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. 2016 Aug 18;7:12444. doi: 10.1038/ncomms12444

Table 1. The Harwell Ageing screen phenotyping pipeline.

Test Phenotypic Area Group Age (weeks)
ECG Cardiac All 12
SHIRPA Neurological Females (males) 13, 66
Grip strength Musculoskeletal/neurological All 13, 66
Slit lamp/opthalmoscope Vision All 15, 49, 65, (73)
Optokinetic drum Vision/neurological All 15, 49, 65, (73)
Click box Hearing Non ahl* 14, 26, 39, 50
Auditory brainstem response+click stimulus Hearing Non ahl* 14, 39
Echo-MRI Growth/body composition Males (females) 16, 27, 51, 71
DEXA Musculoskeletal/body composition Females (males) 16, 51,
X-ray Musculoskeletal Females (males) 16, 51, 74
Pupillometry Vision/neurobehaviour All 18, 68
Sleep tracking Neurobehaviour Females (males) 18, 68
Clinical chemistry Pathology Females (males) 28, 53, 80
Fasted bleed Diabetes/metabolism Males (females) 17, 28, 52, 80
Fasted insulin Diabetes/metabolism Males (females) 33, 57, 72
IPGTT Diabetes/metabolism Males (females) 33, 57, 72

ECG, electrocardiogram; DEXA, dual energy X-ray analysis; IPGTT, intraperitoneal glucose tolerance test; MRI, magnetic resonance imaging; SHIRPA, SmithKline Beecham, Harwell, Imperial College and Royal London Hospital phenotype assessment.

A summary and timetable of the core phenotyping tests in the Harwell Ageing Screen, indicating screening time points. In addition to the documented phenotype tests mice are weighed every 3 months up until the age of 12 months and then monthly from 12 months onwards. For the tests where a single sex was initially tested the other sex was screened when outliers were suspected. The screening timetable is flexible and additional screens can be added to confirm outliers depending on the phenotype detected.

*G3 mice mothered by G2 females that do not carry the Cdh23ahl allele.