Degenerative arthritis is a common joint disease that affects many elderly people and is typically diagnosed through radiography. However, the need for remote diagnosis is increasing because knee pain and walking disorders caused by degenerative arthritis make face-to-face treatment difficult. This study collects three-dimensional joint coordinates in real time using Azure Kinect DK and calculates 6 gait features through visualization and one-way ANOVA verification. The random forest classifier, trained with these characteristics, classified degenerative arthritis with an accuracy of 97.52%, and the model's basis for classification was identified through classification algorithm by features. Overall, this study not only compensated for the shortcomings of existing diagnostic methods, but also constructed a high-accuracy prediction model using statistically verified gait features and provided detailed prediction results.

Current studies have revealed the capacity of mesenchymal stem cells (MSCs) in term of immunomodulatory properties, and this distinct potential is downgraded according to the disease duration of patients-derived MSCs. In order to enhance the immunomodulatory and anti-tumorigenic properties of the rheumatoid arthritis (RA) joints-derived MSCs, we aggregate synovial fluid-derived MSCs from RA joints (RA-hMSCs) into 3D-spheroids by the use of hanging drop culture method. Cells were isolated from synovial fluids of RA joints with longstanding active status over 13 years. For aggregation of RA-hMSCs into 3D-spheroids, cells were plated in hanging drops in 30 μL of advanced DMEM (ADMEM) containing 25,000-30,000 cells/ drop and cultured for 48 h. To analyze the comparative immunomodulatory effects of 3D-spheroid and 2D monolayer cultured RA-hMSCs and then cells were cultured in ADMEM supplemented with 20% of synovial fluids of RA patients for 48 h and were evaluated by qRT-PCR for their expression of mRNA levels of inflammatory and antiinflammatory markers. Cellular aggregation of RA-hMSCs was observed and cells were aggregate into a single sphere. Following treatment of RA patient’s synovial fluids into the RA-hMSCs, spheroids formed RA-hMSCs showed significantly (p < 0.05) higher expression of TNFα stimulated gene/protein 6 (TSG-6) than the monolayer cultured RAhMSCs. Therefore, the 3D-spheroid culture methods of RA-hMSCs were more effective than 2D monolayer cultures in suppressing inflammatory response treated with 20% of RA-synovial fluids by expression of TNFα (TSG-6) according to the immune response and enhanced secretion of inflammatory factors.

목적: 국민건강영양조사 제7기(2016~2018) 원시자료를 이용하여 관절성 질환이 안질환에 영향을 미칠 수 있는지 와 그 연관성 정도를 파악하고자 하였다. 방법: 국민건강영양조사 제7기(2016~2018) 자료 중 관절성 질환과 안과 질환 진단여부에 응답한 만 50세 이상 의 성인 총 3,243명을 대상으로 두 질병간의 연관성을 분석하였으며, p<0.050인 경우 유의한 것으로 판단하였다. 결과 : 백내장, 녹내장, 황반변성의 주요 3대 안과 질환은 관절염 및 골관절염과 유의한 관련성이 있었다. 모든 변수를 보정한 상태에서 관절염은 1.296배(95% CI: 1.054~1.594) 정도 백내장의 위험을 증가시키는 것으로 나 타났으며, 황반변성은 2.413배(95% CI: 1.172~4.968) 위험을 증가시키는 것으로 나타났다. 또한 골관절염은 2.758배(95% CI: 1.342~5.668) 황반변성의 위험을 증가시키는 것으로 나타났다. 관절염과 골관절염은 녹내장에 영향을 미치지 않는 것으로 나타났다. 결론 : 관절염과 골관절염은 황반변성의 위험을 증가시키는 것으로 나타났고, 관절염은 백내장에도 영향을 미 치는 것으로 나타났다.

본 연구는 CIA에 의해 유발된 DBA/1 마우스를 통해 류마티스관절염 바이오마커에 대한 두 충 추출물의 효과를 평가하였다. 평가를 위해 류마티스관절염 동물모델 제작 후 100 ㎎/㎏/day로 4주간 경구 투여하고 혈청 바이오마커, 방사선, 구조적 매개변수 분석을 통해 치료 효과를 확인하였다. 음성대 조군과 비교하여, 두충 추출물은 염증 및 면역글로불린 마커(TNF-α, IgG 및 hs-CRP)의 생성을 유의 하게 감소시켰고, 백혈구의 단핵구 수를 유의적으로 감소시켰다. 또한, 두충 추출물은 관절 파괴를 효과 적으로 보존하고 관절 변형을 줄였으며, 골 밀도의 증가와 유의적으로 골 염증을 감소시켰다. 이러한 결 과는 두충 추출물이 류마티스관절염 증상을 개선하는 것을 나타낸다. 따라서, 두충 추출물은 류마티스관 절염 관리를 위한 새로운 치료 옵션이 될 수 있음을 보여준다.

본 연구는 방사선 형질전환 차조기와 백출복합물(차조기 복합물)이 퇴행성관절염 관련 매개체에 미치는 영향을 확인하고자 MIA(monosodium iodoacetate)로 퇴행성관절염을 유도한 랫드로 평가 하였다. 차조기 복합추출물을 2주 동안 25, 50, 100 ㎎/㎏/day의 용량으로 경구 투여하고 랫드의 우측 관절 내 공간에 MIA를 주입한 후 동일 용량을 4주 동안 지속 투여하였다. 이후, 혈청 바이오마커와 무 릎 관절 분석의 형태학 및 조직병리학적 분석에 기초한 치료 효과를 평가하였다. 대조군 랫드와 비교하였을 때 차조기 복합추출물은 혈청 내 염증 및 골 대사 마커(TNF-α, MMP-3, COX-2, PGE2, COMP, Aggrecan)의 생성량을 유의하게 감소시켰다. 이와는 반대로 연골 흡수 매개체인 CTX-2 생성을 증가시켰으며, 방사선 형질전환 차조기는 무릎 연골과 활막을 효과적으로 보존하였다. 그 결과, 차조기 복합물은 퇴행성관절염 증상을 개선하였다. 따라서, 차조기 복합물은 퇴행성관절염 관리를 위한 식품 소재로 사용될 수 있다.

본 연구는 CIA로 유도된 류마티스 관절염 모델에서 지골피 추출물이 류마티스관절염 관련 인자에 미치는 영향을 평가하였다. 동물 모델에 류마티스관절염을 유발한 후 지골피 추출물을 4주간 200 ㎎/㎏/day 용량으로 경구 투여하였다. 이후 혈액, 방사선 및 조직 분석에 기초하여 효과를 평가하였다. 그 결과, 대조군에 비해 지골피 추출물은 사이토카인, 케모카인 및 면역글로불린 생성을 유의하게 감소시켰다. 또한, 지골피 추출물은 중족골을 효과적으로 보존하였으며, H&E 및 M&T 염색에서도 대조군에 비해 조직 병리학적 개선이 있음을 보여주었다. 이와 같은 결과는 지골피 추출물이 류마티스관절염 증상을 완화시켰음을 나타내고 있다. 따라서 지골피 추출물은 류마티스 관절염 관리를 위한 새로운 치료옵션이 될 수 있다.

The purpose of this study was to investigate the lesions of a mouse collagen antibody-induced arthritis (CAIA) model using fluorescence bioimaging and micro-computed tomography (micro-CT) and to compare it with histopathological examination. Twelve mice were randomly divided into three groups: group 1 (G1) as control, group 2 (G2) as fluorescence probe control and group 3 (G3) as collagen antibodyinduced arthritis. The mice of G3 intravenously received anti-type II collagen 5-clone antibody cocktail (2 mg/mouse) on day 0 and intraperitoneally received lipopolysaccharide (50 μg/mouse) on day 3. On the while, the mice of G1 and G2 received 0.9% saline in equal volumes at equivalent times. Fluorescence bioimaging and micro-CT analysis were carried out to assess arthritis. Treatment with the collagen antibody cocktail increased the paw thickness of mice compared to those in both the control and probe-treated groups. Fluorescence bioimaging using a near infrared imaging agent showed high intensity in the joints of collagen antibody- treated mice, whereas those of control mice showed no signal. Micro-CT analysis of the knee joints of collagen antibody-treated mice showed rough and irregular articular appearance, whereas those of control mice showed normal appearance. Histopathological examination of the knee joints of collagen antibody-treated mice revealed destruction of cartilage and bony structure, synovial hyperplasia and infiltration of inflammatory cells. No cartilage destruction or inflammation was observed in control or probe control mice. Taken together, it is concluded that analyses of fluorescent bioimaging made it possible to evaluate CAIA lesions, comparable with those by micro-CT and histopathological examination in mice.

The anti-inflammatory effects of the glycosaminoglycan (GAG) derived from cricket (G. bimaculatus, Gb) were investigated in complete Freund’s adjuvant (CFA) treated chronic arthritis rat model. This GAG produced a meaningful anti-edema effect showing inhibition of C-reactive protein (CRP) and rheumatoid factor. This GAG also inhibited the atherogenesis and pro-inflammatory cytokine levels of VEGF production in HUVEC cells, IL-6, prostaglandin E2 stimulated lipopolysaccharide in LAW 264.7 cells and TNF-α production in normal splenocytes, with dose dependent manner. This GAG was also found to be an inducer of NO production from the HUVEC cells and a stimulator of endothelial nitric oxide synthase. In the histological finding, the LV dorsal root ganglion, linked to the paw treated Gb GAG, was repaired against CFA induced cartilage destruction. The combined Indomethacin (5 mg/kg)-Gb GAG (10 mg/kg) also more effectively inhibited CFA-induced paw edema at 3h, 2nd and 3rd day to levels comparable to anti-inflammatory drug, indomethacin.

Calcineurin-binding protein 1 (Cabin1) regulates calcineurin phosphatase activity as well as the activation, apoptosis, and inflammatory responses of fibroblast-like synoviocytes (FLSs), which actively participate in the chronic inflammatory responses in rheumatoid arthritis (RA). However, the mechanism of action of Cabin1 in FLS apoptosis is not clear. The aim of this study was to define the regulatory role of Cabin1 in FLSs of mice with collagen-induced arthritis (CIA). Transgenic mice overexpressing human Cabin1 in joint tissues, under the control of a type II collagen promoter, were generated. hCabin1 expression in joints and FLSs was determined by reverse transcriptase-polymerase chain reaction (RT-PCR) and Western blot analysis. The expression of cytokines, matrix metalloproteinases (MMPs), and apoptosis-related genes in FLSs was determined by enzyme- linked immunosorbent assay, gelatin zymography, and RT-PCR, respectively. Joints were histologically examined after H&E and TRAP staining. hCabin1-transgenic CIA mice had less severe arthritis than wild-type CIA mice, based on hind paw thickness and histology. This was accompanied by significantly enhanced apoptosis in transgenic mice, evidenced by significantly more TUNEL-positive cells in synovial tissues. The expression of inflammatory cytokines and MMPs was reduced, and the transgenic CIA mice exhibited decreased Akt activation and increased expression of p53, caspase-3, caspase-9, and Bax. hCabin1 plays a critical role in promoting apoptosis of FLSs and in attenuating inflammation and the destruction of cartilage and bone in RA. These findings help elucidate the pathogenic mechanisms of RA and suggest that Cabin1 is a potential target for RA treatment.

Clinical arthritis is typically divided into rheumatoid arthritis (RA) and osteoarthritis (OA). Arthritis-induced muscle weakness is a major problem in aged people, leading to a disturbance of balance during the gait cycle and frequent falls. The purposes of the present study were to confirm fiber type-dependent expression of muscle atrophy markers induced by arthritis and to identify the relationship between clinical signs and expression of muscle atrophy markers. Mice were divided into four experimental groups as follows: (1) negative control (normal), (2) positive control (CFA+acetic acid), (3) RA group (CFA+acetic acid+type Ⅱ collagen), and (4) aging-induced OA group. DBA/1J mice (8 weeks of age) were injected with collagen (50 μg/kg), and physiological (body weight) and pathological (arthritis score and paw thickness) parameters were measured once per week. The gastrocnemius muscle from animals in each group was removed, and the expression of muscle atrophy markers (MAFbx and MuRF1) and myosin heavy chain isoforms were analyzed by reverse transcription-polymerase chain reaction. No significant change in body weight occurred between control groups and collagen-induced RA mice at week 10. However, bovine type Ⅱ collagen induced a dramatic increase in clinical score or paw thickness at week 10 (p<0.01). Concomitantly, the expression of the muscle atrophy marker MAFbx was upregulated in the RA and OA groups (p<0.01). A dramatic reduction in myosin heavy chain (MHC)-Iβ was seen in the gastrocnemius muscles from RA and OA mice, while only a slight decrease in MHC-Ⅱb was seen. These results suggest that muscle atrophy gene expression occurred in a fiber type-specific manner in both RA- and OA-induced mice. The present study suggests evidence regarding why different therapeutic interventions are required between RA and OA.

Arthritis is a common disease in aged people, and is clinically divided into rheumatoid arthritis (RA) and osteoarthritis (OA). Although common symptoms such as pain are present, the underlying pathological mechanisms are slightly different. Therefore, the objectives of the present study were to compare joint damage induced by RA and OA by analyzing the major morphological and molecular differences, and to propose a suitable therapeutic intervention based on the pathophysiological conditions of bones and joints. For the RA animal model, 8-week-old DBA1/J mice were immunized with bovine type II collagen emulsified in complete Freund’s adjuvant (CFA). Normal C57BL/6 mice (over 2 years of age) were used for OA. The clinical arthritis score was calculated using a subjective scoring system, and paw thicknesses were measured using calipers. The serum TNFα level was analyzed using an ELISA kit. Micro- CT was used to identify pathological characteristics and morphological changes. In collagen-induced RA mice, there were increased ankle joint volumes and clinical scores (p<0.01). The concentration of TNFα was significantly increased from 3 to 7 weeks after immunization. Micro-CT images showed trabecular bone destruction, pannus formation, and subchondral region destruction in RA mice. OA among aged mice showed narrowed joint spaces and breakdown of articular cartilage. This study suggests that a careful therapeutic intervention between RA and OA is required, and it should be based on morphological alteration of bone and joint.

목적 : 본 연구는 노인 관절염환자를 대상으로 일상생활수행능력에 따른 방문재활서비스에 대한 요구도를 파악하 여 노인 관절염환자에 대한 방문재활치료모델개발의 기초자료로 활용하기 위한 것이다. 연구방법 : 2009년 8월 현재 대전광역시에 위치한 3개의 노인복지관과 1개의 주간보호센터에 등록된 재가 관절염 환자를 대상으로 설문을 실시하였다. 설문지는 총 150부를 배부하여 110부가 회수되었고, 회수된 설문지 중 79부 (72%)가 분석에 사용되었다. 설문지는 방문재활서비스 요구도(10문항)와 관절염상태를 평가하기 위한 한국형 WOMAC(Western Ontario and McMaster University Osteoarthritis)검사와 수정 바텔지수(Modified Barthel Index: MBI)로 구성하였다. 한국형 WOMAC과 수정바텔지수(MBI), 시각적통증검사(Visual Analogue Scale: VAS)의 상관성을 알아보기 위해 피어슨 상관분석을 실시하였고, 한국형 WOMAC의 기능 수준에 따른 일반적 사 항, 의학적 사항, 방문재활서비스 인식도, 방문재활서비스의 필요성과 이유, 방문재활서비스의 구체적 욕구에 대하 여 교차분석(3XR)을 통해 분석하였다. 유의수준 α는 .05로 하였다. 결과 : 대상자 79명의 진단명은 퇴행성관절염 환자가 61명(79.2%)이었으며, 통증이 가장 많이 발생하는 부위는 슬 관절로 나타났다. 방문재활서비스에 대한 인식도는 낮았지만 응답자의 93.7%(74명)가 필요하다고 응답하였고, 기능별로는 1등급에서는 15명(19.0%), 2등급에서는 44명(55.7%), 3등급에서는 15명(19.0%)이 방문재활서비 스가 필요하다고 하였다. 결론 : 본 연구의 결과에서 재가 노인 관절염 환자는 가정에서 제공되는 재활서비스에 대해 높은 요구도를 갖고 있 음을 알 수 있다. 향후, 재가 관절염 노인들을 위한 실증적인 방문재활서비스에 대한 연구가 지속적으로 보완되어 야 할 것이다.