Skip to main content
. 2009 Jul 9;30(5):494–535. doi: 10.1210/er.2009-0010

Table 1.

Magnitude of skeletal changes in mice lacking total, local bone, liver-derived, and endocrine IGF-I actions

Total IGF-I KOa Local bone IGF-I KO
Liver IGF-I KOd Endocrine IGF-I KOe
Chondrocyte IGF-I KOb Osteoblast IGF-I KOc
Serum IGF-I 100% ↓ Normal Normal 75% ↓ 97.5% ↓
Length 40% ↓ 7% ↓ 14% ↓ Normal 6% ↓
Cortical bone width 38% ↓ 7% ↓ 20% ↓ 9% ↓ 18% ↓
Cortical vBMD 30% ↓ 4% ↓ 5% ↓ 7% ↓ 11% ↓
Trabecular BV/TV 55% ↑ ND 20% ↓f 10–20% ↓ 8% ↓f
Bone formation rate 70% ↓ ND 48% ↓ ND ND
Mineral apposition rate 40% ↓ ND 38% ↓ ND ND

ND, Not determined; vBMD, volumetric BMD; BV/TV, bone volume/ total volume. 

a

Data for length, bone width, and cortical vBMD were derived from Mohan et al. (50), whereas data for trabecular BV/TV, bone formation rate, and mineral apposition rate were derived from Bikle et al. (153). 

b

Data for chondrocyte IGF-I KO mice were derived from Govoni et al. (52). 

c

Data for osteoblast IGF-I KO mice were derived from Govoni et al. (53). 

d

Data for liver-specific IGF-I KO are summaries of the main findings from several studies using mice with liver-specific IGF-I KO (11,12,58,61,62,155). 

e

Data for length and bone width of endocrine IGF-I KO were derived from triple KO mice lacking liver-derived IGF-I, total IGFBP-3, and total ALS (61), whereas data for cortical vBMD and trabecular BV/TV were derived from double KO mice lacking liver-derived IGF-I and ALS (62). 

f

Not significant.