cellular
• osteoblast surface is increased 1007% in males and 189% in females compared to in wild-type mice
|
skeleton
• osteoblast surface is increased 1007% in males and 189% in females compared to in wild-type mice
|
long femur
(
J:150166
)
• female mice exhibit a slightly longer femur than wild-type females
|
• mice exhibit increased radiodensity throughout the skeleton compared to in wild-type mice
(J:150166)
• whole body bone mineral density is increased
(J:213541)
|
• areal bone mineral density in male mice is increased 62% for lumbar vertebrae and 55% for the whole leg compared with wild-type mice
|
• muCT analysis of distal femoral metaphysis and femur shaft shows increase in trabecular volumetric bone mineral density (+149% in males and +281% in female) compared to wild-type
|
• bone volume fraction (BV/TV) is increased
|
• static histomorphometric analysis shows increased cortical area (+78% in males and +55% in females) and periosteal perimeter (+17% in males, +21% in females) compared to in wild-type mice
• static histomorphometric analysis shows decreased endocortical perimeter (-20% in males and -14% in females) compared to in wild-type mice
|
• the metaphyseal region of distal femur exhibits an increase in trabecular bone compared to in wild-type mice
|
• static histomorphometric analysis shows that trabecular bone volume is increased (+237% in males and +391% in females) compared to in wild-type mice
• muCT analysis of distal femoral metaphysis and femur shaft shows increase in trabecular bone volume (+146% in males and +224% in females) compared to in wild-type mice
|
• static histomorphometric analysis shows that trabecular number is increased (+37% in males and +57% in females) compared to in wild-type mice
|
• static histomorphometric analysis shows that trabecular thickness is increased (+146% in males and +219% in females) compared to in wild-type mice
|
• dynamic histomorphometric analysis of the femur midshaft shows increased cortical bone formation with increase periosteal mineralization surface (+194% in males, 249% in females), periosteal mineral apposition rate (143% in males), periosteal bone formation rate (+396% in males), endocortical minearal apposition rate (+1402% in males, +269% in females), endocortical mineral apposition rate (+1249% in males, +102% in females), and endocortical bone formation (+7891% in males and +499% in females) compared to in wild-type mice
• bone volume is increased in the trabecular and cortical compartments compared to in wild-type mice
|
• mineral apposition rates and bone formation rates are increased
|
• in a compression testing, lumbar vertebrae exhibit a higher maximum load (+243% in males and +188% in females), stiffness (+93% in males), and energy failure (+415% in males and +556% in females) compared to in wild-type mice
(J:150166)
• in a three-point bend testing, femur diaphysis exhibit a higher maximum load (+132% in males and +154% in females), stiffness (+87% in males and +119% in females), and energy failure (+83% in males and +198% in females) compared to in wild-type mice
(J:150166)
• bones show increased ultimate force, energy to failure, and stiffness, indicating enhanced bone strength
(J:213541)
|
growth/size/body
• female mice exhibit a slightly higher body weight than wild-type females
|
limbs/digits/tail
long femur
(
J:150166
)
• female mice exhibit a slightly longer femur than wild-type females
|
Mouse Models of Human Disease |
DO ID | OMIM ID(s) | Ref(s) | |
sclerosteosis 1 | DOID:0060756 |
OMIM:269500 |
J:213541 |