Qianwen Gong1,2, Longqian Liu1,3, and Miroslaw Janowski2,4
1Department of Optometry and Visual Science, West China Hospital, Sichuan University, Chengdu, People's Republic of China, 2Department of Radiology and Radiological Science, Johns Hopkins University School of Medicine, Baltimore, MD, United States, 3Department of Ophthalmology, West China Hospital, Sichuan University, Chengdu, People's Republic of China, 4NeuroRepair Department, Mossakowski Medical Research Centre PAS, Warsaw, Poland
Synopsis
The cause of primary eye movement abnormality is unknown.
The functional MRI of superior and inferior oblique muscles was instrumental to
investigate the cause of overaction. We have shown similar size of superior
oblique muscle in patients and controls in the resting state, while the MRI
performed during gazes revealed differences in the contractility, what suggests
the abnormal innervation as a cause of primary superior oblique muscles. In
contrast, the inferior oblique muscle was larger in resting state, without a
difference in contractility what indicates the hypertrophy as a basis for
primary inferior oblique muscle overaction.
Purpose
Oblique muscle overaction is typically diagnosed based on
physical examination, and interferes with binocular vision and quality of life.
However, the clinical examination poorly distinguishes SO overaction from other
scenarios, such as heterotopic rectus extraocular muscles (EOM) pulleys, or
other orbital or structural EOM abnormalities (1). The current progress in magnetic
resonance imaging (MRI) permits addressing the functional anatomy of the eye,
which was exploited in the studies of SO palsy (2-3). We aim to quantitatively
determine the size and contractility of the superior oblique muscle and
inferior oblique muscle in primary superior oblique overaction
(PSOOA) and primary inferior oblique
muscle overaction (PIOOA), to
facilitate the differential diagnosis, thus open the way for more targeted
treatment.Methods
A prospective, observational study was
conducted on twelve patients with PSOOA, 7 cases with PIOOA, and 10 healthy,
orthotropic subjects. Sets of contiguous, 2 mm slice thickness, quasi-coronal and
sagittal magnetic resonance imaging (MRI) were
obtained during different gazes, giving pixel resolution of 0.391 mm. The
globe–optic nerve junction was localized as plane zero for SO measurement (Fig.
1). For IO, the scanning plane was parallel to the long axis of the orbit, and
plane zero was defined from the nasal side to the temporal side through the
midpoint of the inferior rectus. Cross sectional areas of the superior oblique
(SO) and inferior oblique (IO) muscles were determined in primary position,
supraduction and infraduction to evaluate size and contractility. The cross
sectional areas of SO and IO muscle were compared with those of controls in the
primary position to detect hypertrophy or atrophy and changes in contractility
could be detected during the vertical gaze.
All statistical calculations were performed using PROC MIXED (SAS 9.4).Results and Discussion
In
the primary position, the greatest SO cross-sections occurred about midorbit, 6
mm posterior to the globe-optic nerve junction. In down gaze, the SO
cross-sectional area increased, and the plane in which the maximum
cross-sectional area observed was more posterior. In up gaze, the SO
cross-sectional area decreased, and the plane in which the maximum
cross-sectional area observed was more anterior (Fig. 3). There was no
difference between the ipsilesional (affected eye), contralesional (unaffected
eye) and normal SO muscle cross-sections: 0.176 ± 0.018 cm2, 0.175 ±
0.005 cm2, and 0.173 ± 0.015 cm2, respectively (P=0.82). The maximum contractility of SO
muscle on the ipsilesional (affected) side was 0.097 ± 0.024 cm2,
and was different than on the contralesional (unaffected) side: 0.067 ± 0.015
cm2 and in control subjects: 0.063 ± 0.018 cm2 (P=0.0002)
(Figure 4).
For
PIOOA, compared IO of the patient group and control group of subjects,
ipsilesional IO maximum cross-sectional area (0.150
± 0.021 cm2) was greater than that of normal IO maximum
cross-sectional area (0.131 ± 0.016 cm2) (P=0.023) (Fig. 4).
However, ipsilesional IO maximum contractility (0.052 ± 0.013 cm2)
did not differ from that of normal subjects (0.0430 ± 0.011 cm2)
(P=0.080).
It
is reported that the cause of EOM overaction includes excessive innervation, an
increase in muscle’s cross-sectional area (hypertrophy), and changes in muscle
fiber types within the muscle (1, 4). It seems that muscle hypertrophy is the
likely reason for PIOOA, not for the PSOOA. On the contrary, a difference was
found in contractility between eyes with SO overaction and control eyes, which
may indicate abnormal innervation resulting in increased muscle stimulation. The
excess innervation may primarily act on the posterior half of SO, where the
contractile changes mainly occurred, which is in accordance with the anatomy of
SO (5). Later studies would be recommended to further illustrate oblique muscle
and other EOMs cross-section, contractility, and pulley locations to get a
better understanding of PSOOA and PIOOA, thus
helping choose more appropriate operation method.Conclusions
In PSOOA, the ipsilesional superior oblique is more
contractile than the contralesional SO muscle and different than in controls,
with no difference in SO muscle size in primary position, which suggests that
excessive innervation rather than muscle hypertrophy underlies PSOOA. In PIOOA,
IO cross-section area of the case group was greater than that of the normal
group, while there was no significantly difference in contractility between the
two groups, indicating that primary inferior oblique muscle overaction
associated with IO muscle hypertrophy.Acknowledgements
The study was supported by Department of Science and Technology of Sichuan Province, grant number 2012SZ0138.References
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