Sense of coherence in mothers and children, family relationships and participation in decision-making at home: an analysis based on Japanese parent-child pair data

Children in early adolescence and their mothers were studied to clarify the association between a child's sense of coherence (SOC) and its mother's SOC, the quality of family relationships as gauged by the mother, and the child's positive life experiences at home. An anonymous self-administered group questionnaire was given to all 1540 students of a high school in Tokyo, and a similar questionnaire was sent by mail to their legal guardians. Responses were received from 1505 students (response rate: 97.7%) and 989 legal guardians (response rate: 64.2%); questionnaires completed by legal guardians who were the mothers of the students were paired with the corresponding child's questionnaire. The SOC scores of mothers and students were calculated, and hierarchical multiple regression analysis was performed with the student's SOC as a dependent variable. Results for boys revealed that a mother's SOC was directly related to the child's SOC, regardless of family relationships and participation in decision-making at home. For girls, a mother's SOC was related to family relationships and was indirectly related to the child's SOC through the child's participation in decision-making at home. Results revealed that for both boys and girls, a mother's SOC had an effect on the child's SOC, and this corroborates the hypothesis of Antonovsky.     

Atrial fibrillation induced by post-parathyroidectomy transient thyrotoxicosis

We describe a 59-year-old Japanese woman with post-parathyroidectomy transient thyrotoxicosis and atrial fibrillation. She underwent parathyroidectomy for secondary hyperparathyroidism due to chronic renal failure. Three days after surgery, she complained of palpitation and chest pain due to atrial fibrillation. Results of thyroid function tests were compatible with thyrotoxicosis. Twelve days after parathyroidectomy, the elevated level of free thyroxine decreased spontaneously to the normal range. These features were compatible with post-parathyroidectomy transient thyrotoxicosis. No further recurrences of thyrotoxicosis or atrial fibrillation were observed for one year. This is the first report of atrial fibrillation induced by post-parathyroidectomy transient thyrotoxicosis.     

A 12-year, prospective study of extraocular muscle imaging in complex strabismus

INTRODUCTION: Diagnostic imaging by magnetic resonance imaging (MRI) or computed x-ray tomography (CT) has become the standard of care in many medical fields. Clinical imaging of the extraocular muscles (EOMs) can now provide insight into some causes of strabismus, in some cases challenging traditional concepts of etiology and suggesting alternative treatments. METHODS: Between 1990 and 2001, 62 orthotropic volunteers and 261 strabismic patients underwent orbital imaging under a prospective protocol. Surface coil MRI was performed with fixation control with slice thickness of 1.5 to 3 mm; CT was performed with 1-mm slice thickness. Images were correlated with ophthalmological examinations. RESULTS: MRI was performed in 267 and CT in 56 subjects. Comparison with normal orbits commonly demonstrated abnormalities of EOM size or location in strabismic patients. These included absence (5 patients) or atrophy (33 patients) of the superior oblique (SO) muscle in SO palsy; abnormalities of the trochlea or SO tendon in Brown's syndrome (8 patients); heterotopy of the rectus pulleys associated with incomitant strabismus (46 patients), including instability of pulleys (9 patients); trauma to rectus EOMs (16 patients); atrophy of the lateral rectus (10 patients), inferior rectus (4 patients), medial rectus (4 patients), superior rectus (4 patients), and inferior oblique (1 patient) muscles; and EOMs disinserted by scleral buckles (3 patients). EOM abnormalities correlated closely with clinically abnormal patterns of ocular motility. CONCLUSIONS: With the appropriate technique, EOM imaging is a valuable adjunct in clinical evaluation of complex strabismus. Because imaging can provide unique information unavailable from the clinical examination alone, it should be performed when indicated to evaluate patients with strabismus more complex than concomitant esotropia and exotropia.     

Reduced current density,partially rescued by mexiletine,and depolarizing shift in activation of SCN5A W374G channels as a cause of severe form of Brugada syndrome

Background

SCN5A-related Brugada syndrome (BrS) can be caused by multiple mechanisms including trafficking defects and altered channel gating properties. Most SCN5A mutations at pore region cause trafficking defects, and some of them can be rescued by mexiletine (MEX).

Objective

We recently encountered symptomatic siblings with BrS and sought to identify a responsible mutation and reveal its biophysical defects.

Methods

Target panel sequencing was performed. Wild-type (WT) or identified mutant SCN5A was transfected into tsA201 cells. After incubation of transfected cells with or without 0.1 mM MEX for 24–36 hr, whole-cell sodium currents (I_Na) were recorded using patch-clamp techniques.

Results

The proband was 29-year-old male who experienced cardiopulmonary arrest. Later, his 36-year-old sister, who had been suffering from recurrent episodes of syncope since 12 years, was diagnosed with BrS. An SCN5A W374G mutation, located at pore region of domain 1 (D1 pore), was identified in both. The peak density of W374G-I_Na was markedly reduced (WT: 521 ± 38 pA/pF, W374G: 60 ± 10 pA/pF, p < .01), and steady-state activation (SSA) was shifted to depolarizing potentials compared with WT-I_Na (V_1/2-WT: −39.1 ± 0.8 mV, W374G: −30.9 ± 1.1 mV, p < .01). Incubation of W374G-transfected cells with MEX (W374G-MEX) increased I_Na density, but it was still reduced compared with WT-I_Na (W374G-MEX: 174 ± 19 pA/pF, p < .01 versus W374G, p < .01 versus WT). The SSA of W374G-MEX-I_Na was comparable to W374G-I_Na (V_1/2-W374G-MEX: −31.6 ± 0.7 mV, P = NS).

Conclusions

Reduced current density, possibly due to a trafficking defect, and depolarizing shift in activation of SCN5A W374G are underlying biophysical defects in this severe form of BrS. Trafficking defects of SCN5A mutations at D1 pore may be commonly rescued by MEX.

     

Phosphorylated Smad2/3 immunoreactivity in sporadic and familial amyotrophic lateral sclerosis and its mouse model

Phosphorylated Smad2/3 (pSmad2/3), the central mediators of transforming growth factor (TGF)-beta signaling, were recently identified in tau-positive inclusions in certain neurodegenerative disorders. To clarify whether the localization of pSmad2/3 is altered in amyotrophic lateral sclerosis (ALS), we immunohistochemically examined spinal cords from sporadic ALS (SALS), from familial ALS (FALS) patients with the A4V mutation in their Cu/Zn superoxide dismutase (SOD1) gene, and from G93A mutant SOD1 transgenic (mSOD1 Tg) mice. In control spinal cords, pSmad2/3 immunoreactivity was observed exclusively in neuronal and glial nuclei. In SALS and FALS patients the nuclei showed increased immunoreactivity for pSmad2/3. Noticeably, round hyaline inclusions (RHIs) and skein-like inclusions of SALS patients were immunoreactive for pSmad2/3. Double immunofluorescence staining for pSmad2/3 and transactive response-DNA-binding protein (TDP)-43 revealed co-localization of these proteins within RHIs. In contrast, Bunina bodies in SALS and Lewy body-like hyaline inclusions (LBHIs) in FALS were devoid of labeling for pSmad2/3. Similarly, in the mSOD1 Tg mice pSmad2/3 immunoreactivity was increased in the nuclei, while LBHIs were not labeled. These findings suggest increased TGF-beta-Smad signaling in SALS, FALS, and mSOD1 Tg mice, as well as impaired TGF-beta signal transduction in RHI-bearing neurons of SALS patients, presumably at the step of pSmad2/3 translocation into the nucleus. The pathomechanisms, including the process of inclusion development, appears to be different between SALS and mSOD1-related FALS or Tg mice.