Dogs are amazing for many reasons. One reason is their range in size within one species – from less than 1 kg right up to nearly 100kg – a one-hundred-fold increase.
Another reason is their lifespan. Smaller dogs – on average – live more than twice as long as giant breeds despite near-identical physiology, diet and environmental conditions.
For cats, lifespan is on a much more linear trajectory. Members of the Felidae family range from 15 to 30 years old. Larger cats like lions live longer than smaller cats like your own moggie domestic cat.
Why do big dogs die young? And how do small dogs – and cats – manage to avoid this early death trap?
This article is the first in an occasional series on getting older – in pets, animals in general and, of course humans. Obviously, one critical factor that determines a lifespan is lifestyle, and one factor in premature death is discussed in another article HERE. Lifespan is also determined by hormonal and/or genetic factors and, in dogs and cats, by breed-specific vulnerabilities to disease and other environmental factors.
In this article, we explore the biological correlates of ‘normal’ aging in animals. In other words, we ask the question – what determines a natural, healthy lifespan in different species of animals?
It starts with actuarial senescence
In ecological studies of wild animals, the term – actuarial senescence – is often used to describe increasing adult mortality rates with age. Actuarial senescence operates, either through internal degenerative changes that kill the animal regardless of its environment, or through making the animal more vulnerable to hazards in its environment, for example the presence of predators, including other carnivorous animals and, of course, humans – probably the most significant global influence on unnatural death in wild animals.
Cross-species studies on a wide range of animal species have identified several factors that correlate with actuarial senescence including –
1. The gestation period of the animal.
2. The age at which the animal reaches sexual maturity.
3. The adult body mass of the animal.
Across-species comparisons
When comparing one species with another species across the animal kingdom, a larger body mass is a good predictor of a longer lifespan.
Within-species comparisons
In complete contrast, comparing animals of the same species with each other (within-species comparison) shows the reverse – smaller body size in correlated with longer lifespan and larger body mass is correlated with a shorter lifespan, for example in mice and in dogs.
For a wild animal, being small means being vulnerable so there is a selective advantage in being big, and in growing big as quickly as possible. However, the cost of growing fast is a shorter life span.
Birds are an exception to this rule as many species of bird grow fast and live very long lives.
Dogs in particular are hugely valuable as models for research into ageing because of their unprecedented range in size within one species, from less than 1 kg right up to nearly 100kg, a one-hundred-fold increase.
The lifespan of dogs also varies significantly, with smaller dogs living more than twice as long as giant breeds, despite near-identical physiology, diet and environmental conditions.
Why is it that big dogs die younger than small dogs?
There are 3 possible reasons –
1. Big dogs have a shorter lifespan because of an earlier onset of senescence.
2. Big dogs have a shorter lifespan because they are more vulnerable to hazards in their environments.
3. Big dogs have a shorter lifespan because, biologically, they have an increased rate of ageing.
One study on variability of aging in dogs analysed the data collected over 20 years from the deaths of 74,556 dogs, representing 74 different dog breeds.
The results showed that –
1. For every 2kg increase in body weight, there was a one month reduction in lifespan.
2. Senescence onset was earlier in larger dogs, and once it started they aged more rapidly.
How does this influence aging?
Large breeds have to grow rapidly and for an extended period of time to reach their adult weights. This is associated with higher levels of the insulin/insulin-like growth factor-1 (IGF-1), required to stimulate skeletal and muscle development. However, increased IGF-1 is also linked to cancer, diabetes and obesity.
Take-home message
The conclusion that can be drawn from this is that larger dogs die younger because an earlier onset of senescence triggers an accelerated rate of ageing (actuarial senescence) compared to smaller dogs.
© copyright Robert Falconer-Taylor, 2018
This article is an original work and is subject to copyright. You may create a link to this article on another website or in a document back to this web page. You may not copy this article in whole or in part onto another web page or document without permission of the author. Email enquiries to robertft@emotions-r-us.com.
References
Austad SN. 2010. Cats, “rats,” and bats: the comparative biology of aging in the 21st century. Integr Comp Biol. 2010 Nov;50(5):783-92.
Cohen DH, LeRoith D. 2012. Obesity, type 2 diabetes, and cancer: the insulin and IGF connection. Endocr Relat Cancer. 2012 5;19(5):F27-45.
Etnyre E, Lande J, Mckenna A. 2011. Animal Diversity Web: Felidae cats. http://animaldiversity.org/site/accounts/information/Felidae.html. University of Michigan. Accessed 29/01/2018).
Fleming JM, Creevy KE, Promislow DE. 2011. Mortality in North American dogs from 1984 to 2004: an investigation into age-, size-, and breed-related causes of death. J Vet Intern Med. 2011 Mar-Apr;25(2):187-98.
Gems D, Partridge L. 2013. Genetics of longevity in model organisms: debates and paradigm shifts. Annu Rev Physiol. 2013;75:621-44.
Ghirlanda S, Acerbi A, Herzog H, Serpell JA. 2013. Fashion vs. function in cultural evolution: the case of dog breed popularity. PLoS One. 2013 11;8(9).
Greer KA, Hughes LM, Masternak MM. 2011. Connecting serum IGF-1, body size, and age in the domestic dog. Age (Dordr). 2011 Sep;33(3):475-83.
Herzog HA, Bentley RA, Hahn MW. 2004. Random drift and large shifts in popularity of dog breeds. Proc Biol Sci. 2004 7;271 Suppl 5:S353-6.
Kraus C, Pavard S, Promislow DE. 2013. The size-life span trade-off decomposed: why large dogs die young. Am Nat. 2013 Apr;181(4):492-505.
Metcalfe NB, Monaghan P. 2003. Growth versus lifespan: perspectives from evolutionary ecology. Exp Gerontol. 2003 38(9):935-40.
Miller RA, Harper JM, Galecki A, Burke DT. 2002. Big mice die young: early life body weight predicts longevity in genetically heterogeneous mice. Aging Cell. 2002 1(1):22-9.
Patronek GJ, Waters DJ, Glickman LT. 1997. Comparative longevity of pet dogs and humans: implications for gerontology research. J Gerontol A Biol Sci Med Sci. 1997 52(3):B171-8.
Ricklefs RE. 2010. Life-history connections to rates of aging in terrestrial vertebrates. Proc Natl Acad Sci U S A. 2010 1;107(22):10314-9.
Sutter NB, Bustamante CD, Chase K, Gray MM, Zhao K, Zhu L, Padhukasahasram B, Karlins E, Davis S, Jones PG, Quignon P, Johnson GS, Parker HG, Fretwell N, Mosher DS, Lawler DF, Satyaraj E, Nordborg M, Lark KG, Wayne RK, Ostrander EA. 2007. A single IGF1 allele is a major determinant of small size in dogs. Science. 2007 6;316(5821):112-5.
Uauy R, Solomons N. 2005. Diet, nutrition, and the life-course approach to cancer prevention. J Nutr. 2005 135(12 Suppl):2934S-2945S.
Waters DJ. 2011. Aging research 2011: exploring the pet dog paradigm. ILAR J. 2011;52(1):97-105.
Williams PD, Day T, Fletcher Q, Rowe L. 2006. The shaping of senescence in the wild. Trends Ecol Evol. 2006 21(8):458-63.