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Study · Randomized controlled trial · n = 43 · 1998

11 results

Prevention of estrogen deficiency-related bone loss with human parathyroid hormone-(1-34): a randomized controlled trial.

Finkelstein JS, Klibanski A, Arnold AL, Toth TL, Hornstein MD, Neer RM

JAMA1 Sept 1998Cited by 91 (Europe PMC)

Summary

The text of this summary is not shown here, because the article license does not allow reuse. Read it at the source (opens in a new tab)

Text rights: Publisher copyright. Results still quote short attributed sentences.

Results from this study11

9 results from studies that gave the peptide. 9 results from people.

  1. 01HumanRandomized controlled trialEfficacy outcome

    In women with endometriosis, added hPTH prevented femoral neck bone loss during nafarelin therapy.

    In plain wordsIn women with endometriosis, added hPTH prevented femoral neck bone loss compared with nafarelin alone.

    Outcome
    IncreaseFemoral neck bone loss prevention
    Study

    n = 43

    Comparator
    Nafarelin alone
    Analysis
    Primary
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    BMD change from baseline
    4.7%
    Femoral neck, nafarelin alone (comparator arm), lower than baseline at 12 months

    Source sentences

    Summary
    In contrast, coadministration of hPTH-(1-34) increased BMD of the anterior-posterior spine by 2.1% (1.1%) (P=.09) and lateral spine by 7.5% (1.9%) (P=.002) and prevented bone loss from the femoral neck, trochanter, and total body, despite severe estrogen deficiency.
    5 context sentences
    Summary · context
    In the women who received nafarelin alone, the mean (SEM) BMDs of the anterior-posterior spine, lateral spine, femoral neck, trochanter, and total body were 4.9% (0.6%) (P<.001), 4.9% (0.8%) (P<.001), 4.7% (1.1%) (P<.001), 4.3% (0.9%) (P<.001), and 2.0% (0.6%) (P= .003) lower than at baseline after…
    Summary · context
    Randomized controlled trial.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).
    Summary · context
    The primary end points were bone mineral density (BMD) of the anterior-posterior and lateral spine, femoral neck, trochanter, radial shaft, and total body at 12 months of treatment.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
  2. 02HumanRandomized controlled trialEfficacy outcome

    In women with endometriosis, added hPTH prevented trochanter bone loss during nafarelin therapy.

    In plain wordsIn women with endometriosis, added hPTH prevented trochanter bone loss compared with nafarelin alone.

    Outcome
    IncreaseTrochanter bone loss prevention
    Study

    n = 43

    Comparator
    Nafarelin alone
    Analysis
    Primary
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    BMD change from baseline
    4.3%
    Trochanter, nafarelin alone (comparator arm), lower than baseline at 12 months

    Source sentences

    Summary
    In contrast, coadministration of hPTH-(1-34) increased BMD of the anterior-posterior spine by 2.1% (1.1%) (P=.09) and lateral spine by 7.5% (1.9%) (P=.002) and prevented bone loss from the femoral neck, trochanter, and total body, despite severe estrogen deficiency.
    5 context sentences
    Summary · context
    In the women who received nafarelin alone, the mean (SEM) BMDs of the anterior-posterior spine, lateral spine, femoral neck, trochanter, and total body were 4.9% (0.6%) (P<.001), 4.9% (0.8%) (P<.001), 4.7% (1.1%) (P<.001), 4.3% (0.9%) (P<.001), and 2.0% (0.6%) (P= .003) lower than at baseline after…
    Summary · context
    Randomized controlled trial.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).
    Summary · context
    The primary end points were bone mineral density (BMD) of the anterior-posterior and lateral spine, femoral neck, trochanter, radial shaft, and total body at 12 months of treatment.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
  3. 03HumanRandomized controlled trialEfficacy outcome

    In women with endometriosis, added hPTH prevented total body bone loss during nafarelin therapy.

    In plain wordsIn women with endometriosis, added hPTH prevented whole-body bone loss compared with nafarelin alone.

    Outcome
    IncreaseTotal body bone loss prevention
    Study

    n = 43

    Comparator
    Nafarelin alone
    Analysis
    Primary
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    BMD change from baseline
    2%
    Total body, nafarelin alone (comparator arm), lower than baseline at 12 months

    Source sentences

    Summary
    In contrast, coadministration of hPTH-(1-34) increased BMD of the anterior-posterior spine by 2.1% (1.1%) (P=.09) and lateral spine by 7.5% (1.9%) (P=.002) and prevented bone loss from the femoral neck, trochanter, and total body, despite severe estrogen deficiency.
    5 context sentences
    Summary · context
    In the women who received nafarelin alone, the mean (SEM) BMDs of the anterior-posterior spine, lateral spine, femoral neck, trochanter, and total body were 4.9% (0.6%) (P<.001), 4.9% (0.8%) (P<.001), 4.7% (1.1%) (P<.001), 4.3% (0.9%) (P<.001), and 2.0% (0.6%) (P= .003) lower than at baseline after…
    Summary · context
    Randomized controlled trial.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).
    Summary · context
    The primary end points were bone mineral density (BMD) of the anterior-posterior and lateral spine, femoral neck, trochanter, radial shaft, and total body at 12 months of treatment.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
  4. 04HumanRandomized controlled trialEfficacy outcome

    In women receiving nafarelin, added hPTH produced a nonsignificant increase in anterior-posterior spine BMD from baseline.

    In plain wordsIn women receiving nafarelin, added hPTH did not significantly change front-view spine bone density from baseline.

    Outcome
    No significant changeAnterior-posterior spine BMD
    Study

    n: not reported in source

    Comparator
    Baseline
    Analysis
    Primary
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    BMD change
    2.1%
    hPTH plus nafarelin
    P
    0.09
    change from baseline

    Source sentences

    Summary
    In contrast, coadministration of hPTH-(1-34) increased BMD of the anterior-posterior spine by 2.1% (1.1%) (P=.09) and lateral spine by 7.5% (1.9%) (P=.002) and prevented bone loss from the femoral neck, trochanter, and total body, despite severe estrogen deficiency.
    3 context sentences
    Summary · context
    Randomized controlled trial.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).
  5. 05HumanRandomized controlled trialEfficacy outcome

    In women receiving nafarelin, added hPTH increased lateral spine BMD from baseline.

    In plain wordsIn women receiving nafarelin, added hPTH increased side-view spine bone density from baseline.

    Outcome
    IncreaseLateral spine BMD
    Study

    n: not reported in source

    Comparator
    Baseline
    Analysis
    Primary
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    BMD change
    7.5%
    hPTH plus nafarelin

    Source sentences

    Summary
    In contrast, coadministration of hPTH-(1-34) increased BMD of the anterior-posterior spine by 2.1% (1.1%) (P=.09) and lateral spine by 7.5% (1.9%) (P=.002) and prevented bone loss from the femoral neck, trochanter, and total body, despite severe estrogen deficiency.
    3 context sentences
    Summary · context
    Randomized controlled trial.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).
  6. 06HumanRandomized controlled trialEfficacy outcome

    In women receiving nafarelin plus hPTH, bone-specific alkaline phosphatase increased early and then declined.

    In plain wordsIn women receiving nafarelin plus hPTH, a bone formation marker increased from baseline and then declined.

    Outcome
    MixedBone-specific alkaline phosphatase
    Study

    n: not reported in source

    Comparator
    Baseline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    Fold increase
    2 to 3 fold
    nafarelin plus hPTH-(1-34), first 6 to 9 months; range reported jointly for the four bone markers

    Source sentences

    Summary
    Serum bone-specific alkaline phosphatase and osteocalcin concentrations and urinary excretion of hydroxyproline and deoxypyridinoline increased 2-fold to 3-fold during the first 6 to 9 months of therapy in the women who received nafarelin plus hPTH-(1-34) and then declined.
    3 context sentences
    Summary · context
    Randomized controlled trial.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).
  7. 07HumanRandomized controlled trialEfficacy outcome

    In women receiving nafarelin plus hPTH, serum osteocalcin increased early and then declined.

    In plain wordsIn women receiving nafarelin plus hPTH, blood osteocalcin increased from baseline and then declined.

    Outcome
    MixedOsteocalcin
    Study

    n: not reported in source

    Comparator
    Baseline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    Fold increase
    2 to 3 fold
    nafarelin plus hPTH-(1-34), first 6 to 9 months; range reported jointly for the four bone markers

    Source sentences

    Summary
    Serum bone-specific alkaline phosphatase and osteocalcin concentrations and urinary excretion of hydroxyproline and deoxypyridinoline increased 2-fold to 3-fold during the first 6 to 9 months of therapy in the women who received nafarelin plus hPTH-(1-34) and then declined.
    3 context sentences
    Summary · context
    Randomized controlled trial.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).
  8. 08HumanRandomized controlled trialEfficacy outcome

    In women receiving nafarelin plus hPTH, urinary hydroxyproline increased early and then declined.

    In plain wordsIn women receiving nafarelin plus hPTH, urine hydroxyproline increased from baseline and then declined.

    Outcome
    MixedUrinary hydroxyproline
    Study

    n: not reported in source

    Comparator
    Baseline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    Fold increase
    2 to 3 fold
    nafarelin plus hPTH-(1-34), first 6 to 9 months; range reported jointly for the four bone markers

    Source sentences

    Summary
    Serum bone-specific alkaline phosphatase and osteocalcin concentrations and urinary excretion of hydroxyproline and deoxypyridinoline increased 2-fold to 3-fold during the first 6 to 9 months of therapy in the women who received nafarelin plus hPTH-(1-34) and then declined.
    3 context sentences
    Summary · context
    Randomized controlled trial.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).
  9. 09HumanRandomized controlled trialEfficacy outcome

    In women receiving nafarelin plus hPTH, urinary deoxypyridinoline increased early and then declined.

    In plain wordsIn women receiving nafarelin plus hPTH, urine deoxypyridinoline increased from baseline and then declined.

    Outcome
    MixedUrinary deoxypyridinoline
    Study

    n: not reported in source

    Comparator
    Baseline
    Outcome group
    Bone and joint · Musculoskeletal
    Studied dose
    40 microg daily · subcutaneous · 12 monthsAs given in this study (human).

    Measurements

    Fold increase
    2 to 3 fold
    nafarelin plus hPTH-(1-34), first 6 to 9 months; range reported jointly for the four bone markers

    Source sentences

    Summary
    Serum bone-specific alkaline phosphatase and osteocalcin concentrations and urinary excretion of hydroxyproline and deoxypyridinoline increased 2-fold to 3-fold during the first 6 to 9 months of therapy in the women who received nafarelin plus hPTH-(1-34) and then declined.
    3 context sentences
    Summary · context
    Randomized controlled trial.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).

Studies that did not test the peptide alone2

In this study, Teriparatide (PTH 1-34) was a lab tool or a carrier, part of a mix, or the subject of a lab method. These results are not evidence about taking Teriparatide (PTH 1-34).

  1. 10HumanNot a test of Teriparatide (PTH 1-34) aloneRandomized controlled trialEfficacy outcome

    In women with endometriosis, radial shaft BMD did not change significantly in either randomized group.

    In plain wordsIn women with endometriosis, forearm bone density did not change significantly in either group, including nafarelin alone.

    Outcome
    No significant changeRadial shaft BMD
    Study

    n = 43

    Comparator
    Baseline
    Analysis
    Primary
    Outcome group
    Bone and joint · Musculoskeletal

    Source sentences

    Summary
    Radial shaft BMD did not change significantly in either group.
    3 context sentences
    Summary · context
    Randomized controlled trial.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).

    In this study, Teriparatide (PTH 1-34) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Teriparatide (PTH 1-34).

  2. 11HumanNot a test of Teriparatide (PTH 1-34) aloneObservational studyOther

    In women receiving nafarelin plus hPTH, urinary deoxypyridinolone changes predicted spinal BMD changes.

    In plain wordsIn treated women, changes in a urine bone marker were linked to changes in spine bone density.

    Outcome
    IncreaseDeoxypyridinolone change predicts spinal BMD change
    Study

    n: not reported in source

    Outcome group
    Bone and joint · Musculoskeletal

    Measurements

    Correlation
    0.85 r
    deoxypyridinolone and spinal BMD changes

    Source sentences

    Summary
    Changes in urinary deoxypyridinolone excretion were strongly predictive (r= 0.85) of changes in spinal BMD in the women who received nafarelin plus hPTH-(1-34).
    3 context sentences
    Summary · context
    Randomized controlled trial.
    Summary · context
    Forty-three women between the ages of 21 and 45 years with symptomatic endometriosis.
    Summary · context
    Nafarelin alone (200 microg intranasally twice daily) or nafarelin plus human parathyroid hormone-(1-34) (hPTH-[1-34]) (40 microg subcutaneously daily).

    In this study, Teriparatide (PTH 1-34) was a lab tool or a carrier, part of a mix, or the subject of a lab method. This result is not evidence about taking Teriparatide (PTH 1-34).

AI wrote and checked these results. AI can make mistakes, so check important results against the source.

Version history

PepBank keeps every version of the data on this study. Status changes from Retraction Watch, Europe PMC and Crossref are listed with their source.

  1. Version 3Current

    27 Oct 2026, 16:36 UTC

    Study data updated · source update from Europe PMC

  2. Version 2

    22 Oct 2026, 02:26 UTC

    Study results updated

  3. Version 1

    21 Oct 2026, 18:59 UTC

    First added · source update from Europe PMC

Subjects

Terms as the source lists them.

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