Skip to main content
Wiley Open Access Collection logoLink to Wiley Open Access Collection
. 2025 May 19;196(12):e5433. doi: 10.1002/vetr.5433

Long‐term effect of neutering age on body condition score and bodyweight in domestic cats

Rae Foreman‐Worsley 1,, Emily Blackwell 2, Lauren R Finka 1, Elizabeth Skillings 1, Jenni L McDonald 1,2
PMCID: PMC12180291  PMID: 40390198

Abstract

Background

Neutered cats are more predisposed to obesity. However, limited research has explored whether body condition score (BCS) and bodyweight vary across lifestages as a function of age at neutering.

Methods

Longitudinal clinical records of BCS (n = 2410) and bodyweight (n = 2073) were paired with age at neutering and other owner‐reported auxiliary information before analysis using cumulative link mixed‐effects models and linear mixed models to explore which factors influence BCS and bodyweight as cats age.

Results

BCS and bodyweight were age dependent, increasing until 9 years of age and then declining. No differences in BCS or bodyweight were found between cats neutered at 4 months or younger, 5 months or 6 months. Cats neutered at 7‒12 months experienced a less rapid age‐related increase in bodyweight and BCS. Females had lower bodyweight and BCS than males, with differences more pronounced in the summer and autumn. Longhaired cats had a lower BCS than shorthaired cats, but hair length was not significantly associated with bodyweight.

Limitations

It was not possible to measure welfare impacts or incorporate diet and lifestyle measurements.

Conclusion

Cats neutered prepubertally showed no difference in bodyweight or BCS as cats aged compared to cats neutered at 5 or 6 months. Cats neutered at 7‒12 months had a lower risk of bodyweight and BCS gain overall. Postneutering weight management advice is recommended for all cats, and monitoring should utilise a combination of both BCS and bodyweight, particularly for longhaired cats.

Keywords: cats, companion animals, epidemiology, obesity, welfare

INTRODUCTION

Neutering of owned cats (Felis catus) is widely accepted in the UK as good management practice for preventing accidental litters and thus reducing the number of unwanted cats free roaming and relinquished to shelters. 1 Additionally, neutering has behavioural benefits 2 , 3 and positive health outcomes for cats, resulting in increased longevity, 4 such as reducing the risk of mammary neoplasia 5 or reducing infectious disease transmission through a reduction in agonistic and copulatory interactions between conspecifics. 3 Despite high neutering rates in the UK, 6 around 80% of owned cat litters are accidental, 1 resulting in substantial populations of unowned cats both free roaming 7 and within shelters. 8 As cats can reach sexual maturity at 4 months of age, it is recommended that neutering is carried out early enough to prevent unplanned litters. Recently, modelled data have demonstrated that neutering age has a profound impact on the number of unowned cats within the UK, even when neutering rates remain constant. 9

In 2006, the Cat Group published recommendations that the standard age of neutering of owned cats be reduced from 6 months to 4 months, 10 a practice typically referred to as prepubertal neutering. This term also encompasses the neutering of cats younger than 4 months, which is often appropriate and desirable within a shelter or trap‒neuter‒return context. 11 , 12 , 13 Despite prepubertal neutering being supported by both veterinary and animal welfare organisations, 14 , 15 , 16 not all UK veterinarians carry out prepubertal neutering or recommend the practice to owners. 17 , 18 Barriers to the adoption of prepubertal neutering by veterinarians include a lack of confidence in carrying out the procedure and the need for more training opportunities. 17 , 19 Veterinarians also report concerns around the lack of longitudinal studies on the impact of age of neutering on health and welfare, 17 including concerns of increased bodyweight in cats neutered prepubertally. 20 While the body of evidence to date suggests that neutering cats prepubertally has similar effects on long‐term growth and development as neutering cats between 6 and 8 months, 21 and may even be beneficial in aiding healthy bodyweight management by reducing acute changes in feeding behaviour, 22 studies have been limited in either the duration of the follow‐up 20 , 22 or the fact they are based on shelter populations only. 21 , 23

Body condition score (BCS) and bodyweight are considered readily accessible metrics that may act as indicators of relative health for cats at any age. 24 , 25 Having a BCS associated with being overweight or obese has been implicated as a risk factor for a range of diseases, such as diabetes, 26 , 27 skin disease 28 and osteoarthritis. 29 It also has links to mortality 27 and may impede normal feline behaviours such as grooming, playing or accessing high resting spots due to mobility issues. 30 A recent study revealed that animal welfare experts identify obesity in owned cats as one of the top three current priority welfare issues in the UK, based on potential severity and duration of impact on cats’ health. 31 The reported prevalence of overweight and obesity in owned cats varies globally, with estimates of 11.5% in the UK, 32 15.7% in Australia 33 and 41% in the United States. 34 A range of risk factors for obesity have been identified, such as a dry diet, 35 , 36 indoor‐only lifestyles, 36 , 37 certain breed types, 33 acquisition source 37 and neutering. 38 , 39 , 40

Associations between neutering and increased bodyweight are well established and are posited to be caused by hormonal and metabolic changes leading to decreased activity levels and increased food intake postneutering. 41 , 42 Concerns have been raised that cats neutered prepubertally may experience greater long‐term impacts on their health compared to those neutered later. 17 While the literature so far finds no difference in obesity in later life between cats neutered prepubertally and those neutered between 6 and 8 months old, 21 , 23 limitations within the current body of literature must be acknowledged. Few studies to date have considered both BCS and bodyweight. Where bodyweight is used in isolation, the range of what can be considered a healthy or normal bodyweight for each individual must be taken into account, as this may vary based on age, 43 , 44 sex 45 , 46 and breed. 47 BCS is a measure of body fat mass scored by visual analysis and palpation of the ribs. While BCS is a validated measure of body fat mass 48 , 49 with a relatively high rate of intraobserver reliability for trained veterinary professionals, 50 it is still subjective, with observer interpretation shown to be affected by confounding variables such as coat length. 38 When measured by owners or untrained professionals, as is done in many studies due to the relative ease of accessing larger amounts of data in this way (e.g., as described by Rowe et al 36 ), the reliability of BCS may be reduced or subject to reporter bias. 38 , 40 , 51 Additionally, analysis of BCS often either incorrectly treats the variable as numeric rather than categorical (e.g., as in Alexander et al 52 ) or distills the variation down to a binary measure of whether the cat is obese or not (e.g., as in Rowe et al. 35 ), thus not understanding the full spectrum of body types and the probability of moving between each of them. Studies may also not take into consideration other cat attributes or contributory factors that may influence a cat's propensity to gain bodyweight or increase their BCS, such as season of measurement or sex. Finally, many studies utilise bodyweight or BCS measurements taken at a single time point or during a limited timeframe rather than exploring long‐term changes across a cat population.

Understanding the influence of age at neutering on the bodyweight and body condition of owned cats is important, with results from such studies providing veterinarians with the necessary understanding to tailor and guide bodyweight management advice for cat owners. As such, this study aimed to determine associations between age‐related increases in bodyweight and BCS and the age at neutering in owned cats. Specifically, using observational, longitudinal veterinary clinical measurements paired with owner‐reported auxiliary information, a range of potential risk factors was considered when asking whether the age at which a cat is neutered affects their BCS and bodyweight as they age.

MATERIALS AND METHODS

Data collection

Data for this study were obtained as part of the Bristol Cats Study, a longitudinal cohort study of cats in the UK. Cats and owners were recruited to the Bristol Cats Study between 2010 and 2013, when cats were between 8 and 16 weeks old. Regular questionnaires were sent to owners registered in the study as their cat reached specific ages until owners reported that they were no longer in possession of their cat (due to death, loss or other reasons) or opted to stop participation in the study. In addition to the owner‐reported data, cards to record BCS and bodyweight, alongside the date of recording, were sent to owners at the end of each year to be completed by a veterinarian at their cat's next veterinary visit, with records returned up to February 2023 included. The Bristol Cats Study received ethical approval from the University of Bristol Animal Welfare and Ethical Review Body (reference UB/17/049). For more detailed information on the Bristol Cats Study, see Murray et al. 53

Data cleaning

The BCS system used by veterinarians was a five‐point scale. 49 Although not validated against an objective measure of body fat, it has similarities with the nine‐point BCS scale, which has been validated. 48 Responses provided on the nine‐point scale were excluded, due to a lack of validated conversion between the five‐ and nine‐point scales. As BCS is an ordinal, and therefore a non‐numeric scale, any responses that included a decimal point or a range were rounded down to the nearest whole number, given that such scores indicate that the cat does not fully meet the criteria for the higher bracket, for example, a score of 2.5 would be coded as 2, or a response ‘between 4 and 5’ would be coded as 4. Bodyweight (in kg) was included to two decimal places where provided. The dates at which the BCS and bodyweight measurements were recorded were also coded into seasons as follows: spring—March, April and May; summer—June, July and August; autumn—September, October and November; winter—December, January and February.

The data from the owner questionnaires were cleaned as follows. The cat's age at each BCS and/or bodyweight measurement was calculated using the date of recording and the date of birth. The date of birth was used as reported or, if unknown, calculated by subtracting the age reported at the time of the survey from the date of survey completion. Due to version differences in questionnaires, age at the time of neutering was used as reported where available; otherwise, it was calculated. Where calculated, the length of time owners reported had passed since the neutering operation was subtracted from the date of questionnaire completion to give a neuter date. Then, the date of birth was used with the neuter date to calculate age at neutering. The owner‐reported acquisition source was grouped into biologically relevant categories with adequate sample sizes, resulting in three separate categories: rescue centre/shelter, feral/stray and other (e.g., purchased online, acquired from a breeder). Hair length and sex were used as provided by the owner. As owner‐reported and veterinarian‐reported data were not collected at the same time point, all owner‐reported explanatory variables used were fixed variables, specifically, demographic details. Within questionnaires, owner‐reported time‐relative variables such as outdoor access, multicat households or diet did not align with the time of recording BCS and bodyweight and so were not included.

Data exclusions

From an initial dataset of 832 individual cats for whom veterinary recordings of BCS on a five‐point scale and bodyweight were available, 584 were taken forward for analysis. First, due to morphological differences in cats of different breeds, 47 , 54 , 55 cats reported by owners as purebred, or those where the owners did not know if the cat was purebred, were excluded (n = 226). Second, cats reported to have been pregnant at any point were excluded (n = 5), as pregnancy may impact BCS and bodyweight both during and after pregnancy, 56 while also predisposing them to be neutered at an older age. Data on other potentially confounding factors predisposing cats to being neutered at an older age were unavailable, precluding their exclusion. Next, cats whose neutering age was unknown were excluded (n = 15). Finally, BCSs recorded when cats were less than 1 year old were excluded from the analysis, which led to the removal of 22 cats from the dataset.

Data were checked to ensure sufficient sample sizes for categorical variables and that continuous variables were biologically reasonable. As only a single incidence of a BCS of 1 occurred throughout the entire dataset, this datapoint was excluded (n = 1); however, as this cat had other recorded BCSs above 1, the individual was retained within the dataset. Additionally, no hair length data for cats that were reported to have medium hair length were included in the analysis, both due to the small sample size of this group and the ambiguity in the interpretation of this category (n = 7).

Data analysis

Dataset amalgamation, coding, cleaning and exclusions were completed in Microsoft Excel for Microsoft Office 365 (version 2407). 57 Descriptive statistics for demographic details, absolute counts of veterinary visits and BCSs, and means, medians and ranges for BCS and bodyweight measurements were also calculated in Microsoft Excel. All further data analysis was carried out in R (version 4.2.2). 58 Cumulative link mixed‐effects models (CLMMs) were used to test variables for effects on BCS using the CLMM function within the package ‘ordinal’ (version 2022.11‐16). 59 Each CLMM included a random effect of cat ID, nested within owner ID, to account for non‐independent correlated data across individual measurements and among cats within the same household. CLMMs are able to deal with the ranked variable of BCS, whereby BCS has an ordered but not numeric structure.

Linear mixed models (LMERs) with a random effect of cat ID nested within owner ID were used to test variables for effects on cat bodyweight using the lmer function within the R package ‘lme4’ (version 1.1‐30). 60

For both analyses (CLMMs and LMERs), sex, age at neutering, acquisition source, hair length and season were incorporated as categorical fixed effects, and the age of the cat was incorporated as a continuous fixed effect within the model. Age was incorporated as a non‐linear function using a quadratic term to test whether bodyweight or BCS changes non‐linearly as cats age, as we may expect an increase early in life and a decline later in life.

Model validation

Within both CLMMs and LMERs, the significance of the coefficients was assessed with likelihood ratio tests (which use a chi‐squared statistic), while model comparison was made according to the Akaike information criterion (AIC), where the most parsimonious (lowest AIC) is favoured. Each predictor variable was considered separately, along with testing of individual interaction terms. Furthermore, a multivariable model using identified predictors was used to build a model via stepwise backwards elimination. To validate the age at neutering categories, we explored support for alternative categorisation as indicated by the data (Figures S1 and S2). Statistical comparisons were made between the same datasets that comprised complete records for the predictor of interest, which ranged between 94.8% and 100% complete (see Table S1 for further details).

To further check the validity of our model outcomes, we used a combination of approaches. For the LMER models, variables were checked for influential outliers, normality, homoscedasticity and collinearity using the ‘performance’ package (version 0.12.2), 61 with all terms showing low correlation according to the variance inflation factors (all variables VIF < 1.5). Modelled bodyweight data at 80 weeks were additionally compared to validated, published growth charts for both male and female, intact and neutered cats, 20 , 62 and weights were comparable to anticipated predictions when considering the evidence that neutered cats typically weigh more than intact cats (see Table S2 for values).

Model checking procedures are not as developed for CLMMs. However, we performed multiple checks to test the sensitivity of our data. First, we checked for multicollinearity and influential outliers by recreating the model the lmer function within the R package ‘lme4’, assuming that the BCS was a numeric term and applying a similar approach to LMER model checks. Second, we checked the sensitivity of the findings to the inclusion of BCS 2 data, given that this represented underweight cats, which may have a disproportionate impact on our findings. Finally, comparison of results with weight analysis provides an additional form of sensitivity analysis, with alignment in results providing further model validation. The most supported models were then plotted using ggplot2 (version 3.4.2). 63

RESULTS

Demographics

Following data cleaning, a total of 2410 veterinary visit data points were retained, with BCS recorded at each visit and bodyweight recorded at 2073 visits. The total dataset included 584 individual cats residing with 466 owners. Forty‐six percent (n = 270) of the cats were female, and 80% (n = 468) were shorthaired. Twenty‐five percent (n = 144) were homed from a shelter environment and 12% (n = 68) were previously stray or feral, with the remaining falling into the ‘other’ category. Twenty‐one percent (n = 120) were neutered at 4 months or under, 36% (n = 209) at 5 months, 33% (n = 194) at 6 months and 9% (n = 52) between 7 and 12 months. The dataset contained between one and 12 BCSs for each cat, with 73% (n = 426) having at least two recorded BCSs, and the median being three.

During the 2410 veterinary visits included in the study, a BCS of 3 (ideal) was recorded at 67% of visits (n = 1608), with 85% (n = 498) of cats having at least one recorded BCS of 3. In contrast, at 30% of veterinary visits (n = 714), signs of the cats being above ideal body condition were reported. Specifically, 48% (n = 279) of cats had at least one recorded BCS of 4 (overweight), comprising 26% (n = 628) of all veterinary visits. Nine percent (n = 52) of cats had at least one recorded BCS of 5 (obese), making up 3% (n = 86) of all veterinary visits. Additionally, 13% (n = 76) of cats had a BCS of 2 (underweight) recorded, comprising 4% (n = 88) of veterinary visits (Table 1). The bodyweights of 528 cats were recorded, with between 1 and 10 measurements per cat, and 74% (n = 392) of cats having at least two weight measurements recorded. The mean bodyweight recorded across all veterinary visits was 4.73 kg. The full details of the attributes of cats with BCS and bodyweight recorded at veterinary visits are shown in Table 1.

TABLE 1.

Descriptive statistics of 584 individual cats with 2410 body condition score (BCS) measurements and 2073 bodyweight measurements recorded by veterinary professionals, and associated sample sizes of different characteristics

BCS (n = 2410) Bodyweight (n = 2073)
Variables N % Mean (range) N % Mean (range)
Response variables
BCS
2 88 4
3 1608 67
4 628 26
5 86 3
Bodyweight (kg) 4.73 (2.20‒11.20)
Time‐varying explanatory variables
Age (years) 5.40 (1.04‒12.89) 5.89 (1.04‒12.89)
Season of veterinary visit
Spring (March‒May) 410 17 353 17
Summer (June‒August) 648 27 533 26
Autumn (September‒November) 657 27 560 27
Winter (December‒February) 695 29 622 30
Fixed explanatory variables
Sex
Female 1065 44 927 45
Male 1338 56 1139 55
Hair length
Short 1950 85 1673 85
Long 335 15 295 15
Source
Stray or feral 269 11 222 11
Shelter or rescue 676 29 602 29
Other 1425 60 1215 60
Neuter age
4 months or under 503 21 452 22
5 months 822 34 697 34
6 months 845 35 722 35
7‒12 months 217 9 185 9

Body condition score

In the best supported model, season and its interaction with sex (χ 2(3) = 7.94, p = 0.04, ΔAIC = 2), age and its interaction with age at neutering (χ 2(2) = 158.14, p < 0.001, ΔAIC = 154) and hair length (χ 2(1) = 4.50, p = 0.03, ΔAIC = 2.5) were predictive of BCS, according to both significance testing and AIC model selection. These findings were supported both with and without BCS 2 included in the model, so full results, including those for BCS 2, are discussed here. For details of all tested variables and associated statistics, see Table S3.

The age at neutering was a significant factor. Where four age at neutering categories (Figure S1) were included in the model, the probability of being a certain BCS overlapped for cats neutered at 4 months or under, 5 months and 6 months. These four discrete age at neutering categories did not significantly improve model fit (χ 2(6) = 5.74, p = 0.45), with the simplified model with two age at neutering categories (6 months and under and 7‒12 months) also supported by AIC selection (ΔAIC = 6.3). Figure 1 highlights the most supported results in terms of the effect of age at neutering on BCS.

FIGURE 1.

FIGURE 1

Predicted effect of the interaction between age at neutering and the age of a cat on the probability of attaining a body condition score (BCS) of (a) 2, (b) 3, (c) 4 or (d) 5, calculated for male and female cats. The fitted line represents the effect from the cumulative link mixed‐effects models, assuming that the BCS was recorded in winter for shorthaired cats

BCS changed non‐linearly with age, increasing in earlier life and decreasing in later life; however, the rate of increase was significantly less for cats neutered between 7 and 12 months (Figure 1). Male and female cats had significantly different BCSs, and this was associated with season. Males had an increased probability of a higher BCS; however, females had a higher probability of having a decreased BCS in summer and autumn (Figure 2). Additionally, cats with shorter hair had an increased probability of having a higher BCS.

FIGURE 2.

FIGURE 2

Predicted effect of the interaction between sex and the season of measurement of body condition score (BCS) on the probability of attaining a BCS of (a) 2, (b) 3, (c) 4 and (d) 5 at different ages. The fitted line represents the effect from the cumulative link mixed‐effects models, assuming that cats were neutered before the age of 7 months and were shorthaired

Bodyweight

For predictors of bodyweight, season and its interaction with sex (χ 2(3) = 9.36, p = 0.02, ΔAIC = 3.3) and age and its interaction with age at neutering (χ 2(2) = 14.21, p < 0.001, ΔAIC = 10.3) were found to be important, according to both significance testing and AIC model selection. For details of all tested variables and associated statistics, see Tables S4 and S5.

The age at neutering was a significant factor. Modelling that included four age at neutering categories suggested this was driven by cats neutered between 7 and 12 months having a lower bodyweight. As with the BCS analysis, the modelled bodyweights of cats neutered at 4 months or under, 5 months and 6 months overlapped (Figure S2). Using four age at neuter categories did not significantly improve model fit (χ 2(6) = 8.47, p = 0.21), and the simplified model containing only two age at neutering categories (6 months and under and 7‐12 months) was also supported by AIC selection (ΔAIC = 3.5). Figure 3 highlights the most supported results in terms of the effect of age at neutering on bodyweight.

FIGURE 3.

FIGURE 3

Predicted effect of the interaction between (a) age at neutering and age on the bodyweight of male and female cats, assuming that bodyweight was recorded in winter and (b) sex and the season of measurement on the bodyweight of cats at different ages, assuming that cats were neutered before the age of 7 months. The fitted line represents the results from the linear mixed models. Raw bodyweight values are also shown for (a)

Age was a significant factor, following a non‐linear relationship whereby bodyweight increased in early life and decreased in later life. Cats neutered after 7 months weighed less and their bodyweight did not increase as much as that of cats neutered at 6 months and under. Additionally, male cats were significantly heavier than female cats, and bodyweight was affected by season, with females having lower bodyweight in summer and autumn (Figure 3).

DISCUSSION

In this large contemporary cohort, several principal risk factors governing the BCS and bodyweight of companion cats have been described. BCS and bodyweight were dependent on age, increasing up to around 8‒9 years of age and then decreasing. No appreciable difference between cats neutered at 4 months or under, 5 months or 6 months was found, with all three age groups following similar bodyweight trajectories throughout their lifetime. However, cats neutered between 7 and 12 months did not experience such a rapid rate of increase as those neutered at 6 months or under. Additionally, the results corroborated that sex is an important factor, along with its interaction with season. These findings were consistent across separate analyses of BCS and bodyweight. However, hair length was associated with BCS only, potentially due to the subjective nature of BCS measurements. 38 , 40 , 51

Concerns over the lack of long‐term clinical research on the risks and benefits of prepubertal neutering have been highlighted as a barrier to uptake by some veterinarians. 17 Addressing this, this longitudinal study found no difference in BCS or bodyweight between cats neutered at 4 months or under, 5 months or 6 months. These findings add to the growing body of literature suggesting cats neutered prepubertally are at no greater risk of developing obesity than those neutered at around 6 months old. 20 , 23 , 64 Therefore, from a weight management perspective, proactive dietary management and other lifestyle approaches recommended within the veterinary literature 18 should be encouraged for all cats neutered at 6 months old or younger.

Differences were observed between cats neutered at 6 months old or younger and cats neutered between 7 and 12 months old, with cats neutered later experiencing a slower rate of growth in early life, and typically weighing less throughout adulthood. This result is comparable to a study that found cats neutered between 29 weeks (∼6.7 months) and 18.4 months old had reduced growth in early life following neutering compared to cats neutered prior to 29 weeks. 20 While it is possible that neutering at an older age may be protective against excess weight gain later in life, it is not yet clear why cats neutered later may show size differences postneutering when compared to cats neutered before 7 months old. Changes postneutering have been shown to include increased fat and lean mass, as well as increased ribcage length and abdominal girth when compared to unneutered populations, 20 potentially due to changes in growth hormones or satiety hormones and consequently food intake. However, an early study highlighted that neutering at around 4 months compared to 7 months may be advantageous for weight management by reducing the likelihood of acute changes in eating behaviour. 22 As decisions on age at neutering also need to account for the positive impact of prepubertal neutering on population control, 9 and thus subsequent welfare, of domestic cats, in addition to other individual benefits, the current balance of evidence supports prepubertal neutering, especially given that proactive dietary management can be used to maintain a healthy weight.

It is possible that age at neutering may be a proxy measure for the physiological state of an individual at the time of neutering, with potential key physiological differences present in cats aged 6 months and under compared to those aged 7‒12 months. As neutering norms typically result in most cats being neutered by 6 months old (approximately 90% within this study), neuters taking place between 7 and 12 months may have been performed out of necessity, such as cats being smaller initially or having health concerns. Some physiological confounders in relation to age at neutering were accounted for by removing cats reported to be or have been pregnant; however, further exploration of other health‐related factors, such as illness in early life, would require access to clinical records. The reverse may also be true, in that cats neutered earlier may have reached a greater weight sooner than others in the cohort. Both human 65 and feline studies 46 , 66 suggest that bodyweight in early life may be predictive of bodyweight throughout adulthood, with excess juvenile weight reported as a risk factor for adult obesity. However, it must be considered that the underlying mechanisms for this are likely complex and include genetic and epigenetic factors, as well as resource availability. Future studies with a larger sample size for cats neutered at 7 months or older may choose to explore potential explanations for why cats neutered later than 6 months appear to weigh less throughout their lives, and whether this may have any detrimental impact as cats age into their senior years and typically lose weight. 33 , 67 , 68

It should be noted that the accuracy of the owner‐reported date of birth for their cat and subsequently the calculated age at neutering and age at the time of each BCS and bodyweight measurement may not be exact due to potential recall errors. 69 This was reduced as far as possible by using the first incidence of owner‐reported date of birth and date of neutering to increase recall accuracy or likelihood that the initial date provided would have been referenced against an appointment or calendar. Additionally, cats with an unknown date of birth were excluded from the study. Age at neutering was also grouped and analysed as a categorical variable, rather than a continuous numerical variable, to further reduce any impact of inaccurate reporting.

Age at time of record was a significant predictor of BCS and bodyweight, with BCS and bodyweight increasing from birth, peaking at around 8‒9 years, and then beginning to decrease. This finding agrees with other studies reporting decreasing bodyweight in older cats, 33 , 67 , 68 which has been documented as starting at around 8 years of age. 70 In some individuals, this decrease may be due to sarcopenia (i.e., the gradual loss of lean body mass that occurs due to age). While well documented in people, little literature currently exists around sarcopenia in cats; however, it has been reported to be seen in 37.6% of cats over 7 years of age. 71 These decreases in BCS or bodyweight in later life are thought to be the result of changes to metabolism 44 and activity levels. 72 Decreased bodyweight in older cats may also be symptomatic of diseases such as hyperthyroidism 73 or chronic kidney disease (CKD). 74 While 8 years is younger than the average age of diagnosis for these diseases, it has been suggested that low levels of weight loss may be apparent 3 years before a diagnosis of CKD. 75 Additional longitudinal studies following cats throughout their midlife and into their senior years and recording any incidences of disease may be useful in evaluating whether this weight decrease is predictive of disease.

Sex was found to be significant, whereby males generally weighed more than females at any given time point. It is likely that this weight difference is due to overall size differences between the sexes. This finding is in concordance with the literature, which suggests that sexual dimorphism is present in the species, with male cats being typically larger and heavier than females. 55 , 62 , 68 , 76 , 77 The BCS of male cats was also typically greater than that of female cats. Previous literature has shown inconsistency regarding BCS and associations with sex postneutering, with studies suggesting that both males 38 and females 20 may be at greater risk of higher BCS postneutering. The present study revealed that differences were seemingly driven by seasonal effects, with female cats displaying lower BCSs and bodyweights in the summer and autumn, while the BCS of male cats remained more consistent throughout all seasons. This interaction of sex and season may help to explain inconsistencies in the results of other studies that have not used longitudinal data to explore BCS or bodyweight trends through time or considered the effect of season.

Seasonal changes may be due to variation in food intake throughout the year. While the literature is inconsistent regarding reported levels of food intake and the correlation with season, likely due to factors such as variation in environment, age and lifestyle, some evidence has reported that cats consume more food during colder months, 78 although this has not been shown to correlate with bodyweight changes where investigated. 79 There is also evidence that this may be sex specific. Alegría‐Morán et al. 80 found that female cats significantly increased their energy intake in colder months (autumn and winter), although the effect on bodyweight was not explored. A lag effect of this increased intake may explain the increased bodyweight during the winter and spring. Activity levels and energy expenditure in cats have also been found to vary seasonally, with increased activity levels sometimes demonstrated during summer months, when there is an increased photoperiod 81 and weather is more favourable. 82 Hunting may also vary seasonally due to differences in prey abundance and type 83 , 84 ; however, any impact on bodyweight is unclear and is likely to be complex due to changes to both energy expenditure and intake of prey and human‐provided food. Due to timing differences in the collection of owner‐reported versus veterinarian‐reported information, it was not possible to link bodyweight and BCS directly with parameters such as diet, outdoor access or multicat households, and as such, these data were not included as explanatory variables within the models. However, with improved understanding of potential lag effects of energy intake or expenditure on bodyweight and BCS, future models may better accommodate these temporally and individually variable data.

Hair length was the only variable not predictive of both BCS and bodyweight. Hair length was only predictive of BCS, potentially due to the subjectivity of BCS. Wolf and Drobatz 85 reported that long hair in dogs was a risk factor for veterinary professionals overestimating bodyweight for lower‐weight dogs and underestimating bodyweight for higher‐weight dogs. In cats, long hair is a reported risk factor for being underweight, 33 likely due to owners presuming their cat is larger than they are. In this study, cats with long hair were more likely to be given a lower BCS than shorthaired cats. As no bodyweight association was found, it is likely that this represents inaccurate BCS estimates due to the thicker layer of fur. This finding is in concordance with Courcier et al., 38 who found that owners were more likely to underestimate the BCS of longhaired cats than shorthaired cats. Long hair may distort the perspective of cat body shapes, leading both owners and veterinary professionals to perceive the fur to be responsible for more of the cat's size than it is. These findings highlight the benefits of using both BCS and bodyweight in clinical assessments and when formulating appropriate recommendations on nutrition and bodyweight management for cats.

It should be noted that while the five‐point BCS system was used in this study, the nine‐point scale would have been more ideal if available. It is possible that veterinarians habitually round down when deciding between rankings on a BCS chart, leading to underreporting of cats being overweight or obese. This is somewhat evidenced by the number of veterinarians who provided BCSs that were not a whole number, that is, ‘3 to 4’ or ‘3.5’. Alongside being a validated measure of body fat mass, the nine‐point scale means veterinarians can be more nuanced in their grading, which may reduce reporting bias. No literature is currently available to give an indication as to the extent of this potential reporting bias; however, it is possible that BCS in this study is underestimated.

Overall, this study highlights that bodyweight gain is not greater for cats neutered prepubertally when compared to cats neutered at the historically recommended 6 months; however, the future risk of BCS and bodyweight increase was least in cats neutered between 7 and 12 months. Despite this, given the number of veterinary records that scored cats within this population as overweight or obese, veterinarians should endeavour to provide postoperative weight management advice to owners. Although BCS and bodyweight may be useful as general health indicators when triangulated with other metrics, this study cannot infer the welfare of any of the cat subpopulations. However, timely neutering is known to have beneficial impacts on population control, long‐term prevention of disease and the reduction of owner‐reported undesirable behaviours. This, coupled with the current lack of evidence of any long‐term negative impacts on health, provides a case for prepubertal neutering at the general population level as a positive cat welfare intervention.

In conclusion, this study has provided evidence of the influence of various exogenous and endogenous factors on BCS and bodyweight, including age, sex, seasonality and coat length. The practicalities of recording BCS in longhaired cats and the importance of season when assessing bodyweight changes for female cats in clinical practice have also been highlighted. The underlying mechanisms by which these factors influence BCS and bodyweight are largely unknown but are likely mediated by the diet and activity levels of individual cats. More research into the mechanisms by which BCS and bodyweight are impacted by exogenous and endogenous factors would be beneficial, along with the wider consideration of how these factors translate to welfare implications across a cat's lifetime.

AUTHOR CONTRIBUTIONS

Conceptualisation, data curation, methodology, writing—original draft preparation and writing—review and editing: Rae Foreman‐Worsley. Resources and writing—review and editing: Emily Blackwell. Conceptualisation and writing—review and editing: Lauren R. Finka and Elizabeth Skillings. Conceptualisation, formal analysis, methodology and writing—review and editing: Jenni L. McDonald.

CONFLICT OF INTEREST STATEMENT

The authors declare they have no conflicts of interest.

ETHICS STATEMENT

The Bristol Cats Study received ethical approval from the University of Bristol Animal Welfare and Ethical Review Body (reference UB/17/049).

Supporting information

Supporting Information

VETR-196-e5433-s001.pdf (331.7KB, pdf)

ACKNOWLEDGEMENTS

The authors would like to thank all veterinarians, owners and their cats for their ongoing participation in the Bristol Cats Study, as well as the Bristol Cats Study team for project support and data acquisition. We appreciate the assistance of the Feline Welfare Research Team and Clinical Services team at Cats Protection for their constructive comments. This project received no specific funding. The Bristol Cats Study is funded by Cats Protection and the Waltham Petcare Science Institute.

Foreman‐Worsley R, Blackwell E, Finka LR, Skillings E, McDonald JL. Long‐term effect of neutering age on body condition score and bodyweight in domestic cats. Vet Rec. 2025;e5433. 10.1002/vetr.5433

DATA AVAILABILITY STATEMENT

The data that support the findings of this study are available from the corresponding author upon reasonable request.

REFERENCES

  • 1. Welsh CP, Gruffydd‐Jones TJ, Roberts MA, Murray JK. Poor owner knowledge of feline reproduction contributes to the high proportion of accidental litters born to UK pet cats. Vet Rec. 2014;174:118. [DOI] [PubMed] [Google Scholar]
  • 2. Cafazzo S, Bonanni R, Natoli E. Neutering effects on social behaviour of urban unowned free‐roaming domestic cats. Animals. 2019;9:1105. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 3. Finkler H, Gunther I, Terkel J. Behavioral differences between urban feeding groups of neutered and sexually intact free‐roaming cats following a trap‐neuter‐return procedure. J Am Vet Med Assoc. 2011;238:1141–1149. [DOI] [PubMed] [Google Scholar]
  • 4. O'Neill DG, Church DB, McGreevy PD, Thomson PC, Brodbelt DC. Longevity and mortality of cats attending primary care veterinary practices in England. J Feline Med Surg. 2015;17:125–133. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 5. Overley B, Shofer FS, Goldschmidt MH, Sherer D, Sorenmo KU. Association between ovarihysterectomy and feline mammary carcinoma. J Vet Intern Med. 2005;19:560–563. [DOI] [PubMed] [Google Scholar]
  • 6. Cats Protection . Cats and Their Stats report 2023. https://www.cats.org.uk/about-cp/cats-report (2023). Accessed 15 Apr 2025. [Google Scholar]
  • 7. McDonald JL, Skillings E. Human influences shape the first spatially explicit national estimate of urban unowned cat abundance. Sci Rep. 2021;11:1–12. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 8. Stavisky J, Brennan ML, Downes M, Dean R. Demographics and economic burden of un‐owned cats and dogs in the UK: results of a 2010 census. BMC Vet Res. 2012;8:163. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 9. McDonald J, Finka L, Foreman‐Worsley R, Skillings E, Hodgson D. Cat: empirical modelling of Felis catus population dynamics in the UK. PLoS One. 2023;18:e0287841. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 10. The Cat Group . Policy statement 1: timing of neutering. http://www.thecatgroup.org.uk/policy_statements/neut.html (2006). Accessed 15 Apr 2025.
  • 11. Crawford HM, Calver MC, Fleming PA. A case of letting the cat out of the bag—why trap‒neuter‒return is not an ethical solution for stray cat (Felis catus) management. Animals. 2019;9:171. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 12. Tan K, Rand J, Morton J. Trap‒neuter‒return activities in urban stray cat colonies in Australia. Animals. 2017;7:46. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 13. Farnworth MJ, Adams NJ, Seksel K, Waran NK, Beausoleil NJ, Stafford KJ. Veterinary attitudes towards pre‐pubertal gonadectomy of cats: a comparison of samples from New Zealand, Australia and the United Kingdom. N Z Vet J. 2013;61:226–233. [DOI] [PubMed] [Google Scholar]
  • 14. British Veterinary Association . Neutering of cats and dogs policy statement. https://www.bva.co.uk/take-action/our-policies/neutering-of-cats-and-dogs/ (2019). Accessed 15 Apr 2025. [Google Scholar]
  • 15. British Small Animal Veterinary Association . Position statement ‐ Neutering of dogs, cats, rabbits and ferrets. https://www.bsava.com/position-statement/neutering-of-dogs-cats-rabbits-and-ferrets/ (2021). Accessed 15 Apr 2025. [Google Scholar]
  • 16. RSPCA . Advice and Welfare ‐ Neuter your cat. https://www.rspca.org.uk/adviceandwelfare/pets/cats/health/neutering. Accessed 15 Apr 2025.
  • 17. McDonald J, Clements J. Contrasting practices and opinions of UK‐based veterinary surgeons around neutering cats at four months old. Vet Rec. 2020;187:317. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 18. Godfrey H, Morrow S, Abood SK, Verbrugghe A. Identifying the target population and preventive strategies to combat feline obesity. J Feline Med Surg. 2024;26:1098612X241228042. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 19. Spain CV, Scarlett JM, Cully SM. When to neuter dogs and cats: a survey of New York state veterinarians’ practices and beliefs. J Am Anim Hosp Assoc. 2002;38:482–488. [DOI] [PubMed] [Google Scholar]
  • 20. Salt C, Butterwick RF, Henzel KS, German AJ. Comparison of growth in neutered domestic shorthair kittens with growth in sexually‐intact cats. PLoS One. 2023;18:e0283016. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 21. Porters N, Polis I, Moons CPH, Van de Maele I, Ducatelle R, Goethals K, et al. Relationship between age at gonadectomy and health problems in kittens adopted from shelters. Vet Rec. 2015;176:572. [DOI] [PubMed] [Google Scholar]
  • 22. Allaway D, Gilham M, Colyer A, Morris PJ. The impact of time of neutering on weight gain and energy intake in female kittens. J Nutr Sci. 2017;6:e19. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 23. Spain CV, Scarlett JM, Houpt KA. Long‐term risks and benefits of early‐age gonadectomy in cats. J Am Vet Med Assoc. 2004;224:372–379. [DOI] [PubMed] [Google Scholar]
  • 24. Vojtkovská V, Voslářová E, Večerek V. Methods of assessment of the welfare of shelter cats: a review. Animals. 2020;10:1527. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 25. Taylor S, Roberts G, Evans M, German AJ. Recording of body weight and body condition score of cats in electronic health records from UK veterinary practices. J Feline Med Surg. 2022;24:e380–e393. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 26. Häring T, Haase B, Zini E, Hartnack S, Uebelhart D, Gaudenz D, et al. Overweight and impaired insulin sensitivity present in growing cats. J Anim Physiol Anim Nutr. 2013;97:813–819. [DOI] [PubMed] [Google Scholar]
  • 27. Teng KT, McGreevy PD, Toribio JALML, Raubenheimer D, Kendall K, Dhand NK. Associations of body condition score with health conditions related to overweight and obesity in cats. J Small Anim Pract. 2018;59:603–615. [DOI] [PubMed] [Google Scholar]
  • 28. Tarkosova D, Story MM, Rand JS, Svoboda M. Feline obesity—prevalence, risk factors, pathogenesis, associated conditions and assessment: a review. Vet Med. 2016;61(2016):295–307. [Google Scholar]
  • 29. Kocabağli N, Kutay HC, Dokuzeylül B, Nathalie I, Süer INE, Alp M. The analysis of computer data regarding obesity and associated diseases in cats examined at private veterinary practices. Acta Sci Vet. 2017;45:5. [Google Scholar]
  • 30. Maniaki E, Murrell J, Langley‐Hobbs SJ, Blackwell EJ. Associations between early neutering, obesity, outdoor access, trauma and feline degenerative joint disease. J Feline Med Surg. 2021;23:965–975. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 31. Rioja‐Lang F, Bacon H, Connor M, Dwyer CM. Determining priority welfare issues for cats in the United Kingdom using expert consensus. Vet Rec Open. 2019;6:365. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 32. Courcier EA, Mellor DJ, Pendlebury E, Evans C, Yam PS. An investigation into the epidemiology of feline obesity in Great Britain: results of a cross‐sectional study of 47 companion animal practices. Vet Rec. 2012;171:560. [DOI] [PubMed] [Google Scholar]
  • 33. Teng KT, McGreevy PD, Toribio JALML, Raubenheimer D, Kendall K, Dhand NK. Risk factors for underweight and overweight in cats in metropolitan Sydney, Australia. Prev Vet Med. 2017;144:102–111. [DOI] [PubMed] [Google Scholar]
  • 34. Chiang CF, Villaverde C, Chang WC, Fascetti AJ, Larsen JA. Prevalence, risk factors, and disease associations of overweight and obesity in cats that visited the Veterinary Medical Teaching Hospital at the University of California, Davis from January 2006 to December 2015. Top Companion Anim Med. 2022;47:100620. [DOI] [PubMed] [Google Scholar]
  • 35. Rowe EC, Browne WJ, Casey RA, Gruffydd‐Jones TJ, Murray JK. Early‐life risk factors identified for owner‐reported feline overweight and obesity at around two years of age. Prev Vet Med. 2017;143:39–48. [DOI] [PubMed] [Google Scholar]
  • 36. Rowe E, Browne W, Casey R, Gruffydd‐Jones T, Murray J. Risk factors identified for owner‐reported feline obesity at around one year of age: dry diet and indoor lifestyle. Prev Vet Med. 2015;121:273–281. [DOI] [PubMed] [Google Scholar]
  • 37. Wall M, Cave NJ, Vallee E. Owner and cat‐related risk factors for feline overweight or obesity. Front Vet Sci. 2019;6:266. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 38. Courcier EA, O'Higgins R, Mellor DJ, Yam PS. Prevalence and risk factors for feline obesity in a first opinion practice in Glasgow, Scotland. J Feline Med Surg. 2010;12:746–753. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 39. Harper EJ, Stack DM, Watson TDG, Moxham G. Effects of feeding regimens on bodyweight, composition and condition score in cats following ovariohysterectomy. J Small Anim Pract. 2001;42:433–438. [DOI] [PubMed] [Google Scholar]
  • 40. Colliard L, Paragon BM, Lemuet B, Bénet J‐J, Blanchard G. Prevalence and risk factors of obesity in an urban population of healthy cats. J Feline Med Surg. 2009;11:135–140. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 41. Vester BM, Sutter SM, Keel TL, Graves TK, Swanson KS. Ovariohysterectomy alters body composition and adipose and skeletal muscle gene expression in cats fed a high‐protein or moderate‐protein diet. Animal. 2009;3:91287–91298. [DOI] [PubMed] [Google Scholar]
  • 42. Belsito KR, Vester BM, Keel T, Graves TK, Swanson KS. Impact of ovariohysterectomy and food intake on body composition, physical activity, and adipose gene expression in cats. J Anim Sci. 2009;87:594–602. [DOI] [PubMed] [Google Scholar]
  • 43. Bellows J, Center S, Daristotle L, Estrada AH, Flickinger EA, Horwitz DF, et al. Ageing in cats: common physical and functional changes. J Feline Med Surg. 2016;18:533–550. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 44. Laflamme DP. Nutrition for ageing cats and dogs and the importance of body condition. Vet Clin North Am Small Anim Pract. 2005;35:713–742. [DOI] [PubMed] [Google Scholar]
  • 45. Merenda MEZ, Sato J, Scheibel S, Uemoto AT, Rossoni DF, dos Santos MP, et al. Growth curve and energy intake in male and female cats. Top Companion Anim Med. 2021;44:100518. [DOI] [PubMed] [Google Scholar]
  • 46. Opsomer H, Liesegang A, Brugger D, Wichert B. Growth curves and body condition of young cats and their relation to maternal body condition. Animals. 2022;12:1373. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 47. Kienzle E, Moik K. A pilot study of the body weight of pure‐bred client‐owned adult cats. Br J Nutr. 2011;106(Suppl. 1):S113‒S115. [DOI] [PubMed] [Google Scholar]
  • 48. Bjornvad CR, Nielsen DH, Armstrong PJ, McEvoy F, Hoelmkjaer KM, Jensen KS, et al. Evaluation of a nine‐point body condition scoring system in physically inactive pet cats. Am J Vet Res. 2011;72:433–437. [DOI] [PubMed] [Google Scholar]
  • 49. Laflamme D. Development and validation of a body condition score system for cats: a clinical tool. Feline Pract. 1997;25:13–18. [Google Scholar]
  • 50. Shoveller AK, DiGennaro J, Lanman C, Spangler D. Trained vs untrained evaluator assessment of body condition score as a predictor of percent body fat in adult cats. J Feline Med Surg. 2014;16:957–965. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 51. Blanchard T, Hoummady S, Banuls D, Roche M, Bynens A, Meunier M, et al. The perception of the body condition of cats and dogs by French pet owners and the factors influencing underestimation. Animals. 2023;13:3646. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 52. Alexander LG, Salt C, Thomas G, Butterwick R. Effects of neutering on food intake, body weight and body composition in growing female kittens. Br J Nutr. 2011;106(Suppl. 1):S19‒S23. [DOI] [PubMed] [Google Scholar]
  • 53. Murray JK, Casey RA, Gale E, Buffington CAT, Roberts C, Kinsman RH, et al. Cohort profile: the ‘Bristol Cats Study’ (BCS)—a birth cohort of kittens owned by UK households. Int J Epidemiol. 2017;46:1749–1750. [DOI] [PubMed] [Google Scholar]
  • 54. Künzel W, Breit S, Oppel M. Morphometric investigations of breed‐specific features in feline skulls and considerations on their functional implications. Anat Histol Embryol. 2003;32:218–223. [DOI] [PubMed] [Google Scholar]
  • 55. Monteiro CLB, Campos AIM, Madeira VLH, Silva HVR, Freire LMP, Pinto JN, et al. Pelvic differences between brachycephalic and mesaticephalic cats and indirect pelvimetry assessment. Vet Rec. 2013;172:16. [DOI] [PubMed] [Google Scholar]
  • 56. Wichert B, Schade L, Gebert S, Bucher B, Zottmaier B, Wenk C, et al. Energy and protein needs of cats for maintenance, gestation and lactation. J Feline Med Surg. 2009;11:808–815. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 57. Microsoft Corporation . Microsoft Excel. Available from: https://office.microsoft.com/excel
  • 58. R Core Team . R: a language and environment for statistical computing. Available from: https://www.R‐project.org [Google Scholar]
  • 59. Christensen R. Ordinal—regression models for ordinal data. R package version. 2022. p. 11‒16. Available from: https://CRAN.R‐project.org/package=ordinal
  • 60. Bates D, Mächler M, Bolker BM, Walker S. Fitting linear mixed‐effects models using lme4. J Stat Softw. 2015;67:1–48. [Google Scholar]
  • 61. Lüdecke D, Ben‐Shachar MS, Patil I, Waggoner P, Makowski D. Performance: an R package for assessment, comparison and testing of statistical models. J Open Source Softw. 2021;6:3139. [Google Scholar]
  • 62. Salt C, German AJ, Henzel KS, Butterwick RF. Growth standard charts for monitoring bodyweight in intact domestic shorthair kittens from the USA. PLoS One. 2022;17:e0277531. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 63. Wickham H. ggplot2: elegant graphics for data analysis. New York: Springer‐Verlag. 2016. [Google Scholar]
  • 64. Howe LM, Slater MR, Boothe HW, Hobson HP, Fossum TW, Spann AC, et al. Long‐term outcome of gonadectomy performed at an early age or traditional age in cats. J Am Vet Med Assoc. 2000;217:1661–1665. [DOI] [PubMed] [Google Scholar]
  • 65. Simmonds M, Llewellyn A, Owen CG, Woolacott N. Predicting adult obesity from childhood obesity: a systematic review and meta‐analysis. Obes Rev. 2016;17:95–107. [DOI] [PubMed] [Google Scholar]
  • 66. Serisier S, Feugier A, Venet C, Biourge V, German AJ. Faster growth rate in ad libitum‐fed cats: a risk factor predicting the likelihood of becoming overweight during adulthood. J Nutr Sci. 2013;2:1–8. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 67. Caney S. Weight loss in the elderly cat. Appetite is fine and everything looks normal. J Feline Med Surg. 2009;11:738–746. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 68. Bermingham EN, Thomas DG, Morris PJ, Hawthorne AJ. Meta‐analysis: energy requirements of adult cats. Br J Nutr. 2010;103:1083–1093. [DOI] [PubMed] [Google Scholar]
  • 69. Choi BCK, Pak AWP. A catalog of biases in questionnaires. Prev Chronic Dis. 2005;2:A13. [PMC free article] [PubMed] [Google Scholar]
  • 70. Campigotto AJ, Poljak Z, Stone EA, Stacey D, Bernardo TM. Investigation of relationships between body weight and age among domestic cats stratified by breed and sex. J Am Vet Med Assoc. 2019;255:205–212. [DOI] [PubMed] [Google Scholar]
  • 71. Peterson ME, Little SE. Cachexia, sarcopenia, and other forms of muscle wasting: Common problems of senior and geriatric cats and cats with endocrine disease. In: Proceedings of the Companion Animal Nutrition Summit (Gerontology: An Inside Out Perspective). Purina Institute; 2018:67–75. [Google Scholar]
  • 72. Smit M, Corner‐Thomas RA, Weidgraaf K, Thomas DG. Association of age and body condition with physical activity of domestic cats (Felis catus). Appl Anim Behav Sci. 2022;248:105584. [Google Scholar]
  • 73. Peterson ME, Castellano CA, Rishniw M. Evaluation of body weight, body condition, and muscle condition in cats with hyperthyroidism. J Vet Intern Med. 2016;30:1780–1789. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 74. Castro MCN, Vieira AB, Santos MCS, Kriangwanich W, Gershony LC, Soares AMB, et al. Body condition score as an indicator of prognosis for cats with chronic renal disease. Ciência Rural. 2010;40:335–340. [Google Scholar]
  • 75. Freeman LM, Lachaud MP, Matthews S, Rhodes L, Zollers B. Evaluation of weight loss over time in cats with chronic kidney disease. J Vet Intern Med. 2016;30:1661–1666. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 76. Verdugo MR, Rahal SC, Agostinho FS, Govoni VM, Mamprim MJ, Monteiro FO. Kinetic and temporospatial parameters in male and female cats walking over a pressure sensing walkway. BMC Vet Res. 2013;9:1–7. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 77. Pitakarnnop T, Buddhachat K, Euppayo T, Kriangwanich W, Nganvongpanit K. Feline (Felis catus) skull and pelvic morphology and morphometry: gender‐related difference? Anat Histol Embryol. 2017;46:294–303. [DOI] [PubMed] [Google Scholar]
  • 78. Thomas DG, Hekman M, Weidgraaf K, Bermingham EN. Seasonal effects on energy requirements in young cats in a temperate environment. Adv Anim Biosci. 2010;1:111. [DOI] [PubMed] [Google Scholar]
  • 79. Serisier S, Feugier A, Delmotte S, Biourge V, German AJ. Seasonal variation in the voluntary food intake of domesticated cats (Felis catus). PLoS One. 2014;9:e96071. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 80. Alegría‐Morán RA, Guzmán‐Pino SA, Egaña JI, Sotomayor V, Figueroa J. Food preferences in cats: effect of dietary composition and intrinsic variables on diet selection. Animals. 2019;9:372. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 81. Kappen KL, Garner LM, Kerr KR, Swanson KS. Effects of photoperiod on food intake, activity and metabolic rate in adult neutered male cats. J Anim Physiol Anim Nutr. 2014;98:958–967. [DOI] [PubMed] [Google Scholar]
  • 82. Jensen HA, Meilby H, Nielsen SS, Sandøe P. Movement patterns of roaming companion cats in Denmark—a study based on GPS tracking. Animals. 2022;12:1748. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 83. Thomas RL, Fellowes MDE, Baker PJ. Spatio‐temporal variation in predation by urban domestic cats (Felis catus) and the acceptability of possible management actions in the UK. PLoS One. 2012;7:e49369. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 84. Castañeda I, Forin‐Wiart M‐A, Pisanu B, de Bouillane de Lacoste N. Spatiotemporal and individual patterns of domestic cat (Felis catus) hunting behaviour in France. Animals. 2023;13:3507. [DOI] [PMC free article] [PubMed] [Google Scholar]
  • 85. Wolf JM, Drobatz KJ. Body condition and hair coat length impact weight estimation in dogs and cats presented to an emergency department. J Am Vet Med Assoc. 2023;261:353–357. [DOI] [PubMed] [Google Scholar]

Associated Data

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

Supplementary Materials

Supporting Information

VETR-196-e5433-s001.pdf (331.7KB, pdf)

Data Availability Statement

The data that support the findings of this study are available from the corresponding author upon reasonable request.


Articles from The Veterinary Record are provided here courtesy of Wiley

RESOURCES