X. Guo, W.-J. Ma, F. Zhang, F.-L. Ren, C.-J. Qu, M.J. Lammi 

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Recent advances in the research of an endemic osteochondropathy in China: Kashin- Beck disease  X. Guo, W.-J. Ma, F. Zhang, F.-L. Ren, C.-J. Qu, M.J. Lammi  Osteoarthritis and Cartilage  Volume 22, Issue 11, Pages 1774-1783 (November 2014) DOI: 10.1016/j.joca.2014.07.023 Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 1 Two KBD children aged 7 (A) and 15 (B) years old manifested the deformed joints in the limbs, had especially a knee varus deformity and the shortened humeri and the stature. The flexion of the terminal finger joints or the deformed fingers (C–E) was mostly occurring first in the children. The radiographic findings in the right hand of the KBD patients aged 13 (F), and 45 (G), and the feet of 9 years old one (H), respectively. In the growth plate cartilage of the KBD children, the large chondronecrotic areas without cells were typically observed in the deep zone of the cartilage (arrows in J and K). Such findings were not seen in the control cartilage (I). The chondrocyte size was significantly reduced in the KBD (J), but the cell membranes were intact. The nuclei were dissolved, broken and compressed, and associated with a red staining in the chondrocyte cytoplasm (K), and the cellular fibrillated areas (arrowhead) appeared. In contrast to the control cartilage (L), the chondrocyte clusters and the foci of chondronecrosis, the compressed nucleus and the incomplete cell membrane appeared in the upper and the middle zone in the articular cartilage of the KBD adults (M, N). Hematoxylin–eosin staining, 100 × 20. Osteoarthritis and Cartilage 2014 22, 1774-1783DOI: (10.1016/j.joca.2014.07.023) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 2 The ultrastructure of the KBD and the normal chondrocyte shown in the transmission electron microscopic images. The KBD chondrocytes displayed the swollen mitochondria (A) compared to the normal one (B), and had the distended endoplasmic reticulum with detached ribosomomes (C) compared to the normal cells (D). The KBD chondrocytes has the distended Golgi apparatus (E) in contrast to normal ones (F). Osteoarthritis and Cartilage 2014 22, 1774-1783DOI: (10.1016/j.joca.2014.07.023) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 3 The prevalence in the first offspring generation of the KBD families depended on the clinical phenotype of parents' status and the types of the KBD areas. In the same KBD area, the first offspring generation from the families whose both parents were the KBD patients (A) displayed a higher prevalence of the disease than the ones from families with a single parent suffering from the KBD (B, C); and higher than the one from families with a non-KBD history (D). Osteoarthritis and Cartilage 2014 22, 1774-1783DOI: (10.1016/j.joca.2014.07.023) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 4 An analysis of the allele frequencies of 63 STR loci in the chromosomes 2, 11 and 12. * There were significant differences in the allele frequencies between the KBD patients and the normal residents living in the KBD areas, marked with *. Osteoarthritis and Cartilage 2014 22, 1774-1783DOI: (10.1016/j.joca.2014.07.023) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 5 The relationship between the hair selenium content and the KBD prevalence with the X-ray positive rate in the children aged 7–12 years old in the Shaanxi province of China. The rate of the X-ray positive for the KBD decreased, while the selenium content increased in the hair during years 1990–1999. Osteoarthritis and Cartilage 2014 22, 1774-1783DOI: (10.1016/j.joca.2014.07.023) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions

Fig. 6 The scheme of the environmental risk factors, the pathophysiological processes and the cartilage damage linked to the development of the KBD. Osteoarthritis and Cartilage 2014 22, 1774-1783DOI: (10.1016/j.joca.2014.07.023) Copyright © 2014 Osteoarthritis Research Society International Terms and Conditions