies report the use of hydrolysed diets for chronic vomiting and diarrhoea, inflammatory bowel disease and AFR with gastrointestinal signs, yet, to the authors’ knowledge, there are no studies reporting the use of hydrolysed diets for the diagnosis of AFR in cats with dermatological signs.14, 15 Recently, a hydrolysed fish protein (herring) and rice starch diet (Vet Life Canine UltraHypo, Farmina Pet Food; Nola, NA, Italy) claiming the absence of peptides >6 kDa in size, was considered suitable for the diagnosis of AFR in dogs.16 A feline formulation of the same diet is commercially available. The aim of this study was to evaluate the performance of Vet Life Feline UltraHypo (FUH) diet for the diagnosis of AFR in cats with nonseasonal pruritic dermatitis. We hypothesised that this hydrolysed fish and rice starch diet would be well‐tolerated by cats, including those sensitised to fish and/or rice.

Methods and materials

Animals

Inclusion criteria

Nonseasonally pruritic cats were recruited by four veterinarians in eight referral clinics and included whenever they showed clinical signs compatible with feline allergic dermatitis such as self‐induced alopecia, self‐inflicted excoriations, miliary dermatitis and lesions of the eosinophilic granuloma complex. Owing to the fact that some of the included cats could have suffered flea bite allergy, whenever no preventive measures effective against fleas or other parasites had been adopted previously, a fluralaner‐moxidectin topical solution (Bravecto Plus, MSD; Milan, Italy) was administered one month before inclusion, in order to exclude flea bite allergy as a confounder of the study results.

Exclusion criteria

Cats were not enrolled whenever they showed seasonal pruritic flares or concurrent systemic diseases at the time of inclusion, or if they had been treated with short‐acting glucocorticoids or oclacitinib (off‐label) in the previous two weeks or with long‐lasting glucocorticoids or ciclosporin within the previous two months. Presence of a skin or ear canal infection was not an exclusion criterion.

Evaluation of cats

At the time of inclusion (Visit 1, V1) all cats underwent a dermatological examination, including (when necessary) a cytological evaluation for bacterial and/or yeast infections. The investigators then recorded the historical information and assessed the skin lesions by means of the Scoring Feline Allergic Dermatitis system (SCORFAD; range 0–16).17 Owners were requested to assess their cats’ pruritus using a not yet validated double (licking and scratching) 10 cm Visual Analog Scale (pVAS) with descriptors.18 In addition, they were asked to complete a validated feline quality of life (QoL) questionnaire (range 0–45; the higher the score, the worse the QoL).19 After inclusion, owners were instructed to feed FUH exclusively for at least eight weeks. In case of bacterial or yeast infection, systemic antibiotic or antifungal drugs and/or topical antiseptic treatments were prescribed for the first three to four weeks together with the diet, starting from the inclusion day onwards. Whenever necessary, oral prednisolone 0.5–2 mg/kg daily or every other day (Prednicortone, Dechra; Northwich, UK) or off‐label oclacitinib 1 mg/kg twice daily (Apoquel, Zoetis; Rome, Italy) were permitted during the first six weeks to control pruritus. Long‐lasting glucocorticoids, ciclosporin or supplements of any kind were not permitted during the study. Any concomitant drug, with the exception of ectoparasiticides, had to be stopped two weeks before the end of the ED trial and final assessment. If for any reason the adjunct treatments were not stopped or skin infections were still present at the end of the ED trial, the diet was prolonged until two weeks after discontinuation of therapies and resolution of infections.

After at least eight weeks of ED (V2), cats were re‐evaluated by the same veterinarian. After assessing the absence of concurrent infections through a dermatological examination, clinicians re‐evaluated skin lesions by means of SCORFAD, and owners completed the dual pVAS and the feline QoL questionnaire.

Whenever the owner‐assessed pVAS had decreased by ≥50% compared to V1 and/or lesions had resolved at V2, owners were instructed to perform a diet provocation test to confirm the diagnosis of AFR. Owners were instructed to add home‐cooked rice, fish (usually either canned tuna or boiled cod) and the prior diet, individually and one after the other, for a maximum of 14 days each. If a relapse was observed during the provocation phase, owners were instructed to stop the provocative food and feed the ED exclusively until clinical improvement was achieved again, and then to proceed to the next provocation test. In case of relapse with the prior diet, fish and/or rice, followed by a new improvement with the elimination diet, the cats were diagnosed with AFR.

Cats in which pruritus and lesions did not improve were fed another ED (Anallergenic, Royal Canin; Milan, Italy) for two further months and re‐evaluated at the end of the diet.

Informed consent and animal use

In order for their cats to be included in the study, owners needed to give oral informed consent. The food was marketed and labelled for the purpose of AFR diagnosis at the time the study was conducted. Additionally, the procedure of feeding a hypoallergenic diet for eight weeks, followed by challenge periods with the original diet or with single ingredients, was deemed to be the standard of care for the diagnosis of AFR.

Statistical analysis

With the aim of identifying possible clinical parameters that could predict response to ED and/or to provocation tests, several pre‐study variables were compared between cats with confirmed AFR, those with doubtful diagnosis and those not responding to the diet. ANOVA was used for age, SCORFAD, pVAS and QoL scores, while Fisher's test was used for sex and reproductive state. Changes in SCORFAD, pVAS and QoL between V1 and V2 in each group, were expressed as means. All statistical analyses were performed using SAS 9.2 (SAS Institute Inc.; Cary, NC, USA). Significance was set at P < 0.05.

Results

Thirty‐two cats were included in the study: 24 European shorthair, two Devon rex, two British shorthair, and one each of European longhair, Persian, Chartreux and Maine coon. The mean age was 5.2 years (range five months–14 years). Ten were male (all castrated) and 22 were female (of which four were intact). Further historical data are given in Supporting information Tables S1 and S2.

Twenty‐five cats completed the eight week trial with FUH (Figure 1 and Table S3). Of these, eight did not improve, while 17 (70.8%) were considered to have improved. All 17 cats which improved underwent the provocation test. Upon provocation, nine demonstrated a relapse of clinical signs and a relief of pruritus after reintroduction of the ED and were thus diagnosed with AFR. Among the nine cats with confirmed AFR, four reacted to rice and two to fish. Eight of the 17 cats that improved with the ED relapsed neither with the old diet, nor with fish or with rice, and a diagnosis of AFR was considered to be doubtful.

Figure 1.

Figure 1

Summary of results of feeding a hydrolysed fish and rice starch diet to 32 cats suspected of having adverse food reactions.

Eight cats did not improve with the ED (Figure 1 and Table S3). Of these, four underwent the second eight week hydrolysed ED period, and none of these improved.

Seven cats did not complete the elimination trial period (Figure 1 and Table S3). One refused to eat the diet owing to low palatability, one was euthanised as a consequence of a malignant tumour, one was lost to follow‐up, and four had signs of vomiting and/or diarrhoea. Of these four cats, one improved on another hydrolysed ED (Royal Canin Anallergenic), while the others went back to their original diet and were treated symptomatically.

For humane reasons, concurrent antipruritic and or antibiotic treatments were administered to 15 of the 25 cats that completed the diet (Table S4). Of these, five were diagnosed with AFR, in three AFR was excluded and seven had a doubtful diagnosis. Administered molecules comprised methylprednisolone 1 mg/kg once daily), betamethasone (0.1 mg/kg once daily), topical hydroxycortisone aceponate, maropitant (2 mg/kg once daily), oclacitinib (1 mg/kg twice daily), cephalexin (20 mg/kg twice daily) and amoxicillin/clavulanic acid (15 mg/kg twice daily). In every case, with exception of one cat (Case 26 with a doubful AFR diagnosis), all treatments were withdrawn ≥14 days before the final visit. Details on concomitant treatments in cats which completed the diet are reported in Table S4.

No statistically significant differences in age, sex, reproductive state or double pVAS scores were observed at V1 between cats that were ultimately confirmed with AFR, those that failed to respond to the diet, and those that failed to respond to provocative challenges.

Mean pruritus, lesional and quality of life scores are given in Table 1. In the nine cats with confirmed AFR, pVAS scores improved by a mean of 68.6%, SCORFAD scores by a mean of 87.5% and QoL by a mean of 48.6% at V2 (Table 2). The percentage improvements in other study animals are reported in Table 2. Improvements of all parameters in cats with confirmed or doubtful AFR were statistically significant (Table 1).

Table 1.

Mean pruritus score, lesional score and quality of life score before and after a two month hydrolysed fish and rice starch elimination diet in 25 cats with signs of cutaneous allergy

Number of cats pVAS V1 pVAS V2 pVAS P‐value SCORFAD V1 SCORFAD V2 SCORFAD P‐value QoL V1 QoL V2 QoL P‐value
Confirmed AFR 9 7.0 2.2 0.000 4.8 0.6 0.000 22.0 11.3 0.019
Improved, no relapse upon provocation 8 6.2 2.4 0.003 4.9 1.6 0.032 20.1 10.6 0.063
Nonresponders 8 6.1 6.3 0.835 5.6 4.4 0.239 15.3 16.0 0.801

AFR, adverse food reaction; pVAS, double pruritus Visual Analog Scale score (range 0–10); SCORFAD, Scoring Feline Allergic Dermatitis lesion index (range 0–16); QoL, quality of life score (range 0–45); V1, visit 1; V2, visit 2, at the end of the elimination diet.

Table 2.

Mean percentage improvement of pruritus score, lesional score and quality of life score after a two month hydrolysed fish and rice starch elimination diet in 25 cats with signs of cutaneous allergy

Mean percentage improvement Number of cats pVAS SCORFAD QoL
Confirmed AFR 9 68.6 87.5 48.6
Improved, no relapse upon provocation 8 61.3 67.3 47.3
Nonresponders 8 –3.3 21.4 –4.6

AFR, adverse food reaction; pVAS, double pruritus Visual Analog Scale score (range 0–10); SCORFAD, Scoring Feline Allergic Dermatitis lesion index (range 0–16); QoL, quality of life score (range 0–45).

Discussion

There are only two studies evaluating the efficacy of a particular diet in cats with food allergy. One study evaluated the efficacy of two commercial limited antigen diets in maintaining the remission obtained with a home‐cooked diet in cats with dermatological manifestations of AFR.20 The other study investigated the efficacy of a hydrolysed diet in cats with gastroenteric signs of AFR.14 To the best of the authors’ knowledge, this is the first study to evaluate a hydrolysed ED for the diagnosis of AFR in cats with dermatological signs. Similar to the canine study with the same product, this study suggests that FUH is suitable for use as an ED for the diagnosis of feline AFR.16

A decrease of pruritus and clinical signs was observed in 17 of 25 (68%) cats that completed the ED, in line with what was observed in dogs.16 However, only nine of 17 (53%) cats that improved on the ED and completed provocative challenges reacted to other foods. This resulted in an AFR prevalence of approximately 36% in cats with signs of cutaneous allergy (nine of 25 cats that completed the ED trial), similar to the percentage described in dogs, and higher than that reported previously in cats.2 This discrepancy could depend on the low number of studies and of cats analysed, as well as on different diagnostic procedures, including diets used for obtaining the diagnosis.

Two cats improving on the ED did not relapse on their old food, and recurred when fed whole rice. The reason for this is not completely understood: they may have been exposed to more than one diet in the past and not have been fed the culprit diet during the provocation test. This also could be a reason for improving during the ED and not deteriorating during the provocation phase in “doubtful” cases. In fact, similar to the canine study, several cats improved on the diet and did not relapse upon provocation, maybe as a result of a wrong choice of provocation diet, or administration of concomitant treatments (see discussion below) during the first month of ED, or thanks to the good‐quality balanced formula of the ED. Those cats with a doubtful diagnosis of AFR were nearly as numerous as those with confirmed AFR, and this finding underpins the importance of performing several provocation tests at the end of the ED trial, for the confirmation of the diagnosis of AFR. A false positive diagnosis of AFR could possibly imply pointlessly keeping a cat on an hypoallergenic diet for the rest of its life.

Fifteen of the 25 cats that completed the diet were treated with concomitant antipruritic and/or antibiotic therapy in the first period of the ED. Ideally, in order to precisely evaluate the efficacy of an ED, no treatment should be allowed during its administration; however, it would not have been ethical to leave the patients with pruritus and infections for such a long period of time. Short‐acting topical and systemic antipruritic therapies and antibiotics thus were allowed, as generally prescribed in everyday practice, with a withdrawal of at least two weeks before the final evaluation visit. A washout period of two weeks was considered sufficient for the observation of re‐occurrence of pruritus and/or lesions in nonresponding cats, similar to what recently has been suggested in dogs.25 Pruritus was considered to relapse earlier than skin lesions upon drug withdrawal, and its improvement at the end of the dietary trial was taken as major outcome of ED success. In just two AFR confirmed cases (cases 3 and 17) pruritus scores did not improve by >50%, and lesional improvement was used to define ED efficacy instead. The first cat (Case 3) had received no treatment during the ED and in the second case (Case 17) topical aceponate spray was withdrawn >28 d before the final visit, so that the lesional improvement observed cannot be considered a consequence of concomitant therapy in either case. Interestingly, seven of eight doubtful AFR cases (versus five of nine cats with AFR and three of eight cats without AFR) had been treated with concomitant therapy in the first month on the ED, which could have been responsible for their improvement during the ED trial period.

Four cats of nine (44%) with confirmed AFR relapsed with rice and two of nine (22%) to fish. These prevalences are much higher than what has been reported previously in food‐allergic cats, and the reason for this discrepancy is unknown.26 Differences may depend on geographical variations in feeding habits, and no study was yet been performed in the authors’ country to allow a direct comparison of allergen prevalences.

The fact that cats that did not tolerate rice or fish could tolerate FUH suggests that the level of hydrolysis is adequate in FUH or that fish fed during the provocation test was antigenically different to the herring contained in the ED. The producer declares that FUH contains hydrolysed proteins with a low molecular weight (<6 kDa) as unique source of proteins, a limit considered acceptable for a hydrolysed diet in dogs, while no data are available in cats.22 Extensive hydrolysation may impact palatability, which can, in turn, affect compliance. Surprisingly in this study, only one cat refused the diet, a percentage (3%) much lower than what has been described previously in dogs fed FUH and other hydrolysed diets.16, 23 Gastrointestinal signs associated with this diet were represented by vomiting and diarrhoea in three cases and just diarrhoea in a fourth one, for a total of 12.5% of cats, in line with a previous canine report in which constipation, soft faeces or diarrhoea were observed in 10% of dogs fed hydrolysed diets.24

Cats not improving on the first ED trial were prescribed a second diet trial with a different hydrolysed protein and starch food, in order to minimise false negative diagnoses of AFR. Of four nonresponsive cats that underwent a second ED trial, none improved. However, the numbers are too low to draw a definitive conclusion on the sensitivity of FUH for the diagnosis of AFR in cats. In a previous canine study, 10% of dogs needed a second ED trial for the confirmation of AFR, yet no such data are available for the feline species.21

Similar to the study on dogs fed FUH or other studies on the efficacy of therapeutical interventions for pruritus in allergic cats, it is interesting to note that pruritus and lesions decreased by >60% to approximately 90%, while QoL did not reach 50% improvement in cats with confirmed or doubtful AFR.16, 18, 19 This observation confirms the need to measure QoL together with clinical parameters when evaluating therapeutic interventions in animals with allergic dermatoses: clinical improvement may not reflect a better quality of life, owing to the burden of the treatment on the pet and/or the owner.

There are several limitations in this study, besides the low number of included cats and the fact that the study was not controlled. One of these is that some of the animals were indoor–outdoor cats and may not have improved owing to uncontrolled access to nonpermitted food sources. Furthermore, in cats that were not on routine parasite control, a systemic parasiticide (fluralaner) was chosen, which could not have provided adequate flea control in flea allergic cats living under high environmental parasite pressure. In these cases pruritus due to flea bite allergy could have negatively influenced the evaluation of the efficacy of the diet. Last, and not least, the dual pVAS (licking and scratching) for the evaluation of feline pruritus used in this study is not yet validated, and may thus not provide a precise quantification of pruritus in cats. To the best of the authors’ knowledge, currently there are no validated feline pruritus scales. Among those used in other studies, the dual pVAS was considered the most reliable one, as it is based on the common observation that cats scratch and/or lick when feeling pruritus, and on the assumption that the two different behaviours should be evaluated separately. Even though the dual pVAS has not yet undergone complete validation procedures, its performance was substantiated by correlation analyses in a previous study.18

In conclusion, the low prevalence of gastrointestinal adverse effects (12.5%) and the excellent palatability (97%) make FUH a useful option for the diagnosis of AFR in cats, if fed exclusively for at least eight weeks. In the case of failure, it is advisable to undertake a second diet trial with different protein and carbohydrate sources. Provocation tests with several diets or ingredients are always necessary to confirm the diagnosis of AFR.

Supporting information

Table S1. Onset of pruritus, history of otitis, gastrointestinal signs and anal pruritus in 25 cats with AFR and in cats where this diagnosis was excluded or was doubtful.

Table S2. Signalment and historical data of 32 cats included in the study.

Table S3. Pruritus scores, lesional scores and quality of life scores of 32 cats with signs of cutaneous allergy that underwent a two month elimination diet with a hydrolysed fish and rice starch hypoallergenic diet.

Table S4. Molecules, doses, duration and withdrawal time of concomitant treatments in 25 cats with signs of cutaneous allergy undergoing an elimination diet.

Acknowledgements

The authors thank Luisa Cornegliani for the statistical analysis, Silvia Colombo for critically reviewing the manuscript, and Vera Luciano, Alice Restagno and Antonella Varina for including some of the cases.

Source of Funding: This study was funded by Farmina Pet Food, Nola, NA, Italy

Conflicts of Interest: Chiara Noli received consulting and speakers fees from Farmina Pet Food.

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Associated Data

This section collects any data citations, data availability statements, or supplementary materials included in this article.

Supplementary Materials

Table S1. Onset of pruritus, history of otitis, gastrointestinal signs and anal pruritus in 25 cats with AFR and in cats where this diagnosis was excluded or was doubtful.

Table S2. Signalment and historical data of 32 cats included in the study.

Table S3. Pruritus scores, lesional scores and quality of life scores of 32 cats with signs of cutaneous allergy that underwent a two month elimination diet with a hydrolysed fish and rice starch hypoallergenic diet.

Table S4. Molecules, doses, duration and withdrawal time of concomitant treatments in 25 cats with signs of cutaneous allergy undergoing an elimination diet.


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