Mechanisms Accounting for Unexplained Anemia in the Elderly
| Status: | Completed |
|---|---|
| Conditions: | Anemia |
| Therapuetic Areas: | Hematology |
| Healthy: | No |
| Age Range: | 18 - Any |
| Updated: | 12/26/2018 |
| Start Date: | March 29, 2012 |
| End Date: | July 30, 2015 |
Assessing Mechanisms Accounting for Unexplained Anemia in the Elderly
Background:
- Anemia occurs commonly and is associated with poor outcomes in the elderly. In about a
third of anemia cases in older people (over age 65), the cause of anemia is unexplained.
Anemia in older adults may be caused by the bone marrow's inability to produce red blood
cells fast enough to replace older red blood cells that have died. Researchers want to look
at unexplained anemia by studying the life span of red blood cells in younger adults and
older adults. To do so, a vitamin called Biotin will be used as a marker on the red blood
cells.
Objectives:
- To investigate possible causes of unexplained anemia in older people.
Eligibility:
- Individuals in the following groups:
- Men and women between 18 and 50 years of age who do not have anemia
- Men and women at least 70 years of age who do not have anemia.
- Men and women at least 70 years of age who have iron-deficiency anemia.
- Men and women at least 70 years of age who have anemia with no known cause.
Design:
- Participants will be screened with a physical exam and medical history. Blood and urine
samples will be collected.
- Participants will have an overnight stay for the first study visit. They will provide a
blood sample to which Biotin will be added. The blood sample with Biotin will then be
returned to the participant. Twenty-four hours later, another blood sample will be
collected.
- Participants will have up to 14 additional study visits. At each visit, blood samples
will be collected to measure the amount of Biotin remaining in the blood.
- Participants may also provide a separate blood sample for genetic testing. These tests
may provide more information about genetic causes of unexplained anemia.
- Anemia occurs commonly and is associated with poor outcomes in the elderly. In about a
third of anemia cases in older people (over age 65), the cause of anemia is unexplained.
Anemia in older adults may be caused by the bone marrow's inability to produce red blood
cells fast enough to replace older red blood cells that have died. Researchers want to look
at unexplained anemia by studying the life span of red blood cells in younger adults and
older adults. To do so, a vitamin called Biotin will be used as a marker on the red blood
cells.
Objectives:
- To investigate possible causes of unexplained anemia in older people.
Eligibility:
- Individuals in the following groups:
- Men and women between 18 and 50 years of age who do not have anemia
- Men and women at least 70 years of age who do not have anemia.
- Men and women at least 70 years of age who have iron-deficiency anemia.
- Men and women at least 70 years of age who have anemia with no known cause.
Design:
- Participants will be screened with a physical exam and medical history. Blood and urine
samples will be collected.
- Participants will have an overnight stay for the first study visit. They will provide a
blood sample to which Biotin will be added. The blood sample with Biotin will then be
returned to the participant. Twenty-four hours later, another blood sample will be
collected.
- Participants will have up to 14 additional study visits. At each visit, blood samples
will be collected to measure the amount of Biotin remaining in the blood.
- Participants may also provide a separate blood sample for genetic testing. These tests
may provide more information about genetic causes of unexplained anemia.
Anemia occurs commonly and is associated with adverse outcomes in the elderly. In
approximately one third of anemia cases in patients over the age of 65 years, the cause of
anemia is not readily apparent (unexplained anemia or UA). Of the various causes of anemia in
young adults, overt hemolysis (either acute or chronic) is very uncommon. However, we
speculate that older persons tend to develop a low grade hemolytic process which
significantly reduces RBC survival, and when this is not adequately countered by increased
bone marrow RBC production, anemia (UA) is the consequence. This hypothesis is supported by a
few clinical observations. For example, red cells in patients with UA are generally not small
and when the peripheral blood smear is examined microscopically, anisocytosis (varying cell
size) is observed, as is typical in patients with hemolytic anemia. Similarly, UA is
frequently associated with an elevated red cell distribution width (RDW) on electronic
measurement. Furthermore, serum erythropoietin levels gradually rise with advancing age (1),
and this would be consistent either with a smoldering hemolytic process or a decreased
responsiveness to erythropoietin. To address the hypothesis that UA is due, at least in part,
to shortened RBC survival, we propose to directly measure red blood cell survival and to
correlate this with aspects of red blood cell physiology that may increase susceptibility to
the hemolytic process.
approximately one third of anemia cases in patients over the age of 65 years, the cause of
anemia is not readily apparent (unexplained anemia or UA). Of the various causes of anemia in
young adults, overt hemolysis (either acute or chronic) is very uncommon. However, we
speculate that older persons tend to develop a low grade hemolytic process which
significantly reduces RBC survival, and when this is not adequately countered by increased
bone marrow RBC production, anemia (UA) is the consequence. This hypothesis is supported by a
few clinical observations. For example, red cells in patients with UA are generally not small
and when the peripheral blood smear is examined microscopically, anisocytosis (varying cell
size) is observed, as is typical in patients with hemolytic anemia. Similarly, UA is
frequently associated with an elevated red cell distribution width (RDW) on electronic
measurement. Furthermore, serum erythropoietin levels gradually rise with advancing age (1),
and this would be consistent either with a smoldering hemolytic process or a decreased
responsiveness to erythropoietin. To address the hypothesis that UA is due, at least in part,
to shortened RBC survival, we propose to directly measure red blood cell survival and to
correlate this with aspects of red blood cell physiology that may increase susceptibility to
the hemolytic process.
- INCLUSION CRITERIA:
- Ambulatory, community dweller
- Age greater than or equal to 70 years or older or between the ages of 18 and 50 years.
- Able to understand English
- Able to complete study questionnaires as determined by the investigator
- Evidence for recent (within 1 year) clinical evaluation for blood loss directed by
primary care physician or consultant in subjects referred with microcytic anemia or
with referring laboratories indicative of iron deficiency. Furthermore, subjects found
to have microcytic anemia will be eligible but will be referred to their primary
doctor for evaluation of blood loss.
- Provide informed consent
EXCLUSION CRITERIA:
- Hemoglobin (Hb) less than 9 g/dL during screening
- History of red blood cell transfusion withinthe 3 month period prior to accrual to
this study, or evidence for active bleeding as ascertained by medical history (e.g.,
persistent melena, hematuria or dysfunctional uterine bleeding).
- Patients for whom oral iron supplementation has been prescribed within the past two
months. (Patients on a stable dose of oral iron for more than two months may be
eligible).
- ALT or AST more than 3 times upper normal limitation of the time of screening
- B12 or folate deficiencies during screening period
- Estimated GFR less than 30 ml/min/1.73m(2)during screening period (by the 4-variable
Modification of Diet in Renal Disease [MDRD] equation).
- Receiving hemodialysis or peritoneal dialysis for renal failure, or history of kidney
transplant
- Use of exogenous erythropoietin during the past 3 months
- Any major surgery requiring general anesthesia within the past 3 months
- Treatment with chemotherapy or radiotherapy in the past 12 months
- Current diagnosis of active cancer, other than non-melanoma skin cancer and, stable
prostate cancer
- History of blood disorders including thalassemia, sickle cell disease or
myelodysplasia
- Current severe (NYHA Class III - IV) congestive heart failure or advanced chronic
obstructive pulmonary disease
- Positive serum monoclonal protein and immunofixation
- Women who are pregnant or women planning to get pregnant during the duration of the
study or those with a positive pregnancy test during screening
- Active infection requiring antibiotic treatment or HIV, Hepatitis B or C
- History of overt chronic inflammation, active Crohn s disease, rheumatoid arthritis,
or diabetes(HbA1C greater than 7),
- Known hemolytic anemia
- History of prosthetic heart valve
- History of participation in biotinylation studies or handling biotinylated reagent
products.
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