Automated assessment of sperm samples
20190293545 ยท 2019-09-26
Inventors
- Assaf Ben Shoshan (Kibbutz Barkai, IL)
- Vitaly Strongin (Nesher, IL)
- Lior Shriki (Haifa, IL)
- Marcia Deutsch (Los Angeles, CA, US)
- Benihu Cohen (Nesher, IL)
Cpc classification
C12M41/36
CHEMISTRY; METALLURGY
H04N23/55
ELECTRICITY
International classification
C12M3/00
CHEMISTRY; METALLURGY
Abstract
A method for testing includes capturing a sequence of video images of a sample comprising semen. The sequence of video images is analyzed by a processor so as to compute and output a motile sperm concentration of the sample.
Claims
1. A method for testing, comprising: capturing a sequence of video images of a sample comprising semen; and analyzing the sequence of video images by a processor so as to compute and output a motile sperm concentration of the sample.
2. The method according to claim 1, wherein the sequence of video images is captured by a camera module in a Smartphone, and wherein analyzing the sequence of video images comprises processing the captured video images using application software running on the processor in the Smartphone.
3. The method according to claim 2, wherein analyzing the sequence of video images comprises presenting an assessment of the sample on a display screen of the Smartphone.
4. The method according to claim 1, wherein analyzing the sequence of video images comprises selecting a region of interest (ROI) within the images, and detecting sperm cells within the ROI.
5. The method according to claim 4, wherein selecting the ROI comprises computing gradients of gray-level change at pixels in the images, and choosing a region of maximal gradient values as the ROI.
6. The method according to claim 5, wherein choosing the region comprises identifying all pixels in the captured video images that had a gradient of at least 50% of a maximal gradient at least once in the sequence, and centering the ROI at a center of gravity of the identified pixels.
7. The method according to claim 1, wherein analyzing the sequence of video images comprises identifying respective locations of blobs of pixels in a first image in the sequence as sperm cells, and detecting movement of the sperm cells by comparing the respective locations of the blobs in a second image in the sequence, subsequent to the first image, to the respective locations in the first image.
8. The method according to claim 7, wherein detecting the movement comprises counting a number of the blobs that have moved in each of the images in the sequence relative to a preceding image, and computing the motile sperm concentration as a function of the number of the blobs that have moved over all of the images in the sequence.
9. The method according to claim 8, wherein the motile sperm concentration is equal to a median of the number of the blobs that have moved in each of the images in the sequence, scaled by a volume of the semen in a region of the sample analyzed by the processor.
10. Testing apparatus, comprising: a camera module, which is configured to capture a sequence of video images of a sample comprising semen; and a processor, which is configured to analyze the sequence of video images so as to compute and output a motile sperm concentration of the sample.
11. The apparatus according to claim 10, comprising a Smartphone, which comprises the camera module, wherein the sequence of video images is processed using application software running on the processor in the Smartphone.
12. The apparatus according to claim 11, wherein the Smartphone comprises a display screen, and the processor is configured to present an assessment of the sample on the display screen.
13. The apparatus according to claim 10, wherein the processor is configured to select a region of interest (ROI) within the images, and to detect sperm cells within the ROI.
14. The apparatus according to claim 13, wherein the processor is configured to select the ROI by computing gradients of gray-level change at pixels in the images, and choosing a region of maximal gradient values as the ROI.
15. The apparatus according to claim 14, wherein the processor is configured to identify all pixels in the captured video images that had a gradient of at least 50% of a maximal gradient at least once in the sequence, and to center the ROI at a center of gravity of the identified pixels.
16. The apparatus according to claim 10, wherein the processor is configured to identify respective locations of blobs of pixels in a first image in the sequence as sperm cells, and to detect movement of the sperm cells by comparing the respective locations of the blobs in a second image in the sequence, subsequent to the first image, to the respective locations in the first image.
17. The apparatus according to claim 16, wherein the processor is configured to count a number of the blobs that have moved in each of the images in the sequence relative to a preceding image, and to compute the motile sperm concentration as a function of the number of the blobs that have moved over all of the images in the sequence.
18. The apparatus according to claim 17, wherein the motile sperm concentration is equal to a median of the number of the blobs that have moved in each of the images in the sequence, scaled by a volume of the semen in a region of the sample analyzed by the processor.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
[0022]
[0023]
[0024]
[0025]
[0026]
[0027]
[0028]
DETAILED DESCRIPTION OF EMBODIMENTS
[0029] In view of the high incidence of male fertility problems, sperm testing should be performed at an early stage in most cases in which a couple has difficulty in conceiving. Such testing requires, however, that the man either ejaculate a semen sample at the laboratory, which can be difficult and embarrassing, or rush the sample from his home to the laboratory, with the risk that the sperm may die in transit.
[0030] Embodiments of the present invention that are described herein address this problem by providing an automated sperm testing apparatus that can be operated conveniently and reliably in the privacy of one's home. The apparatus comprises an optical adapter, which fits onto an existing mobile computing device, such as a smart phone, and converts the device into a video microscope. The apparatus takes advantage of the existing resources of the mobile computing device, including camera (and its internal optics), illumination source, processor and display screen, and thus provides a low-cost solution that enables the user to test his semen at home at any stage, even before going to see a doctor.
[0031] In the disclosed embodiments, a clip-on optical adapter device comprises a case, which fits over at least the part of a mobile computing device, such as a Smartphone, where the light source and camera module are located. The case of the adapter device has a receptacle for a sample, such as a semen sample or other liquid sample, contained in a suitable sample holder, such as a transparent slide. When inserted into this receptacle, the sample is positioned within the field of view and focal range of the camera module, in proximity to the face of the mobile computing device where the entrance and exit apertures are located. In the disclosed embodiments, the desired focus and magnification of the sample are achieved with the assistance of internal optics in the adapter device, as described below.
[0032] To capture a suitable electronic image of the sample for analysis, it is desirable that the sample be back-illuminated. In all common Smartphones, as well as other, similar devices, however, the exit aperture of the light source and the entrance aperture of the camera module are located on the same face of the device, not facing one another as required for back-illumination. A separate light source could be provided for this purpose, but this approach increases the size and cost of the adapter and also requires it to provide power to the light source.
[0033] Instead, the disclosed embodiments of the present invention exploit the existing light source in the mobile computing device itself, using illumination optics in the case of the adapter device to receive and turn the beam emitted by the light source so as to back-illuminate the sample. Thus, the camera module (with the assistance of the optics in the adapter device) captures back-illuminated images of the sample, which are processed by the mobile computing device in order to compute and output an assessment of the sample. Typically, the adapter device also comprises a lens mounted in the case in a location between the sample and the entrance aperture of the camera module, which magnifies the images captured by the camera module.
[0034] A clip-on adapter of this sort, which takes advantage of the light source and camera module in a Smartphone or other mobile computing device, can be useful in various methods for automated testing. Thus, embodiments of the present invention also provide a method in which a sample is inserted into a transparent sample holder, the transparent sample holder with the sample is inserted into an optical adapter, and the optical adapter is fitted over a mobile computing device. (Alternatively, the adapter may first be fitted over the mobile computing device, after which the sample holder is inserted into the adapter.) The camera module captures one or more electronic images of the sample, which is illuminated by the beam emitted by the light source in the Smartphone. An application program running on the mobile computing device actuates the light source and camera module, and causes the processor in the device to analyze the images so as to compute and output an assessment of the sample.
[0035] In a disclosed embodiment, the sample comprises semen, as noted above, and the processor assesses the motility of the spermatozoa in the semen. Advantageously, the processor may compute and output an assessment of a motility characteristic of the spermatozoa, such as the motile sperm concentration(MSC, also referred to in some publications as motile sperm count), which is the product of the sperm concentration multiplied by the percent motility of the sperm (divided by 100). Because MSC integrates these two parameters, it gives a better screening indication for fertility problems than either sperm concentration or motility alone.
[0036]
[0037] The processor (not shown) in Smartphone 24 analyzes images captured by the camera module in order to make an assessment of the sample, and outputs the assessment to a display screen 28. The images captured by the camera module are referred to interchangeably herein as electronic images or video images. For the sake of clarity in the description that follows, the term first face in reference to Smartphone 24 refers to the side of the Smartphone on which display screen 28 is located, while the reverse face, facing into the page in
[0038] Although the present embodiment and the figures in this patent application refer to a particular type of Smartphone, the features of this embodiment may be adapted, mutatis mutandis, to work with Smartphones of other types and designs, as well as with other mobile devices having suitable imaging and computing capabilities, such as tablet and laptop computers. All such alternative implementations are considered to be within the scope of the present invention.
[0039]
[0040] Test slide 26 fits into a receptacle 31, which is shaped as a slot in the case of adapter device 22. Alternatively, receptacle 31 may be configured to receive samples and sample holders, made of appropriate transparent materials, of any suitable size and shape.
[0041]
[0042] A ball lens 40, held between a pair of lens holders 42, is mounted in case 30 in a location between the sample held by slide 26 and the entrance aperture of camera module 27. Springs 32 hold slide 26 at a fixed, accurate distance from lens 40. Lens 40 serves to magnify the images of the sample that are captured by the camera module. Lens holders 42 are shaped as wings, extending out to either side of ball lens 40, without occluding the small optical aperture of the ball lens. Alternatively, the ball lens and wings may be molded together out of a single piece of optical plastic or glass. Typically, ball lens 40 is about 2 mm in diameter, although larger or smaller elements may alternatively be used. Further alternatively, ball lens 40 may be replaced by other magnifying optics, such as a miniature simple lens (either spherical or aspheric) or even a compound lens, depending on the desired magnification and other optical requirements.
[0043]
[0044] Following reflection from mirrors 36 and 38, beam 54 back-illuminates a sample 56 held by slide 26. Ball lens 40 creates a magnified image of the sample on the image sensor plane in camera module 27. Smartphone 24 captures and processes the image as described further hereinbelow.
[0045]
[0046] Typically, cover slip 60 is glued onto slide 26. For this purpose, the slide may be molded to define one or more grooves 64, into which an adhesive is inserted before applying the cover slip to the slide. Once cured (by ultraviolet illumination, for example), the adhesive fixes the cover slip to the slide. To prevent overflow of the adhesive from grooves 64 into the sample chamber, one or more additional grooves 66 may be molded in locations between grooves 64 and depression 58. Alternatively, as noted above, the cover slip may be placed on top of the shaped double-sided adhesive that creates depression 58.
[0047] The design of slide 26 and its dimensions are shown and described here by way of example. In alternative embodiments (not shown in the figures), adapter device 22 may accommodate sample holders of other dimensions and designs.
[0048]
[0049] The user begins the procedure with the preliminary step of installing testing application software in Smartphone 24. The software may be downloaded from a Web site or app store, as is known in the art. It includes a user interface, which guides the user in carrying out the test and receives user input as required, as well as drive components to operate camera module 27, light source 29, and display screen 28 as needed. The application software also includes image processing and analysis components, which analyze the images of the sample that are captured by the camera module and compute the test results.
[0050] Once the application has been installed, the user collects and prepares a semen sample, at a sample preparation step 70. For this purpose, the user may mix the semen with a liquefying agent, such as chymotrypsin, to reduce its viscosity. The user inserts a small amount of the sample into loading area 62, at a sample transfer step 72, whereupon the sample is drawn into the chamber defined by depression 58, at a sample transfer step 72. For example, the user may draw a small amount of the liquefied semen into a capillary tube, and then place the end of the capillary tube in the loading area so that the semen fills the sample chamber.
[0051] The user inserts slide 26 with the sample into receptacle 42 of optical adapter device 22, so that the slide is held firmly in place, at a slide insertion step 74. The user then clips device 22 over the end of Smartphone 24, as shown in the preceding figures, at a device fitting step 76. Alternatively, the order of steps 74 and 76 may be reversed. In either case, the sample is now ready for imaging.
[0052] The user indicates to the testing application on Smartphone 24 that the sample is in position by pressing a control presented on screen 28, at a measurement actuation step 78. This step causes the application to turn on light source 29 and operate camera module 27 to capture one or more images of the sample. The image processing component of the application causes the processor in Smartphone 24 to process the electronic images in the mobile computing device so as to compute and output an assessment of the sample. The processing performed at this step is described in greater detail hereinbelow with reference to
[0053] Upon completion of processing the captured images, Smartphone 24 outputs the results, typically via display screen 28, at a data output step 80. The measurement results, such as the MSC, may be output as a numerical value. Alternatively or additionally, it may be preferable simply to report the range in which the result falls, so as to indicate to the user viewing the display whether or not there is cause for concern. For example, in the case of MSC, the result may be reported to the user as normal if it is no less than 6 million/ml, or as low if the result is below 6 million/ml. In the latter case, the user may be prompted to run the test again, and to see a doctor if the MSC is again found to be low.
[0054]
[0055] Within the stable video image, the Smartphone processor chooses the area that presents the clearest view of the sperm cells for analysis, at a region of interest (ROI) selection step 92. The inventors have found that an ROI of 700?700 pixels is convenient for analysis and gives reliable results. The processor attempts to select an ROI with good focal quality and contrast. For this purpose, for example, the processor may seek the maximal gradient of gray-level change at every pixel over time (over all processed image frames)and determine the maximum gradient over all the pixels. The processor identifies all pixels in the captured video stream that had a gradient of at least 50% of the maximal gradient at least once in the image sequence. The ROI is then chosen to be the area of 700?700 pixels that is centered at the center of gravity of all of the identified high-gradient pixels.
[0056] The application program next causes the Smartphone processor to detect pixels within the ROI that may belong to sperm cells, at a pixel detection step 94. Pixels belonging to sperm cells are defined as dark pixels surrounded by an area of brighter pixels. These dark pixels are detected by first defining the brightness of the background environment and of the areas that are suspected to contain sperm cells, and then this brightness criterion to sort the pixels in the images.
[0057] The processor aggregates the potential sperm pixels that it has detected into blobs, at a pixel aggregation step 96. This step may use image processing methods that are known in the art for identification of connected components. Typically, groups of adjoining sperm pixels are labeled to identify them as blobs, and the blobs are filtered by size, so that only blobs of a certain minimum size are classified as sperm cells. In each image, the processor marks the center of each blob that satisfies these criteria.
[0058] The processor counts the number of moving sperm in each image frame by comparing the location of each blob relative to its location in the preceding frame, at a movement counting step 98. If a given blob is found to have moved, the sperm movement count is incremented by one. The total number of blobs that have moved thus gives the movement count for each frame. The processor then computes the motile sperm count based on the median count of moving blobs per image frame, at a motility counting step 100. This value is scaled by the volume of semen contained in the ROI in order to give the actual MSC value, as defined above. The result is output to screen 28 at step 80 (
[0059] Alternatively, other methods of image processing that are known in the art may be applied in analyzing the sequence of images of the sample captured by camera module 27. These alternative methods, as well as the method described above, may be applied not only in computing MSC, but also in extracting measures of sperm count and/or motility alone, as well as analyzing other qualities of semen and other sorts of samples.
[0060] Although the embodiments described above refer specifically to sperm testing, and more particularly to assessment of MSC, the principles of the present invention may similarly be applied in testing samples of other sorts, using the capabilities of existing mobile computing devices. It will thus be appreciated that the embodiments described above are cited by way of example, and that the present invention is not limited to what has been particularly shown and described hereinabove. Rather, the scope of the present invention includes both combinations and sub-combinations of the various features described hereinabove, as well as variations and modifications thereof which would occur to persons skilled in the art upon reading the foregoing description and which are not disclosed in the prior art.