WO2005011471A2

WO2005011471A2 - System and method for utilizing shape analysis to assess fetal abnormality

Info

Publication number: WO2005011471A2
Application number: PCT/US2004/024189
Authority: WO
Inventors: David A. Krantz; Francesco Orlandi
Original assignee: Ntd Laboratories, Inc.
Priority date: 2003-07-29
Filing date: 2004-07-28
Publication date: 2005-02-10
Also published as: US20050063576A1; US7244233B2; CA2575517C; US7780600B2; EP1659947A4; US20080077014A1; CA2575517A1; WO2005011471A3; EP1659947A2

Abstract

A method and system for utilizing shape analysis to assess fetal abnormality. According to one embodiment, coordinates of points identifying a shape in a fetal image are received (100), coefficients of one or more mathematical functions that describe the identified shape are determined (110), and the determined coefficients are utilized as markers to assess fetal abnormality (120).

Description

SYSTEM AND METHOD FOR UTILIZING SHAPE ANALYSIS TO ASSESS FETAL ABNORMALITY

Cross Reference To Related Applications

[0001] This application claims the benefit under 35 U.S.C. § 119(e) of U.S. Provisional Application No. 60/490,540, filed July 29, 2003 and U.S. Provisional Application No. 60/493,442, filed August 8, 2003, both of which are hereby incorporated by reference as if repeated herein in their entirety.

Background Of The Invention

[0002] Prenatal screening methods are routinely employed to assess the likelihood of fetal abnormalities, commonly referred to as birth defects. For example, Down syndrome or Trisomy 21 is the most common cause of severe learning disability and accounts for approximately one half of all chromosomal anomalies in live born children.

[0003] Current methods to screen prenatally for trisomy 21 involve maternal serum testing for biochemical markers and/or ultrasound evaluation of biophysical markers. Maternal serum screening involves the quantitative analysis of biochemical markers and risk assessment based on likelihood ratios derived from the population distributions of affected and unaffected pregnancies. Ultrasound evaluation, however, has historically involved visual observation of a fetal image and deciding empirically whether the image looks "normal" or "abnormal" (for example, whether the cerebellum appears as a banana sign for open spina bifida). This approach requires extensive experience in the "art" of ultrasound and the interpretation is necessarily subjective.

[0004] Accordingly, there is a need in the art for a system and method that adequately evaluates the morphological changes observed with birth defects during prenatal screening.

Summary Of The Invention [0005] Embodiments of the present invention provide for utilizing shape analysis to assess fetal abnormality. According to one embodiment, coordinates of points identifying a shape in a fetal image are received, coefficients of one or more mathematical functions that describe the identified shape are determined, and the determined coefficients are utilized as markers to assess fetal abnormality.

Brief Description Of The Drawings [0006] FIG. 1 is a flow chart that depicts a process for utilizing shape analysis to assess fetal abnormality in accordance with an embodiment of the present invention.

[0007] FIG. 2 is a flow chart that depicts a process for utilizing shape analysis to assess fetal abnormality in accordance with an embodiment of the present invention.

[0008] FIG. 3 is a block diagram that depicts a user computing device in accordance with an embodiment of the present invention.

[0009] FIG. 4 is a block diagram that depicts a network architecture in accordance with an embodiment of the present invention.

[0010] FIG. 5 is a flow chart that depicts a process for utilizing shape analysis of a fetal head to determine risk of fetal abnormality in accordance with an embodiment of the present invention.

[0011] FIG. 6 is a screen shot that depicts outlining of a fetal head in accordance with an embodiment of the present invention.

[0012] FIG. 7 is a screen shot that depicts outlining of a fetal head in accordance with an embodiment of the present invention.

[0013] FIG. 8 is a flow chart that depicts a process for utilizing shape analysis of a fetal brow to determine risk of fetal abnormality in accordance with an embodiment of the present invention.

[0014] FIG. 9 is a screen shot that depicts outlining of a fetal brow in accordance with an embodiment of the present invention.

[0015] FIG. 10 is a screen shot that depicts outlining of a fetal brow in accordance with an embodiment of the present invention. [0016] FIG. 11 is a screen shot that depicts outlining of a fetal brow in accordance with an embodiment of the present invention.

[0017] FIG. 12 is a screen shot that depicts outlining of a fetal brow in accordance with an embodiment of the present invention.

Detailed Description OVERVIEW

[0018] FIG. 1 depicts a process for utilizing shape analysis to assess fetal abnormality in accordance with an embodiment of the present invention. Upon receiving coordinates of points identifying a shape in a fetal image (step 100), the coordinates are used to determine coefficients of a mathematical function or functions that describe the identified shape (step 110). These coefficients are used as markers to assess fetal abnormality (step 120).

[0019] As shown in FIG. 2, once the coefficient markers are determined (step 200), they may be used by themselves or with other markers to assess fetal abnormality (step 210). A fetal abnormality may be assessed by comparing a patient's coefficient markers to reference data of coefficient markers by conducting a statistical analysis. The reference data may contain unaffected patients and/or affected patients. The statistical comparison could result in a risk of fetal abnormality, a likelihood ratio for a fetal abnormality or an index value that could be considered within range or outside of range for a fetal abnormality.

[0020] The use of multidimensional coordinates allows for the evaluation of a shape as a whole. In one embodiment, a statistical shape analysis involves the tracing of an outline around the part of a fetal image to be analyzed. The points that make up this curve are then analyzed to derive a function that best fits the individualized points around the outline. The coefficients of this function may be considered random variables and can be determined for each evaluated image. The coefficients may then be analyzed using multivariate statistics to determine if they are outliers compared to the normal population. A subject shape that has coefficients outside the normal ranges observed in control shapes would indicate that the subject shape was significantly different than expected. [0021] Described below are several embodiments within which the present invention may be implemented.

ARCHITECTURE

[0022] FIGS. 3 and 4 illustrate the components of a basic computer and network architecture in accordance with an embodiment of the present invention. FIG. 3 depicts user computing device 300, which may be an ultrasound machine (3-D, 4-D or color), MRI or CAT scan machine, fetoscopy machine, workstation, personal computer, handheld personal digital assistant ("PDA"), or any other type of microprocessor-based device. User computing device 300 may include a processor 310, input device 320, output device 330, storage device 340, client software 350, and communication device 360.

[0023] Input device 320 may include a keyboard, mouse, pen-operated touch screen or monitor, voice-recognition device, or any other device that accepts input. Output device 330 may include a monitor, printer, disk drive, speakers, or any other device that provides output.

[0024] Storage device 340 may include volatile and nonvolatile data storage, including one or more electrical, magnetic or optical memories such as a RAM, cache, hard drive, CD-ROM drive, tape drive or removable storage disk. Communication device 360 may include a modem, network interface card, or any other device capable of transmitting and receiving signals over a network. The components of user computing device 300 may be connected via an electrical bus or wirelessly.

[0025] Client software 350 may be stored in storage device 340 and executed by processor 310, and may include, for example, imaging and analysis software that embodies the functionality of the present invention.

[0026] FIG. 4 illustrates a network architecture in accordance with an embodiment of the present invention. The network architecture allows the imaging and analysis functionality of the present invention to be implemented on more than one user computing device 300. For example, in one embodiment user computing device 300 may be an ultrasound machine that performs all of the imaging and analysis functionality of the present invention. In another embodiment, user computing device 300a may be an ultrasound machine that performs the imaging functionality of the present invention, and then transfers image or coordinate data over network 410 to server 420 or user computing device 300b or 300c for analysis of the data. The analyzed data could further be transferred to another user computing device 300 belonging to the patient or another medical services provider for testing with others markers. <■

[0027] Network link 415 may include telephone lines, DSL, cable networks, Tl or T3 lines, wireless network connections, or any other arrangement that implements the transmission and reception of network signals. Network 410 may include any type of interconnected communication system, and may implement any communications protocol, which may secured by any security protocol.

[0028] Server 420 includes a processor and memory for executing program instructions, as well as a network interface, and may include a collection of servers. In one particular embodiment, server 420 may include a combination of servers such as an application server and a database server. Database 440 may represent a relational or object database, and may be accessed via server 420.

[0029] User computing device 300 and server 420 may implement any operating system, such as Windows or UNIX. Client software 350 and server software 430 may be written in any programming language, such as ABAP, C, C++, Java or Visual Basic.

ANALYSIS OF FETAL HEAD SHAPE EMBODIMENT

[0030] FIG. 5 provides an example embodiment of the present invention in which the shape of a fetal head is analyzed to assess fetal abnormality. Fetal abnormalities identifiable through the use of the present invention may include, among others,

Down syndrome, Spina Bifida, Trisomy 18, Trisomy 13, frontal bossing, unbalanced translocation, other chromosomal abnormalities, heart abnormalities and abnormalities of any major body organ, structural abnormalities and craniofacial abnormalities. [0031] According to this embodiment, a transverse view of the fetal head is obtained by ultrasound (e.g., UCD 300a), saved as a bit-map image and transferred to another computer (e.g., UCD 300b). Then, in step 500, a user (e.g., user 400b) employs digitizing software (e.g., client software 350), such as TPSDIG, DigitX, CalExcel, DSDigit, Digical, Windig or MacMorph, to create an outline of the fetal head to be analyzed. (Digitizing software provides coordinate data when a user clicks on a particular point in a bit-map image.) In creating the outline, the user may identify two landmarks on the bit-map image along the OFD (ocipito-frontal diameter) axis so that the image may be aligned against a consistent axis and to allow for a uniform assessment of points on each image.

[0032] As shown in FIG. 6, prior to placing the coordinates on the outline, a series of 20 lines, each the length of the OFD axis, may be generated utilizing software employing general algorithms. The first line overlays the OFD axis; the remaining lines are centered at the mid-point of the first line and then are rotated at 9 degrees from the previous line in a counterclockwise manner. Once this "fan" is drawn, the user may place points, via the digitizing software, on the outline of the fetal head where it crosses the equidistant lines of the fan. FIG. 7 shows the resulting 40 points representing the outline. Each small circle connected in the loop represents a point on the image clicked by the user to identify the outline, and the two cross-hair symbols next to the number "2"s represent the OFD positioning landmarks. The use of the "fan" allows for more consistency in creating the outlines on different images.

[0033] In step 510, the user-identified outline points are converted into data coordinates by the digitizing software. TABLE 1 represents the landmarks and outline points of FIG. 7 as stored in an output file. The output file lists the coordinate data in a tabular format, with the x-coordinate listed first followed by the y-coordinate. As indicated in TABLE 1, the two landmark coordinates are listed first, followed by the 40 point coordinates. TABLE 1

LM=2

401.00000 304.00000 180.00000 347.00000 CϋRVES=l POINTS=40

401.00000 302.00000 399.00000 322.00000 393.00000 337.00000 386.00000 353.00000 375.00000 365.00000 365.00000 376.00000 356.00000 386.00000 345.00000 395.00000 334.00000 400.00000 320.00000 402.00000 307.00000 402.00000 294.00000 401.00000 283.00000 400.00000 271.00000 397.00000 260.00000 396.00000 247.00000 391.00000 236.00000 387.00000 220.00000 381.00000 209.00000 373.00000 194.00000 364.00000 182.00000 349.00000 178.00000 330.00000 183.00000 313.00000 189.00000 297.00000 198.00000 283.00000 207.00000 270.00000 221.00000 261.00000 236.00000 254.00000 248.00000 248.00000 260.00000 243.00000 272.00000 240.00000 287.00000 236.00000 301.00000 236.00000 315.00000 235.00000 331.00000 238.00000 346.00000 244.00000 359.00000 252.00000 371.00000 264.00000 382.00000 275.00000 391.00000 288.00000 IMAGE=Imagel . bmp ID=1 SCALE=0.140234 [0034] In order to ensure the coordinate data is aligned properly with the two specified landmarks, the user may employ a software program that utilizes general algorithms to adjust the coordinate data by rotating and translating each data point so that the OFD axis lies along the horizontal axis and that the first point lies at the origin, (x,y) = (0,0). These adjustments do not change the shape of the outline being investigated. The software program may employ the following general algorithm:

• Point 1 = Origin: Denote as X_tN_! • Point 2 = Other end of OFD axis: Denote as X ,Y₂ • Determine Slope of Line: (Y₂- Yι)/( X₂- Xi) • Determine the angle of the slope: Theta = arctangent(Slope) • For each point in the shape rotate the point clockwise: • Subtract out the origin such that NewX = X - X_ls NewY = Y - Yi • FinalX = NewX* cos(Theta) + NewY* sin(Theta) • Final Y = newY*cos(theta) - NewX*sin(theta) [0035] The set of FinalX, FinalY values represent the rotated data points such that the OFD axis lies horizontally. In different scenarios, it may be appropriate to rotate the image in a counter clockwise manner; if this is the case then the formulas for FinalX and FinalY are:

• FinalX = NewX*cos(Theta) - NewY*sin(Theta) • FinalY = NewX* sin(Theta) + NewY* cos(Theta)

[0036] In step 520, the user may employ software such as the NTS YSPC program (Exeter Software), which uses an elliptical Fourier analysis program to generate a series of best fit curves to the coordinate data using harmonics. The zero harmonic consists of only 2 coefficients and represents only translation (i.e. movement in the x and y direction) and not shape itself so these 2 coefficients are usually not analyzed. Each harmonic comprises four coefficients of interpolation functions that describe the user-identified outline shape. In general, the more harmonics used, the better the fit to the coordinates; however, if too many harmonics are used the fit may be too good since small differences might appear due to poor placement of the outline point during step 500. In this embodiment, the user evaluates the first harmonic (i.e., the four coefficients al, bl, cl and dl). [0037] The user may choose alternatives to the method described above for aligning the coordinate data. For example, the user could rotate the image so that the long axis of the shape described by the first harmonic is parallel to the x-axis, or the user can align the image such that the first point of the outline is set equal to the end point of the first harmonic to the x-axis, or the user could combine both of these methods. These options are available as part of the Elliptical Fourier Analysis module in the NTSYSPC program.

[0038] In step 530, the determined coefficients may be utilized as markers to assess fetal abnormality by conducting a statistical analysis to compare the patient's determined coefficients with reference parameters derived from reference data of coefficient markers (e.g., a statistical distribution of determined coefficients in the unaffected population and/or affected population). One exemplary method of doing this is to calculate the Mahalanobis Squared Distance (MSD) value for the patient's coefficients.

[0039] Prior to determining the outline coefficients, the coordinates may be adjusted by scaling the coordinates so that the area enclosed inside the outline equals 1. The original areas of the enclosed outline could be included as a separate variable in addition to the coefficients as part of the statistical comparison analysis. Also, many shapes change with growth in the fetus. As a result, it may be necessary to adjust the observed coefficients to account for gestational age of the fetus as part of the statistical analysis.

[0040] Several other shape analysis methods besides elliptical Fourier analysis may be utilized by the present invention. All of the following methods determine coefficients of functions that may be used as markers to assess fetal abnormality. Some examples of outline methods are:

A. polynomials B. cubic splines C. parametric polynomials D. parametric cubic splines E. bezier curves F. Fourier analysis of equally spaced radii G. dual axis Fourier analysis [0041] All of these methods deal with outlines, of which there are four classes - simple open outlines, simple closed outlines, complex open outlines, complex closed outlines. A simple open outline is an open outline that has only one value of y for each x. A complex open outline is an outline that can have more than one y value for each x. Simple closed outlines are closed outlines such that if one draws a line from the center through the outline it only crosses the outline once whereas in a complex outline the line would cross the outline more than once. In most cases an open outline can be analyzed as if it is a closed outline by assuming there is a straight line from the last to first point of the outline or by mirroring all of the coordinates around the x (or y) axis, however the outline can be analyzed as an open outline. Some of the methods above, such as the polynomial method, work with open outlines while others like the elliptical Fourier analysis work with closed outlines. It is also possible to analyze 3 -dimensional outlines (x,y,z) in accordance with an alternative embodiment of the present invention.

[0042] To provide the reference data to which the determined coefficients are compared in step 530, a statistical algorithm may be utilized to determine the statistical distribution of the coefficients in the unaffected population using a set of coefficients for a series of unaffected pregnancies. The distribution may be defined by a series of reference parameters for each coefficient or pair of coefficients such as means, standard deviations and correlations. The coefficients associated with an outline in a particular patient could be compared to these reference parameters and the chance that the coefficients could be equal to or more extreme than their observed values could be determined.

[0043] If affected cases are available then they may be included in the reference data set to determine the statistical distribution of the coefficients in the affected population using a set of coefficients from a series of affected pregnancies. The patient's coefficients could then be compared to the distribution of coefficients in the affected population. Alternatively, the patient's coefficients could be compared to both the unaffected distribution and the affected distribution as defined by the reference parameters. For example, if both the unaffected cases and affected cases are multivariately normally distributed, the distribution function for the multivariate normal distribution can be used with the reference parameters for the unaffected distribution to determine a relative frequency for the unaffected distribution and then again for the affected distribution to determine a relative frequency for the affected distribution, and then a likelihood ratio may be determined. A likelihood ratio equals the quotient of the relative frequency in the affected distribution to the relative frequency in the unaffected distribution. A risk result (e.g., 1 in 100) gives the chance that a patient with the same parameters could have a child with a fetal abnormality. A likelihood ratio gives the relative risk that the patient could have a child with a fetal abnormality.

[0044] The likelihood ratio can be used to multiply a prior risk to determine a posterior risk (after accounting for the minor adjustment between odds and risk, if necessary). For example, the prior risk of Down syndrome is often based on maternal age. If the statistical distribution of the determined coefficients are independent of the distribution of other markers, the likelihood ratio could also be used to adjust the risk of Down syndrome determined by the other markers to determine the overall risk of Down syndrome based on the outline and the other markers. Alternatively, if the coefficients are not independent of the other markers, then risk of Down syndrome could be determined by utilizing reference parameters for a combination of the coefficients and the other markers together using multivariate normal distributions or other distribution functions.

[0045] Examples of other markers include nuchal translucency, free Beta hCG and PAPP-A, Ductus Nenosus, absent or hypoplastic nasal bone observed on ultrasound, maternal blood alpha-fetoprotein, maternal blood hCG, maternal blood imconjugated estriol, maternal blood dimeric inhibin A, maternal urine total estriol, maternal urine beta core f agment, maternal urine hyperglycosylated hCG, maternal blood hyperglycosylated hCG, ultrasound "soft markers" which include for example, nuchal edema or increased nuchal fold, short femur, hyperechogenic bowel, and echogenic foci in the heart, etc.

[0046] As mentioned above, the other markers can be combined statistically with the results from the shape analysis to provide a final result to the patient.

Alternatively, the medical tests for the other markers could be performed prior to the ultrasound exam and then, when the ultrasound exam is completed, the results of the other marker tests can be thereafter combined with the results from the shape analysis.

[0047] For providing reference data according to this embodiment of the present invention, columns 2-5 of TABLE 2A show the results of evaluating the first harmonic (i.e., the four coefficients al, bl, cl and dl) of fetal head outlines in a study of 35 unaffected pregnancies in the first trimester. TABLE 2B lists the reference parameters consisting of the mean and standard deviation of each coefficient and the variance/covariance matrix consisting of the variance (standard deviation squared) and covariance between each pair of coefficients and the formula for calculating a Mahalanobis-Squared Distance (MSD) for each case.

TABLE2A

ID al bl cl dl 1 .618923 -.021438 .017238 .512385

2 .618007 -.00636 .004269 .513899

3 .611512 -.009105 .013914 .519218 4 .620708 .001494 .005816 .511672

5 .620591 -.001878 .002653 .511512 6 .610873 -.005378 .009693 .520104

7 .626065 .002194 .00969 .506797 8 .610239 -.022687 .015904 .520122 9 .619487 -.009327 .000085 .512371

10 .61309 .002649 .013512 .518273

11 .610239 .009847 -.00302 .520935

12 .633193 -.0167 .021139 .500202

13 .617141 -.031007 .009402 .513915

14 .613927 -.003108 .020587 .517351

15 .624268 .010912 .002663 .508347

16 .620115 -.027663 .02827 .510862

17 .613857 -.034757 .023583 .516377

18 .636496 -.010523 .021077 .497571

19 .607668 -.026101 .003049 .522709

20 .614509 .004114 .020143 .517041

21 .627318 -.034898 .014111 .50485

22 .605777 -.018182 .013938 .524513

23 .606093 .009761 .007094 .524719

24 .633498 -.005676 .029437 .500312

25 .634393 -.00556 .013881 .499904

26 .606259 .006939 -.016111 .52415

27 .63582 -.031021 .035875 .497006

28 .607238 -.040385 .006671 .522681

29 .612626 -.023636 -.006856 .518649

30 .6171 .026204 -.001128 .514461

31 .640095 -.022288 .018631 .494486

32 .625569 -.012373 .038643 .506998

33 .611093 -.02788 .032891 .518468

34 .629932 -.03224 .033393 .501638

35 .608294 .041921 -.008744 .522055

TABLE 2B

Variable | Mean Std. Dev. al | -.6189147 .0099677 bl I .0104039 .0183979 cl | -.0128969 .0130582 dl | -.5127587 .00881

Variance/Covariance Matrix (M)

SD = (X-μ)^τ M^"1 (X-μ) where: (X-μ) is a 4 element vector consisting of the patient's 4 coefficients (al,bl,cl,dl minus their respective reference means) . (X-μ) is the transpose of the (X-μ) vector M^"1 is the Inverse of the 4x4 Variance/Covariance Matrix

[0048] TABLE 2C shows the MSD calculation in the 35 unaffected cases. A cutoff beyond 95% of the observed data was established representing a point halfway between the last 2 MSD values (11.714). TABLE 2D shows the results of 2 patients who happened to be carrying a fetus with Down syndrome, both of which based on their MSD calculation are outliers. As more data from Down syndrome pregnancies are gathered, additional reference parameters (e.g., means, standard deviations, and covariances) based on the Down syndrome cases could be calculated along with other statistical techniques such as likelihood ratios to determine the odds that a patient is carrying a fetus with Down syndrome.

TABLE 2C

ID MSD 1 .5453869 2 .72770054 3 .86797516 4 .99110505 5 1.0513294 6 1.1757276 7 1.3182192 8 1.639374 9 1.7719449 10 1.9632445 11 2.0438778 12 2.0904377 13 2.4440608 14 2.5725717 15 2.6427427 16 2.8276119 17 3.255354 18 3.5018765 19 3.6411678 20 3.7887796 21 3.9182202 22 4.0570078 23 4.5657224 24 4.6067905 25 4.9834947 26 5.5061446 27 5.5437792 28 5.877155 29 6.0931487 30 6.2047977 31 6.3209851 32 6.5548075 33 7.4795723 34 9.0892238 35 14.338667

TABLE 2D

Outcome al bl cl dl MSD 36 .570043 -.015975 .01023 .558191 94.220565 37 .58333 .076813 -.056937 .538497 403.86348 [0049] In this embodiment of the present invention, only the data associated with TABLE 2B would have to be stored in the computing device for the statistical comparison analysis of a particular patient to be conducted. This would preserve storage resources in the event of reference data based on very large populations. ANALYSIS OF FETAL BROW EMBODIMENT

[0050] FIG. 8 provides an example embodiment of the present invention in which the shape of a fetal brow is analyzed using 3-D ultrasound to assess fetal abnormality. In traditional 2-D ultrasound the challenge to the sonographer is obtaining an image that is in the proper plane of view. The ability to consistently obtain the same angle and depth of view of the fetus requires subjective decision making during the ultrasound exam. Thus it is difficult to obtain consistent views of each fetus from exam to exam. This increases error when trying to analyze shapes from these images.

[0051] 3D ultrasound allows for the simultaneous visualization of the fetus in 3 separate 2-D planes, as shown in FIG. 9. These three planes are called the sagittal (side-view), coronal (front-view) and transverse (top-view). In FIG. 9, the top left image represents the transverse plane, the top right represents the coronal plane, and the bottom right represents the sagittal plane.

[0052] Misalignment of an image in any given plane distorts the images in the other two planes. Therefore, in order to perform proper 2-D image analysis of any given plane, the image should first be aligned properly in all three planes. For example, to analyze an image in the sagittal plane, a user can assure a proper view by aligning the fetus in the coronal and transverse views. In addition, by choosing a landmark in each plane (e.g. the white dot placed at the bridge of the nose in the FIG. 9) the depth of the section can also be defined. Using landmarks and aligning the fetus in all three planes can insure that the view of each fetus in any given plane is the same and thus reduce variation in shape due to differences in ultrasound technique. Ultimately this will improve the ability to see changes due to biological effects. 3D ultrasound further allows for image manipulation after the completion of the examination. Therefore, after capturing a 3-D image the operator can later rotate that image to the appropriate view. [0053] The use of 3D sonography is a recent advance in prenatal ultrasound. The technique generates a multiplanar display of separate images in the coronal, sagittal and transverse planes obtained by the ascertainment of a single "volume". Once the volume is obtained the images in each plane may be rotated to provide consistent and reproducible planes as part of a "post processing" evaluation. This advance was previously unobtainable using conventional 2D sonographic techniques. Once a given desired image and plane is obtained, it may be superimposed on a digitized screen where geometric morphometric analysis may be performed.

[0054] According to this embodiment, a fetal brow is analyzed in the sagittal plane - from the bridge of the nose to the midportion of the top of the skull. The fetal image of FIG. 9 is obtained by 3-D ultrasound (e.g., UCD 300a), saved as a bit-map image and transferred to another computer (e.g., UCD 300b). The sonographer (e.g., user 400a) places the landmark at the bridge of the nose in each plane.

[0055] In step 800, a user (e.g., user 400b) employs digitizing software to create an outline of the fetal brow to be analyzed. As illustrated in FIG. 10, the user first places two landmark points on the fetal head in the sagittal plane - one at the bridge of the nose and the other at the midportion of the top of the skull. Once these landmarks are correctly in place, the user employs a software program that utilizes a general algorithm to find a point that has the same horizontal component as the landmark on the bridge of the nose, and the same vertical component as the landmark at the top of the head. Once this point is found, a series of 16 lines of equal length are drawn, as shown in FIG. 11.

[0056] The first line in FIG. 11 starts from the center point and goes through the landmark at the bridge of the nose. The remaining lines start at the center point and then are rotated at 6 degrees from the previous line in a counterclockwise manner until a line is drawn through the point at the top of the head which is at a 90 degree angle from the initial line. Once this "fan" is drawn, the user may place points on the outline of the skull where it crossed the equidistant lines of the "fan" using the digitizing software. This method ensures the user to get curves with less human error and more reproducibility. FIG. 12 shows the 16 resulting points placed in the sagittal plane. [0057] In step 810, the user-identified outline points are converted into data coordinates by the digitizing software. The user may choose to use only the first eight points in subsequent analysis since these points more determinatively represent the fetal brow.

[0058] In step 820, an elliptical Fourier analysis is employed using three harmonics (i.e., three sets of coefficients). The determined coefficients are utilized as markers to assess fetal abnormality by conducting a statistical analysis, such as a principal component (PC) analysis.

[0059] In step 830, PC scores are determined based on a PC analysis of the determined Fourier coefficients, and in step 840, the MSD values of the PC scores are calculated. As discussed above, this shape analysis may also be combined with other markers to more completely assess fetal abnormality.

[0060] The PC analysis utilized by this embodiment is a statistical technique used with multivariate data to reduce the number of variables used in further statistical analysis. (It can also be used as an exploratory analysis to see which of the variables are most important). The PC analysis is a standard statistical technique that generates a set of linear combinations of the underlying variables. These linear combinations represent new variables that can be used in other statistical analyses. The first linear combination is the most important variable and so on. Higher numbered principal components can be dropped from further analyses since they tend to represent noise. Once the principle components are determined (e.g., 0.3Xi + 0.2X₂ + O.4X₃...), the PC scores can then be calculated which can be used as the variables in an MSD calculation.

[0061] For providing reference data according to this embodiment of the present invention, TABLE 4 shows the results of evaluating the first three harmonics (i.e., three sets of the four coefficients A, B, C and D) of fetal brow outlines in a study of 32 normal pregnancies. TABLE4 image outcome addnl img al bl cl dl a2 b2 c2 d2 a3 b3 c3 1-4x2 0 0 -1.53 -.0426 -.00609 -.205 .000102 .00658 .0751 -.00803 -.163 -.0141 .00464 -.01 865-16x2 0 0 -1.52 -.0427 .000763 -.204 -.000096 .00607 .071 .000297 -.162 -.014 -.000216 -.01 l-7x 0 0 -1.5 -.0434 .000701 -.208 .00116 .00865 .0756 -.00421 -.161 -.0123 .0103 -.01 1-27x2 0 0 -1.5 -.0478 -.00868 -.209 .000064 .00832 .0771 -.0112 -.161 -.0163 .00577 -.01 1-5x2 0 0 -1.36 -.059 -.00291 -.233 -.000516 .0105 .0887 -.00506 -.14 -.0194 .00354 -.01 l-9x 0 0 -1.38 -.0487 .0112 -.225 -.000699 .00801 .0785 .00928 -.145 -.0153 -.0000916 -.01 865-1x2 0 0 -1.57 -.0347 .0212 -.202 .00101 .00913 .0805 .0202 -.168 -.00939 -.00341 -.007 l-2x 0 0 -1.48 -.0377 .0133 -.215 .000543 .00961 .085 .0106 -.158 -.0104 .00267 -.005 2-20x2 0 0 -1.67 -.0407 -.0159 -.187 -.0000525 .00626 .0685 -.0166 -.18 -.0141 .00452 -.0 865-10x2 0 0 -1.27 -.0647 .00922 -.246 -.00123 .0109 .0872 .0062 -.13 -.02 .00275 -.01 865-15x2 0 0 -1.45 -.0362 .0204 -.218 -.00224 .00905 .082 .0209 -.153 -.0119 -.00631 -.01 1-12x1 0 0 -1.64 -.0383 -.00745 -.187 .000816 .00495 .0604 -.0124 -.177 -.0124 .0108 -.02 1-29x2 0 0 -1.44 -.0539 -.00597 -.216 .00316 .00857 .0763 -.0134 -.152 -.0145 .0165 -.01 865-18x2 0 0 -1.81 -.0216 .00424 -.173 -.000255 .0042 .065 .00434 -.198 -.00702 -.00122 -.009

_* 865-12x2 0 0 -1.54 -.0313 .015 -.205 -.00311 .00838 .0791 .0182 -.165 -.0119 -.0111 -. tsi 1-6x2 0 0 -1.5 -.0455 -.00627 -.21 -.0002 .00953 .0831 -.00785 -.162 -.0151 .00415 -.004

- 865-6x2 0 0 -1.66 -.0336 -.0104 -.191 -.000402 .00666 .0773 -.0113 -.18 -.0119 .0032 -.004 865-11x2 0 0 -1.39 -.0673 -.0116 -.224 .00189 .0084 .0754 -.0158 -.143 -.0205 .00992 -.02 865-7x2 0 0 -1.36 -.0427 .0272 -.234 -.00137 .0128 .092 .0263 -.143 -.0123 -.00534 -.004 865-9x2 0 0 -1.87 -.0212 .00799 -.165 -.0012 .00491 .0558 .00881 -.204 -.00773 -.0034 -.01 1-30x2 0 0 -1.31 -.0799 -.0141 -.239 .0021 .0138 .0851 -.0225 -.134 -.0235 .0205 -.01 1-13x1 0 0 -1.3 -.0583 .^"014 -.24 -.00241 .00913 .0805 .0123 -.131 -.0191 -.00154 -.0 865-3xx2 0 0 -1.99 -.0176 .0217 -.156 -.00203 .00869 .0563 .0251 -.221 -.00685 -.0134 -.007 865-8x2 0 0 -1.9 -.0272 -.0168 -.164 .00109 .0053 .0601 -.0231 -.209 -.00858 .0175 -.009 865-14x2 0 0 -2.16 -.026 -.0209 -.142 .000559 .00425 .0464 -.0211 -.238 -.00879 .00466 -.01 2-18x2 0 0 -1.98 -.0161 .0138 -.154 -.000513 .00284 .0467 .0112 -.215 -.00484 .00322 -.02 1-28x2 0 0 -1.39 -.0642 -.00215 -.22 .000798 .00732 .0643 -.00749 -.144 -.02 .0106 -.0 2-19x2 0 0 -1.4 -.0598 .00756 -.232 .00114 .016 .101 .00485 -.145 -.0183 .0018 .002 1-lx 0 0 -1.14 -.0995 .0115 -.272 -.000611 .0122 .0868 .0042 -.108 -.0301 .00714 -.02 1-11x2 0 0 -1.19 -.111 -.0167 -.266 .000575 .0157 .0974 -.024 -.116 -.0352 .0161 -.01 l-14x 0 0 -1.62 -.028 .0307 -.201 -.00573 .014 .0889 .0371 -.174 -.0128 -.0219 .002 1-10x2 0 0 -1.18 -.0676 .0359 -.271 -.00495 .0222 .102 .0335 -.12 -.0211 -.00789 -.005

[0062] TABLE 5 shows the resulting PC analysis of the Fourier coefficients.

TABLE 5

PRINCIPAL COMPONENT ANALYSIS

. pea al-d3 if outcome==0 & addnl_img ==0, ineigen(l.O) (obs=32)

(principal components; 3 components retained) Component Eigenvalue Difference Proportion Cumulative 1 5 .96194 1.82595 0.4968 0 4968 2 4 13599 3.09719 0.3447 0 8415 3 1 03880 0.57715 0.0866 0 9281 4 0 46165 0.21530 0.0385 0 9665 5 0 24635 0.14543 0.0205 0 9871 6 0 10092 0.06229 0.0084 0 9955 7 0 03863 0.02910 0.0032 0 9987 8 0 .00953 0.00396 0.0008 0 9995 9 0 00558 0.00520 0.0005 0 9999 10 0 00038 0.00022 0.0000 1 0000 11 0 00016 0.00010 0.0000 1 0000 12 0 00006 0.0000 1 0000

-coring Coefficients Variable 1 2 3 al 0.39500 -0.01100 -0 08986 bl -0.36639 0.18716 0 08292 cl 0.06718 0.44499 -0 25403 dl -0.40589 -0.01047 0 07023 a2 -0.03619 -0.41808 0 20309 b2 0.33650 0.17614 0 25352 c2 0.36181 0.14020 0 32808 d2 0.02593 0.46832 -0 22168 a3 0.39740 -0.02115 -0 11651 b3 -0.36383 0.15894 0 08324 c3 0.06250 -0.46168 0 10331 d3 -0.01183 0.28823 0 78874

Variable Mean Std. Dev. al -1.53125 .2485798 bl -.04715 .0221123 cl .0037642 .0151056 dl .2098125 .0330263 a2 -.000394 .0018714 b2 .0091534 .0040555 c2 .0765344 .014202 d2 .0015418 .0170104 a3 -.1625 .0312441 b3 .0149906 .0066018 c3 .0026395 .0092017 d3 .0135719 .0085003 [0063] In this embodiment, the first 3 principal components are retained and used to calculate the associated PC variables. First a z-score for each coefficient is calculated by subtracting the mean of the coefficient and then dividing the difference by the standard deviation of the coefficient from TABLE 5. Each PC variable is then created by multiplying the scoring coefficient for each (al-d3) by the z-score for each variable and then summing the 12 products, as shown in TABLE 6.

TABLE 6 image outcome addnl img [ PCA1 PCA2 PCA3 1-4x2 0 0 -.4907767 -.8738552 .0987127 65-16x2 0 0 -.6085553 -.2783825 -.4990045 l-7x 0 0 -.2317154 -.874534 .4810387 1-27x2 0 0 .0218282 -.9802006 .569997 1-5x2 0 0 1.670697 -.3829324 .4203361 l-9x 0 0 .6840906 .4666384 -.7679284 865-1x2 0 0 -.6142922 1.508776 .3821437 l-2x 0 0 .0732714 .8884591 .8576227 2-20x2 0 0 -1.432505 -1.382093 .4184196 65-10x2 0 0 2.309402 .2540324 -.5981961 65-15x2 0 0 .2062483 2.133314 -.6064944 1-12x1 0 0 -1.716844 -1.812474 -.44028 1-29x2 0 0 .3513637 -2.44019 .2868603 65-18x2 0 0 -2.942221 .4870823 .2135515 65-12x2 0 0 -.5070165 2.407711 -.391572 1-6x2 0 0 .1698279 -.2595708 1.379145 865-6x2 0 0 -1.33174 -.3922991 1.348731 65-11x2 0 0 1.119487 -2.558559 -.6279961 865-7x2 0 0 1.386343 2.689931 .3561011 865-9x2 0 0 -3.317 .6986394 -.8962799 1-30x2 0 0 2.653671 -3.064767 .526195 1-13x1 0 0 1.737869 .6931306 -1.907204 65-3xx2 0 0 -3.596458 2.816385 -.203151 865-8x2 0 0 -3.22584 -2.18013 1.356439 65-14x2 0 0 -4.802877 -1.925512 .2700403 2-18x2 0 0 -4.344046 .1713885 -1.659267 1-28x2 0 0 .7005095 -2.296043 -2.21848 2-19x2 0 0 2.251043 .7969418 2.307821 1-lx 0 0 4.38609 -.9528349 -1.857011 1-11x2 0 0 5.014206 -2.781211 .8650386 l-14x 0 0 -.0283105 5.296726 .5011879 1-10x2 0 0 4.454249 4.126434 .0334842 [0064] The PC variables are used in an MSD calculation to create an atypicality index, as shown in TABLE 7. The PC variables are independent of each other so the variance/covariance matrix is not needed. A cut-off of MSD> 7.81 ( 95^th percentile of the expected X² with 3 d.o.f.) was used to define outliers.

TABLE 7

Variable I Obs Mean Std - Dev - + PCA1 I 35 -l . l≤e-Ofl S . ^ITOI

PCA3 I 35 E ^ Me-OT 1 . OπElL.

MSD = ( PCAl/5 - m70T ) Λδ+ ( PCA5/δ .0337m ) Λ5+ ( PCA3/l - 0π51(-. ) Λδ

[0065] TABLE 8A shows the coefficients from an elliptical Fourier analysis for 6 affected cases and 8 images that represent an additional image from a patient in the reference set. The MSD is calculated using the means and standard deviations of the coefficients, the PC scoring coefficients and the MSD formula for the 32 unaffected patients, the six affected patients and 8 additional images from patients in the group. The results are shown in TABLE 8B. The 3 outliers were all abnormal (trisomy 21, trisomy 18, and one fetus with multiple congenital anomalies). Two trisomy 21 and one case with an unbalanced translocation were not outliers. The affected cases were l-3x Trisomy 18, 2-21x2 campomelic dysplasia, 2-23x2, 2-23x3, 2-23x4 (same patient) Trisomy 21, 865x2 Trisomy 21, 865-5x2 Trisomy 21, 865-17x2 translocation.

TABLE 8A image outcome addnl ._iimmgg al bl cl dl a2 b2 c2 d2 a3 b3 c3 d 865-llxx2 0 1 -1.8 -.0179 .0173 -.174 -.00083 .00425 .0647 .0179 -.196 -.00566 00494 -.010 865-13xx2 0 1 -1.55 -.0308 .0201 -.202 ^■.00266 .00797 .0725 .0213 -.165 -.0111 00747 -.018 1-12x2 0 1 -1.91 -.0263 -.0153 -.163 000187 .00376 .0617 -.0147 -.209 -.00962 .0013 -.0083 1-14x2 0 1 -1.25 -.053 .0353 -.25 -.00137 .0141 .0898 .0317 -.129 -.0138 00302 -.012 1-14x3 0 1 -1.19 -.0866 .0063 -.26 000359 .0105 .0853 .0000546 -.116 -.0263 00843 -.026 1-12x3 0 1 -L.56 -.0535 -.021 -.204 .00453 .0105 .079 -.0298 -.167 -.0141 .0235 -.0098 2-23x2 1 0 -1.43 -.0371 .0264 -.223 -.00117 .0118 .0906 .0265 -.152 -.0107 00682 -.0027 865-17x2 1 0 -1.34 -.0532 .00953 -.24 -.00186 .0136 .0975 .00848 -.138 -.0172 .0011 -.0034

» 865-5x2 1 0 -1.5 -.0568 -.018 -.208 .00261 .00753 .0721 -.024 -.159 -.0172 .0156 -.018--. l-3x 1 0 -1.52 -.0561 -.0255 -.212 .00157 .0125 .0884 -.0314 -.163 -.0181 .0177 .00024 2-21x2 1 0 -1.23 -.0604 .0336 -.252 .00684 .013 .0829 .0362 -.125 -.0213 .0167 -.023 865-2x2 1 0 -1.3 -.0456 .0409 -.242 -.0086 .0146 .0837 .0455 -.133 -.018 -.022 -.020 2-23x4 1 1 -1.5 -.04 .00436 -.211 -.00322 .00833 .0793 .00699 -.158 -.0156 00813 -.013 2-23x3 1 1 -1.58 -.05 -.0167 -.196 .00368 .00868 .0656 -.0284 -.17 -.0133 .0283 -.018

TABLE 8B image outcome addnl img MSD 1-4x2 0 0 .2344088 865-16x2 0 0 .3205591 l-7x 0 0 .4166765 1-27x2 0 0 .5451415 1-5x2 0 0 .6737114 l-9x 0 0 .6988295 865-1x2 0 0 .754262 l-2x 0 0 .8997956 2-20x2 0 0 .9745739 865-10x2 0 0 1.254639 865-15x2 0 0 1.461579 1-12x1 0 0 1.475262 1-29x2 0 0 1.539608 865-18x2 0 0 1.55325 865-12x2 0 0 1.592335 1-6x2 0 0 1.852124 865-6x2 0 0 2.085814 865-11x2 0 0 2.172602 865-7x2 0 0 2.193894 865-9x2 0 0 2.736778 1-30x2 0 0 3.718682 1-13x1 0 0 4.124299 865-3xx2 0 0 4.127046 865-8x2 0 0 4.665785 865-14x2 0 0 4.835767 2-18x2 0 0 5.822632 1-28x2 0 0 6.094747 2-19x2 0 0 6.130581 1-lx 0 0 6.765957 1-11x2 0 0 6.807669 l-14x 0 0 7.025152 1-10x2 0 0 7.445808 65-llxx2 0 1 2.216359 65-13xx2 0 1 2.848514 1-12x2 0 1 2.850898 1-14x2 0 1 2.998304 1-14x3 0 1 4.574026 1-12x3 0 1 7.325252 2-23x2 1 0 2.310336 865-17x2 1 0 2.346174 865-5x2 1 0 2.474172 l-3x 1 0 10.08229 2-21x2 1 0 12.61865 865-2x2 1 0 15.38419 2-23x4 1 1 .6735099 2-23x3 1 1 4.372908

[0066] In this embodiment of the present invention, only the scoring coefficients, means and standard deviations of the coefficients from TABLE 5 and the standard deviations of the PC variables in TABLE 7 would have to be stored in the computing device for the statistical comparison analysis of a particular patient to be conducted. This would preserve storage resources in the event of reference data based on very large populations.

[0067] Several embodiments of the invention are specifically illustrated and/or described herein. However, it will be appreciated that modifications and variations of the invention are covered by the above teachings and within the purview of the appended claims without departing from the spirit and intended scope of the invention.

Claims

What Is Claimed Is:

1. A computer-implemented method for utilizing shape analysis to assess fetal abnormality, comprising: receiving coordinates of points identifying a shape in a fetal image; determining coefficients of one or more mathematical functions that describe the identified shape; and utilizing the determined coefficients as markers to assess fetal abnormality.

2. The method of claim 1 , wherein the fetal abnormality is a chromosomal abnormality.

3. The method of claim 2, wherein the chromosomal abnormality is Down syndrome.

4. The method of claim 1 , wherein the fetal abnormality is Spina Bifida.

5. The method of claim 1 , wherein the points are placed upon a computer monitor.

6. The method of claim 1 , wherein the points are placed upon a 3D ultrasound image.

7. The method of claim 1 , wherein the points trace an outline around a part of the fetal image to be analyzed.

8. The method of claim 1 , wherein the coefficients are determined by a Fourier analysis.

9. The method of claim 1 , wherein the coefficients are determined by a shape analysis method selected from the group consisting of elliptical Fourier analysis, polynomials, cubic splines, parametric polynomials, parametric cubic splines, bezier curves, Fourier analysis of equally spaced radii and dual axis Fourier analysis.

10. The method of claim 1, wherein the determined coefficients are utilized as markers to assess fetal abnormality in the first trimester.

11. The method of claim 1 , wherein utilizing the determined coefficients as markers comprises conducting a statistical analysis on the determined coefficients.

12. The method of claim 11, wherein the statistical analysis compares the determined coefficients with reference parameters derived from a statistical distribution of determined coefficients in the unaffected population and/or affected population.

13. The method of claim 12, wherein the conducted statistical analysis on the determined coefficients includes at least one of a means calculation, a standard deviation calculation and a correlation calculation.

14. The method of claim 12, wherein the conducted statistical analysis on the determined coefficients includes a principal component analysis.

15. The method of claim 12, wherein the conducted statistical analysis results in an indication of risk of fetal abnormality.

16. The method of claim 12, wherein the conducted statistical analysis results in a likelihood ratio for a fetal abnormality.

17. The method of claim 12, wherein the conducted statistical analysis results in an index value to be considered within range or outside of range for a fetal abnormality.

18. The method of claim 1 , comprising utilizing the determined coefficients as markers in combination with one or more additional markers to assess fetal abnormality.

19. The method of claim 18, wherein the one or more additional markers includes at least one biochemical marker selected from the group consisting of free Beta hCG and PAPP-A, maternal blood alpha-fetoprotein, maternal blood hCG, maternal blood unconjugated estriol, maternal blood dimeric inhibin A, maternal urine total estriol, maternal urine beta core fragment, maternal urine hyperglycosylated hCG and maternal blood hyperglycosylated hCG.

20. The method of claim 18, wherein the one or more additional markers includes at least one ultrasound marker selected from the group consisting of nuchal translucency, Ductus Venosus, absent or hypoplastic nasal bone, nuchal edema, short femur, hyperechogenic bowel and echogenic foci in the heart.

21. The method of claim 1, further comprising: adjusting the received coordinates to align the shape according to a particular axis before the coefficients are determined.

22. The method of claim 1, further comprising: adjusting the received coordinates before the coefficients are determined by at least one of translating the coordinates, rotating the coordinates and scaling the coordinates.

23. The method of claim 22, wherein utilizing the determined coefficients as markers comprises conducting a statistical analysis on the determined coefficients.

24. The method of claim 23, wherein the statistical analysis compares the determined coefficients with reference parameters derived from a statistical distribution of determined coefficients in the unaffected population and/or affected population.

25. An apparatus for utilizing shape analysis to assess fetal abnormality, comprising: a processor; and a memory storing instructions adapted to be executed by said processor to: receive coordinates of points identifying a shape in a fetal image; determine coefficients of one or more mathematical functions that describe the identified shape; and utilize the determined coefficients as markers to assess fetal abnormality.

26. A system for utilizing shape analysis to assess fetal abnormality, comprising: a means for receiving coordinates of points identifying a shape in a fetal image; a means for determining coefficients of one or more mathematical functions that describe the identified shape; and a means for utilizing the determined coefficients as markers to assess fetal abnormality.