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A shallow chest correlates with the aortic position in the normal spine: features resembling those observed in structural scoliosis
© Doi et al.; licensee BioMed Central Ltd. 2014
- Received: 3 April 2014
- Accepted: 28 August 2014
- Published: 30 August 2014
Right thoracic curvature, rib cage deformities and aortic left shift are features of adolescent idiopathic scoliosis that are correlated with each other. We recently reported that disturbance of ribcage development results in progressive thoracic scoliosis in mice. Recently, it has been confirmed that the normal spine exhibits right thoracic curvature and rib cage deformities and that these deformities worsen during the adolescent period. The purpose of this study was to examine whether rib cage deformities correlate with thoracic side curvature in the normal spine, as observed in scoliosis, which is important basic knowledge needed to elucidate the causative factors of adolescent idiopathic scoliosis.
To examine the relationship between rib cage deformities and thoracic side curvature in the normal spine, CT scans of 148 consecutive adult females were examined. The anteroposterior chest dimension, aortic location and rib cage rotation were measured on CT scans obtained at the T8 level. The thoracic side curvature (T5-T12) was also measured on chest radiographs.
The anteroposterior chest dimension exhibited a significant correlation with aortic left shift. The aortic location and rib cage rotation were correlated, and the rib cage rotation and thoracic side curvature were correlated.
There was a significant correlation between a shallow chest and the aortic position, between the aortic position and the rib cage rotation and between the rib cage rotation and the thoracic side curvature in the normal spine. These findings suggest the possibility that rib cage development is one of the causative factors of adolescent idiopathic scoliosis.
- Rib cage deformity
- Shallow chest
Adolescent Idiopathic Scoliosis (AIS), which dramatically worsens in the adolescent period, is characterized by the features of right thoracic scoliosis, a shallow chest and aortic left shift[1–6]. The causal relationship between scoliosis and chest deformities is unknown.
Cole AA et al. reported that the anteroposterior chest dimension in thoracic scoliosis patients is significantly smaller than that observed in normal subjects[5, 6]. It is known that a correlation exists between the anteroposterior chest dimension, aortic location and the severity of thoracic curvature in AIS. We previously reported that a disturbance of ribcage development leads to progressive structural scoliosis in a mouse model and demonstrated that the pathomechanisms of rib cage deformities and the associated imbalanced load on the vertebral body result in structural scoliosis. The mice model also demonstrated that the position of the heart is a significant factor influencing the direction of thoracic curvature.
Recently, it has been confirmed that the normal spine exhibits right thoracic curvature[9, 10], vertebral rotation and rib cage deformities and that these deformities worsen during the adolescent period. It remains unknown whether rib cage deformities and thoracic side curvature coexist and/or are correlated with each other. If a shallow chest and the position of the heart and aorta are factors that influence the thoracic side curvature, then these correlations can be observed in the normal spine.
To examine the relationships between rib cage deformities, the aortic position and thoracic side curvature in the normal spine, CT scans of 148 consecutive females 20 to 29 years of age were examined.
The background diseases in the patients
Type of disease
N = 148
The thoracic side curvature in the normal spine was measured according to Cobb’s method, as previously described. Standing chest PA radiographs were obtained. One line was drawn along the superior end plate of T5 and one line was drawn along the lower end plate of T12 on a computer screen using the Fuji Synapse angle measurement system (Fuji Synapse System, Fujifilm holdings, Tokyo, Japan). If the end plate was indistinct, the line was drawn through the pedicles. A right convex curve was assigned a positive value and a left curve was assigned a negative value. Among the 148 patients, 117 patients had right convex curves (> +1 degree), 13 patients had neutral convex curves (from -1 degree to +1 degree), and 18 patients had left convex curves (< -1 degree). We could not find anything unusual about the shallow chest or aortic position in the patients with left curves compared with the patients having either right or neutral curves.
The GraphPad Prism statistical software program (GraphPad Software, CA, USA) was used for the statistical analyses. The statistical methods included Spearman’s rank correlation coefficients. P-values of less than 0.05 were considered to be statistically significant.
Right thoracic curvature, rib cage rotation and thoracic vertebral right rotation have been reported to become dominant after adolescence in the normal spine[9, 12]. The prominence of the right scapula in the normal spine is reported to correspond to right thoracic rotation. In the present study, the significant correlation between a shallow chest and the aortic position were confirmed. These deformities are similar to those observed in patients with AIS.
The presence of a relationship between organ anatomy and thoracic deformities, such as vertebral rotation and thoracic side curvature, is suggested by observations in humans with situs inversus totalis[10, 14]. In patients with situs inversus, thoracic vertebral rotation and thoracic curvature occur in reverse directions. There is a hypothesis that the position of the heart and aorta may be the cause of scoliosis[15–17]. The present findings of a relationship between the aortic position in a shallow chest and right thoracic curvature in the normal spine support the interpretation that a shallow chest and aortic left shift are associated with the initiation process of small thoracic curvatures and possibly also of right thoracic AIS.
Cole AA et al. reported that a decreased AP chest diameter may be a risk factor for the development of AIS by altering the spinal mechanics during movement[5, 6]. We recently reported that disturbance of ribcage development results in progressive thoracic scoliosis in mice. The mouse model also demonstrated that the position of the heart is a significant factor that influences the direction of thoracic curvature, thus indicating that the imbalanced load to the vertebral body is derived from an indirect mechanical effect travelling through the ribs on both sides owing to the asymmetry of the position of the heart in the limited thoracic cavity.
We examined a series of CT scans of patients who visited our institution for investigating other diseases (Table 1). To eliminate the effects of each disease, it is ideal to study healthy volunteers; however, this is difficult due to the risk of irradiation. Furthermore, one of the limitations of this study may be associated with the fact that these findings represent a snapshot in time in mature subjects with minimal curves. In order to evaluate the potential development of AIS, it is ideal to obtain cross-sectional data using thoracic CT scans in healthy juvenile volunteers and follow the time course of the deformities. Such studies are also difficult to performed due to ethical issues.
Kouwenhoven JW et al. previously reported that there are 2.365 degrees of T8 vertebral right rotation in the normal spine. We described the aorta as having a left shift in this study. There may be an argument that the aortic left shift is an only the comparative position because of the right shift of the vertebra. Our measurements using the rib head as a baseline measured the left-posterior direction, and the aortic position ranged from -3.0 mm to 31.8 mm relative to the rib head, and those values are considered to be larger than the right shift of the vertebrae in the normal spine. Furthermore, in a previous study regarding preoperative non-congenital spines, shallow chest significantly correlated with an aortic leftward shift (reference 7, Figure 5). We therefore believe that the influence of the right vertebral rotation was relatively minor, if any at all, and the main cause of the aortic position is thus believed to be the aortic left shift.
There was a significant correlation between a shallow chest and the aortic position, between the aortic position and the rib cage rotation and between the rib cage rotation and the thoracic side curvature in the normal spine. The findings support the interpretation that a shallow chest and aortic left shift are associated with the initiation process of small thoracic curvatures and possibly also of right thoracic AIS. These factors may not be causal for right thoracic AIS.
This work was supported by MEXT KAKEN Grant Number 25462296.
- Sevastik B, Xiong B, Hedlund R, Sevastik J: The position of the aorta in relation to the vertebra in patients with idiopathic thoracic scoliosis. Surg Radiol Anat. 1996, 18 (1): 51-56. 10.1007/BF03207763.View ArticlePubMedGoogle Scholar
- Erkula G, Sponseller PD, Kiter AE: Rib deformity in scoliosis. Eur Spine J. 2003, 12 (3): 281-287.PubMedPubMed CentralGoogle Scholar
- Sucato DJ, Duchene C: The position of the aorta relative to the spine: a comparison of patients with and without idiopathic scoliosis. J Bone Joint Surg Am. 2003, 85-A (8): 1461-1469.PubMedGoogle Scholar
- Qiu Y, He YX, Wang B, Zhu F, Wang WJ: The anatomical relationship between the aorta and the thoracic vertebral bodies and its importance in the placement of the screw in thoracoscopic correction of scoliosis. Eur Spine J. 2007, 16 (9): 1367-1372. 10.1007/s00586-007-0338-6.View ArticlePubMedPubMed CentralGoogle Scholar
- Cole AA, Burwell RG, Dangerfield PH, Grivas TB, Webb JK, Moulton A: Anthropometry. Spine: state of the art reviews. 2000, 14: 411-421.Google Scholar
- Cole AA, Burwell RG, Kirby AS, Polak FJ, Webb JK: Anthropometry and Allometry in Pre-Poerative Adolescent Idiopathic Scoliosis (AIS). Research into Spinal Deformities 1. 1997, Amsterdam: Ios Press, 98-92.Google Scholar
- Doi T, Harimaya K, Matsumoto Y, Iwamoto Y: Aortic location and flat chest in scoliosis: a prospective study. Fukuoka Igaku Zasshi. 2011, 102 (1): 14-19.PubMedGoogle Scholar
- Kubota K, Doi T, Murata M, Kobayakawa K, Matsumoto Y, Harimaya K, Shiba K, Hashizume M, Iwamoto Y, Okada S: Disturbance of rib cage development causes progressive thoracic scoliosis: the creation of a nonsurgical structural scoliosis model in mice. J Bone Joint Surg Am. 2013, 95 (18): e130-View ArticlePubMedGoogle Scholar
- Doi T, Harimaya K, Mitsuyasu H, Matsumoto Y, Masuda K, Kobayakawa K, Iwamoto Y: Right thoracic curvature in the normal spine. J Orthop Surg Res. 2011, 6: 4-10.1186/1749-799X-6-4.View ArticlePubMedPubMed CentralGoogle Scholar
- Tallroth K, Lohman M, Heliovaara M, Aromaa A, Knekt P, Standertskjold-Nordenstam CG: Dextrocardia and coronal alignment of thoracic curve: a population study. Eur Spine J. 2009, 18 (12): 1941-1945. 10.1007/s00586-009-1049-y.View ArticlePubMedPubMed CentralGoogle Scholar
- Kouwenhoven JW, Vincken KL, Bartels LW, Castelein RM: Analysis of preexistent vertebral rotation in the normal spine. Spine. 2006, 31 (13): 1467-1472. 10.1097/01.brs.0000219938.14686.b3.View ArticlePubMedGoogle Scholar
- Grivas TB, Vasiliadis ES, Koufopoulos G, Segos D, Triantafyllopoulos G, Mouzakis V: Study of trunk asymmetry in normal children and adolescents. Scoliosis. 2006, 1: 19-10.1186/1748-7161-1-19.View ArticlePubMedPubMed CentralGoogle Scholar
- Cobb JR: Outline for the Study of Scoliosis. American Academy of Orthopaedic Surgeons. Instructional Course Lectures. 1948, St Lous: CV Mosby, 261-275.Google Scholar
- Kouwenhoven JW, Bartels LW, Vincken KL, Viergever MA, Verbout AJ, Delhaas T, Castelein RM: The relation between organ anatomy and pre-existent vertebral rotation in the normal spine: magnetic resonance imaging study in humans with situs inversus totalis. Spine. 2007, 32 (10): 1123-1128. 10.1097/01.brs.0000261563.75469.b0.View ArticlePubMedGoogle Scholar
- Luke MJ, McDonnell EJ: Congenital heart disease and scoliosis. J Pediatr. 1968, 73 (5): 725-733. 10.1016/S0022-3476(68)80178-7.View ArticlePubMedGoogle Scholar
- Niebauer JJ, Wright WD: Congenital heart disease and scoliosis. J Bone Joint Surg Am. 1956, 38-A (5): 1131-1136.PubMedGoogle Scholar
- Taylor JR: Vascular causes of vertebral asymmetry and the laterality of scoliosis. Med J Aust. 1986, 144 (10): 533-535.PubMedGoogle Scholar
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