Weijie Wang, Yung-Heng Lee, James Cheng-Chung Wei, Philip Mease
doi : 10.1111/1756-185X.14537
Lieh-bang Liou
doi : 10.1111/1756-185X.14538
Muhammad Asim Khan, Su-Boon Yong, James Cheng-Chung Wei
doi : 10.1111/1756-185X.14547
Qinglin Wu, Chuangong Fu, Zhifu Lu
doi : 10.1111/1756-185X.14533
By performing a meta-analysis of published cohort studies, this review aims to evaluate the association between gouty arthritis (GA) and the risk of myocardial infarction (MI) and heart failure (HF), hence providing evidence for clinical management.
Daisuke Uritani, Hitoshi Koda, Yuuka Yasuura, Aya Kusumoto
doi : 10.1111/1756-185X.14536
Subjective knee stiffness is a common symptom in patients with knee osteoarthritis treated conservatively. However, the influencing factors or effects of knee joint stiffness are unknown. The aim of this study was to explore the factors associated with subjective knee stiffness in patients with knee osteoarthritis.
Hossein Azadeh
doi : Hossein Azadeh
Rheumatoid arthritis (RA) has been linked to an increased risk of osteoporosis as well as fractures. Patients diagnosed with RA had a 25% increased risk of osteoporotic fracture, according to a recent population-based cohort study that compared them to people without RA.
Yukiko Takakuwa, Yoshioki Yamasaki, Hiromi Matsushita, Tomofumi Kiyokawa, Machiko Mizushima, Kumiko Tonooka, Hiroko Nagafuchi, Shin Matsuoka, Seido Ooka, Kimito Kawahata
doi : 10.1111/1756-185X.14532
To elucidate the clinical features, long-term survival, and prognostic factors for mortality among patients with microscopic polyangiitis (MPA), including those with anti-neutrophil cytoplasmic antibody-positive interstitial lung disease (ILD) (ANCA-ILD), which could be a subset of its variant phenotype.
Yujun Rao, Nan Xu, Yongbin Zhang, Yuxuan Fang, Longlong Tian, Xingxing Min, Guiyu Chen, Tiantian Dai, Nianxing Liu, Xuanhan Wang, Xiuting Gu, Hanpeng Lai, Wei Wang, Guoqing Li
doi : 10.1111/1756-185X.14528
To evaluate the utility of magnetic resonance imaging (MRI) and magnetic resonance sialography (MRS) for diagnosis of primary Sjögren syndrome (pSS) singly or integrated with 2016 American College of Rheumatology (ACR)/European League Against Rheumatic Diseases (EULAR) classification criteria.
Xiao-Li Huang, Hong-Yu Zheng, Hui-Hui Yang, Ze-Feng Shi, Bing Zhang, Bei Lan, Hong Wang, Ru-Xin Tan
doi : 10.1111/1756-185X.14545
To explore the value of human data from the Zhuang population via predicting the diameter of the hamstring tendon autograft in anterior cruciate ligament (ACL) reconstruction and determining the feasibility of preoperative ultrasound for prediction.
Ping-Han Tsai, Chang-Fu Kuo, Jia-Rou Liu, Pei-Ru Li, Lai-Chu See
doi : 10.1111/1756-185X.14558
To evaluate the influence of febuxostat on adverse events and mortality in gout.
Mariko Hara, Noriko Morimoto, Takahisa Watabe, Naho Morisaki, Kenji Matsumoto
doi : 10.1111/1756-185X.14559
To evaluate the clinical factors associated with the outcome of tonsillectomy in children with periodic fever, aphthous stomatitis, pharyngitis, and cervical adenitis (PFAPA) syndrome, thereby clarifying who would most likely benefit from that surgery.
Sanat Phatak, Aditya Khenat, Mansi Malandkar, Sanjiv Amin
doi : 10.1111/1756-185X.14570
Clinical trial evidence demonstrates the efficacy of tofacitinib in ankylosing spondylitis and psoriatic arthritis (PsA). Real-world data from spondyloarthritis (SpA) patients are scarce; there are few reports of its effectiveness and safety from low- to middle-income countries like India, despite its widespread usage.
Katsuhiko Yoneda, Soshi Takahashi, Kazuhiko Nakayama, Masanori Iwahashi, Noriaki Emoto, Shunichi Kumagai
doi : 10.1111/1756-185X.14576
To determine whether complications of pulmonary hypertension (PH) can be predicted by noninvasive screening tests in systemic sclerosis (SSc).
Faiq I. Gorial, Nabaa Ihsan Awadh, Yasameen Abbas Humadi, Mohammed Tareq Mutar, Mustafa Majid Hameed, Shahlaa B. Ali, Hala Fadhil Hasan, Alyaa N. Aljafr
doi : 10.1111/1756-185X.14584
There is a growing interest in studying the effects of arthritis on a person's work productivity using a growing variety of outcome indicators.
Dominic Seet, Siaw Ing Yeo, Man Hua Aw, Preeti Dhanasekaran, Rosa Mui-San Lim, Li Wearn Koh, Manjari Lahiri
doi : 10.1111/1756-185X.14590
To describe inflammatory arthritis (IA) patients initiating biologic disease-modifying anti-rheumatic drugs (bDMARDs) who use complementary and alternative medicine (CAM), and determine the impact of CAM on predicting modified Health Assessment Questionnaire (mHAQ) at 6Â months.
Özgül Öztürk, Özlem Feyzioğlu, Fatih Sarıtaş
doi : 10.1111/1756-185X.14591
Raida Ben Salah, Sonda Kammoun, Ansar Mefteh, Faten Frikha, Mona Rekik, Amira Trigui, Zouhir Bahloul
doi : 10.1111/1756-185X.14521
Relatively recently, the concept that immunoglobulin G4 (IgG4)-related disease is a distinct chronic inflammatory disorder rather than a subset of Sjögren's syndrome has been accepted.
Napisa Bunnag, Kitwiwat Phuangmali, Sira Vachatimanont
doi : 10.1111/1756-185X.14525
Microscopic polyangiits (MPA) is an autoimmune vasculitis that is challenging to diagnose because it can present with myriad of manifestations. We present a case of a woman who presented with prolonged fever.
Qi Zheng, Qian He, Hongxia Huang, Meiping Lu
doi : 10.1111/1756-185X.14529
To describe venous sinus thrombosis involved in immunoglobulin A (IgA) vasculitis and identify the clinical features and imaging findings of this rare disease.
Muserref Kasap Cuceoglu, Ozge Basaran, Ezgi Deniz Batu, Ummusen Kaya Akca, Erdal Atalay, Seher Sener, Zeynep Balik, Yagmur Bayindir, Emil Aliyev, Rahsan Gocmen, Sibel Kadayifcilar, Umut Akyol, Yelda Bilginer, Seza Ozen
doi : 10.1111/1756-185X.14531
Cogan's syndrome (CS) is a rare inflammatory disease characterized by interstitial keratitis or uveitis, vestibular impairment, and progressive hearing loss, commonly bilateral.
Kento Souma, Junya Fujimura, Atushi Nishiyama, Yoshinobu Oyazato, Shuya Kaneko, Masaki Shimizu, Takeshi Morisawa
doi : 10.1111/1756-185X.14534
Early diagnosis of systemic juvenile idiopathic arthritis (s-JIA) is a prerequisite for therapeutic efficacy. However, it is often challenging because most patients with s-JIA do not show arthritis at disease onset and are simply diagnosed with fever of unknown origin. Serum ferritin levels have commonly been used to diagnose s-JIA because they increase in patients with this condition by more than 5 times their normal value.
Heng Xu, Li Wang, Shufeng Wei, Chen Li, Kai Yuan
doi : 10.1111/1756-185X.14539
Calcinosis and lipodystrophy are severe complications of juvenile dermatomyositis (JDM). Up to 20% of patients have calcinosis, and the onset of calcinosis usually occurs 1 to 3 years after that of the illness.
Fatih Yildirim, Mustafa Erdogan, Melek Yalcin Mutlu, Gamze Akkuzu, Duygu Sevinç Ozgur, Bilgin Karaalioglu, Mesut Ayer, Cemal Bes
doi : 10.1111/1756-185X.14540
VEXAS (vacuoles, E1 enzyme, X-linked, autoinflammatory, somatic) syndrome is a newly defined disorder in which treatment is still unclear.
Yuchen Liu, Xia Wu, Yihan Cao, Shengyan Liu, Mingwei Ma, Chen Li
doi : 10.1111/1756-185X.14542
Synovitis, acne, pustulosis, hyperostosis and osteitis (SAPHO) syndrome is a rare autoinflammatory disease; its primary manifestation includes osteoarthropathy with skin involvement. Janus kinase (JAK) inhibitors, such as tofacitinib, were used for rheumatoid arthritis; however, due to its downregulation of immune cytokines including interleukin (IL)-6 and IL-8, it might be effective for SAPHO patients.
Bhaskar Thakur, Mona Pathak, Pratima Singh, Prasanta Padhan
doi : 10.1111/1756-185X.14535
Thomas Khoo, Simon Burnet
doi : 10.1111/1756-185X.14546
Mayu Fujiwara, Hiroyuki Wakiguchi, Fumiko Okazaki, Yuno Korenaga, Masashi Uchida, Ryota Sato, Masatoshi Omoto, Takashi Kanda, Shunji Hasegawa
doi : 10.1111/1756-185X.14519
Jonathan Kow, Gek Hsiang Lim, York Kiat Tan
doi : 10.1111/1756-185X.14526
Reem Alkilany, Douglas Einstadter, Maria Antonelli
doi : 10.1111/1756-185X.14527
Alexander Troelnikov, Xin Jing Choo, Dimitra Beroukas, Vidya Limaye
doi : 10.1111/1756-185X.14552
Murat BektaÅŸ, OÄŸuzhan TaÅŸ, Melike Ordu
doi : 10.1111/1756-185X.14541
Systemic lupus erythematosus (SLE) has the potential to affect virtually every organ; however, gastrointestinal system manifestations are relatively rare compared to other autoimmune diseases such as systemic sclerosis and inflammatory bowel disease.
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