Osteoporosis (OP) is a chronic metabolic bone disease characterized by the decrease of bone tissue per unit volume under the combined action of genetic and environmental factors, which leads to the decrease of bone strength, makes the bone brittle, and raises the possibility of bone fracture. However, the exact mechanism that determines the progression of OP remains to be underlined. There are hundreds of trillions of symbiotic bacteria living in the human gut, which have a mutually beneficial symbiotic relationship with the human body that helps to maintain human health. With the development of modern high-throughput sequencing (HTS) platforms, there has been growing evidence that the gut microbiome may play an important role in the programming of bone metabolism. In the present review, we discuss the potential mechanisms of the gut microbiome in the development of OP, such as alterations of bone metabolism, bone mineral absorption, and immune regulation. The potential of gut microbiome-targeted strategies in the prevention and treatment of OP was also evaluated. Cite this article:
In developmental dysplasia of the hip (DDH),
a bone defect is often observed superior to the acetabulum after
the reconstruction at the level of the true acetabulum during total
hip replacement (THR). However, the essential amount of uncemented
acetabular component coverage required for a satisfactory outcome
remains controversial. The purpose of this study was to assess the
stability and function of acetabular components with a lack of coverage >
30% (31% to 50%). A total of 760 DDH patients underwent THR with
acetabular reconstruction at the level of the true floor. Lack of
coverage above the acetabular component of >
30% occurred in 56
patients. Intra-operatively, autogenous morcellised bone grafts
were used to fill the uncovered portion. Other than two screws inserted through
the acetabular shell, no additional structural supports were used
in these hips. In all, four patients were lost to follow-up. Therefore,
52 patients (52 hips, 41 women and 11 men) with a mean age of 60.1
years (42 to 78) were available for this study at a mean of 4.8
years (3 to 7). There were no instances of prosthesis revision or
marked loosening during the follow-up. The Harris hip score improved
from a mean of 40.7 points ( Cite this article: