IP Library Granted Patent US 10,317,396
Granted Patent B2
US 10,317,396 · App. 14/116,138 · Granted Jun 11, 2019

Peripheral diagnostic methods for screening Alzheimer's disease using beta amyloid and intercellular communication

Inventors: Florin V. Chirila (Morgantown, WV); Tapan Kumar Khan (Morgantown, WV); Daniel L. Alkon (Bethesda, MD)
Assignee: West Virginia University
G01N33/5091G01N2800/2821
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Quick Facts
Patent No.
US 10,317,396
App. No.
14/116,138
Granted
Jun 11, 2019
Kind
B2
Abstract

The present disclosure relates to a peripheral diagnostic method for screening Alzheimer's disease in patients based on quantitatively measured complexity of skin-sampled fibroblast networks.

Claims (13)

1. A method of diagnosing Alzheimer's disease in a human subject, the method comprising:

(a) treating a first sample of fibroblast skin cells from the subject with an amyloid beta peptide (Aβ);

(b) separately culturing in a culture medium on an extracellular matrix (i) the resulting Aβ-treated first sample, and (ii) a second sample of fibroblast skin cells from the subject that have not been treated with Aβ, wherein the extracellular matrix comprises laminin, collagen, heparin sulfate proteoglycans, entactin/nidogen, or any combination thereof;

(c) obtaining at least one image of each of the resulting cultured first and second samples; and

(d) morphologically analyzing the images of the first and second samples using at least one method selected from the group consisting of determining area per number of aggregates, determining fractal dimension, and determining lacunarity,

wherein the subject has Alzheimer's disease if there is no distinguishable difference between the results of the morphologic analyses of the first and second samples.

2. The method of claim 1 , wherein step (d) comprises morphologically analyzing the images of the first and second samples by determining the area per number of aggregates.

3. The method of claim 1 , wherein step (d) comprises morphologically analyzing the images of the first and second samples by determining fractal dimension.

4. The method of claim 1 , wherein step (d) comprises morphologically analyzing the images of the first and second samples by determining lacunarity.

5. The method of claim 1 , wherein step (d) comprises morphologically analyzing the images of the first and second samples using at least two methods selected from the group consisting of determining area per number of aggregates, determining fractal dimension, and determining lacunarity.

6. The method of claim 1 , wherein step (d) comprises morphologically analyzing the images of the first and second samples by determining area per number of aggregates, determining fractal dimension, and determining lacunarity.

7. The method of claim 1 , wherein the culture medium comprises a growth factor.

8. The method of claim 1 , wherein step (b) comprises culturing the first and second samples for a period of from about 24 hours to about 48 hours.

Assignments (3)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 15, 2021
From: BLANCHETTE ROCKEFELLER NEUROSCIENSES INSTITUTE, INC.
To: WEST VIRGINIA UNIVERSITY
Reel/Frame 055304/0423 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 15, 2018
From: BLANCHETTE ROCKEFELLER NEUROSCIENSES INSTITUTE, INC.
To: WEST VIRGINIA UNIVERSITY
Reel/Frame 045071/0265 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Feb 4, 2014
From: CHIRILA, FLORIN V.; KHAN, TAPAN KUMAR; ALKON, DANIEL L.
To: BLANCHETTE ROCKEFELLER NEUROSCIENCES INSTITUTE
Reel/Frame 032135/0356 →
Continuity (2)
Provisional Application 61485256 · May 12, 2011
Related Publication 20140248648A1 · Sep 4, 2014
Cited By (1)
US 12,405,268