Dose Estimation of Jarlsberg Cheese in Young, Active Norwegian Cross-country Skiers (XCS)

Aim

• To estimate the daily OED of Jarlsberg cheese related to increased total serum Osteocalcin (tOC) level in young, active female and male Cross-country skiers (XCS).
• To estimate the effect of daily Jarlsberg cheese intake on increased, muscle strength, peak VO2 and bone mineral density.

Study population: The study population consists of active Cross-country Skiers (XCS) of both genders above 18 years of age. The study is separated in one female and one male XCS study arm.

Trial treatment:The optimal daily intake of Jarlsberg cheese is assumed to have a dose window of [20 - 100] gram/day and a starting dose of 47 gram/day for both female and male. The cheese is received in package of 250 gram divided in 16 slices of 15.625 gram. 47 gram represents 3 slices of cheese.

Design and randomization: The female and the male arms of the study will be performed equally as an open, two-armed within-patient Response Surface Pathway (RSP) study with three design level and skewed starting dose. The two parts will be performed separately in parallel with identical RSP-design.

The main outcome variable will be categorized in the following four categories:

• Low to moderate increase in the tOC level: [0- 10%> the last 4 weeks
• High increase in the tOC level: ≥10% the last 4 weeks
• Low to moderate decrease in the tOC level: <0 - 10% > the last 4 weeks
• High decrease in the tOC level: ≥ 10% the last 4 weeks

Ten XCS in both arms will be included in the first design level and all receiving the starting dose of Jarlsberg cheese every day in four weeks. The individual increase in tOC from baseline to four weeks will be used to calculate the doses for the XCS in the second design level. The individual increase tOC in the second design will decide the daily doses of cheese to be used in the third design level.

The OED for healthy women in pre-menopausal age was previously estimated to 57-gram Jarlsberg cheese per day. It is unknown if this OED will be different from active XCS and dependent of gender and age.1 The initial dose window in this study was set to [20 - 100] gram based on the previous dose-response study in healthy pre-menopausal women.

Based on prior knowledge, the tOC follows a quadratic function in Jarlsberg cheese dose.1 The Osteocalcin seem to increase with increasing dose until a maximum (OED) and reduces for higher intake of the cheese. OED might be below the midpoint of the initial dose window of 60 gr/day. In order to optimize the estimation procedure with the skewed starting dose of 47g/day or 3 slices of Jarlsberg cheese will be chosen.

This gives an adjusted starting dose window of [20 - 74] gr/day. In case the results from all the five XCS of equal gender in the first design level reports an increase < 10% in the tOC level, the RSP-procedure recommend a maximum escalation in the daily intake of Jarlsberg cheese in the second design level. The new starting dose-window will then be change with the previously used starting dose as lower boundary.2 In the present study the adjusted dose-window for the second design level will then be [47 - 85] g/day with the new starting dose of 66 g/day. In case the results obtained at the design level recommend different doses to be used for the next level, the common RSP procedure will be followed.

Main variables: The main response variable will be the change in the tOC level after four weeks from baseline of the given design level. The osteocalcin ratio R0 defined as the ratio between carboxylated osteocalcin (uOC) and under-carboxylated osteocalcin (ucOC) = [cOC / ucOC], together with vitamin K2 and the different variants MK-7, MK-8,MK- 9 and MK-9(4H) will be used as secondary variables. Diet registration will be performed at screening and every 4 weeks. Additionally, increase in Muscle strength, Peak VO2 and Bone mineral density (BMD) will be measurement at screening and at the end of the study (week 12). Blood samples for measurements of HbA1C and Lipids; Collagen (CTX-1) and Procollagen (PINP); Estradiol and Testosterone; Progesterone and FSH will be taken at screening and at the last visit week 12 in the study. The Common Terminology Criteria for Adverse Events version 4.0 (CTCAE) will be used for registration of Adverse Events (AE) and toxicity score at every investigation visit.

Study procedure: Participants, who fulfil the inclusion criteria, do not meet any of the exclusion criteria and willing to give informed consent to participate will receive an appointment for starting the study. All demographic data, social factors, history of disease and vital signs will be recorded at screening.

Blood samples for measurements of Haematological and biochemical variables, HbA1C and Lipids; Collagen (CTX-1) and Procollagen (PINP); Estradiol and Testosterone; LH, FSH and SHBG will be taken at screening. Additionally, muscle strength, Peak VO2 and BMD will be recorded before starting the clinical part.

The design consists of three design levels within each study arm. Measurement will be taken at screening and every four weeks after daily intake of the decided dose of Jarlsberg cheese. All the participants will be asked not to change anything in their common intake of food during the study except for replacing other cheese with the received daily dose of Jarlsberg. Clinical examination, blood sampling for osteocalcin measurement and diet registration will be performed every fourth week during the study including follow-up. The physical examination includes registration of vital signs, CTCAE and change in concomitant medication. Blood sampling will be taken for measurements of tOC, cOC and ucOC and vitamin K. Blood sampling for measurements of HbA1C and Lipids; Collagen (CTX-1) and Procollagen (PINP); Estradiol and Testosterone; LH and FSH; haematological and bio-chemical variables will be taken at the last visit in the study (week 12). Additionally, muscle strength, Peak VO2 and BMD will be recorded at week 12.

Sample size: Ten female and 10 male XCS divided will be included, perform and complete the study. The minimum number of participants recommended in each arm in a within-patient RSP model is 8

Inclusion criteria

-Healthy active XCS of both genders past the age of 18 years

Exclusion criteria

• Eating disorder
• Pregnancy
• Known gastrointestinal disorder
• Abnormal liver or kidney function.
• Diabetes
• Suffering from verified cancer
• Under systemic treatment with corticosteroids or other immunosuppressive drugs the last 3 weeks before start of the trial treatment.
• Participating in another clinical trial with pharmaceuticals the last six weeks before start of this trial treatment.
• Lactose intolerance or known milk product allergy
• Not able to understand information.
• Do not want or not able to give written consent to participate in the study.