Musculoskeletal Effects of Bicarbonate

NCT ID: NCT01475214

Last Updated: 2015-10-19

Basic Information

• Recruitment Status: COMPLETED
• Clinical Phase: PHASE2
• Total Enrollment: 244 participants
• Study Classification: INTERVENTIONAL
• Study Start Date: 2012-01-31
• Study Completion Date: 2015-08-31

Brief Summary

With aging, men and women develop a mild and progressive metabolic acidosis. This occurs as a result of declining renal function and ingestion of acid-producing diets. There is extensive evidence that severe metabolic acidosis causes bone and muscle loss, but the impact of the chronic, mild acidosis on bone and muscle in older individuals has not been established. In a recent study, administration of a single dose of bicarbonate daily for 3 months significantly reduced urinary excretion of N-telopeptide (NTX), a marker of bone resorption and urinary nitrogen, a marker of muscle wasting and improved muscle performance in the women but not the men. These and other data support a potential role for bicarbonate as a means of reducing the musculoskeletal declines that lead to extensive morbidity and mortality in the elderly. Before proceeding to a long-term bicarbonate intervention study, however, it is important to identify the dose of bicarbonate most likely to be optimal and to characterize the subjects who benefit most from it. This double blind, placebo controlled, dose-finding study will evaluate the effects of placebo and two doses of bicarbonate on urinary NTX and nitrogen excretion and on lower extremity performance over a 3 month period in 138 men and 138 women, age 60 and older. Changes in urinary excretion of NTX and nitrogen and in selected measures of lower extremity performance will be compared across the three groups. The safety and tolerability of the interventions will also be evaluated. This investigation should provide needed information on the appropriate dosing regimen for men and women and on the study population that should be enrolled in a future bicarbonate intervention trial to assess the long-term effects of this simple, low cost intervention on important clinical outcomes including rates of loss in bone and muscle mass, falls, and fractures.

Detailed Description

This dose-finding study will evaluate the effects of placebo and two doses of bicarbonate on urinary NTX and nitrogen excretion and on lower extremity performance over a three month period. The lower dose is similar to the dose shown in our recent trial to be effective. This study is a double blind, randomized, placebo-controlled, parallel-group trial in which 138 healthy men and 138 women, age 60 and older, will take potassium bicarbonate in doses of 1.0 or 1.5 mmol/kg of body weight or placebo daily for three months. Changes in urinary excretion of NTX and nitrogen and in measures of lower extremity performance will be compared across the three groups. The safety and tolerability of the interventions will also be evaluated. This investigation should provide needed information on the appropriate dosing regimen and on the study population that should be enrolled in a future bicarbonate intervention trial to assess the long-term effects of this simple, low cost intervention on important clinical outcomes including rates of loss in bone and muscle mass, falls, and fractures.

Conditions

Muscle Loss; Fractures; Osteoporosis, Age Related; Fall Injury

Study Design

• Allocation Method: RANDOMIZED
• Intervention Model: PARALLEL
• Primary Study Purpose: PREVENTION
• Blinding Strategy: DOUBLE

Study Groups

potassium bicarbonate low dose

potassium bicarbonate in dose of 1.0 mmol/kg per day, given in three even daily doses after meals with a full glass of water

Group Type: ACTIVE_COMPARATOR

potassium bicarbonate

Intervention Type: DIETARY_SUPPLEMENT

potassium bicarbonate in dose of 1.0 mmol/kg per day, given in three even daily doses after meals with a full glass of water

potassium bicarbonate higher dose

potassium bicarbonate in dose of 1.5 mmol/kg per day, given in three even daily doses after meals with a full glass of water

Group Type: ACTIVE_COMPARATOR

potassium bicarbonate

Intervention Type: DIETARY_SUPPLEMENT

potassium bicarbonate in dose of 1.5 mmol/kg per day, given in three even daily doses after meals with a full glass of water

placebo

microcrystalline cellulose

Group Type: PLACEBO_COMPARATOR

Inactive placebo capsule

Intervention Type: OTHER

microcrystalline cellulose

Interventions

potassium bicarbonate

potassium bicarbonate in dose of 1.0 mmol/kg per day, given in three even daily doses after meals with a full glass of water

Intervention Type: DIETARY_SUPPLEMENT

potassium bicarbonate

potassium bicarbonate in dose of 1.5 mmol/kg per day, given in three even daily doses after meals with a full glass of water

Intervention Type: DIETARY_SUPPLEMENT

Inactive placebo capsule

microcrystalline cellulose

Intervention Type: OTHER

Eligibility Criteria

Inclusion Criteria

• men and women
• age 60 and older
• community dwelling
• women 1 yr since last menses

Exclusion Criteria

Medications:

1. Oral glucocorticoids for > 10 days in the last 3 months

• Cortef (hydrocortisone)
• Prednisone

2. Parenteral glucocorticoids

• Decadron (dexamethasone)

3. Osteoporosis medications in the last 6 months

• Forteo (teriparatide)
• Calcimar, Miacalcin (calcitonin)
• Evista (raloxifene)

4. Osteoporosis medications in the last 2 years

• Fosamax (alendronate)
• Didronel (etidronate)
• Aredia (pamidronate)
• Actonel (risedronate)
• Reclast (zoledronate)

5. Tamoxifen in the last 6 months

6. Calcium/Parathyroid

• Rocaltrol (calcitriol)
• Zemplar (paricalcitol)
• Drisdol, Ergocalciferol

7. Diuretics currently

• hydrocholorothiazide (HCTZ)
• Diuril (chlorothiazide)
• Thalitone (chlorthalidone)
• Zaroxolyn (metolazone)
• Dyazide
• Maxide
• Moduretic
• Lasix (forosamine)
• Dyrenium (triamterene)
• Midamor

8. Testosterone or estrogen in the last 6 months (vaginal estrogen okay)

9. Angiotensin converting enzyme (ACE) inhibitors currently

• Benazepril (Lotensin)
• Captopril (Capoten)
• Enalapril (Vasotec)
• Fosinopril (Monopril)
• Lisinopril (Prinivil, Zestril)
• Moexipril (Univasc)
• Perindopril (Aceon)
• Quinapril (Accupril)
• Ramipril (Altace)
• Trandolapril (Mavik)

10. Angiotensin II receptor blockers currently

• Candesartan (Atacand)
• Eprosartan (Teveten)
• Irbesartan (Avapro)
• Losartan (Cozaar)
• Olmesartan (Benicar)
• Telmisartan (Micardis)
• Valsartan (Diovan)

Over-the-Counter Drugs currently

1. Antacids - any antacid that contains calcium carbonate, aluminum hydroxide, magnesium hydroxide, or calcium acetate - selected examples include

• TUMS
• Mylanta
• Maalox
• Titralac
• Rolaids
• Sodium bicarbonate (baking soda)
• Note: magaldrate or Riopan® is allowed

2. Potassium supplements

3. Salt substitutes

Conditions/Diseases

1. renal disease including kidney stones in the past 5 years or glomerular filtration rate (GFR) < 60 ml/min/1.73 m2

2. hyperkalemia (serum potassium >5.3 meq/L; normal range 3.5-5.3 meq/L)

3. elevated serum bicarbonate (serum bicarbonate > 29 mmol/L; normal range 22-29 mmol/L)

4. cirrhosis

5. gastroesophageal reflux disease (GERD) requiring treatment with alkali-containing antacids (TUMS, Mylanta, Maalox, Titralac, Rolaids, or sodium bicarbonate)

6. hyperparathyroidism

7. untreated thyroid disease

8. significant immune disorder such as rheumatoid arthritis

9. current unstable heart disease

10. active malignancy or cancer therapy in the last year

11. fasting spot urine calcium/creatinine > 0.38 mmol/mmol after 1 wk off of calcium supplements

12. congestive heart failure, arrhythmias (surgically treated arrhythmias acceptable), or myocardial infarction in last 12 months

13. serum calcium outside the normal range of 8.3-10.2 mg/dl

14. uncontrolled diabetes mellitus (fasting blood sugar > 130)

15. alcohol use exceeding 2 drinks/day

16. peptic ulcers or esophageal stricture

17. weight <45 or >113.5 kg (<99 or >249.7 lbs)

18. other abnormalities in screening labs, at discretion of the study physician (the PI)

• Minimum Eligible Age: 60 Years
• Eligible Sex: ALL
• Accepts Healthy Volunteers: Yes

Sponsors

National Institute of Arthritis and Musculoskeletal and Skin Diseases (NIAMS)

NIH

Sponsor Role: collaborator

Tufts University

OTHER

Sponsor Role: lead

Responsible Party

Bess Dawson-Hughes

Professor of Medicine

Responsibility Role: PRINCIPAL_INVESTIGATOR

Principal Investigators

Bess Dawson-Hughes, M.D.

Role: PRINCIPAL_INVESTIGATOR

Tufts University

Locations

Jean Mayer USDA Human Nutrition Research Center on Aging at Tufts University

Boston, Massachusetts, United States

Countries

United States

References

Shea MK, Dawson-Hughes B. Association of Urinary Citrate With Acid-Base Status, Bone Resorption, and Calcium Excretion in Older Men and Women. J Clin Endocrinol Metab. 2018 Feb 1;103(2):452-459. doi: 10.1210/jc.2017-01778.

Reference Type: DERIVED

PMID: 29211866 (View on PubMed)

Ceglia L, Dawson-Hughes B. Increasing alkali supplementation decreases urinary nitrogen excretion when adjusted for same day nitrogen intake. Osteoporos Int. 2017 Dec;28(12):3355-3359. doi: 10.1007/s00198-017-4196-8. Epub 2017 Aug 25.

Reference Type: DERIVED

PMID: 28842733 (View on PubMed)

Other Identifiers

R01AR060261

Identifier Type: NIH

Identifier Source: secondary_id

View Link

2705

Identifier Type: -

Identifier Source: org_study_id