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REVIEW ARTICLE Table of Contents   
Year : 2010  |  Volume : 44  |  Issue : 1  |  Page : 9-13
The natural history of adolescent idiopathic scoliosis


University Spine Center, University Orthopedics, Hand and Reconstructive Microsurgery Cluster, National University Health System, Singapore

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Date of Web Publication31-Dec-2009
 

   Abstract 

There have been great advances in the conservative and surgical treatment for adolescent idiopathic scoliosis in the last few decades. The challenge for the physician is the decision for the optimal time to institute therapy for the individual child. This makes an understanding of the natural history and risk factors for curve progression of significant importance. Reported rates of curve progression vary from 1.6% for skeletally mature children with a small curve magnitude to 68% for skeletally immature children with larger curve magnitudes. Although the patient's age at presentation, the Risser sign, the patient's menarchal status and the magnitude of the curve have been described as risk factors for curve progression, there is evidence that the absolute curve magnitude at presentation may be most predictive of progression in the long term. A curve magnitude of 25º at presentation may be predictive of a greater risk of curve progression. Advances in research may unlock novel predictive factors, which are based on the underlying pathogenesis of this disorder.

Keywords: Adolescent idiopathic scoliosis, curve progression, natural history

How to cite this article:
Wong HK, Tan KJ. The natural history of adolescent idiopathic scoliosis. Indian J Orthop 2010;44:9-13

How to cite this URL:
Wong HK, Tan KJ. The natural history of adolescent idiopathic scoliosis. Indian J Orthop [serial online] 2010 [cited 2014 Dec 20];44:9-13. Available from: http://www.ijoonline.com/text.asp?2010/44/1/9/58601

   Introduction Top


Adolescent idiopathic scoliosis (AIS) is defined by the Scoliosis Research Society as scoliosis whose onset occurs after ten years of age and whose cause is essentially unknown. It is a relatively common condition among adolescents.

AIS has been described as having a prevalence of about 0.35 to 13%, depending on the defined Cobb's angles, screening age and sex. [1],[2],[3] Stirling et al., in a school screening study, reported prevalence rates of 0.4 and 2.2% in English girls of 9 to 11 years of age and 12 to 14 years of age, respectively. The boys had prevalence rates of 0.1 and 0.3% in the two age groups. [4]

Soucacos et al. reported on the results of screening of 82,900 Greek schoolchildren of 9 to 14 years old during a 1-year prospective study. He reported a prevalence of 1.7% in his study. In total, 2.6% of the girls and 0.9% of the boys had radiographic evidence of a Cobb's angle of 10 or more. He also described the prevalence to vary according to age. A total of 0.07% of the children had scoliosis by the age of 9, 0.2% by age 10 and 0.4% at age 14. [5]

Wong et al., reporting on the prevalence of idiopathic scoliosis in Singaporean school children, found that 0.04% of the children had scoliosis by the age of 7, 0.19% by the age of 10 and 1.44% by the age of 14, while the overall predicted prevalence rate for children 9 to 14 years of age (comprising 9- to 10-, 11- to 12-, 13- to 14-year-old groups) was 0.78% (1.23% in girls and 0.33% in boys). [6]


   Long-term Complications of Untreated Scoliosis Top


If left undetected and untreated, AIS can lead to many potential complications. Nachemson, [7] Nilsonne and Lundgren, [8] Pehrsson et al. [9] and Fowles et al. [10] described a poor prognosis for untreated scoliosis with increased mortality rates related to cor pulmonale and back pain, increased disability and socioeconomic effects on work and marital status. In Nachemson's study, he reported on the outcome of a 38-year follow-up of 130 patients with untreated scoliosis. About 38% were disabled due to their deformity and the mortality rate was 100% above that of the normal population. About 37% had constant backache and 14% complained of cardiopulmonary symptoms. Nilsonne and Lundgren, reporting on a 50-year follow-up of 113 patients, also reported a mortality rate twice that of the general population. Of the remaining patients, half were unable to work, 90% had back pain and 30% were on disability pensions for back pain or scoliosis. However, it should be noted that these studies included patients with other causes of scoliosis, and a significant number of cases of idiopathic scoliosis were of infantile and juvenile types. Therefore, the conclusions may not completely apply to children with AIS who may have a more benign long-term natural history.

Hence, the natural history of AIS in the long-term would be better analyzed in studies that only include patients who have AIS. Weinstein and Ponseti reported on the long-term outcome of a group of 194 patients with untreated AIS. The patients were an average of 53 years of age and out of the 194, all but 4 were normally active. About 21% had mild psychological reactions to their deformity, such as unwillingness to wear tight fitting clothing or a bathing suit. Backache was described as being somewhat more common compared to a matched group of 100 patients but was not disabling. They did not find an increased mortality rate compared to a match group and cor pulmonale was implicated as a cause of death only in one patient. [11]


   School-based Screening Top


There have been significant improvements in both the conservative as well as operative treatment of AIS in the last few decades. However, it has become apparent that despite these advances, the success of treatment still depends on early detection of this condition. Both conservative treatments as well as spinal instrumentation have the best results before the curve has progressed to a large magnitude.

This has been an important reason behind the institution of screening programs in many countries that allow for the early detection of curves of smaller magnitude. [1],[2],[3],[6] However, this presents the treating physician with the challenge of predicting the risk of curve progression and deciding on appropriate management as well as follow-up intervals and duration for this group of patients.


   Curve Progression During Skeletal Growth Top


The decision on the optimal time to institute bracing or surgical treatment as well as when observation of the curve alone is sufficient can only be confidently made with an understanding of the natural history of adolescent idiopathic scoliosis. However, accurate prediction of curve progression is still not available. Reported rates of curve progression have varied considerably [Table 1]. There is also no agreement on the associated risk factors. Some of the factors quoted by previous studies include magnitude of the curve, the patient's age at presentation, the Risser sign and the patient's menarchal status.

This is compounded by the issue of differences in the criteria for progression, the institution of treatment during follow-up and the length of follow-up. As a result, it is not clear to what extent these factors may be used to accurately predict the natural history of AIS. To date, there has been no agreement and definitive guidelines have yet to be established in the prediction of curve progression and when to institute treatment for each child.

Indeed, it has been reported that a significant number of idiopathic curves may actually improve during the follow-up period. Brooks et al., who studied 474 children with AIS defined at a Cobb's angle of 5 or more, reported that spontaneous improvement was observed in approximately 22% of those on follow-up for an average of one year. In the same study, he reported only a 5% incidence of progression of an average of 7. There was also no difference in the age, gender or curve location between those that improved or progressed. [12]

Soucacos et al. reported a 14.7% incidence of curve progression defined as an increase in Cobb's angle of 5 or more. The authors also reported that an unexpected 9.5% of children in his study showed complete spontaneous resolution of the scoliotic curve, while over 35% of the patients with a left thoracic or left and right thoracolumbar curves showed a spontaneous decrease in the magnitude of their curve of at least 10. In this study, the authors found that the factors that were most associated with the natural history of the scoliotic curve were gender, curve pattern and maturity. They found that girls showed a higher incidence of progression overall and that the difference was even more pronounced in curves that progressed between 5 and 10. In addition, curves that developed before menarche were found to have almost twice as great a risk for progression. [5]

In cases detected through school screening, Rougala et al. followed 603 children for at least 2 years and reported a 6.8% progression of 5 or more. In addition, 15.4% of the skeletally immature girls with initial curves of 10 or more progressed but he also observed that there was no progression in 20% of the skeletally immature curves with an initial magnitude of 20 or more. [2]

Lonstein and Carlson retrospectively reviewed the progression of 727 children with idiopathic scoliosis defined by a single radiograph showing scoliosis of 29 or less. Due to the varying definitions of curve progression in previous studies which varied from 5 to 10, Lonstein and Carlson instead defined curve progression in their study as an initial curve of 19 or less that increased at least 10 with the final magnitude being greater than 20 and an initial curve of between 25 and 29 that increased by 5 or more. They reported a curve progression rate of 23.2% and found that curve magnitude, skeletal immaturity and curve pattern were associated with progression. [13]

The various factors associated with progression have also been combined for more useful model for prediction of curve progression. Lonstein and Carlson used a combination of curve magnitude and the Risser sign to calculate the probability of curve progression. They found that for children with a Risser grade of 0-1, those with a curve magnitude of 5-19 had a 22% progression rate compared to a 68% progression rate for those with a curve magnitude of 20-29. Similarly, for children with a Risser grade of 2-4, those with a curve magnitude of 20-29 had a progression rate of 23%, while those with a curve magnitude of 5--19 had only a 1.6% progression rate [13] [Table 2]. Nachemson and Peterson used a combination of age and curve magnitude. They observed that in children of 16 years of age with an initial curve magnitude of less than 19, none of the curves progressed. However, in children aged 10-12 years with a curve magnitude of 60 there was a 100% progression rate. [14] [Table 3].


   Genetic Profiling as a Means to Predict Curve Progression Top


There is an increasing evidence that genetic factors have a part to play in the development in idiopathic scoliosis. [15] Together with new studies that have investigated the role of hormonal factors such as melatonin and estrogens, there has been interest in studying the genetic polymorphisms of these hormones in an attempt to predict curve development and progression. [16],[17],[18] However, there is still no clear genetic marker that can be reliably used to predict progression of the curve. Qiu et al. performed genetic association studies to investigate variation of the melatonin receptor 1A (MTNR1A) and 1B genes in girls with adolescent idiopathic scoliosis (AIS) patients compared to normal controls. He found an association with the 1B gene but not the 1A gene polymorphism. [16],[17] Inoue et al. analyzed the estrogen receptor gene in 304 girls with idiopathic scoliosis whom he followed up till skeletal maturity. He found that the Xbal site polymorphism was associated with curve progression defined as an increase of more than 5 from initial evaluation. [18]

More recently, there has been progress in using a combination of multiple genes associated with the development of severe curves to predict curve progression. Ogilvie has developed a saliva-based test for a combination of multiple genetic markers that have been linked with curve progression in clinical trials as a prognostic test for AIS. This allows for the calculation of a quantitative score that correlates with a low, medium or high risk of curve progression. [19]


   Curve Progression After Skeletal Maturity Top


Once the child has attained skeletal maturity, it was generally thought that the curves are less likely to progress. However, this may not always be the case. It is now established that curves due to idiopathic scoliosis do not necessarily stop progressing after skeletal maturity. In a long-term follow-up study of patients with idiopathic scoliosis, Collis and Ponseti found that curves of a larger degree did increase after skeletal maturity. [20] In a separate study with an average follow-up of 40 years, Weinstein and Ponseti also found that a significant number of idiopathic curves increased after skeletal maturity. They reported that in thoracic curves, the Cobb's angle, apical vertebral rotation and the Mehta angle were important prognostic factors. For lumbar curves, the degree of apical vertebral rotation, the Cobb's angle, the direction of the curve and the relationship of the fifth lumbar vertebra to the inter-crest line were of prognostic value. However, they also observed that curves that were less than 30 at skeletal maturity tended not to progress regardless of curve pattern. [21]

Given the varying definitions of curve progression, this suggests that curves with a Cobb's angle of 30 are an important threshold magnitude and may serve as an endpoint for prediction of curve progression rather than predefined units of curve progression quoted in previous studies. In addition, it must be appreciated that the various associated factors and predictions described only apply to the likelihood of a curve progressing in adolescence. They are only averages and correlations and do not allow us to answer the key issue of how much the curve of an individual child is going to progress.

In a recent study, Tan and Wong reported on a group of 279 patients with idiopathic scoliosis detected by school screening, and who were followed-up until skeletal maturity using a 30 Cobb's angle at skeletal maturity as a threshold instead of predefined units of curve progression during shorter periods of growth. They found that an initial Cobb's angle of 25 was the most predictive factor for curve progression to this threshold magnitude. Initial age, gender and pubertal status were less important prognostic factors. [22] When different factors were combined, it was also possible to generate different risk progression profiles [Table 4].


   Conclusion and Future Perspective Top


Adolescent idiopathic scoliosis is a relatively common condition that if left untreated can lead to significant morbidity and possibly mortality. Early detection of curves has been facilitated by school-based screening but has resulted in a need for the understanding of the natural history and reliable prediction of curve progression to decide on the appropriate treatment and timing of intervention. Individual factors such as the patient's age at presentation, the Risser sign, the patient's menarchal status and the magnitude of the curve have been used as predictive factors as well as using a combination of factors to predict curve progression. However, the relative importance of each factor and how they may interact is as yet not defined. Based on current evidence, we recommend closer follow-up of skeletally immature children with a curve magnitude of 25 or more at presentation and also continuing to follow-up children with a curve magnitude of 30 or more even after skeletal maturity. Moving forward, the ideal prognostication model needs to be one that allows for prediction of the amount of progression that is likely to be observed over the whole period of remaining growth and should be individualized to the child. This may only be attained by the introduction of novel predictive factors rather than factors that are surrogate markers of potential remaining skeletal growth that have been used in the literature thus far. This may only be realized by unlocking the underlying pathogenesis of AIS.

 
   References Top

1.Lonstein JE, Bjorklund S, Wanninger MH, Nelson RP. Voluntary school screening for scoliosis in Minnesota. J Bone Joint Surg Am 1982;64:481-8.  Back to cited text no. 1  [PUBMED]  [FULLTEXT]  
2.Rogala EJ, Drummond DS, Gurr J. Scoliosis incidence and natural history: a prospective epidemiological study. J Bone Joint Surg Am 1978;60:173-6.  Back to cited text no. 2  [PUBMED]  [FULLTEXT]  
3.Brooks HL, Azen SP, Gerberg E, Brooks R, Chan L. Scoliosis: A prospective epidemiological study. J Bone Joint Surg Am 1975;57:968-72.  Back to cited text no. 3  [PUBMED]  [FULLTEXT]  
4.Stirling AJ, Howel D, Millner PA, Sadiq S, Sharples D, Dickson RA. Late-onset idiopathic scoliosis in children six to fourteen years old: A cross-sectional prevalence study. J Bone Joint Surg Am 1996;78:1330-6.  Back to cited text no. 4  [PUBMED]  [FULLTEXT]  
5.Soucacos PN, Zacharis K, Gelalis J, Soultanis K, Kalos N, Beris A, et al. Assessment of curve progression in idiopathic scoliosis. Eur Spine J 1998;7:270-77.  Back to cited text no. 5  [PUBMED]  [FULLTEXT]  
6.Wong HK, Hui JH, Rajan U, Chia HP. Idiopathic scoliosis in Singapore schoolchildren: A prevalence study 15 years into the screening program. Spine 2005;30:1188-96.  Back to cited text no. 6  [PUBMED]  [FULLTEXT]  
7.Nachemson A. Adult scoliosis and back pain. Spine 1979;4:513-7.  Back to cited text no. 7  [PUBMED]  [FULLTEXT]  
8.Nilsonne U, Lundgren KD. Long-term prognosis in idiopathic scoliosis. Acta Orthop Scand 1968;39:456-65.  Back to cited text no. 8  [PUBMED]  [FULLTEXT]  
9.Pehrsson K, Larsson S, Oden A, Nachemson A. Long-term followup of patients with untreated scoliosis: A study of mortality, causes of death, and symptoms. Spine 1992;17:1091-6.  Back to cited text no. 9  [PUBMED]  [FULLTEXT]  
10.Fowles JV, Drummond DS, L′Ecuyer S, Roy L, Kassab MT. Untreated scoliosis in the adult. Clin Orthop Relat Res 1978;134:212-7.  Back to cited text no. 10  [PUBMED]  [FULLTEXT]  
11.Weinstein SL, Zavala DC, Ponseti IV. Idiopathic scoliosis: Long-term follow- up and prognosis in untreated patients. J Bone Joint Surg Am 1981;63:702-12.  Back to cited text no. 11  [PUBMED]  [FULLTEXT]  
12.Brooks HL, Azen SP, Gerberg E, Brooks R, Chan L. Scoliosis: A prospective epidemiological study. J Bone Joint Surg Am 1975;57:968-72.  Back to cited text no. 12  [PUBMED]  [FULLTEXT]  
13.Lonstein JE, Carlson JM. The prediction of curve progression in untreated idiopathic scoliosis during growth. J Bone Joint Surg Am 1984;66:1061-71.  Back to cited text no. 13  [PUBMED]  [FULLTEXT]  
14.Nachemson AL, Peterson LE. Effectiveness of treatment with a brace in girls who have adolescent idiopathic scoliosis: A prospective, controlled study based on data from the Brace Study of the Scoliosis Research Society. J Bone Joint Surg Am 1995;77:815-22.  Back to cited text no. 14  [PUBMED]  [FULLTEXT]  
15.Lowe TG, Edgar M, Margulies JY, Miller NH, Raso VJ, Reinker KA, et al. Etiology of idiopathic scoliosis: current trends in research. J Bone Joint Surg Am 2000;82-A:1157-68.  Back to cited text no. 15  [PUBMED]  [FULLTEXT]  
16.Qiu XS, Tang NL, Yeung HY, Lee KM, Hung VW, Ng BK, et al. Melatonin receptor 1B (MTNR1B) gene polymorphism is associated with the occurrence of adolescent idiopathic scoliosis. Spine 2007;32:1748-53.  Back to cited text no. 16  [PUBMED]  [FULLTEXT]  
17.Qiu XS, Tang NL, Yeung HY, Cheng JC, Qiu Y. Lack of association between the promoter polymorphism of the MTNR1A gene and adolescent idiopathic scoliosis. Spine 2008;33:2204-7.  Back to cited text no. 17  [PUBMED]  [FULLTEXT]  
18.Inoue M, Minami S, Nakata Y, Kitahara H, Otsuka Y, Isobe K, et al. Association between estrogen receptor gene polymorphisms and curve severity of idiopathic scoliosis. Spine 2002;27:2357-62.  Back to cited text no. 18  [PUBMED]  [FULLTEXT]  
19.Ogilvie. Axial Biotech [Internet]. Available from http://www.axialbiotech.com/ .  Back to cited text no. 19      
20.Collis DK, Ponseti IV. Long-term follow-up of patients with idiopathic scoliosis not treated surgically. J Bone Joint Surg Am 1969;51:425-45.  Back to cited text no. 20  [PUBMED]  [FULLTEXT]  
21.Weinstein SL, Ponseti IV. Curve progression in idiopathic scoliosis. J Bone Joint Surg Am 1983;65:447-55.  Back to cited text no. 21  [PUBMED]  [FULLTEXT]  
22.Tan KJ, Moe MM, Vaithinathan R, Wong HK. Curve progression in idiopathic scoliosis: Follow-up study to skeletal maturity. Spine 2009;34:697-700.  Back to cited text no. 22  [PUBMED]  [FULLTEXT]  

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Correspondence Address:
Hee-Kit Wong
National University Hospital, 5, Lower Kent Ridge Road 119 074
Singapore
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DOI: 10.4103/0019-5413.58601

PMID: 20165671

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    Tables

  [Table 1], [Table 2], [Table 3], [Table 4]

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    Abstract
    Introduction
    Long-term Compli...
    School-based Scr...
    Curve Progressio...
    Genetic Profilin...
    Curve Progressio...
    Conclusion and F...
    References
    Article Tables
 

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