Evaluation of New Markers to Assess Kidney Function

General description: The overall study procedure requires assessment of eligibility and
safety for inclusion in the study through a) the screening questionnaire; b) medical
history, which will be derived from subject and combined with a review of his/her medical
record after signing the consent; and c) interview, physical examination and laboratory
tests from screening visit if required.

Screening questionnaire: All subjects, whether they are interviewed during a clinic visit or
call in response to fliers, will be given the pre-screening questionnaire. This will be
given to people who voluntarily express interest in the study. Participants who do not
disclose any conditions that would exclude them from participating will be invited to a
health screening visit.

Health screening visit: The purpose of the pre-study health screening is to perform a more
detailed assessment than is provided in the screening questionnaire to determine if
potential subjects are eligible to participate in the study. A member of the research team
will first read the consent form with the subject, describe the health screening and study
visits, and answer any questions that the subject has regarding the nature of the study
and/or study procedures. The screening visit will consist of the following:

- Reading and signing the study consent. The subject will be given a copy of the consent.

- Collection of information on demographics and current and past health history.

- Ascertain participants medical history through participant interview and a review of
his/her medical record

- A physical exam, which will include measuring and recording vital signs (temperature,
blood pressure, heart rate, breathing rate), height, weight (if not documented in
medical record in past 3 months).

- Collection of a blood sample for laboratory testing, if required.

- Pre-menopausal women of child-bearing potential we will undergo a serum pregnancy test,
using a small amount of blood from the sample collected above.

- Ascertainment of current and recent past medications.

If the subject is a patient at Tufts Medical Center, a research team member may access the
potential participant's medical record after the subject has signed the consent form to
further screen for potential exclusion criteria, ascertain laboratory test results that are
necessary for determining eligibility, and confirm the medical history provided by the
potential participant and medication list. If the participant is not a patient at Tufts
Medical Center, then the research team member will obtain permission to obtain the
participant's medical record from his/her physician.

For non-pregnant women of childbearing age (pre-menopausal) who are sexually active, use of
an acceptable birth control method will be required for participation. They will be
requested to sign a statement of compliance prior to participating in the study stating that
they are employing one of the below-listed forms of contraception between the screening and
study visits.

- condoms with spermicide

- diaphragm with spermicide

- injectable contraceptives (Depoprovera)

- transdermal contraceptives (Ortho-Evra and Nuvaring)

- intrauterine device (IUD)

- permanent sterilization (i.e. tubal ligation, vasectomy, essure)

- abstinence from sexual activity

- hysterectomy

- oral contraceptives

If the study visit occurs 3 weeks or more after the health screening, the female subjects
will undergo a second, urine-based pregnancy test on the morning of the study visit. In
addition, healthy women will be required to continue employing an accepted birth control
method and not attempt to become pregnant for at least one month following completion of the
final study visit. Women with CKD will be requested to continue employing an accepted birth
control method for at least two months following completion of the final study visit.

If a potential subject is taking trimethoprim containing medications or cimetidine, the
study physician will discuss with the attending physician whether it is safe for the person
to stop these medications for one week prior to the study. If not, then the person will be
excluded from participation. If a potential subject is taking non-steroidal
anti-inflammatory agents or medications that block the renin-angiotensin system, the study
physician will discuss with the potential participant and the attending physician whether
maintenance of stable dose of these medications is possible. If a change in the subject's
medication regimen is required immediately prior to the study visit, the subject will be
rescheduled for a later date.

Eligibility will be determined by the principal investigator or other physician
co-investigators based on the medical history obtained from the participant, and their
medical records and the results of the laboratory test that were included in the medical
record or obtained during the health screening visit). Eligible subjects will be contacted
to see if they remain interested in participating in the study. A study visit date will then
be scheduled. All subjects will receive a stipend for the health screening.

Screening prior to at-home dosing of KI The main concern when subjects are asked to take KI
on the morning prior to the study visit is the possibility that the patient is allergic to
iodine and will thus have a reaction to the KI in the unobserved environment at home. The
research team will identify subjects with known allergies in advance by screening the
subjects' medical records (if available) and through the health-history interview conducted
via telephone by the study coordinator. Subjects who are not sure if they have an iodine
allergy because they have not eaten shellfish or have never received contrast dye and,
therefore, cannot say with sureness that they are not allergic will be excluded from
participation.

Supplying the KI tablet to the subject prior to the study visit The KI tablet will be
supplied to the study participant from 2 days to approximately 2 weeks prior to the study
visit. The tablet and the instruction sheet will be mailed to the subject or supplied
during the health screening visit at the Clinical and Translational Research Center (CTRC);
however, if the subject is a patient at the KBPC and has an appointment with their physician
within approximately 2 weeks of the study visit, a member of the research team may provide
the KI tablet and instruction sheet at the clinic visit. Otherwise, all subjects will be
asked to provide their mailing address during the phone interview to ensure that the tablet
is sent to the correct address.

Per the IosatTM package insert, the tablet should be stored in a dry place at room
temperature and out of direct sunlight. Subjects will also be instructed to keep the tablet
in a place where someone else cannot accidentally consume it (i.e., a child, spouse, etc).
These storage techniques will be conveyed to the subject in the included instructions. The
tablets are available individually wrapped in foil blister packs to protect them from the
effects of UV light, which can damage the KI. To further decrease the likelihood of damage
to the tablet due to improper storage or handling, all tablets will be packaged in a
secondary pill bottle with child-safe caps by the Tufts Medical Center pharmacy.

Subjects will be instructed to take the KI tablet on the morning of the day before the study
visit between 6:00 AM and 10:00 AM. Instructions with the tablet will include:

- An additional warning, in bold typeface, instructing the subject to not take the tablet
if they even suspect that they might have an iodine allergy.

- Proper administration. Per the package insert, the tablet can be consumed with water,
low fat milk, low fat chocolate milk, or orange juice.

- Symptoms of an allergic reaction and steps to take in the event that the subject
experiences a reaction (per the IosatTM package insert).

In addition to listing the emergency phone number '911' on the package, the contact numbers
of Dr. Stevens (PI) and the study coordinator will be included in the event that the subject
has any questions or concerns. On the morning of the study visit, the research staff will
ask the subject to give verbal confirmation that they have taken the KI dose and record the
approximate time at which the subject took it.

Subjects taking medications that interfere with creatinine, who can safely cease taking the
medication, as described in the exclusion criteria, will be reminded to stop these
medications 1 week prior to the study visit at this time. In addition, a member of the
research team will contact the subject 2-3 days prior to the visit date to ensure that the
subject is clear on all directions and has no questions or concerns. During this call, the
subject will be reminded to take the KI tablet at the specified time. When possible, the
study personnel will also call the subject at approximately 9:00 AM on the morning of the
day before the study visit to ensure that the subject took the tablet.

Non-diabetic subjects will be requested to fast overnight and to avoid changes in
non-steroidal anti-inflammatory agents or medications that block the renin-angiotensin
system. Subjects with diabetes will be asked to eat a light breakfast the morning of the
study visit. Subjects will be asked to maintain adequate oral hydration and to ingest two
to three glasses of non-caffeinated beverages prior to arrival to facilitate the collection
of a baseline urine collection and an additional two to five glasses upon arrival at the
CTRC.

Upon arrival on the morning of the study visit, the nursing staff will ask the study subject
to provide verbal confirmation that they took the KI pill and will document and record on
the study flow sheet the approximate time that the subject took the tablet. If the pill
was not taken within the allowed time range of 6:00 AM to 10:00 AM, the subject will not be
able to participate in the study visit. A research team member will obtain informed consent
from the participant and a copy of the consent will be given to the subject. The nursing
staff will measure and record the subject's height, weight, blood pressure, temperature,
pulse rate, respiration rate; confirm that the subject has not experienced any changes in
physical/psychological health since the screening; and collect a baseline urine sample. As
outlined above, if three weeks or more has elapsed since the health screening, women of
childbearing age will be administered a urine pregnancy test, prior to the insertion of the
IV lines, using an aliquot of the baseline urine sample. The test kits used will be
purchased from a local pharmacy by the site principal investigator or her delegate and
provided to the CTRC staff. Nursing will interpret the results of the test and the
principal investigator will verify a negative result prior to initiation of the GFR
measurement. If the test yields a positive result, the study visit will be immediately
terminated.

Subjects with diabetes will be requested to bring their own testing devices. The CTRC has
their own testing devices if the subject forgets to bring his or her own. Subjects will be
asked to check their blood sugar upon arrival at the CTRC. If they are unable to perform
the measurement, the nurses will do so. The study physician will be informed of low (less
100 mg/dl) or high (greater than 200) blood sugars. Otherwise, the participant will follow
their normal routine for checking blood sugar. For example, if they check after each meal,
then they will be asked to do so. If they only check once a day, then they will not be
asked to check again. Participants will be fed breakfast and lunch and therefore there is
no concern for hypoglycemia over the course of the study visit.

A saline lock and intravenous line will be inserted at two different sites and two drops of
saturated solution of potassium iodide (SSKI) will be administered at least 30 minutes and
no more than six hours prior to the administration of 125I-iothalamate to prevent uptake by
the thyroid. Baseline laboratory tests will include serum creatinine, cystatin C, blood
urea nitrogen (BUN), C-reactive protein (CRP), electrolytes and albumin.

The markers to be administered will be prepared by a pharmacist at the Tufts Medical Center
Pharmacy. The pharmacist will prepare the markers such that they can be administered
directly by the nurse. That is, the correct dose will be placed in a syringe that can be
administered directly to the participant. A member of the research team will obtain the
drugs and bring them to the CTRC for administration by the nurse.

After collection of the baseline blood sample and a separate sample for tissue banking
(optional), 50 mg Inulin/kg will be administered by bolus IV, followed by a sustaining dose
of 18.8 mg/square area/min. Approximately 30 minutes later, 35 µCuries of 125I-iothalamate
will be injected subcutaneously to allow for a 60 minute equilibrium time. After a further
30 minutes, 5 ml of Iohexol (Omnipaque 300, 300mg/mL of organic iodine) and 10 uL/kg of
Gd-DTPA will be administered via a bolus IV injection through the same IV line as inulin.
Iohexol will be given first over 1 minute, followed by saline flush of the intravenous line,
followed by Gd-DTPA over one minute. Subjects with an eGFR < 30 mL/min/1.73 m2, as
determined from their medical record or the serum creatinine measurement from the health
screening, will not receive Gd-DTPA. The syringes used to administer the iohexol and
Gd-DTPA will be weighed to the nearest tenth gram on the same scale before and after
injection. Nurses at the CTRC will monitor the participant at the time of the
administration and throughout the study.

Blood samples for plasma clearance measurements will be obtained from the second IV line,
which will also remain in place throughout the course of the study visit. To maintain the
patency of the IV access for the purpose of the serial blood collections, normal saline will
be administered at a rate of approximately 20-30 c.c. per hour from a 500 c.c. bag of normal
saline.

The administration of inulin will be considered time 0. Following the iohexol
administration, blood samples will be taken at approximately 10, 30, 120, and 240 minutes
from the second intravenous line. For participants with estimated GFR less than 45 ml/min
per 1.73 m2, as determined from the screening visit or the subject's medical record, a
sample will be drawn at 360 minutes. The exact time of the sample will be recorded.

Following the 180-minute timed void, all voluntary voids will be collected but the volume of
oral fluid intake will match the urine output (i.e. water loading to stop). The nursing
staff will continue to monitor fluid balance. For all urine samples, a bladder scan will be
conducted immediately before and immediately after the subject urinates to assess the
completeness of bladder emptying. Following the equilibration period for inulin (90
minutes) and 125I-iothalamate (60 minutes), four timed urinary clearance periods of at least
30 minutes will begin. Blood samples for urinary clearance measurements will be taken
following each bladder emptying. Blood samples for plasma clearance measurements will be
taken at approximately 10, 30, 120, 150, and 240 min. For patients with estimated GFR <30
mL/min per 1.73 m2, an additional blood sample will be collected at 360 min. Subjects are
free to move around during the GFR test.

Participants will be fed a breakfast consisting of a standardized protein content following
collection of the 30 minute blood sample and a lunch of similar protein content. Subjects
with diabetes will be given a meal that is consistent with their treatment regimen and asked
to administer their medications and check their blood sugar levels during the course of the
study visit as they would normally do, in the manner prescribed by their treating physician.

At the conclusion of the study, both intravenous lines will be removed. Subjects will
remain at the CTRC for at least 30 minutes following removal of the IV lines. During that
time, nursing staff will re-measure and record the subject's vital signs (height, weight,
blood pressure, temperature, pulse rate, respiration rate). Upon successful completion of a
study visit, subjects will receive a stipend

Subjects will undergo repeat study visits with a target time of one month between visits.
The second study visit will proceed in an identical manner with the exception that urinary
clearance of inulin will only be measured in a subset of the study participants during the
second visit.