Method of treating proteinuria in pregnancy
A therapeutic agent for the treatment of toxemia, preeclampsia and eclampsia and a method for preparing the therapeutic agent are disclosed. The therapeutic agent is a stable pharmaceutical preparation containing, but not limited to, digestive/pancreatic enzymes. The therapeutic agent may be manufactured by a variety of encapsulation technologies. Delivery of the therapeutic agent may be made orally, through injection, by adherence of a medicated patch or by other methods. Further, a method of using the presence of chymotrypsin in the maternal GI tract as a biomarker, to determine the likelihood of developing preeclampsia, a pregnancy induced hypertension, and eclampsia/toxemia is disclosed.
1. A method for treating an individual exhibiting pregnancy-related elevated proteinuria, the method comprising administering to the individual a therapeutically effective amount of a pharmaceutical preparation comprising digestive enzymes, wherein the digestive enzymes comprise an amylase, a lipase, a protease, or a combination thereof, whereby pregnancy-related elevated proteinuria is treated.
2. The method of claim 1 , wherein the digestive enzymes comprise the protease, wherein the protease comprises chymotrypsin or trypsin.
3. The method of claim 1 , wherein the digestive enzymes comprise an amylase, a lipase, and a protease.
4. The method of claim 3 , wherein the digestive enzymes are provided as pancreatin.
5. The method of claim 1 , wherein the digestive enzymes are animal enzymes, plant enzymes, synthetic enzymes, or a combination thereof.
6. The method of claim 1 , wherein the pharmaceutical preparation is administered orally.
7. The method of claim 1 , wherein the pharmaceutical preparation is a dosage formulation selected from the group consisting of a pill, a tablet, a capsule, a microcapsule, a mini-capsule, a time released capsule, a mini-tab, a sprinkle, and a combination thereof.
8. The method of claim 1 , wherein the digestive enzymes comprise the amylase, and wherein an amount of the amylase in the pharmaceutical preparation ranges from about 10,000 to about 60,000 U.S.P. units/dose.
9. The method of claim 1 , wherein the digestive enzymes comprise the protease, and wherein an amount of the protease in the pharmaceutical preparation ranges from about 10,000 to about 70,000 U.S.P. units/dose.
10. The method of claim 1 , wherein the digestive enzymes comprise the lipase, and wherein an amount of the lipase in the pharmaceutical preparation ranges from about 4,000 to about 30,000 U.S.P. units/dose.
11. The method of claim 4 , wherein an amount of the pancreatin in the pharmaceutical preparation ranges from about 2,000 to about 6,000 U.S.P. units/dose.
12. The method of claim 2 , wherein the protease comprises chymotrypsin, and wherein an amount of the chymotrypsin in the pharmaceutical preparation ranges from about 2 to about 5 mg/dose.
13. The method of claim 2 , wherein the protease comprises trypsin, and wherein an amount of the trypsin in the pharmaceutical preparation ranges from about 60 to about 100 mg/dose.
14. The method of claim 1 , wherein the digestive enzymes comprise the protease, the amylase and the lipase.