Does Potassium Bicarbonate Improve the Effect of Dietary Protein on Bone and Muscle?

Tufts University

Status: Completed

Conditions: Osteoporosis; Sarcopenia

Treatments: Dietary Supplement: potassium bicarbonate; Dietary Supplement: Placebo (microcrystalline cellulose)

Study type: Interventional

Funder types: Other

Identifiers

NCT00730184

2510

7937

Details and patient eligibility

About

The purpose of this study is to examine whether adding the basic salt potassium bicarbonate to the diet will have a positive effect on how dietary protein affects your bone and muscle.

Full description

The balance between the amount of protein in the diet (anabolic component) and the net acid load of the diet (catabolic component) in part determines whether the diet as a whole has a net anabolic or catabolic effect on bone and muscle. This study will investigate whether the addition of an alkaline salt of potassium, potassium bicarbonate, will allow dietary protein to have a more favorable net impact on intermediary indices of bone and muscle conservation than is observed with protein in the usual acidic environment.

Men and postmenopausal women, age 50 and older, will be enrolled in this 42-day study in order to have 20 completers. Subjects may continue in the study for up to an additional two weeks should this be necessary for reasons related to intercurrent illness (unrelated to the research) or scheduling circumstances. Over the first 15 days, subjects will be placed on gradually increasing doses, up to a maximum of 90 mmol/d of potassium bicarbonate or placebo. They will remain on this dose for the rest of the study. Subjects will then have two 10-day metabolic diet cycles each, in random order, as follows:

Group 1 - low protein diet (0.5 g/kg/d) then high protein diet (1.5 g/kg/d) Group 2 - high protein diet (1.5 g/kg/d) then low protein diet (0.5 g/kg/d)

There will be a 5-day period between the two metabolic diets in which subjects consume their usual diets but continue to take the study pills.

Enrollment: 23 patients

Sex: All

Ages: 50+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

• This study will be conducted in subjects with body mass index < 38 kg/m2.
• Women must be at least 6 months since last menses.
• Subjects must be willing to maintain their usual exercise level and agree not to attempt to gain or lose weight or change their diets substantially during the study.
• Subjects will not be allowed to take their own calcium or vitamin D supplements from one week before their screening visit through the end of the study.
• They must also agree not to ingest bicarbonate- or potassium-rich products such as selected antacids and salt substitutes during the study.
• They must also agree not to consume alcohol during the study.

Exclusion criteria

Medications

• Oral glucocorticoid use for > 10 days in the last 3 months
• Estrogen, raloxifene, or calcitonin use in the last 6 months, bisphosphonate or teriparatide use in the last 2 years
• Current use of diuretics
• Regular use of NSAIDS (> 3 times per wk) or anabolic drugs (steroids or other). Note that subjects may use acetominophen for joint or other discomforts during the study.

Conditions/Diseases

• Renal disease including kidney stones in the past 5 years or creatinine clearance < 50 ml/min/1.73 X m2 of body surface area
• Cirrhosis
• GERD requiring treatment with alkali-containing antacids (use of Lowsium okay)
• Hyperparathyroidism
• Untreated thyroid disease
• Significant immune disorder such as rheumatoid arthritis, SLE
• Current unstable heart disease
• Active malignancy or cancer therapy in the last year
• 24-hr urine calcium > 300 mg/d after 1 wk off of calcium supplements
• Subjects with arrythmias (surgically treated arrythmias acceptable), or myocardial infarction in last 12 months
• Total hip T score of < -3.0
• Abnormal serum calcium; alkaline phosphatase >10% above the upper end of the reference range
• Adrenal insufficiency, primary aldosteronism, Bartter's syndrome
• Diabetes mellitus (fasting blood sugar > 130)
• Alcohol use exceeding 2 drinks/day
• Peptic ulcers or esophageal stricture
• Screening serum 25(OH)D levels below 16 ng/ml
• Vegetarians
• Other abnormalities in screening labs, at discretion of the study physician (principal investigator)

Trial design

Primary purpose: Prevention

Allocation: Randomized

Interventional model: Parallel Assignment

Masking: Quadruple Blind

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23 participants in 2 patient groups, including a placebo group

1

Active Comparator group

Description:

Participants receive potassium bicarbonate in dosage of 90 mmol/d. This compound has no other name.

Treatment:

Dietary Supplement: potassium bicarbonate

2

Placebo Comparator group

Description:

Participants receive placebo as microcrystalline cellulose. This compound has no other name.

Treatment:

Dietary Supplement: Placebo (microcrystalline cellulose)