Documente Academic
Documente Profesional
Documente Cultură
2011
Dr. Dottie Laflamme received her Doctor of Veterinary Medicine degree, Master of Science degree in ruminant nutrition, and PhD in philosophy in physiology and nutrition from the University of Georgia. She also completed her nutritional residency there, as an ALPO Fellow in Clinical Nutrition. She is a diplomate in the American College of Veterinary Nutrition. Dr. Laflamme is currently a senior research scientist at Nestl Purina PetCare Research.
Dr. Joseph Wakshlag received his Doctor of Veterinary Medicine degree and PhD in pharmacology from Cornell University, where he is now an assistant professor of clinical nutrition. He is also a diplomate in the American College of Veterinary Nutrition and American College of Veterinary Sports Medicine and Rehabilitation.
2011 Nestl Purina. The views and opinions in this publication are those of the participants and do not necessarily represent the views of the sponsor. Cover art Getty Images/Ryan Kramer. To view online, visit www.dvm360.com/Purina2011.
Veterinary Symposium
WHATS INSIDE:
2 9 14 23
Understanding pet owner behavior to achieve weight loss in companion animals Debra F. Horwitz, DVM, DACVB Clinical and research experiences with probiotics in cats Michael R. Lappin, DVM, PhD, DACVIM When pieces are better than the whole: Hydrolyzed protein diets Dottie Laflamme, DVM, PhD, DACVN From fat to fitAvoiding six common mistakes while helping pets combat obesity Joseph Wakshlag, DVM, PhD, DACVN, DACVSMR
Obesity in companion animals has become a serious medical problem. Data published in Australia found 33.5% of dogs were classed as overweight, whereas 7.6% were judged to be obese, findings which are likely comparable to those in the USA.1,2 The prevelance of obesity in cats appears to be similar.3 Overweight animals may experience orthopedic problems, metabolic diseases, a reduced quality of life, and a shorter life span. Even with a plethora of weight-loss diets available to them, some pet owners seem unable to help their companion animals lose weight. When owners try a weight-loss diet for their pet, and the pet does not lose weight, the owners may conclude the diet or your advice is ineffective. Considering the behavioral factors in weight loss will improve owner compliance and benefit the pet with better overall health.
Veterinary Symposium
Feeding ecology of dogs and cats Because of the feeding ecology of canids, a dogs food-seeking behavior may not be hunger driven, but the natural foodscavenging behavior of dogs. Dogs tend to eat in a feast or famine mode, eating large quantities when food is available since hunting and catching prey is unreliable. In life, food is an important commodity; some dogs will ask for food even if they receive adequate daily nutrition. The smell or presence of food is enough to elicit this response in most dogs. If they
Social factors in food consumption Social factors within the home can have a profound influence on consumptive behavior in dogs and cats. Group eating in dogs results in social facilitation of eating and for some dogs an increase in consumption. Dogs may threaten, fight, or intimidate other dogs when food is being prepared and consumed, altering the amount consumed or the eating pattern of other dogs. Common signs may include an altered consumption rate; faster
A dogs food-seeking behavior may not be hunger driven, but the natural food-scavenging behavior of dogs.
Satiety versus meeting caloric needs Another issue is satiety, the sensation of fullness, which may not be achieved or noted by the pet. When the pet is fed a food that is highly palatable it may be stimulated to consume more than it needs. Alternately, if the food has high caloric density per piece, resulting in smaller portions being offered, the animal may not feel full. Although ideally an animal should eat to meet its caloric needs, if it does not feel full, begging and foodseeking behavior may persist. Learning contingencies Most behavior is influenced by the if/then relationshipif I do behavior A, then outcome B occurs. The stronger the relationship is between the behavior and outcome, the more difficult it will be to change the behavior. In weight-loss issues, several if/ then situations arise that may be obstacles to success. In fact, the mere presence of the owner may be a signal that food is forthcoming, resulting in a classically conditioned response. For the owner, the pets apparent delight at receiving food is the reward for giving treats or tidbits from the table. The owner might be unaware of how to provide bonding and enrichment for the pet without using food. Appropriate enrichment and owner-pet activities can be another way to strengthen the human-animal bond. In addition,
Many owners are unaware that cats would naturally eat multiple small meals daily rather than one or two larger ones.
Veterinary Symposium
ommendations may make compliance easier. (See Table 2.) For some dogs, slowing down the rate of eating and having the dog work for its food can increase satiety and decrease begging. The best options for doing this are fooddispensing toys. These must be used cautiously in a multipledog home since fighting over food-dispensing toys can occur. (See Table 3 for a resource list.) If food-seeking behavior and begging occur while human food is being prepared and eaten, then the dog should be confined elsewhere during these activities. However, owners are often unable or unwilling to comply with this recom-
mendation. One alternative is to use part of the pets daily ration as table treats that are given when the dog begs at the table. Another is to feed the dog during these times using a fooddispensing toy or a long-lasting treat. A more useful tip is to explain to the owners that the begging behavior is reinforced by the dog intermittently receiving food, which makes the dog hopeful that this will occur again. Therefore, when they stop feeding the dog from the table, begging behavior is likely to continue and actually may increase, until it finally goes away if no food is given. If food sharing is a large component of the human-animal
bond, create an acceptable food-sharing plan that includes the approved diet or some low-calorie substitute such as carrots or apples. Identifying and dealing with this problem is likely to increase compliance overall. In some situations, countersurfing and garbage-raiding will test the owners patience. Discussions about how to keep these items away from the dog can help. These include keeping garbage under the sink, rather than in an accessible garbage can, and placing bread in a covered breadbox. Treats are almost always an issue. Many dogs get treats for simply being cute or just coming inside. These can add up to
many additional calories over the course of a day. Although we would like owners to stop giving the pet treats, realistically most will not. By calculating the number of treats given each day, it is possible to ask the owners to break each treat in half and decrease the number of treats by 50%. Once they realize that the size of the treat does not seem to matter to the pet, it is often easy to substitute something else or switch to a low-calorie option. Owner and pet become conditioned to use food as a bond-
ing exercise. Replacing this bonding exercise with another is crucial to success. Increasing exercise, bonding, and play is critical. It is often assumed that a dog with a fenced yard will exercise itself, but once the dog is out of adolescence, this is simply not so. Therefore, the owner needs to find a way to increase activity levels. Walks are a good alternative. In many situations, the owner is unable or unwilling to walk the dog due to its behavior on a leash. Appropriate control products,
such as head halters or no-pull body harnesses, can be used to address leash-walking problems. As part of the weight-loss plan, the owner could meet with a veterinary technician to learn how to use these devices for more pleasurable walks. Walks do not need to be long, but should be frequent. Be sure to counsel owners that an increase in exercise does not mean that the dog can increase its intake of food. If the dog likes to play with toys, then the owner and the dog can play fetch. Most owners have a difficult time getting the dog to drop the ball so that the game can continue. This can be overcome by using two objects. When the dog returns with one object, the owner holds up the second one, asks the dog to drop the object and when it does, the new object is thrown. Other games are possible, such as hide and seek or even basic training or tricks to keep the pet moving.
Veterinary Symposium
Table 3. Resources
Food-dispensing toys for dogs and cats Kong Products (www.kongcompany.com) Kong and Kong Wobbler Premier Pet Products (www.premier.com) Busy Buddy, Kibble Nibble, Twist n Treat, and Linkables for dogs Funkitty Twist n Treat and Egg-Cersizer for cats Purina Pet Gear (www.purinapetgear.com) The Gratifier, Kitty Treat Ball Control products for dogs and cats Canny Collar (www.cannyco.us) Halti Training Head Collar (most pet supply stores) Premier Pet Products (www.premier.com) Easy Walk Harness Gentle Leader Headcollar Come with Me Kitty Harness & Bungee Leash
resources all over the home is essential because some cats may have their movement and access to resources restricted by another cat. Exercise and increased activity can aid in weight loss in cats. Some cats enjoy interactive play with their owners and the use of toys can greatly enhance this activity. (See Table 3.) Owners should realize that when active play wanes after a short time, removal of the toy and substitution with another would restimulate play activity.12 Adding climbing towers and placing food bowls in outof-the-way places can increase activity. Some cats will use food-dispensing toys and can have at least one meal a day provided in this manner.
References
1. McGreevy PD, Thomson PC, Pride C, et al. Prevalence of obesity in dogs examined by Australian veterinary practices and the risk factors involved. Vet Rec 2005;156:695-707. 2. Burkholder WJ, Toll PW. Obesity. In: Hand MS, Thatcher CD, Remillard RL, et al, eds. Small animal clinical nutrition, 4th ed. Topeka, Kan.: Mark Morris Institute, 2000;401-430. 3. Colliard L, Paragon BM, Lemuet B, et al. Prevalence and risk factors of obesity in an urban population of healthy cats. J Feline Med Surg 2009;11:135-140. 4. Impellizeri JA, Tetrick MA, Muir P. Effect of weight reduction on clinical signs of lameness in dogs with hip osteoarthritis. J Am Vet Med Assoc 2000;216:1089-1091. 5. Kealy RD, Lawler DF, Ballam JM, et al. Effects of diet restriction on life span and age-related changes in dogs. J Am Vet Med Assoc 2002;220:1315-1320. 6. Scarlett JM, Donoghue S. Associations between body condition and disease in cats J Am Vet Med Assoc 1998;212:1725-1731. 7. Slingerland LI, Fazilova VV, Planting EA, et al. Indoor confinement and physical inactivity rather than the proportion of dry food are risk factors in the
development of feline type 2 diabetes mellitus. Vet J 2009;179:247253. 8. Harperd EJ, Stack MT, Watson TGD, et al. Effects of feeding regimens on a bodyweight, composition and condition score in cats following ovariohysterectomy. J Small Anim Pract 2001;42:433-438. 9. Kienzle E, Berglert R. HumanAnimal Relationship of Owners of Normal and Overweight Cats. J Nutr 2006;136(suppl):1947S-1950S. 10. Kienzle E, Bergler R, Mandernack A. Comparisons of the feeding behavior and the human-animal relationship in owners of normal and obese dogs. J Nutr 1998;12(suppl):128. 11. Bissot T, Servet E, Vidal S, et al. Novel dietary strategies can improve the outcome of weight loss programmes in obese client-owned cats. J Feline Med Surg 2010 Feb;12(2):104-12. 12. Hall SL, Bradshaw JWS, Robinson IH. Object play in adult domestic cats: the roles of habituation and disinhibition. App Anim Behav Sci 2002;79:263-271. 13. Roudebush P, Schoenherr WD, Delaney SJ. An evidence-based review of the use of therapeutic foods, owner education, exercise and drugs for the management of obese and overweight pets. J Am Vet Med Assoc 2008;233:717-725.
DVM, PhD,
College of Veterinary Medicine and Biomedical Sciences Colorado State University Fort Collins, Colo.
10
Veterinary Symposium
11
equilibration period, mild stress was induced over time by changing the housing of the cats from cages to gang housing repeatedly over a five-month period. The SF68 was well tolerated by all cats. Fecal microbial diversity was maintained throughout the study in cats given SF68, but decreased in cats fed the placebo, indicating a more stable microbiome in cats fed SF68. Upper respiratory signs of disease were not exacerbated by the induced stress, but those fed SF68 had fewer episodes of conjunctivitis than the placebo group during the supplementation period, suggesting that administration of the probiotic lessened morbidity from chronic FHV-1 infection (see Figure 2).
12
Veterinary Symposium
35 30 25 20 15 10 5 0
Percent conjunctivitis
P<0.0001
Supplementation/stress period
dogs and cats were divided into groups and housed in separate rooms (two groups of dogs and two groups of cats). The cats and dogs were all fed a standardized diet by species. Animals in one room were supplemented daily with FortiFlora and animals in the alternate room were supplemented daily with placebo. Otherwise, management of the rooms was identical. Before the room was cleaned each morning, one of the investigators would score the feces in each animals cage using the Purina Fecal Scoring System for Dogs and Cats (see Table 1). Feces from dogs and cats with a score of 4 or greater were collected and transported to Colorado State University (CSU) for infectious disease testing. The testing at CSU included microscopic examination for parasite eggs, cysts, and oocysts and immunofluorescent antibody testing for Cryptosporidium oocysts and Giardia cysts.
Diarrhea prevalence rates were low for all dogs in the study and so statistical differences were not detected. However, the percentage of cats with diarrhea of two or more days was 7.7% for the probiotic group and 20.7% for the placebo group. These results suggest that administering SF68 to cats housed in shelters may reduce the number of days with diarrhea. Since this was a shortterm study, this effect was likely from the probiotics influences on intestinal flora rather than its systemic immune-enhancing effects.
Summary
Controlled studies evaluating the use of probiotics in cats is limited and inconclusive. However, there is evidence that SF68 is well tolerated and may have various clinical applications. Further research is ongoing in this area.
References
1. Schrezenmeir J, de Vrese M. Probiotics, prebiotics, and synbioticsapproaching a definition. Am J Clin
13
When pieces are better than the whole: Hydrolyzed protein diets
Clinical signs of food allergy in dogs and cats
Dottie Laflamme,
DVM, PhD, DACVN
Senior Research Scientist Nestl Purina PetCare Research St. Louis, Mo.
Food allergy and food intolerance imply abnormal reactions to a normal food or ingredient. Food allergy is immune-mediated, while food intolerance is considered to be an idiosyncratic reaction. Other forms of adverse reactions to foods can include food intoxication or food poisoning. Unlike food allergy or intolerance, which are abnormal responses to normal foods or ingredients, food poisoning refers to normal, biological reactions to the toxins or infectious agents in foods, rather than to normal foods. Food allergy may manifest with dermatologic or gastrointestinal (GI) signs, or both. Dermatologic signs of food allergy (Table 1) are similar to those of atopic dermatitis, and both food allergy and atopic dermatitis commonly occur together.1 GI signs can include vomiting, diarrhea, and borborygmus. According to veterinary dermatologists, the majority of dogs and cats with food allergies manifest dermatologic signs, although 15% to 50% are now recognized to also have GI signs.1-4 Moreover, veterinary gastroenterologists recognize that a large percentage of patients with GI signs have some form of food allergy or intolerance.2,5,6 In one study of 70 cats with chronic GI signs, 29% were diagnosed as food allergic based on elimination and challenge testing.5 An additional 20% of cats in the study showed a positive response to diet but did not relapse upon challenge. Similarly, another study demonstrated that 50% of dogs with chronic GI signs were food responsive, although only 20% of these were confirmed by challenge to be food allergic.6 Another study evaluating 128 cats with either pruritus, GI signs, or both, identified 22 (17%) cats that were confirmed food allergic by elimination and subsequent challenge testing.2 Among the cats confirmed to be food allergic, 45% exhibited dermatologic signs, 32% expressed GI signs, and 23% exhibited both signs. It appears that patients expressing both dermatologic and GI signs are more likely to be diagnosed as food allergic.2-4 In a study of 418,422 dogs in Switzerland, 259 allergic dogs were identified.4 Of these, 65 were identified as food responsive, while 183 were considered atopic. Concurrent GI signs occurred in 31% of the food-responsive dogs, but in only 10% of the atopic dogs. Similarly, cats with both dermatologic and GI signs (42%) were more likely to be food allergic than those with only dermatologic (16%) or GI signs (13%).2
14
Veterinary Symposium
fold cells (M cells) located on the Peyers patches. M cells take up antigens from the intestinal lumen and present them directly to lymphocytes within the Peyers patch. This allows the immune system to develop an appropriate recognition and response to that particular antigeneither to develop a tolerance to a food protein or to mount a defense against an invading organism. Errors in this process can result in development of a food allergy or an infection.
nisms, immunoglobulins (Ig), and the cells involved. Although type I and III reactions are mediated by IgE or IgG and type IV is a T-cellmediated reaction, other cells play a role in these reactions. Advances in the past decade have contributed to a greater understanding of the pathophysiology of allergy: the key lies in CD4+ and CD8+ T cells and related cytokines.10 Two major subsets of CD4+ T cells are the Th1 and Th2 subsets, which are distinguishable on the basis of their expressed cytokines. Th1 cells stimulate cell-mediated immune functions and inhibit IgE synthesis, whereas Th2 cells produce interleukin (IL)-4, which stimulates IgE production by B
15
When pieces are better than the whole: Hydrolyzed protein diets
cells. A proper balance between these cell types is necessary for normal immune function, and a number of immunopathologies have been associated with an exaggerated Th1 or Th2 response. The cytokines IL-10, transforming growth factor- (TGF-), and others play an important role in maintaining the Th1-Th2 ratio and promoting allergen tolerance. Increased IL-4, IL-6, and tumor necrosis factor- (TNF-) production and a reduced Th1-Th2 ratio associated with increased Th2 cells are found in atopic and food-allergic people. Immunoglobulin and T-cell responses appear to differ between food allergy and atopy, at least in dogs. One study confirmed an increase in IgE in atopic dogs and an increase in IgG in dogs with food-allergic and other forms of gastroenteritis.11 Though no differences were found in the T-cell status of the GI tract between normal dogs and food-allergic dogs, significant changes occurred within the skin of dogs with cutaneous adverse food reactions.12,13 These changes included a pronounced CD8+ T cell-dependent inflammatory response, and increased expression of IL-4, IL-13, and other genes suggestive of a Th2-skewed immune status.14 These changes remained even after clinical resolution of signs, suggesting a continuing pre-activated immune status in dogs with food allergies.14 This is consistent with results from food-allergic children, who have ongoing activation of Th2 cells with increased release of inflammatory cytokines.15 contribute to clinical signs of allergy. This appears to be associated with clinical or subclinical intestinal inflammation. In cats and dogs, food allergy often manifests with primary GI signs, and up to 30% of patients with cutaneous manifestations also develop GI signs. The percentage with subclinical GI involvement is unknown; thus, it is likely that some degree of GI compromise exists in dogs and cats with food allergies. Another factor that may influence the manifestation of clinical signs is the pruritic threshold, which refers to the variation in response to a given allergen. It may relate to the concept of summation, which suggests that multiple allergies or nonallergenic pruritic stimuli are additive in effect. For example, a pruritic dog with concurrent atopy and food allergy may drop below the pruritic threshold by effective control of only one of these conditions. Nonallergenic factors, such as stress, dry skin, and hot weather, can also contribute to pruritus via nonimmunologic means and must be considered in the diagnosis and management of pruritic pets.17
16
Veterinary Symposium
allergy. However, it is necessary to rule out other causes of GI or dermatologic signs that may be confused with food allergies (Table 3). Location and type of skin lesions can help identify or rule out other conditions. For example, lesions predominantly located on the caudal half of the body are more consistent with flea allergy. In nearly 25% of food-allergic dogs, pruritus in the ear region may be the only clinical sign. In pruritic patients, skin cytology should be evaluated for bacterial and Malassezia infections. Unfortunately, medical history does not help differentiate food allergy from atopic disease. The clinical signs of these conditions can be identical, and they may exist concurrently. For patients with GI signs, blood, urine, and feces should be examined to rule out systemic or parasitic causes of vomiting or diarrhea. If food allergy is suspected, a dietary trial (Table 4) using an appropriate elimination diet is required. Most patients with
dermatologic signs respond within four to eight weeks. If only partial improvement is seen, an additional four to six weeks may be needed for maximum resolution.7,20 If concurrent therapy is provided, such as antibiotics or corticosteroids, the trial must be continued for at least three to six weeks after completion of these therapies. If only GI signs are present, a two- to four-week trial is sufficient.5,7 Improvement in dermatologic signs is typically defined in terms of changes in pruritus. Most studies consider a decrease of 50% or more to be a positive response.7,20,21 If the patient responds positively to the elimination diet, a provocative challenge with the prior diet is needed to confirm the diagnosis. Though many will occur within 48 hours, allow up to two weeks to document adverse responses during the challenge period.1 A diagnosis of food allergy is confirmed if the patient improves while on the elimination diet, recrudesces during the challenge, and
17
When pieces are better than the whole: Hydrolyzed protein diets
Table 3. Differential diagnoses for pruritic dogs and cats
Atopy Flea allergy dermatitis Food allergy Drug reaction Lice infestation (pediculosis) Intestinal parasite hypersensitivity Mite infestation (Sarcoptes, Cheyletiella, Demodex, Notoedres, etc.) Malassezia dermatitis Seborrheic skin disease Viral infection Contact dermatitis Primary pyoderma Autoimmune disease
improves again when returned to the elimination diet. If desired, identification of specific protein sources to which the patient is sensitive can be done by challenging with individual ingredients, one at a time, while maintaining the patient on the elimination diet.
do not appear to be common.1 Some limitations to homeprepared diets typically used for elimination trials include: laborintensive preparation (compared with feeding commercial diets); excessive costs; diet acceptance; the possibility of GI upsets; and nutritional completeness.3,7 Because of nutritional imbalances, home-prepared diets are not recommended for use in growing animals nor for long-term use.1,3,7 Published studies using homemade diets suggest a drop-out rate from 15% to 36%, with the most common reasons being patient refusal, difficult preparation, and development of diarrhea.3,21,23 The proportion of dogs enrolled in the eliminationchallenge tests that were diagnosed as food allergic in these studies averaged 35.7%.
Diet selection
The goal in conducting a dietary trial with an elimination diet is to eliminate any exposure to allergens to which the patient may be sensitive. In addition, because the diet may be fed for an extended period of time, it should also provide complete and balanced nutrition and be palatable and convenient for the owner to feed. Controlled intake during the trial period includes the main meal as well as treats, flavored medications, bits of food used to give medications, and access to any other foods.
18
Veterinary Symposium
tein and carbohydrate sources. While allergies to carbohydrates are uncommon, allergies to the protein contained in these ingredients (e.g., potato, rice, corn, wheat) can occur.5,24,25
Most commercial novel protein diets provide complete and balanced nutrition and they are easy to prepare. Because of this, the proportion of patients completing the elimination
study may be increased.2,5 Commercial novel protein diets are recommended when owners do not wish to cook for their pets, when pets do not tolerate home-prepared diets, and when
19
When pieces are better than the whole: Hydrolyzed protein diets
the cost of a home-prepared diet is prohibitive.7 A few published studies have shown that these diets can be used with good success to diagnose food allergy.2,5 However, several studies have documented adverse reactions in 15% to 85% of confirmed food-allergic dogs offered various commercial novel protein diets.8,22,23,26 One study indicated that 22 of 40 dogs reacted only against one of three diets, while an additional eight dogs reacted against two different novel diets.26 Such results confirm the critical importance of a good dietary history prior to selecting a diet for a suspected food-allergic patient. They also are the reason some researchers discourage the use of novel commercial diets during the elimination trial.7,22,26 While there are limitations to using novel protein diets during the diagnostic period, it appears that 84% to 95% of confirmed food-allergic dogs can be maintained on a commercial novel protein diet.22,26 This provides a viable way to control clinical signs while providing complete and balanced nutrition. If the patients specific allergies are not known, it may be necessary to test several novel protein diets until a suitable diet is found. Unfortunately, it is still possible for the patient to develop a hypersensitivityeven to the novel dietat a later time.1
In addition to protein hydrolysis, hypoallergenic diets should be formulated using carbohydrate sources containing minimal to no protein to reduce risk of new allergenic responses. While grains are typically considered carbohydrate sources, they also contain varying amounts of intact proteins that could trigger allergic responses. In recent years, a number of diets made with hydrolyzed proteins have been introduced into the marketplace. If these diets could be used even in dogs allergic to the parent (intact) protein, they could be used as elimination diets without consideration of the dietary history. Several studies specifically designed to look at the impact of hydrolyzed protein diets in dogs allergic to the parent protein documented that the reaction to hydrolyzed proteins is significantly reduced.19,30-33 For example, 10 of 12 confirmed chicken-allergic dogs had at least a 50% reduction in CADESI (Canine Atopic Dermatitis Extent and Severity Index) score when fed a chicken hydrolysate diet.32 In two different studies of dogs with confirmed soy or corn allergies, or both, the reaction to a hydrolyzed soy and corn starch diet was significantly reduced versus intact soy or corn, and no different from the reactions to corn- and soy-free control diets.30,33 Multiple hypersensitivities may occur in one-third to one-half of dogs or cats with food-allergies.7
20
Veterinary Symposium
In one study, most food allergic dogs reacted to two food ingredients while one dog reacted to seven.24 This situation presents a challenge when attempting to develop effective novel protein diets, and becomes less important when a hydrolyzed hypoallergenic diet is used. Furthermore, because the hydrolyzed proteins are truly hypoallergenic, it is less likely that a new allergy will form when these diets are fed longterm. Other advantages of hydrolyzed protein diets are that they can provide complete and balanced nutrition and avoid client concerns about the difficulties in preparing homemade diets. A further advantage of hydrolyzed protein diets is the effect on digestibility. The use of highly digestible proteins has long been recommended for managing food allergies. One of the natural defenses against food allergy is the breakdown of food allergens during digestion. Under normal circumstances, very little intact protein is absorbed. However, if there is increased GI permeability, or digestive function is compromised, larger peptides and proteins may be absorbed intact, contributing to development or exacerbation of food allergy.9,25 Hydrolysis of a protein enhances digestive efficiency. For example, when soy protein hydrolysates were administered to dogs, the small intestinal absorption rate increased three-fold compared
with administration of intact soy protein.34 Thus, feeding hydrolyzed protein diets may avoid aggravation or perpetuation of allergies in animals with compromised GI tracts. Several studies suggest that about 90% of dogs with food allergy will be detected using hydrolysate diets, although a few dogs or cats might have an adverse reaction to the hydrolyzed diets.18,35 (Sousa C, unpublished data 2001) While this falls short of 100%, it compares favorably with home-prepared or commercial novel diets.
Summary
Food allergies may cause dermatological or GI signs, or both. A diagnosis of food allergy is made by performing a dietary elimination trial using an appropriate diet, followed by a food challenge using the patients prior diet or specific food ingredients. Following diagnosis and identification of the offending allergens, dogs and cats can be maintained on diets that exclude the identified antigens or on commercial novel protein or hypoallergenic diets. As the immune system remains primed for an allergic response, it is possible for an allergy to additional proteins to develop over time with recurrence of clinical signs. This risk may be reduced by feeding hydrolyzed protein diets to at-risk patients.
21
When pieces are better than the whole: Hydrolyzed protein diets
mal and atopic dogs, and dogs with gastrointestinal disease. Vet Immunol Immunopathol 2003;92:113-124. Veenhof EZ, Rutten VP, van Noort R, et al. Evaluation of T-cell activation in the duodenum of dogs with cutaneous food hypersensitivity. Am J Vet Res 2010;71:441-446. German AJ, Hall EJ, Day MJ. Immune cell populations within the duodenal mucosa of dogs with enteropathies. J Vet Intern Med 2001;15:14-25. Veenhof EZ, Knol EF, Schlotter YM, et al. Characterization of T cell phenotypes, cytokines and transcription factors in the skin of dogs with cutaneous adverse food reactions. Vet Journal 2010. doi:10.1016/i. tvil.2010.02.005. Available at: www.sciencedirect.com/science?_ ob=ArticleURL&_udi=B6WXN4YM7N2N-1&_user=3550545&_ coverDate=03%2F15%2F2010&_ rdoc=1&_fmt=high&_ orig=search&_origin=search&_ sort=d&_docanchor=&view=c&_ acct=C000065267&_version=1&_urlVersion=0&_userid=3550545&md5= 44c2bdacee7020760e91c4a9549c65 7e&searchtype=a. Accessed Feb. 16, 2011. Frischmeyer-Guerrerio PA, Guerrerio AL, Chichester KL, et al. Dendritic cell and T cell responses in children with food allergy. Clin Exp Allergy 2011;41:61-71. Hillier A, Griffin CE. The ACVD task force on canine atopic dermatitis (X): is there a relationship between canine atopic dermatitis and cutaneous adverse food reactions? Vet Immunol Immunopathol 2001;81:227-231. Chalmers SA, Medleau L. An update on atopic dermatitis in dogs. Vet Med 1994;89:326-341. Biourge VC, Fontaine J, Vroom MW. Diagnosis of adverse reactions to food in dogs: efficacy of a soy-isolate hydrolyzate-based diet. J Nutr 2004;134:2062-2064. Puigdemont A, Brazis P, Montserrat S, et al. Immunological responses against hydrolyzed soy protein in dogs with experimentally induced soy hypersensitivity. Am J Vet Res 2006;67:484-488. Chesney CJ. Systematic review of evidence for the prevalence of food sensitivity in dogs. Vet Rec 2001;148:445-448. Proverbio D, Perego R, Spada E, et al. Prevalence of adverse food reactions in 130 dogs in Italy with dermatological signs: a retrospective study. J Sm Anim Pract 2010;51:370-374. Jeffers JG, Shanley KJ, Meyer EK. Diagnostic testing of dogs for food hypersensitivity. J Am Vet Med Assoc 1991;198:245-250. Tapp T, Griffin C, Rosenkrantz W, et al. Comparison of a commercial limited-antigen diet versus homeprepared diets in the diagnosis of canine adverse food reaction. Vet Therapeutics 2003;3:244-251. Kawarai S, Ishihara J, Masuda K, et al. Clinical efficacy of a novel elimination diet composed of a mixture of amino acids and potatoes in dogs with non-seasonal pruritic dermatitis. J Vet Med Sci 2010;72:1413-1421. Roudebush P, Guilford WG, Jackson HA. Adverse reactions to food. In: Hand MS, Thatcher CD, Remillard RL, et al, eds. Small animal clinical nutrition, 5th ed. Topeka, Kan.: Mark Morris Institute, 2010;609-635. Leistra MHG, Markwell PJ, Willemse T. Evaluation of selected-proteinsource diets for management of dogs with adverse reactions to food. J Am Vet Med Assoc 2001;219:1411-1414. Awazuhara H, Kawai H, Maruchi N. Major allergens in soybean and clinical significance of IgG4 antibodies investigated by IgE- and IgG4-immunoblotting with sera from soybean-sensitive patients. Clin Exp Allergy 1997;27:325-332. Wilson S, Blaschek K, Gonzalez de Mejia E. Allergenic proteins in soybeans: processing and reduction of P34 allergenicity. Nutr Rev 2005;63:47-58. Olson ME, Hardin JA, Buret AG, et al. Hypersensitivity reactions to dietary antigens in atopic dogs. In: Reinhart GA, Carey DP, eds. Recent advances in canine and feline nutrition, Vol III, 2000 Iams Nutrition Symposium Proceedings. Wilmington, Ohio: Orange Frazer Press, 2000:69-77. Beale KM, Laflamme DP. Comparison of a hydrolyzed soy protein diet containing corn starch with a positive and negative control diet in corn- or soy-sensitive dogs, in Proceedings. 16th Annual AAVD and ACVD Meeting 2001;12:237. Serra M, Brazis P, Fondati A, et al. Assessment of IgE binding to native and hydrolyzed soy protein in serum obtained from dogs with experimentally induced soy protein hypersensitivity. Am J Vet Res 2006;67:1895-1900. Ricci R, Hammerberg B, Paps J, et al. A comparison of the clinical manifestations of feeding whole and hydrolyzed chicken to dogs with hypersensitivity to the native protein. Vet Derm 2010;21:358-366. Jackson HA, Jackson MW, Coblentz L, et al. Evaluation of the clinical and allergen specific serum immunoglobulin E responses to oral challenge with cornstarch, corn, soy and a soy hydrolysate diet in dogs with spontaneous food allergy. Vet Derm 2003;14:181-187. Zhao XT, McCamish MA, Miller RH, et al. Intestinal transit and absorption of soy protein in dogs depend on load and degree of protein hydrolysis. J Nutr 1997;127:2350-2356. Olivry T, Bizikova P. A systematic review of the evidence of reduced allergenicity and clinical benefit of food hydrolysates in dogs with cutaneous adverse food reactions. Vet Derm 2010;21:31-40.
12.
20.
30.
21.
13.
14.
22.
31.
23.
32.
24.
33.
25.
15.
34.
26.
16.
35.
27.
17.
18.
28.
19.
29.
22
From fat to fitAvoiding six common mistakes while helping pets combat obesity
We veterinarians are all aware that weight problems affect 30% to 40% of our patients. The effects of obesity are far-reaching, predisposing our patients to insulin resistance, type II diabetes, orthopedic disease, and possibly even cancer.1-3 We all know that a pet is not in ideal health if it is not at its ideal weight, but many of us have also discovered how difficult it can be to motivate clients to help their pets lose weight. In this article, I will describe six common mistakes veterinarians make when implementing weight-management programs and explain how best to avoid them.
23
From fat to fitAvoiding six common mistakes while helping pets combat obesity
Recent results from our data set and now from an Australian group suggest that adiponectin and HMW adiponectin concentrations are not affected during weight loss in dogs.6,7 However, even in obese dogs, it appears that adiponectin is continually secreted at high concentrations into the blood. Could this be part of the reason why insulin resistance in dogs is hard to define in clinical investigations? And is this why type II diabetes is rarely observed in dogs? Further research is needed to elucidate the clinical ramifications of adiponectin secretion in dogs and cats. Table 1 shows results from a recent study examining adipokine concentrations before and after a weight-loss program in dogs. The results show that all of the aforementioned adipokines except for adiponectin decrease after about 25% weight loss in a group of dogs, similar to other reports.8,9 This decrease in inflammatory adipokines corresponds with a drop in the systemic marker of inflammation, the acute phase protein called C-reactive protein (CRP). In obese people, the increased inflammation is associated with an increased risk of heart disease and type II diabetes.10 The chronic health ramifications of this slightly elevated inflammatory response in dogs and cats still need to be investigated. Although there is much left to be studied, we do know that obesity has a multitude of systemic effects and predisposes pets to many problems. We can do a better job of communicating to clients what is definitively known about the short- and long-term health risks of obesity in pets. tion or management. We ask clients to exert a great deal of effort for the health of their pets, and so we should be willing to do the same. Fortunately, the major pet food companies make software that allows us to track our patients progress. This tracking can be entrusted to a technician who is familiar with your weightloss software program. When you dispense the first bag of a therapeutic diet, it is best to have your technician schedule several monthly weigh-in sessions for the animal. These are usually free office visits, but you will find that the client typically buys another bag of food or another item, such as a flea control product or heartworm preventive, which more than justifies the time spent in these cases. Reminder calls before each weigh-in session are a good idea. Time and time again, plans without weigh-in appointments fail because of client noncompliance. If veterinary professionals do not take a longterm interest in these cases, then clients are also less likely to comply or come back for that second bag of weight-loss-formula food, and the battle is lost.
Fortifying food with 150 mg to 500 mg carnitine can improve retention of lean mass during a weightreduction protocol.
24
Veterinary Symposium
patients maintenance energy requirement (MER). For animals weighing less than 30 kg, the MER is calculated in kilocalories (kcal) by first using the linear equation to calculate the resting energy requirement (RER):11 RERkcal = 30(BWkg) + 70. Then, to determine the MER, a multiplier is applied to the RER. This multiplier is based on the animals activity level, and it is frequently around 1.5. With this equation, you should use the pets ideal body weight. Other weight-loss equations use current body weight and/or body condition score to calculate the daily caloric amount. For more information on one such method, visit Purinaveterinarydiets.com, or call the Veterinary Resource Center at 1-800-222-VETS (8387). Regardless of the methods used, it is ideal to target between 1-3% weekly weight loss for dogs and between 0.5-2.0% in cats. One common mistake in using this equation is calculating the
RER using the animals current body weight instead of its ideal or goal body weight. You should use the pets ideal body weight. A second error can occur with the activity level multiplier. Using 1.5 as the multiplier is acceptable for young active dogs or indoor/outdoor cats, but it is not appropriate for inactive dogs or indoor cats. Often the multiplier should be less than 1.5, particularly in cases in which a previous weight-loss program was unsuccessful. Recent research suggests that obese, inactive cats should start at their RER (that is, with a multiplier of 1.0), because they are not active enough to have an MER. The multiplier should be closer to 1.0 or 1.2 in the typical inactive, neutered, overweight dog.12,13 Unfortunately, the linear RER equation only works for dogs that weigh less than 30 kg. If used for an obese 50-kg Rottweiler, then the dogs kilocalorie needs would be overestimat-
ed right from the start. For larger dogs, the RER is calculated by plugging the ideal body weight into this exponential equation:13-15 95(BWkg)0.75. Be sure you begin a patients weight-loss program based on correct calculations. Use the pets ideal body weight in your RER calculations and be sure to use an appropriate multiplier to calculate a pets MER.
25
From fat to fitAvoiding six common mistakes while helping pets combat obesity
Figure 1.
Mistake #5 Not addressing problems with the pets behavior and satiety
Undesirable behaviors, such as begging, breaking into pet food bags, and food protectiveness, can develop or worsen during a weight-loss program. Owners are less likely to comply with your recommendations if they see these negative behaviors develop or worsen. Because of my involvement with a fairly extensive obesity trial and routine obesity clinic work, I feel that switching some pets to a canned therapeutic food or a combination of canned and dry foods can sometimes result in progress. An 8-oz portion of dry kibble has between 225 and 275 kcal for dogs and a half cup of food (4 oz) has 125 to 175 kcal for cats, while a 13-oz can for dogs has 175 to 275 kcal and a 6-oz can for cats has 110 to 130 kcal. Therefore, the cans contain fewer calories but more volume. Clients will appreciate being able to feed the increased quantity, and the canned food is likely to provide more immediate gastric fill, increasing the dogs or cats satiety. Another trick for adding volume to a dogs diet is to substitute green beans for dog food. We have gone as high as 1 cup of green beans per cup of dog food. The owners appreciate the extra volume given, which creates the needed gastric fill.
is true.6 In the second study, we also measured steps taken with a pedometer during a weightloss program, and we found that pedometer readings were virtually unchanged when the dogs average BCS dropped from 8 to 5.5. That is, weight loss did not increase their activity level. This, unfortunately, really points the finger at owners. From our data, we predict that the owners activity and willingness to increase the dogs physical activity may play a role in the success of a canine weight-loss program. Another question is whether active dogs lose weight quicker than less active dogs do. Our study showed that active dogs could eat approximately 5 more
This scatter plot shows the relationship of baseline body condition score and average daily steps. Analysis of these values revealed a significant negative nonparametric correlation (P value <0.0001).
kcal/kg of metabolic body weight (not kg of true body weight) during weight loss. Thus, activity does play a role in calorie consumption and weight loss. In our study, active dogs averaged about 5,000 more steps per day than inactive dogs did. This equates to about a 2-mile walk each day.6 It is, without a doubt, more challenging to increase the activity level of cats, especially obese cats. Veterinarians should encourage owners to work at this, and share their own ideas about ways to boost the cats activity level in the home. Although most cats quickly grow bored with the same activities, if owners are willing to be creative, they can pique a cats interest by rotating toys or using laser pointers and treat dispensers.
26
Veterinary Symposium
27
From fat to fitAvoiding six common mistakes while helping pets combat obesity
to low in protein and are usually not fortified with carnitine.
and drugs for the management of obese and overweight pets. J Am Vet Med Assoc 2008;233:717-725. 3. Laflamme DP. Understanding and managing obesity in dogs and cats. Vet Clin North Am 2006;36:12831295. 4. Chiarugi P, Fiaschi T. Adiponectin in health and diseases: From metabolic syndrome to tissue regeneration. Expert Opin Ther Targets 2010;14:193-206. 5. Linscheid P, Christ-Crain M, Stoeckli R. Increase in high molecular weight adiponectin by bariatric surgery-induced weight loss. Diab Obes Metab 2008;20:1266-1270. 6. Wakshlag JJ, Bushey JJ, Struble AM, et al. The effects of weight loss on adipokines and markers of chronic inflammation in dogs. Br J Nutr (in press). 7. Rand J. Companion Animal Clinical Sciences, University of Queensland, St. Lucia, QLD 72, Australia: Personal communication, 2011. 8. German AJ, Hervera M, Hunter L, et al. Improvement in insulin resistance and reduction in plasma inflammatory adipokines after weight loss in obese dogs. Domest Anim Endo 2009;37:214-226. 9. Eirmann LA, Freeman LM, Laflamme DP, et al. Comparison of adipokine concentrations and markers of inflammation in obese versus lean dogs. Int J Appl Res Vet Med 2009;7:196-205. 10. Gustafson B. Adipose tissue, inflammation and athelosclerosis. J Atheroscler Thromb 2009;17:332341. 11. Chan DL. Parenteral support. In: Ettinger SJ, Feldman EC, eds. Textbook of veterinary internal medicine, 6th ed. Saunders Elsevier, St. Louis, Mo.: WB Saunders, 2005;587-591. 12. Chen CA, Hill RC, Scott KC, et al. Energy requirements of indoor adult pet cats (abst). 9th Annu Am Acad of Vet Nut Symp 2009;4. 13. Wakshlag JJ, Struble AM, Warren BS, et al. The effects of physical activity on kilocalorie intake during a successful canine weight reduction protocol. J Am Vet Med Assoc (in press). 14. Saker KE, Remillard RL. Performance of a canine weight-loss program in clinical practice. Vet Ther 2005;6:291-302. 15. Kienzle, E. Energy. In: Beitz DC, ed. National Research Council nutrient requirements of dogs and cats. Washington DC: National Academies Press, 2006;28-48 16. Warren BS, Wakshlag JJ, Maley M, et al. Use of pedometers to measure the relationship of dog walking to body condition score in obese and non-obese dogs. Br J Nutr (in press). 17. Linder DE, Freeman LM. Evaluation of calorie density and feeding directions for commercially available diets designed for weight loss in dogs and cats. J Am Vet Med Assoc 2010;236:74-77. 18. Jeusette I, Torre C, Salas A, et al. Effects of consuming diets containing various fats or citrus flavanones on plasma lipid and urinary F2-isoprostane concentrations in overweight cats. Am J Vet Res 2010;71:1039-1044. 19. Cave NJ, Backus RC, Marks SL, et al. Oestradiol and genistein reduce food intake in male and female overweight cats after gonadectomy. N Z Vet J 2007;55:113-119. 20. Cave NJ, Backus RC, Marks SL, et al. Oestradiol, but not genistein, inhibits the rise in food intake following gonadectomy in cats, but genistein is associated with an increase in lean body mass. J Anim Physiol Anim Nutr 2007;91:400-410. 21. Center SA, Harte J, Watrous D, et al. The clinical and metabolic effects of rapid weight loss in obese pet cats and the influence of supplemental oral L-carnitine. J Vet Intern Med 2000;14:598-608. 22. German AJ, Holden SL, Bissot T, et al. A high protein high fiber diet improves weight loss in obese dogs. Vet J 2010;183:294-297.
Conclusion
As a profession we are on the cusp of new and exciting product innovations that will help our patients combat obesity not only with greater success, but also in a healthier way. The adage that calories in must equal calories out is still the key to successful weight loss. But we veterinarians can help ensure the success of our patients weight-loss programs by avoiding the six common mistakes reviewed in this article. In summary, we should back up our recommendations for a weight-loss program with the science at hand, devote adequate time to obesity prevention and management in our practice, ensure the accuracy of the initial calculations on which our caloric recommendations are based, take into account the activity level of our patients, acknowledge that we may need to alter feeding recommendations for some pets to sate them and prevent negative behaviors, and help clients choose the best food for a patients weight-loss program.
References
1. German AJ. The growing problem of obesity in dogs and cats. J Nutr 2006;136:1940S-1946S. 2. Roudebush P, Schoenherr, WD, Delaney SJ. An evidence-based review of the use of therapeutic foods, owner education, exercise,
28