Article Text


Marfan syndrome in children and adolescents: predictive and prognostic value of aortic root growth for screening for aortic complications


Objective To assess and measure the diagnostic and prognostic value of individual aortic root growth in children and adolescents with Marfan syndrome.

Design From 1983 to 1996, 250 children were screened for Marfan syndrome. Serial echocardiographic aortic root measurements of 123 children (57 Marfan, 66 control) were available for evaluation of aortic root growth. Aortic root diameters were correlated with body surface area. Based on individual growth of the aortic root a discrimination formula was derived to distinguish Marfan patients from control subjects.

Results Sensitivity and specificity of this method, which were dependent on the number of measurements, were 84% and 73%, respectively, for three serial measurements. The discrimination score also predicted a five year complication free survival in all patients.

Conclusions In children and adolescents with Marfan syndrome, aortic root growth differs significantly from subjects in whom Marfan syndrome was definitely ruled out during screening. Measurement of individual aortic root growth may serve to establish diagnosis at an early stage and is of prognostic value for occurrence of aortic complications.

  • Marfan syndrome
  • aortic root growth
  • echocardiography
  • children
  • adolescents

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Marfan syndrome is an autosomal dominantly inherited disorder of connective tissue associated with mutations in the fibrillin I gene,1in which ocular, skeletal, cardiovascular, integumentary, pulmonary, and neurological features may be present in a highly variable degree.2 3 Until recently, the diagnosis was based on fulfilment of diagnostic criteria established in Berlin in 1986.4 In 1995 these criteria were revised in Gent.5 Prevalence has been estimated to be 1 in 3000 to 5000,6 15–30% of whom represent new mutations.3 4 7

Prognosis is mainly determined by progressive aortic root dilatation, potentially leading to aortic type A dissection and aortic rupture, which are the major causes of death.2 3 Prophylactic composite graft repair of the aortic root is usually performed before the aortic root diameter reaches 55 mm in adults, thereby raising life expectancy from 40 years in 1972 to approximately 60 years in 1993.8 Nevertheless, 60% of all mortality is still caused by aortic complications9 and hence several studies with respect to aortic complications have been focused on the identification of specific risk groups in the Marfan population.10 11

Whereas aortic root complications are rare in childhood, early identification of the diagnosis of Marfan syndrome and the identification of patients at a high risk for aortic complications are still important. Particularly in childhood, clinical signs vary in onset and severity, and long term follow up examinations may be necessary before a definite diagnosis can be established.12 Furthermore, treatment with β adrenergic blocking agents, which are reported to slow down the rate of aortic dilatation,13 14 should be started as soon as possible to delay or even prevent critical dilatation requiring surgical intervention. Although the beneficial effects of this treatment on the aortic root dilatation rate have only been investigated in adults, one could argue that the same protective mechanism occurs in children. Thus, since 1996 we have increasingly prescribed β blocker treatment for Marfan children in our institution. We perform prophylactic surgery at an aortic root diameter of 50 mm.

Screening in children relies mainly on aortic root size. Aortic root diameter is measured by echocardiography at the sinuses of Valsalva and related to height,15 16 weight,16 17 and body surface area,14 16 18-23 the latter being considered as the most significant reference in children and adolescents.19 21-27 With serial measurements of the aortic root diameter, individual aortic root growth curves can be constructed. Our aim in this study was threefold: (1) to assess individual growth of the aortic root diameter relative to body surface area; (2) to predict at an early stage a probable diagnosis of Marfan syndrome by measuring individual aortic root growth; and (3) to examine the prognostic importance of aortic root growth on aortic complications in children and adolescents with Marfan syndrome.



From 1983 until 1996, 250 children have been referred to the multidisciplinary Marfan team of the Academic Medical Centre of Amsterdam. Indications for screening included family history, excessive height, chest or spine anomalies, hypermobile joints, and lens luxation. None of these subjects was referred for aortic root enlargement. Of the 250 children, 71 eventually had a definite diagnosis of Marfan syndrome according to the Berlin criteria4 and in 104 the diagnosis Marfan syndrome could definitely be excluded on clinical grounds at some time during this 13 year period. A control group excluded any child with aortic disease or connective tissue disease. In 75 children the diagnosis remained uncertain, which also prevented inclusion in the study.

Of 175 children initially included, 52 were ruled out for various reasons (table 1), leaving 123 children for final analysis (57 Marfan patients and 66 controls). None of these 123 children had ever used β blocking agents because up to 1996 no obvious advantage of this treatment in children with Marfan syndrome was recognised in our institution. In the Marfan group, four patients (7%) were diagnosed before the third year of age. Mean age at definite diagnosis in the entire Marfan group was 7 years (range 1 to 18 years). Follow up was continued until the subjects reached 21 years of age. The baseline characteristics of the study population, expressed as ranges and means (SD), are shown in table 2.

Table 1

Numbers of children evaluable for analysis of 250 children referred for screening

Table 2

Clinical characteristics


Echocardiographic measurements of the aortic root diameter of the patients and control subjects were made by M mode echocardiography and cross sectional echocardiography. The number of measurements per patient and control subject varied from two to 19 (mean (SD) 6.6 (3.9)) and from two to six (3.1 (1.2)), respectively. We measured the aortic root at the level of the sinuses of Valsalva with both methods. The measurements by M mode echocardiography were made according to the recommendations of the American Society of Echocardiography (ASE)28 and guided by cross sectional mode. With cross sectional echocardiography the aortic root diameter was imaged in long axis parasternal views.

We used all the measurements made by both modes interchangeably, because in an earlier study from our institution29 no clinically relevant difference was found in assessing the aortic root diameter by either of these two echocardiographic methods.


To construct aortic root growth curves we first calculated body surface area by the Dubois formula.30 Aortic root diameters from each individual were then correlated with body surface area to yield aortic root growth curves. Previous studies have shown that individual growth curves related to body surface area can be described by means of linear regression analysis.19 26 27 31 Differences in individual aortic root growth between patients and control subjects were analysed by individual specific intercepts and slopes from linear regression lines, resulting in a discrimination formula to predict Marfan syndrome (see statistical analysis below). To examine the possible value of aortic root growth in addition to absolute dilatation for early diagnosis, we selected 26 Marfan patients who had had at least three echocardiographic measurements before dilatation of the aortic root occurred. The discrimination formula was used to identify aortic root involvement in these 26 patients, based on the aortic root growth before the aortic root became dilated. We used the nomogram previously reported by our group29 to examine whether the aortic root was dilated. This was done to rule out the effects of differences in anthropometric measurements and growth rate between a population being screened for Marfan syndrome and a standard population, which we showed in a previous study.29


The discrimination formula was also tested to predict increased risk for aortic complications in the Marfan group. End points were defined as cardiovascular death, aortic root surgery for dissection or rupture of the ascending aorta, and critical ascending aortic root dilatation beyond 50 mm in children requiring prophylactic repair of the aortic root. Aortic root growth was not considered to be a standard indication for prophylactic surgery in our institution. In Marfan patients we calculated the complication rate from the second echocardiographic measurement in relation to the discrimination score.


Data on baseline characteristics and serial echocardiographic measurements are presented as range and mean (SD) unless otherwise reported. The differences of the mean values were compared with the Student’s t test. In all 123 children the individual aortic root growth curve in relation to body surface area was examined and quantified using linear regression analysis. The relation between aortic root diameter and body surface area was analysed using a random coefficient linear growth model.32 “Proc.mixed” from SAS 6.11 for Windows was used for the calculations. Differences in individual aortic root growth between patients and control subjects were analysed by individual-specific intercepts and slopes, following quadratic discriminant analysis.33 This statistical model was modified to take into account differences between subjects regarding the precision of the intercepts and slopes caused by the different numbers of measurements per subjects and the differences in body surface area values. The analysis resulted in a discriminant score function, which includes the slope and intercept, number of measurements, and mean and standard deviation of body surface area of a subject. Further details are given in the .

Depending on a chosen cut off point an optimal balance between the sensitivity and specificity of the discrimination score can be obtained. A cut off point at −0.7 of the discrimination score was chosen, indicating that a score larger than −0.7 was predictive of Marfan syndrome—that is, involvement of the aortic root—while a score below −0.7 indicated absence of aortic root disease. We examined the sensitivity and specificity for subjects with at least two, three, and four serial measurements, respectively, at the cut off point of −0.7.

The log rank test was used to test the differences in complication rate between the patients stratified according to the score. The complication-free event rate was expressed in percentages with one standard error (SE). To obtain similar sample sizes, two approximate groups were prespecified to define the categories in the plot: 29 patients with a discrimination score of less than 2, and 28 patients with a score above 2.

All analyses including aortic growth rate and risk stratification were made in SPSS 6.0. A p value < 0.05 was considered significant.



In all 123 children the individual growth curves were analysed in relation to body surface area. The mean interval between measurements was significantly shorter for the Marfan group than for the controls (Marfan 1.3 (0.7) years v control 2.3 (0.9) years, p <  0.01)) but there were no significant differences within the groups between subjects with two, three, or more measurements. The mean regression line of the 57 patients was steeper than in the 66 control subjects and there was a significant discrimination between the two different groups (y = 13.4x + 14.5 and y = 9.3x + 12.1 respectively, p < 0.001). The mean regression lines for growth of the aortic root in relation to body surface area are shown in fig 1.

Figure 1

Regression lines of mean aortic root growth in relation to body surface area (BSA) of the Marfan patients (n = 57) and the control subjects (n = 66).


At a cut off point of −0.7 (fig 2), the diagnostic accuracy for the subjects with at least two, three, and four serial echocardiographic measurements was examined. For subjects with at least two serial measurements the observed sensitivity and specificity were 81% and 69% respectively; for subjects with at least three serial measurements, 84% and 73% respectively; and for subjects with at least four serial measurements, 90% and 73% respectively.

Figure 2

Cumulative percentage plot of discrimination score of patients and control subjects with at least two (uninterrupted line), three (short dashes), and four (long dashes) measurements per subject. The cut off point at −0.7 shows a different sensitivity and specificity for at least two (81% and 69%, respectively), three (84% and 73%, respectively) and four (90% and 73%, respectively) measurements.

Of the 46 patients with at least three serial measurements, 26 showed no aortic root dilatation during the first three measurements. Among these 26 patients, abnormal aortic root growth was identified in 18 by means of the discrimination formula (69%), suggesting Marfan syndrome before aortic root dilatation.


During 13 years’ follow up, 12 patients developed complications in the cardiovascular system (table 3). At five years’ follow up after the second echocardiographic measurement, the estimated probabilities of no complications were 100% (SE = 0%) for a score < 2, and 85% (SE = 7%) for a score ⩾ 2. At 10 years’ follow up after the second echocardiographic measurement these figures were 90% (SE = 9%) for a score < 2, and 56% (SE = 13%) for a score ⩾ 2, p = 0.069 (fig 3).

Table 3

Discrimination score of 12 patients with aortic complications

Figure 3

Complication rate for the patients in relation to the discrimination scores distinguishing two groups of similar sample size. The numbers of patients in each group on whom the calculations are based are given at the bottom. Patients with a discrimination score < 2 (n = 29) filled squares; patients with a score ⩾ 2 (n = 28) empty circles.

Table 4 shows data on the family history of Marfan syndrome and aortic dissection of the two different risk groups (score ⩾ 2 and score < 2). Patients with a score ⩾ 2 were younger (9.4 (5.1) and 10.2 (4.6) years, respectively), less often had a positive family history of Marfan syndrome (60% and 83%, respectively), and more often had a positive family history of aortic dissection (36% and 21%, respectively), compared with patients with a score < 2.

Table 4

Comparison of clinical findings in 57 patients with a discrimination score ⩾ 2 and < 2


Marfan syndrome remains a difficult nosological entity requiring a multidisciplinary approach in specialised centres. Our study shows that with a formula based on paired echocardiographic and anthropometric data, measurement of aortic root growth may establish the diagnosis at an early stage, and predict aortic complications in children and adolescents with Marfan syndrome.

An early diagnosis may be important but is still often not easily made. In our population of 250 children who were initially referred for screening, the diagnosis of Marfan syndrome could not be established with absolute certainty in a substantial group (75 subjects) after a follow up of several years (range 0 to 11; mean 2 years). This indicates the difficulty in establishing the diagnosis Marfan syndrome using the standard diagnostic criteria. Hence additional information that can provide a tool for diagnosis at an earlier stage is of great importance. For the purpose of the present study we selected only those patients in whom no doubt remained about the diagnosis of Marfan syndrome. Subsequent studies will have to be performed to evaluate the formula in patients in whom the diagnosis remains questionable.

The relation of aortic root growth to body surface area has previously been analysed in 17 Marfan patients by Hirata et al 34 and in 19 children with Marfan syndrome by Vetter et al.26 In these small groups of patients a positive correlation was found between initial aortic root dilatation and the rate of aortic growth. In 89 Marfan patients studied by Legget et al an aortic diameter of 30% or more above normal was found to be related to an increased risk of aortic complications.11 Furthermore, in 62 Marfan patients studied by serial echocardiograms, an annual change in aortic diameter of more than 5% appeared to be a risk factor for aortic complications.11

Identification of a higher risk group during follow up is important and may have implications for management and treatment. The prevalence of serious cardiovascular complications in childhood is low (4.3% of 186 patients as reported by El Habbal35). There is, however, a risk of rupture or dissection of the aorta around adolescence (approximately 20%).10 11 35 36

Our Marfan population could be divided into two groups with different growth rates. Patients with a higher growth rate—that is, with a score ⩾ 2 and a higher risk of aortic complications—were younger at initial evaluation, less often had a positive family history of Marfan syndrome, and more often had a family history of aortic dissection than patients with a score < 2. This is in line with previous studies that showed that new mutations, younger age at presentation, and a family history of severe aortic disease in Marfan patients are important predictors of aortic complications.7 10 33 34 There was a significant discrimination in the occurrence of mitral valve prolapse between the two groups (p = 0.01). No other studies, however, showed a correlation between the occurrence of mitral valve prolapse and aortic complications in Marfan syndrome. Therefore the significance of this feature remains unclear. More accurate measurements of aortic root diameter with magnetic resonance imaging (MRI) may improve the predictive power of aortic root growth in Marfan syndrome.37 Further specification of diagnostic criteria, for instance skeletal features and dural ectasia as proposed by De Paepe et al,5 may also make diagnosis easier. Until a fully reliable molecular based approach that will identify patients at higher cardiovascular risk is widely available, echocardiographic and MRI variables will be the most important prognostic indicators. Patients with Marfan syndrome and a discrimination score ⩾ 2 should be followed closely, because of the increased risk of serious complications.

None of the study subjects used β blocking agents before or during our study. Whether the use of these drugs would have invalidated the discrimination score can only partly be answered by making assumptions on theoretical grounds, as no research in this specific direction has yet been performed. Aortic dilatation in Marfan syndrome will occur when degenerative changes take place in the aortic tunica media, with defragmentation of elastic tissue and mucoid pooling. These alterations in the tunica media resemble degenerative changes in the elderly,38 39 and gradual aortic dilatation (with the risk of aortic dissection or rupture) also takes place when people grow older. Thus media changes in the Marfan aorta could be regarded as accelerated aging. We do not know to what extent this is the case in children with Marfan syndrome. When tests of elasticity are performed in vivo (by measuring distensibility), the aorta is found to be less elastic in Marfan patients and in the elderly, independent of aortic size.40 41 However, in the few studies that have been performed to test the effect of β blocking agents on aortic elasticity in children with Marfan syndrome, no significant difference in aortic distensibility between those with and without β blocker treatment was shown.42 If we assume that aortic dilatation will follow decreased aortic elastic function, no effect of β blocking agents on aortic root growth in children is to be expected, and the value of the discrimination formula will be unaffected. Knowing, on the other hand, that β blocking agents can reduce aortic dilatation in adult Marfan patients and that Marfan syndrome is characterised by a great variability in clinical features, there might be a subgroup of children with Marfan syndrome in whom β blocker treatment results in decreased aortic growth rate. This would, of course, have an effect on the validity of the discrimination formula.


The number of patients with aortic complications may have been too small to assess the true prognostic value, as can be seen from the large standard errors. There is, however, a clear trend with respect to the occurrence of aortic complications and the family history. Furthermore, rapid growth of the aortic root could incidentally have played a role in the decision to perform prophylactic surgery.

One could argue that there was no absolute certainty of excluding Marfan syndrome on clinical grounds during a screening period. Moreover, there is a possibility that Marfan patients were diagnosed after the 21st year of age and wrongly classified as controls in our study. As Lipscomb et al have recently shown,43 the variance in evolving Marfan phenotype causes diagnostic problems in childhood. Most patients in their study were, however, diagnosed before their 15th year and it seems reasonable to assume that there will be very few patients in whom the signs are not present after the 21st year (when growth ceases to be an important disturbing factor). As stated, patients in whom any doubt remained were excluded from analysis. If, however, any patients were wrongly left in the control group, the true difference between the two groups could only be more clear than we showed in the current study.

As can be seen from table 2, follow up was significantly shorter in the control group than in the Marfan group, which could involve a possible source of error. A subject classified as a control might, when followed for a longer period, develop aortic dilatation. Mean age at the end of follow up, however, was the same (14 years) in both groups (table 2) and most patients will be diagnosed before that age. Moreover, as the mean interval between measurements was larger for the control subjects, one could argue that aortic root growth rate was investigated more reliably in the controls, which would counterbalance the shorter period of follow up.

In our study, the sensitivity and specificity of the diagnosis of Marfan syndrome, based on aortic root growth, are favourably reflected in the population from which the calculation variables were taken. The cut off point was chosen to achieve an optimal balance between sensitivity and specificity in the test population, which was also the study population. It is thus to be expected that the discriminating power will be somewhat lower when our score function is applied to an independent dataset, but to what extent it is difficult to estimate owing to the rather complex statistical methods. Our discrimination formula may still need to be tested in a different Marfan population to find true sensitivity and specificity values.

Another limitation of the study is the relatively complex nature of the discrimination formula, which necessitates the use of computerised assistance in daily clinical practice. On the other hand, the importance of early and accurate diagnosis might justify such an additional effort. In our hands, the proper score and subsequent diagnosis could be established within five minutes using a hand held calculator.


We conclude that the individual growth rate of the aortic root of Marfan patients is significantly greater than in controls without Marfan syndrome. Quantification of individual aortic root growth using a newly developed formula may serve to establish the diagnosis at an early stage and is of prognostic value with respect to the occurrence of aortic complications in children and adolescents with Marfan syndrome.


The individual aortic root growth curves related to body surface area are described as linear regression lines:

AoDij = ai + bi * BSAij + eij where AoDij is the aortic root diameter of subject i at evaluation day j, BSAij is the body surface area of subject i at evaluation day j, ai is the intercept of the regression line of subject i, bi is the slope of the regression line of subject i, and eij is the deviation of point j for subject i from the subject specific regression line given by ai and bi.

One can plot the observed bi values versus aivalues for both Marfan patients and control subjects. If it is possible to discriminate between Marfan patients and control subjects on the basis of the aortic root growth curves, one may expect to find two clusters of points in such a plot—one for the patients and one for the control subjects. Hence one can try to find a line that optimally separates the two clusters. The prediction would be that a subject is a Marfan patient (or control subject) if his (ai,bi) point lies on the same side of the line as the Marfan (or control subject) cluster.

Similarly, the dividing line can be described by the equation e = c* ai + d * bi, where e is the cut off point, and c and d are coefficients. For each subject one can calculate a discrimination score and predict that the subject will be a Marfan patient if the result is larger than e or a control subject if the result is lower than e. One way to find such a dividing line is by means of quadratic discriminant analysis.31 In that method, the coefficients c, d, and e are calculated from the means, standard deviations, and correlations of the ai and bi values within each group. However, all points are assumed to have the same precision. This is not the case in the present study design, because different subjects have different numbers of points at different values of body surface area, resulting in different precisions of the ai and bi values. Two sources of variation have to be taken into account: (1) variations of points around the regression line within subjects, and (2) variations of the regression lines (ai and bi) between subjects. With regard to the latter, it was assumed that this variation within each group (Marfan patients and control subjects) can be described by a bivariate normal distribution, one for each group.

Within a subject, the aortic root diameters—given the body surface area values—are assumed to be independently normally distributed, with a standard deviation only depending on the group. The effect of this within subject variation on the standard deviations and the correlation of the observed ai and bi values can be calculated by standard methods, as can the combined effect of the within subject and between subject variation. The result is a modified Fisher discriminant score function, that is a log likelihood ratio based on a bivariate normal distribution using the same basic formula as in Fisher’s discriminant analysis, but substituting adapted values for the standard deviations and correlations. The necessary parameters are derived from the data using restricted maximum likelihood (REML) estimation in a random coefficient linear growth curve model,36 using a different model for each group. Calculations were performed using the SAS 6.11 procedure “Proc Mixed.”


The following symbols are used:

number of (aortic root diameter vbody surface area) points for a subject
mean value of body surface area for a subject
SD of body surface area for a subject
intercept of the regression line for a subject
slope of the regression line for a subject
group (Marfan patients or control subjects) αg, mean intercept for group g βg, mean slope for group g ςα,g, population SD of intercept in group g ςβ,g, population SD of slope in group g ςαβ,g, population covariance of intercept and slope in group g ςεg, SD of point from regression line in group g
natural log of x.

The estimates showed in table 5 are derived from the data using REML estimation in a random coefficient linear growth curve model. The following formulas can then be used to calculate the discrimination score for each subject:

V11 = 1/N + m2/(N−1)s2
V12 = −m/(N−1)s2
V22 = 1/(N−1)s2
Z11,g = ςα,g 2 + ςε,g 2 * V11
Z12,g = ςαβ,g + ςε,g 2 * V12
Z22,g = ςβ,g 2 + ςε,g 2 * V22
Dg = Z11,g *Z22,g − Z12,g 2
W11,g = Z22,g /Dg
W12,g = −Z12,g/Dg
W22,g = Z11,g/Dg
Cg = −1/2 *[(a−αg)2 W11,g + 2(a−αg)(b−βg) W12,g + (b−βg) 2 W22,g + ln(Dg)]
Discrimination score = CMarfan patients− Ccontrol subjects
Table 5

Estimates (SE) derived from the data for Marfan syndrome patients and controls


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