2.Incidence of upper respiratory tract infection and duration of weekly training among Japanese collegiate male and female athlete
Ayaka Sunami ; Kazuto Sasaki ; Osamu Ezaki ; Ayumi Nakai ; Jun Yasuda ; Yuri Yokoyama ; Takahiro Yoshizaki ; Yuki Tada ; Azumi Hida ; Yukari Kawano
Japanese Journal of Physical Fitness and Sports Medicine 2016;65(1):189-196
Strenuous exercise induces upper respiratory tract infection (URTI), whereas moderate exercise prevents URTI. This study aimed to assess the incidence of URTI and the association between URTI episodes and exercise duration in Japanese collegiate athletes. A cross-sectional survey was conducted with 1,740 participants; 1,235 responses were eligible for analysis. Participants were classified into three groups: control group (weekly total exercise duration <60 min, n=405), exercise group (weekly total exercise duration >60 min, n=193), and athlete group (joined a sports club and weekly exercise frequency >5 days, n=637). We requested the following information from participants: basic characteristics, incidence of URTI symptoms (fever, runny or plugged nose, sore throat, and cough) or influenza for each month over the past year, day of the week exercise is typically performed, and duration of exercise per week. The incidence of URTI episodes per year was significantly lower in the athlete group (2.0 ± 2.4 episodes) compared to the control group (2.6 ± 2.4 episodes, p<0.001). The incidence of URTI episodes did not significantly differ between the control group and exercise group (2.9 ± 2.9 episodes, p=0.607). Although the frequency of URTI episodes and exercise duration were not significantly associated among male athletes (p=0.209), they were positively associated in female athletes (p=0.027). These results indicate that Japanese collegiate athletes experience fewer URTI episodes than non-athletes, but athletes who exercise for long durations may frequently experience URTI, particularly female athletes.
3.A Systemic Lupus Erythematosus Patient with Cutaneous Mycobacterium haemophilum Infection under Belimumab Treatment: A Case Report
Jonghun KIM ; Toshio HASEGAWA ; Kurisu TADA ; Yuki UEHARA ; Yukiko FUKUI ; Ayako NAKAMURA ; Satomi TAKEI ; Satoshi MITARAI ; Akio AONO ; Shigaku IKEDA
Annals of Dermatology 2023;35(Suppl1):S63-S66
A 38-year-old female with systemic lupus erythematosus (SLE) initiated belimumab treatment. One month later, she presented with a reddish painful swelling on her right lower leg.She was treated with ceftriaxone and vancomycin. However, novel erythematous papules and indurated nodules appeared on both her lower legs. Skin biopsy revealed microabscess formation with mixed cell granuloma surrounded by inflammatory cell infiltration within the dermis with subcutaneous fat tissue. A large number of acid-fast bacilli were observed with Ziehl–Neelsen staining. DNA sequencing of both the hsp65 and the 16S rRNA sequences showed a 100% match with the corresponding region of Mycobacterium haemophilum. Mycobacterial culture revealed satellite growth enhancement on Middlebrook 7H11 agar plates around a paper strip containing hemin. She was treated with levofloxacin, rifabutin, and ethambutol. Within 13 months, her cutaneous lesions improved markedly without any side effects. The B cell-targeted biologic belimumab, a fully humanized IgG1γ monoclonal antibody that inactivates B lymphocyte stimulator, has been considered to be beneficial for active SLE. However, this therapy could increase the risk for the development of biologic therapy-associated mycobacterial infections, both tuberculosis and nontuberculous mycobacteria infections.
4.Two cases of bilateral reverse shoulder arthroplasty performed in patients with rheumatoid arthritis
Takuya TADA ; Yuki KOBAYASHI ; Misaki WATANABE ; Akito NISHIMURA ; Kenji TAKAGISHI
Journal of Rural Medicine 2023;18(3):194-199
Bilateral shoulder joint disorders caused by rheumatoid arthritis significantly impair daily functioning owing to a lack of contralateral compensation. In Japan, reverse shoulder joint prostheses were approved in 2014. This was expected to improve the surgical outcomes of rheumatoid shoulder arthroplasty. We report two patients with rheumatoid arthritis who underwent bilateral reverse shoulder arthroplasty. This study aims to evaluate their postoperative clinical outcomes and activities of daily living. The patients were women in their 70s with stage III class 2 rheumatoid arthritis. Their treatment and postoperative activities of daily living were retrospectively reviewed. The first patient underwent the inlay type and experienced a residual limitation of external rotation postoperatively; therefore, she was restricted to dress with front-open clothes. However, she was able to undress after the lining of the garment was changed to a slippery material. The second patient underwent the onlay type and showed almost no limitations in postoperative activities of daily living. She was able to undress with an external rotation of 40–50°. Bilateral reverse shoulder arthroplasty improved range of motion, the Japanese Orthopaedic Association shoulder score, and functional outcomes. Only a few difficulties were encountered in the activities of daily living.
5.Phenotypic diversity of hereditary sensory and autonomic neuropathy type IE: a case series and review of the literature
Noriyuki Miyaue ; Yuki Yamanishi ; Satoshi Tada ; Rina Ando ; Hayato Yabe ; Noriko Nishikawa ; Masahiro Nagai ; Hiroshi Takashima ; Masahiro Nomoto
Neurology Asia 2019;24(1):15-20
Objective: DNA methyltransferase 1 (DNMT1) is crucial to maintaining methylation during DNA
replication and DNA repair. DNMT1 mutations have been identified in two neurological syndromes,
including hereditary sensory and autonomic neuropathy type IE (HSAN IE) with dementia and
hearing loss and autosomal dominant cerebellar ataxia, deafness and narcolepsy. It is likely that
DNMT1 mutations lead to various symptoms of the central and peripheral nervous system. The aim
of this study was to examine the clinical characteristics, especially the initial symptoms, in the cases
of DNMT1 mutations. Methods: We investigated the clinical manifestation and examination findings
of four cases of HSAN IE from one family with the DNMT1 mutation c.1531Y>C (p.Try511His).
Results: All four cases exhibited sensory neuropathy, cerebellar ataxia, and hearing loss, all of which
were demonstrated by the audiograms. The initial symptoms of the four cases included hearing loss
(n=1), gait disturbance (n=1), and depressive mood (n=2). Depressive symptoms are reported in some
cases with HSAN IE, however, there are currently no published reports that describe them as primary
symptoms. The CSF orexin level was measured in three cases, revealing normal values in two cases
and intermediate values in one case, in which the patient exhibited rapid eye movement (REM) sleep
behavior disorder.
Conclusion: Our findings suggest that in cases with HSAN IE or the DNMT1 mutation, psychiatric
symptoms should be taken into account as one of the initial manifestations of the disease.